| FcγR2B B2.4 haplotype predicts increased risk of red blood cell alloimmunization in sickle cell disease patients. | Costa Neto A, Santos F, Ribeiro I, Oliveira V, Dezan M, Kashima S, Covas D, Pereira A, Fonseca G, Moreira F, Krieger J, Gualandro S, Rocha V, Mendrone A, Dinardo CL | Transfusion | 2020 |
| Individual red blood cell fetal hemoglobin quantification allows to determine protective thresholds in sickle cell disease. | Hebert N, Rakotoson MG, Bodivit G, Audureau E, Bencheikh L, Kiger L, Oubaya N, Pakdaman S, Sakka M, Di Liberto G, Chadebech P, Vingert B, Pirenne F, Galactéros F, Cambot M, Bartolucci P | Am J Hematol | 2020 |
| Hematological Diseases and Osteoporosis. | Gaudio A, Xourafa A, Rapisarda R, Zanoli L, Signorelli SS, Castellino P | Int J Mol Sci | 2020 |
| Label-free detection of thalassemia and other ROS impairing diseases. | Chakraborty A, Chatterjee SK, Dasgupta AK | Med Biol Eng Comput | 2020 |
| Effectiveness of a home-based therapeutic exercise program on lower back pain and functionality in Sickle Cell Disease (SCD) patients. | Zanoni CT, Galvão F, Maria RM, Zulli R, Ricciardi JB, Cliquet A, Saad STO | Hematol Transfus Cell Ther | 2020 |
| Effect of Inhaled Cannabis for Pain in Adults With Sickle Cell Disease: A Randomized Clinical Trial. | Abrams DI, Couey P, Dixit N, Sagi V, Hagar W, Vichinsky E, Kelly ME, Connett JE, Gupta K | JAMA Netw Open | 2020 |
| Young Adults With Sickle Cell Disease: Challenges With Transition to Adult Health Care. | Varty M, Popejoy LL | Clin J Oncol Nurs | 2020 |
| Analysis of the foveal microvasculature in sickle cell disease using swept-source optical coherence tomography angiography. | Mokrane A, Gazeau G, Lévy V, Fajnkuchen F, Giocanti-Aurégan A | Sci Rep | 2020 |
| The safety and effectiveness of genetically corrected iPSCs derived from β-thalassaemia patients in nonmyeloablative β-thalassaemic mice. | Xian Y, Xie Y, Song B, Ou Z, Ouyang S, Xie Y, Yang Y, Xiong Z, Li H, Sun X | Stem Cell Res Ther | 2020 |
| A high frequency of Gilbert syndrome (UGT1A1*28/*28) and associated hyperbilirubinemia but not cholelithiasis in adolescent and adult north Indian patients with transfusion-dependent β-thalassemia. | Shrestha O, Khadwal AR, Singhal M, Trehan A, Bansal D, Jain R, Pal A, Hira JK, Chhabra S, Malhotra P, Das R, Sharma P | Ann Hematol | 2020 |
| CTLA4Ig in an Extended Schedule along with Sirolimus Improves Outcome with a Distinct Pattern of Immune Reconstitution Following Post-Transplantation Cyclophosphamide-Based Haploidentical Transplantation for Hemoglobinopathies. | Jaiswal SR, Bhakuni P, Aiyer HM, Soni M, Bansal S, Chakrabarti S | Biol. Blood Marrow Transplant. | 2020 |
| Hemoglobin SS Nigerian Woman First Diagnosed at the Age of 52 years with Manifestation Mimicking Tuberculosis of the Spine. | Ugwu NI, Nna EO, Egwu AN, Okoye EA | Niger Med J | 2020 |
| The Effect of Five Single Nucleotide Polymorphisms on Hb F Variation of β-Thalassemia Traits and Hematologically Normal Individuals in Southeast Turkey. | Genc A, Tastemir Korkmaz D, Bayram S, Rencuzogullari E | Hemoglobin | 2020 |
| Hematological Characteristics of β-Globin Gene Mutation -50 (G>A) (: c.-100G>A) Carriers in Mainland China. | Zhao Y, Jiang F, Li DZ | Hemoglobin | 2020 |
| Voxelotor: A Novel Treatment for Sickle Cell Disease. | Herity LB, Vaughan DM, Rodriguez LR, Lowe DK | Ann Pharmacother | 2020 |
| Antioxidant nutrients and hemolysis in sickle cell disease. | Delesderrier E, Curioni C, Omena J, Macedo CR, Cople-Rodrigues C, Citelli M | Clin Chim Acta | 2020 |
| Computer Algorithm-Based Hydroxyurea Dosing Facilitates Titration to Maximum Tolerated Dose in Sickle Cell Anemia. | Oldham M, Conrey A, Pittman C, Fisher C, Hargrett S, West K, Jackson M, Martin S, Hsieh MM, Jeffries N, Kaplarevic M, Johnson D, Olkhanud P, Fitzhugh CD | J Clin Pharmacol | 2020 |
| Stable renal function in children and adolescents with sickle cell disease after nonmyeloablative hematopoietic stem cell transplantation. | Pedersen SJV, Monagel DA, Mammen C, Lewis VA, Guilcher GMT, Bruce AA | Pediatr Blood Cancer | 2020 |
| Longitudinal follow-up of patients with thalassaemia intermedia who started transfusion therapy in adulthood: a cohort study. | Ricchi P, Meloni A, Pistoia L, Spasiano A, Rita Gamberini M, Maggio A, Gerardi C, Messina G, Campisi S, Allò M, Renne S, Righi R, Midiri M, Positano V, Filosa A, Pepe A | Br. J. Haematol. | 2020 |
| Cost of health care for paediatric patients with sickle cell disease: An analysis of resource use and costs in a European country. | Thielen FW, Houwing ME, Cnossen MH, Al Hadithy-Irgiztseva IA, Hazelzet JA, Groot CAU, de Pagter APJ, Blommestein HM | Pediatr Blood Cancer | 2020 |
| Osteomyelitis in sickle cell disease: You know it when you see it? | Rothman JA | Pediatr Blood Cancer | 2020 |
| Two Novel and Five Rare Mutations in the Non Coding Regions of the β-Globin Gene in the Iranian Population. | Hamid M, Zargan Nezhad E, Keikhaei B, Galehdari H, Saberi A, Sedaghat A, Mohammadi-Anaei M, Shariati G | Hemoglobin | 2020 |
| Update in Laboratory Diagnosis of Thalassemia. | Munkongdee T, Chen P, Winichagoon P, Fucharoen S, Paiboonsukwong K | Front Mol Biosci | 2020 |
| A cross-sectional study of awareness and practices regarding thalassemia among parents of thalassemic children. | Jain A, Singla S, Lakhanpal S, Jain I | J Family Med Prim Care | 2020 |
| Impact of SARS CoV-2 in Hemoglobinopathies with Immune Disfunction and Epidemiology. A Protective Mechanism from Beta Chain Hemoglobin Defects? | Torti L, Maffei L, Sorrentino F, De Fabritiis P, Miceli R, Abruzzese E | Mediterr J Hematol Infect Dis | 2020 |
| Preliminary Data on COVID-19 in Patients with Hemoglobinopathies: A Multicentre ICET-A Study. | de Sanctis V, Canatan D, Corrons JLV, Karimi M, Daar S, Kattamis C, Soliman AT, Wali Y, Alkindi S, Huseynov V, Nasibova A, Tiryaki TO, Evim MS, Gunes AM, Karakas Z, Christou S, Campisi S, Zarei T, Khater D, Oymak Y, Kaleva V, Stoyanova D, Banchev A, Galati MC, Yassin MA, Kakar S, Skafida M, Kilinc Y, Alyaarubi S, Verdiyevas N, Stoeva I, Raiola G, Mariannis D, Ruggiero L, Di Maio S | Mediterr J Hematol Infect Dis | 2020 |
| Creating New β-Globin-Expressing Lentiviral Vectors by High-Resolution Mapping of Locus Control Region Enhancer Sequences. | Morgan RA, Ma F, Unti MJ, Brown D, Ayoub PG, Tam C, Lathrop L, Aleshe B, Kurita R, Nakamura Y, Senadheera S, Wong RL, Hollis RP, Pellegrini M, Kohn DB | Mol Ther Methods Clin Dev | 2020 |
| Seroprevalence of HBV, HCV and HIV-1 and Correlation with Molecular Markers among Multi-Transfused Thalassemia Patients in Western India. | Mishra K, Shah A, Patel K, Ghosh K, Bharadva S | Mediterr J Hematol Infect Dis | 2020 |
| Association of rs4701 Variant, but not -α Over-Expression with Bone Mineral Density in Pediatric Well-Chelated β-Thalassemia Patients. | Sahmoud S, Ibrahim MS, Toraih EA, Kamel N, Fawzy MS, Elfiky S | Mediterr J Hematol Infect Dis | 2020 |
| Prevalence and predictors of chronic pain intensity and disability among adults with sickle cell disease. | Matthie N, Jenerette C, Gibson A, Paul S, Higgins M, Krishnamurti L | Health Psychol Open | 2020 |
| Health-Related Quality of Life in Thai Children with Thalassemia as Evaluated by PedsQL and EQ-5D-Y: A Single-Center Experience. | Sinlapamongkolkul P, Surapolchai P | Mediterr J Hematol Infect Dis | 2020 |
| Re: Renal medullary carcinoma and its association with sickle cell trait: a case report and literature review. | Riminucci M, Corsi A | Curr Oncol | 2020 |
| Effects of α-tocopherol on hemolysis and oxidative stress markers on red blood cells in β-thalassemia major. | Sovira N, Lubis M, Wahidiyat PA, Suyatna FD, Gatot D, Bardosono S, Sadikin M | Clin Exp Pediatr | 2020 |
| Reduction of Liver Iron Load in Adult Patients with β-Thalassemia Major Treated with Modern Chelation Modalities. | Georgiev PG, Sapunarova KG, Goranova-Marinova VS, Goranov SE | Folia Med (Plovdiv) | 2020 |
| Inadequate Pre-conception Counseling is a Major Challenge for Antenatal Management of β-Thalassemia: Experience from a Referral Centre in India. | Shetty M, Balakrishna S, Hegde S | Indian J Hematol Blood Transfus | 2020 |
| Thalidomide in Patients with Transfusion-Dependent E-Beta Thalassemia Refractory to Hydroxyurea: A Single-Center Experience. | Nag A, Radhakrishnan VS, Kumar J, Bhave S, Mishra DK, Nair R, Chandy M | Indian J Hematol Blood Transfus | 2020 |
| Association of HMIP1 C-893A polymorphism and disease severity in patients with sickle cell anemia. | Pereira-Martins DA, Domingos IF, Belini-Junior E, Coelho-Silva JL, Weinhäuser I, Araújo AS, Lobo CL, Bonini-Domingos CR, Bezerra MA, Lucena-Araujo AR | Hematol Transfus Cell Ther | 2020 |
| β-Globin Gene Mutations in Pediatric Patients with β-Thalassemia in the Region of Çukurova, Turkey. | Guzelgul F, Seydel GS, Aksoy K | Hemoglobin | 2020 |
| Cost-utility of new film-coated tablet formulation of deferasirox vs deferoxamine among major beta-thalassemia patients in Iran. | Saiyarsarai P, Khorasani E, Photogeraphy H, Ghaffari Darab M, Seyedifar M | Medicine (Baltimore) | 2020 |
| Promising Response to Thalidomide in Symptomatic β-Thalassemia. | Yassin AK | Indian J Hematol Blood Transfus | 2020 |
| Alternative Strategies in Thalassemia: Focus on Thalidomide. | Naithani R, Jeyaraman P, Mahapatra M | Indian J Hematol Blood Transfus | 2020 |
| A New α Chain Variant, Hb Heilongjiang (: c.49A>C), Found During Hb A Measurement. | Xu A, Chen W, Xie W, Ji L, Wang Y, Xu M | Hemoglobin | 2020 |
| Marijuana use and health behaviors in a US clinic sample of patients with sickle cell disease. | Wilson JD, Pecker LH, Lanzkron S, Bediako SM, Han D, Beach MC | PLoS One | 2020 |
| Serum folate and cytokines in heterozygous β-thalassemia. | Paniz C, Lucena MR, Bertinato JF, Dos Santos MNN, Gomes GW, Figueiredo MS, Sonati MF, Blaia-D Avila VLN, Green R, Guerra-Shinohara EM | Int J Lab Hematol | 2020 |
| Self-management recommendations for sickle cell disease: A content analysis of websites. | Druye AA, Nelson K, Robinson B | Nurs Health Sci | 2020 |
| Efficacy and Safety of Combined Oral Chelation with Deferiprone and Deferasirox on Iron Overload in Transfusion Dependent Children with Thalassemia - A Prospective Observational Study. | DivakarJose RR, Delhikumar CG, Ram Kumar G | Indian J Pediatr | 2020 |
| Haptoglobin: From hemoglobin scavenging to human health. | di Masi A, De Simone G, Ciaccio C, D'Orso S, Coletta M, Ascenzi P | Mol Aspects Med | 2020 |
| Extensive Extramedullary Hematopoiesis in Thalassemia: Soft Tissue Uptake on 99mTc-MDP SPECT/CT. | Usmani S, Ahmed N, Muzaffar S, Al Kandari F | Clin Nucl Med | 2020 |
| Hemoglobin S/Hemoglobin Quebec-Chori Presenting as Sickle Cell Disease: A Case Report. | Goode E, Boruchov D, Oliveira JL, Lau CC | J Pediatr Hematol Oncol | 2020 |
| Vulnerability of sickle cell disease persons to the COVID-19 in sub-Saharan Africa. | Tonen-Wolyec S, Marini Djang'eing'a R, Kambale-Kombi P, Tshilumba CK, Bélec L, Batina-Agasa S | Hematology | 2020 |
| Whole blood viscosity and red blood cell adhesion: Potential biomarkers for targeted and curative therapies in sickle cell disease. | Kucukal E, Man Y, Hill A, Liu S, Bode A, An R, Kadambi J, Little JA, Gurkan UA | Am J Hematol | 2020 |
| The effect of dietary nitrate supplementation on the speed-duration relationship in mice with sickle cell disease. | Ferguson SK, Redinius KM, Harral JW, Pak DI, Swindle DC, Hirai DM, Blackwell JR, Jones AM, Stenmark KR, Buehler PW, Irwin DC | J Appl Physiol (1985) | 2020 |
| Men with sickle cell disease experience greater sexual dysfunction when compared with men without sickle cell disease. | Idris IM, Abba A, Galadanci JA, Mashi SA, Hussaini N, Gumel SA, Burnett AL, DeBaun MR | Blood Adv | 2020 |
| Cohort profile: targeted antenatal screening for haemoglobinopathies in Basel. | Amstad Bencaiova G, Geissler F, Hoesli I | BMJ Open | 2020 |
| Improving self-management in adolescents with sickle cell disease. | Crosby LE, Hood A, Kidwell K, Nwankwo C, Peugh J, Strong H, Quinn C, Britto MT | Pediatr Blood Cancer | 2020 |
| A Case of COVID-19 in a Patient with Asymptomatic Hemoglobin D Thalassemia and Glucose-6-Phosphate Dehydrogenase Deficiency. | Sasi S, Yassin MA, Nair AP, Al Maslamani MS | Am J Case Rep | 2020 |
| The CYB5R3 and G6PD A alleles modify severity of anemia in malaria and sickle cell disease. | Gordeuk VR, Shah BN, Zhang X, Thuma PE, Zulu S, Moono R, Reading NS, Song J, Zhang Y, Nouraie M, Campbell A, Minniti CP, Rana SR, Darbari DS, Kato GJ, Niu M, Castro OL, Machado R, Gladwin MT, Prchal JT | Am J Hematol | 2020 |
| Socio-religious Prognosticators of Psychosocial Burden of Beta Thalassemia Major. | Ul Hassan Rashid MA, Abbasi SS, Manzoor MM | J Relig Health | 2020 |
| Mild Thalassemia Intermedia Due to Interaction of δβ-Thalassemia with Triplicated α-Globin Genes. | Payán-Pernía S, Bernal Noguera S, Rojas Rodríguez E, Serra Ferrer M, Remacha Sevilla ÁF | Hemoglobin | 2020 |
| Rare Anaemias, Sickle-Cell Disease and COVID-19. | Vives Corrons JL, De Sanctis V | Acta Biomed | 2020 |
| Implications of SARSr-CoV 2 infection in thalassemias: Do patients fall into the | Karimi M, De Sanctis V | Acta Biomed | 2020 |
| Analysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia. | Horri-Naceur A, Timson DJ | Hemoglobin | 2020 |
| Chronic opioid use can be reduced or discontinued after haematopoietic stem cell transplantation for sickle cell disease. | Han J, Holden CC, Ahluwalia AY, Molokie RE, Gowhari M, Sweiss K, Patel PR, Gordeuk VR, Rondelli D, Saraf SL | Br J Haematol | 2020 |
| Molecular Understanding of Severe Cases of β-Thalassemia in the Nablus Region, West Bank, Palestine. | Samha L, Sirdah MM, Reading NS, Karmi B, Agarwal AM | Hemoglobin | 2020 |
| Long-Molecule Sequencing: A New Approach for Identification of Clinically Significant DNA Variants in α-Thalassemia and β-Thalassemia Carriers. | Xu L, Mao A, Liu H, Gui B, Choy KW, Huang H, Yu Q, Zhang X, Chen M, Lin N, Chen L, Han J, Wang Y, Zhang M, Li X, He D, Lin Y, Zhang J, Cram DS, Cao H | J Mol Diagn | 2020 |
| Persons With Thalassemia Major May Have Increased Risk of Gingival Inflammation. | Ayilavarapu S | J Evid Based Dent Pract | 2020 |
| Novel dose escalation to predict treatment with hydroxyurea (NDEPTH): A randomized controlled trial of a dose-prediction equation to determine maximum tolerated dose of hydroxyurea in pediatric sickle cell disease. | George A, Dinu B, Estrada N, Minard CG, Hurwitz R, Mahoney DH, Yates AM, Vaughan M, Carmouche A, Airewele G, Kirk SE, Fasipe T, Uwaezuoke P, Ware RE | Am. J. Hematol. | 2020 |
| [Effect of high-throughput sequencing for the prevention and control of thalassemia]. | Chen Y, Zhang S, Wang C, Chen S, Feng N, Liu H, Tang X, Wang J | Zhonghua Yi Xue Yi Chuan Xue Za Zhi | 2020 |
| Racism and Health-Related Quality of Life in Pediatric Sickle Cell Disease: Roles of Depression and Support. | Mougianis I, Cohen LL, Martin S, Shneider C, Bishop M | J Pediatr Psychol | 2020 |
| Non-myeloablative matched sibling stem cell transplantation with the optional reinforced stem cell infusion for patients with hemoglobinopathies. | Shin SH, Park SS, Park S, Jeon YW, Yoon JH, Yahng SA, Cho BS, Kim YJ, Lee S, Kim HJ, Min CK, Cho SG, Kim DW, Lee JW, Eom KS | Eur. J. Haematol. | 2020 |
| Use of nonopioid agents for inpatient pain management of sickle cell disease. | Austin Szwak J | Am J Health Syst Pharm | 2020 |
| Assessment of Patient and Caregiver Attitudes and Approaches to Decision-Making Regarding Bone Marrow Transplant for Sickle Cell Disease: A Qualitative Study. | Bakshi N, Katoch D, Sinha CB, Ross D, Quarmyne MO, Loewenstein G, Krishnamurti L | JAMA Netw Open | 2020 |
| Perceptions of US Adolescents and Adults With Sickle Cell Disease on Their Quality of Care. | Kanter J, Gibson R, Lawrence RH, Smeltzer MP, Pugh NL, Glassberg J, Masese RV, King AA, Calhoun C, Hankins JS, Treadwell M | JAMA Netw Open | 2020 |
| Improving the Quality of Care for Adolescents and Adults With Sickle Cell Disease-It's a Long Road. | Oyedeji C, Strouse JJ | JAMA Netw Open | 2020 |
| Influenza vaccine effectiveness and disease burden in children and adolescents with sickle cell disease: 2012-2017. | Kao CM, Lai K, McAteer JM, Elmontser M, Quincer EM, Yee MEM, Tippet A, Jerris RC, Lane PA, Anderson EJ, Bakshi N, Yildirim I | Pediatr Blood Cancer | 2020 |
| Effect of point mutation on structure-function correlation of hemoglobin variants, HbE and HbD Punjab. | Narayanan S, Mathew B, Srinivasu BY, Bhat V, Ross C, Mandal AK | Amino Acids | 2020 |
| Busulfan clearance does not predict the development of hepatic veno-occlusive disease in patients undergoing hematopoietic stem cell transplantation. | Salman B, Al-Khabori M, Al-Huneini M, Al-Rawas A, Dennison D, Al-Za'abi M | Int. J. Hematol. | 2020 |
| Graft Versus Host Disease Prophylaxis With Abatacept Reduces Severe Acute Graft Versus Host Disease in Allogeneic Hematopoietic Stem Cell Transplant for Beta Thalassemia Major with Busulfan, Fludarabine, and Thiotepa. | Khandelwal P, Yeh RF, Yu L, Lane A, Dandoy CE, El-Bietar J, Davies SM, Grimley MS | Transplantation | 2020 |
| Hemoglobin switching in mice carrying the variant. | Korporaal A, Gillemans N, Heshusius S, Cantú I, van den Akker E, van Dijk TB, von Lindern M, Philipsen S | Haematologica | 2020 |
| Metabolomic Profiling of Plasma and Erythrocytes in Sickle Mice Points to Altered Nociceptive Pathways. | Dembélé KC, Mintz T, Veyrat-Durebex C, Chabrun F, Chupin S, Tessier L, Simard G, Henrion D, Mirebeau-Prunier D, Chao de la Barca JM, Tharaux PL, Reynier P | Cells | 2020 |
| Growth hormone therapy for people with thalassaemia. | Ngim CF, Lai NM, Hong JY, Tan SL, Ramadas A, Muthukumarasamy P, Thong MK | Cochrane Database Syst Rev | 2020 |
| Pulmonary functions in children and adolescents with sickle cell disease. | Al Biltagi M, Bediwy AS, Toema O, Al-Asy HM, Saeed NK | Pediatr. Pulmonol. | 2020 |
| Vitamin D supplementation for sickle cell disease. | Soe HHK, Abas AB, Than NN, Ni H, Singh J, Said ARBM, Osunkwo I | Cochrane Database Syst Rev | 2020 |
| Sodium, Magnesium, Calcium, Manganese, Iron, Copper, and Zinc in Serums of Beta Thalassemia Major Patients. | Şahin A, Er EÖ, Öz E, Yıldırmak ZY, Bakırdere S | Biol Trace Elem Res | 2020 |
| Hemoglobinopathies in Iran: An Updated Review. | Nasiri A, Rahimi Z, Vaisi-Raygani A | Int J Hematol Oncol Stem Cell Res | 2020 |
| Long--Term Free Survival of Two Class III β-Thalassemic Patients after Non-Myeloablative Stem Cell Transplantation. | Adib Sereshki MM, Bahar B, Ghavamzadeh A, Mousavi SA, Alimoghaddam K | Int J Hematol Oncol Stem Cell Res | 2020 |
| Genetic Variation in SOD1 Gene Promoter Ins/Del and Its Influence on Oxidative Stress in Beta Thalassemia Major Patients. | Tripathi P, Agarwal S, Sarangi AN, Tewari S, Mandal K | Int J Hematol Oncol Stem Cell Res | 2020 |
| Origin of complexity in haemoglobin evolution. | Pillai AS, Chandler SA, Liu Y, Signore AV, Cortez-Romero CR, Benesch JLP, Laganowsky A, Storz JF, Hochberg GKA, Thornton JW | Nature | 2020 |
| Homozygous sickle cell disease in Central India & Jamaica: A comparison of newborn cohorts. | Jain D, Tokalwar R, Upadhye D, Colah R, Serjeant GR | Indian J. Med. Res. | 2020 |
| A cost-of-illness analysis of β-Thalassaemia major in children in Sri Lanka - experience from a tertiary level teaching hospital. | Reed-Embleton H, Arambepola S, Dixon S, Maldonado BN, Premawardhena A, Arambepola M, Khan JAM, Allen S | BMC Pediatr | 2020 |
| BETA THALASSEMIA MINOR PATIENTS: NOT TIRED, BUT DEPRESSED AND ANXIOUS. | Eren R, Karışmaz A, Aslan C, Doğu MH, Altındal Ş, Yokuş O, Suyani E | Med Princ Pract | 2020 |
| Outcomes of a preoperative risk-based transfusion assignment protocol in sickle cell disease patients: a single-center retrospective study from Saudi Arabia. | Albolowi N, Mustafa O, Almohammadi M, Al-Hindi MY, Jastaniah W | Pediatr Hematol Oncol | 2020 |
| Sleep disturbance in adults with sickle cell disease: relationships with executive and psychological functioning. | Rhodes A, Martin S, Wolters P, Rodriguez Y, Toledo-Tamula MA, Struemph K, Fitzhugh C, Hsieh M, Tisdale J | Ann. Hematol. | 2020 |
| The Case of an Adolescent Male With Sickle Cell Disease and Atypical Leg Pain. | Millan J, Karrs J, Helou M, Dunbar EE | Clin Pediatr (Phila) | 2020 |
| Placental histopathology in sickle cell disease: A descriptive and hypothesis-generating study. | Malinowski AK, Dziegielewski C, Keating S, Parks T, Kingdom J, Shehata N, Rizov E, D'Souza R | Placenta | 2020 |
| Fifteen years of newborn sickle cell disease screening in Madrid, Spain: an emerging disease in a European country. | García-Morín M, Bardón-Cancho EJ, Beléndez C, Zamarro R, Béliz-Mendiola C, González-Rivera M, Vecilla C, Llorente-Otones L, Pérez-Alonso V, Román SS, Sebastián E, Dulín E, Cela E | Ann. Hematol. | 2020 |
| A biomathematical model of human erythropoiesis and iron metabolism. | Schirm S, Scholz M | Sci Rep | 2020 |
| Synthesis and evaluation of resveratrol derivatives as fetal hemoglobin inducers. | Bosquesi PL, Melchior ACB, Pavan AR, Lanaro C, de Souza CM, Rusinova R, Chelucci RC, Barbieri KP, Fernandes GFDS, Carlos IZ, Andersen OS, Costa FF, Dos Santos JL | Bioorg. Chem. | 2020 |
| Patient-reported outcomes in sickle cell disease and association with clinical and psychosocial factors: Report from the sickle cell disease implementation consortium. | Knisely MR, Pugh N, Kroner B, Masese R, Gordeuk V, King AA, Smith SM, Gurney JG, Adams R, Wun T, Snyder A, Glassberg J, Shah N, Treadwell M, | Am. J. Hematol. | 2020 |
| Potential Markers of Dietary Glycemic Exposures for Sustained Dietary Interventions in Populations without Diabetes. | Feskens E, Brennan L, Dussort P, Flourakis M, Lindner LME, Mela D, Rabbani N, Rathmann W, Respondek F, Stehouwer C, Theis S, Thornalley P, Vinoy S | Adv Nutr | 2020 |
| Sickle cell disease clinical phenotypes in Nigeria: A preliminary analysis of the Sickle Pan Africa Research Consortium Nigeria database. | Isa H, Adegoke S, Madu A, Hassan AA, Ohiaeri C, Chianumba R, Brown B, Okocha E, Ugwu N, Diaku-Akinwumi I, Adeyemo T, Kuliya-Gwarzo A, Dogara L, Lawal H, Tanko Y, Ladu A, Kangiwa U, Ekwem L, Oniyangi S, Wakama T, Umoru D, Olanrewaju O, Akinola N, Nnebe-Agumadu U, Asala S, Adekile A, Olaniyi J, Sangeda R, Sickle Africa Data Coordinating Center SADaCC , Nnodu O | Blood Cells Mol. Dis. | 2020 |
| Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania. | Nkya S, Mwita L, Mgaya J, Kumburu H, van Zwetselaar M, Menzel S, Mazandu GK, Sangeda R, Chimusa E, Makani J | BMC Med. Genet. | 2020 |
| Wrist Joint Skeletal Changes in Children With Transfusion-dependent Thalassemia. | Dhawan P, Kanojia RK, Chandra J, Kumar A, Anand R, Gupta S | J Pediatr Orthop | 2020 |
| The curious case of hemoglobin DC disease masquerading as sickle cell anemia. | Hirani S, Gupta S, Veillon D, Patan S, Master S, Mansour R | Hematol Rep | 2020 |
| Portal Vein Thrombosis with Splenic Infarct in β-Thalassemia Minor at High Altitude. | Yanamandra U, Bahl R, Mishra K, Kumar S | High Alt. Med. Biol. | 2020 |
| Severe α-Thalassemia Due to Compound Heterozygosity for Hb Adana (α59 Gly>Asp) (: c.179G > A) and Codon 127 (A > T) (: c.382A > T) in an Iranian Family. | Azimi A, Tahmasebi S, Moradi K, Nejati P, Alibakhshi R | Hemoglobin | 2020 |
| Probing the structure-function relationship of hemoglobin in living human red blood cells. | Dybas J, Bokamper MJ, Marzec KM, Mak PJ | Spectrochim Acta A Mol Biomol Spectrosc | 2020 |
| Comparative analysis of lentiviral gene transfer approaches designed to promote fetal hemoglobin production for the treatment of β-hemoglobinopathies. | Daniel-Moreno A, Lamsfus-Calle A, Wilber A, Chambers CB, Johnston I, Antony JS, Epting T, Handgretinger R, Mezger M | Blood Cells Mol. Dis. | 2020 |
| Characteristics and potential biomarkers of adult sickle cell patients with chronic pain. | Albo C, Kumar S, Pope M, Kidwell KM, Xu H, Bowman L, Wells L, Barrett N, Fields S, Bora P, Patel N, Kutlar A | Eur. J. Haematol. | 2020 |
| Sexual health of French adolescents with sickle cell disease. | Gros M, Jung C, Fourmaux C, Kamdem A, Arnaud C, Hau I, Pondarre C, Carlier-Gonod A | Eur J Contracept Reprod Health Care | 2020 |
| Fusobacterium nucleatum Multiple Liver Abscesses in an Adolescent With Hemoglobin SC Disease. | Pincez T, Ovetchkine P, Pastore Y | J. Pediatr. Hematol. Oncol. | 2020 |
| The effect of mother's β-thalassemia minor on placental histology and neonatal outcomes. | Vafaei H, Karimi S, Akbarzadeh Jahromi M, Asadi N, Kasraeian M | J. Matern. Fetal. Neonatal. Med. | 2020 |
| Effects of Alpha-Lipoic Acid Supplementation on Cardiovascular Disease Risk Factors in β-Thalassemia Major Patients: A Clinical Trial Crossover Study. | Jamshidi K, Abdollahzad H, Nachvak M, Rezaei M, Golpayegani MR, Sharifi Zahabi E | J Blood Med | 2020 |
| Brodie's Abscess Masquerading as Vaso-occlusive Crisis in a Sickle-cell Disease Patient. | Sheikh T, Fatima R, Aziz M, Balla M, Georgescu C | Cureus | 2020 |
| Zinc supplementation improves markers of glucose homeostasis in thalassaemia. | Fung EB, Ahmad T, Killilea DW, Hussain R, Lal A | Br. J. Haematol. | 2020 |
| Fetal haemoglobin H-Constant Spring disease: a role for intrauterine management. | Luewan S, Charoenkwan P, Sirichotiyakul S, Tongsong T | Br. J. Haematol. | 2020 |
| Alloimmunization and autoimmunization in adult transfusion-dependent thalassemia patients: a report from a comprehensive center in Israel. | Pazgal I, Yahalom V, Shalev B, Raanani P, Stark P | Ann. Hematol. | 2020 |
| Baseline and Disease-Induced Transcriptional Profiles in Children with Sickle Cell Disease. | Creary S, Shrestha CL, Kotha K, Minta A, Fitch J, Jaramillo L, Zhang S, Pinto S, Thompson R, Ramilo O, White P, Mejias A, Kopp BT | Sci Rep | 2020 |
| Leukocyte telomere length in patients with transfusion-dependent thalassemia. | Nanthatanti N, Tantiworawit A, Piriyakhuntorn P, Rattanathammethee T, Hantrakool S, Chai-Adisaksopha C, Rattarittamrong E, Norasetthada L, Tuntiwechapikul W, Fanhchaksai K, Charoenkwan P, Kumfu S, Chattipakorn N | BMC Med Genomics | 2020 |
| Pulmonary disease burden in Hispanic and non-Hispanic children with sickle cell disease. | Chen L, Gong J, Matta E, Morrone K, Manwani D, Rastogi D, De A | Pediatr. Pulmonol. | 2020 |
| A Nested Asymmetric PCR Melting Curve Assay for One-Step Genotyping of Nondeletional α-Thalassemia Mutations. | Qin J, Xu M, Zhang Q, Wen X, He S, Zhou Y, Liu H, Zhou W | J Mol Diagn | 2020 |
| Association of Hb A Variants with Several Forms of α- and β-Thalassemia in Thailand. | Panyasai S, Pornprasert S | Hemoglobin | 2020 |
| Mn porphyrins as a novel treatment targeting sickle cell NOXs to reverse and prevent acute vaso-occlusion in vivo. | Thamilarasan M, Estupinan R, Batinic-Haberle I, Zennadi R | Blood Adv | 2020 |
| Can CSF spectrophotometry for | Siu WY, Thomas W, Trivedi R, Hogan A, Siddiqi U, Sarker A, Besser MW | Clin Case Rep | 2020 |
| Renal failure in thalassemia: Thinking outside the box. | Kasinathan G | Clin Case Rep | 2020 |
| Locomotor mal-performance and gait adaptability deficits in sickle cell mice are associated with vascular and white matter abnormalities and oxidative stress in cerebellum. | Almeida LEF, Wang L, Kamimura S, Zerfas PM, Smith ML, Neto OLA, Vale T, Quezado MM, Horkayne-Szakaly I, Wakim P, Quezado ZMN | Brain Res. | 2020 |
| Development of the Thalassaemia Adult Life Index (ThALI). | Kantaris X, Shevlin M, Porter J, Myers L | Health Qual Life Outcomes | 2020 |
| JPP Student Journal Club Commentary: Review of Psychological Interventions Targeting Adherence Among Pediatric Sickle Cell Disease. | Durkin LK, Neff Greenley R | J Pediatr Psychol | 2020 |
| Delta-Globin Gene Expression Is Enhanced by Interferon Type I. | Manchinu MF, Simbula M, Caria CA, Musu E, Perseu L, Porcu S, Steri M, Poddie D, Frau J, Cocco E, Manunza L, Barella S, Ristaldi MS | Front Med (Lausanne) | 2020 |
| Trends in the Development of Diagnostic Tools for Red Blood Cell-Related Diseases and Anemias. | Kaestner L, Bianchi P | Front Physiol | 2020 |
| Allosteric control of hemoglobin S fiber formation by oxygen and its relation to the pathophysiology of sickle cell disease. | Henry ER, Cellmer T, Dunkelberger EB, Metaferia B, Hofrichter J, Li Q, Ostrowski D, Ghirlando R, Louis JM, Moutereau S, Galactéros F, Thein SL, Bartolucci P, Eaton WA | Proc. Natl. Acad. Sci. U.S.A. | 2020 |
| Comment on | Olatunya OS | Br. J. Haematol. | 2020 |
| Nights with sickle cell. | Mattingly DT | Fam Syst Health | 2020 |
| Genotypic-phenotypic heterogeneity of δβ-thalassemia and hereditary persistence of fetal hemoglobin (HPFH) in India. | Hariharan P, Kishnani P, Sawant P, Gorivale M, Mehta P, Kargutkar N, Colah R, Nadkarni A | Ann. Hematol. | 2020 |
| Neglected Pulmonary Arterial Hypertension in Sickle Cell Anaemia during Prenatal Care. | Karimi MB | Eur J Case Rep Intern Med | 2020 |
| Interocular asymmetry of foveal avascular zone morphology and parafoveal capillary density in sickle cell retinopathy. | Zhou DB, Scott AW, Linz MO, Han IC, Castanos MV, Lynch G, Andrade Romo JS, Linderman RE, Carroll J, Rosen RB, Chui TY | PLoS ONE | 2020 |
| Fetal Cardiac Cellular Damage Caused by Anemia in Utero in Hb Bart's Disease. | Jatavan P, Kumfu S, Tongsong T, Chattipakorn N | Curr. Mol. Med. | 2020 |
| Advances in Sickle Cell Disease Treatments. | Pavan AR, Dos Santos JL | Curr. Med. Chem. | 2020 |
| Optical coherence tomography (OCT) and OCT angiography allow early identification of sickle cell maculopathy in children and correlate it with systemic risk factors. | Grego L, Pignatto S, Alfier F, Arigliani M, Rizzetto F, Rassu N, Samassa F, Prosperi R, Barbieri F, Dall'Amico R, Cogo P, Lanzetta P | Graefes Arch. Clin. Exp. Ophthalmol. | 2020 |
| Risk score to predict event-free survival after hematopoietic cell transplant for sickle cell disease. | Brazauskas R, Scigliuolo GM, Wang HL, Cappelli B, Ruggeri A, Fitzhugh CD, Hankins JS, Kanter J, Meerpohl JJ, Panepinto JA, Rondelli D, Shenoy S, Walters MC, Wagner JE, Tisdale JF, Gluckman E, Eapen M | Blood | 2020 |
| Progressive vasoconstriction with sequential thermal stimulation indicates vascular dysautonomia in sickle cell disease. | Veluswamy S, Shah P, Khaleel M, Thuptimdang W, Chalacheva P, Sunwoo J, Denton CC, Kato R, Detterich J, Wood JC, Sposto R, Khoo MCK, Zeltzer L, Coates TD | Blood | 2020 |
| SEN virus genotype H distribution in β-thalassemic patients and in healthy donors in Iraq: Molecular and physiological study. | Al-Ouqaili MTS, Majeed YH, Al-Ani SK | PLoS Negl Trop Dis | 2020 |
| Moderate fixed-dose hydroxyurea for primary prevention of strokes in Nigerian children with sickle cell disease: Final results of the SPIN trial. | Galadanci NA, Abdullahi SU, Ali Abubakar S, Wudil Jibir B, Aminu H, Tijjani A, Abba MS, Tabari MA, Galadanci A, Borodo AM, Belonwu R, Salihu AS, Rodeghier M, Ghafuri DL, Covert C Greene BV, Neville K, Kassim AA, Kirkham FJ, Jordan LC, Aliyu MH, DeBaun MR | Am. J. Hematol. | 2020 |
| Recent Advances in the Treatment of Sickle Cell Disease. | Salinas Cisneros G, Thein SL | Front Physiol | 2020 |
| I Polymorphism in Sickle Cell Disease in North Morocco. | Alaoui-Ismaili FZ, Laghmich A, Ghailani-Nourouti N, Barakat A, Bennani-Mechita M | Hemoglobin | 2020 |
| Sickle cell disease perceptions of caregivers, adolescent, and adult patients: Barriers and facilitators to medical care adherence. | Hoegy D, Guilloux R, Bleyzac N, Gauthier-Vasserot A, Cannas G, Bertrand Y, Hot A, Dussart C, Janoly-Dumenil A | J Adv Nurs | 2020 |
| Development of the Next Generation Sequencing-Based Diagnostic Test for β-Thalassemia and its Validation in a Pashtun Family. | Sabiha B, Haider SA, Jan H, Yousafzai YM, Afridi OK, Khan AA, Ali J | Hemoglobin | 2020 |
| Rheumatoid arthritis and sickle cell disease: A potential association. | Roizenblatt S, Cabañas-Pedro AC, Figueiredo MS | Br J Haematol | 2020 |
| Manual erythroexchange in sickle cell disease: multicenter validation of a protocol predictive of volume to exchange and hemoglobin values. | Gianesin B, Pinto VM, Casale M, Corti P, Fidone C, Quintino S, Voi V, Forni GL | Ann Hematol | 2020 |
| Determination of von Willebrand factor level in patient with sickle cell diseasein vaso-occlusive crisis. | Akaba K, Nwogoh B, Oshatuyi O | Res Pract Thromb Haemost | 2020 |
| Association between Vaso-occlusive Crises and Opioid Prescriptions among Patients with Sickle Cell Disease: A Retrospective Claims-based Study. | Kang HA, Barner JC, Richards KM, Bhor M, Paulose J, Kutlar A | J Health Econ Outcomes Res | 2020 |
| Medical Resource Use and Costs of Treating Sickle Cell-related Vaso-occlusive Crisis Episodes: A Retrospective Claims Study. | Shah N, Bhor M, Xie L, Paulose J, Yuce H | J Health Econ Outcomes Res | 2020 |
| The First Asian, Single-Center Experience of Blastocyst Preimplantation Genetic Diagnosis with HLA Matching in Thailand for the Prevention of Thalassemia and Subsequent Curative Hematopoietic Stem Cell Transplantation of Twelve Affected Siblings. | Tiewsiri K, Manipalviratn S, Sutheesophon W, Vanichsetakul P, Thaijaroen P, Ketcharoon P, Bradley CK, McArthur SJ, Krutsawad W, Marshall JTA, Papadopoulos KI | Biomed Res Int | 2020 |
| Corrigendum to | Amin SS, Jalal SD, Ali KM, Mohammed AI, Rasool LK, Osman TJ | Biomed Res Int | 2020 |
| Frequency of thyroid nodules in patients with β-thalassemias in Southern Iran. | Haghpanah S, Pishdad P, Zarei T, Shahsavani A, Amirmoezi F, Ilkhanipoor H, Ilkhanipoor H, Safaei S, Setoodegan F, De Sanctis V, Karimi M | Acta Endocrinol (Buchar) | 2020 |
| The Predictor Role of Perceived Social Support and Spiritual Intelligence in Hope Among Thalassemia Patients. | Pasyar N, Rambod M, Behrouzi Z | Malays J Med Sci | 2020 |
| The Use of Extracorporeal Membrane Oxygenation During Acute Chest Crisis in an Adult Sickle Cell Disease Patient: Identification of Pearls and Pitfalls. | Tanenbaum MT, Shvygina A, Sridhar V, Vaughn JE, Joseph M | Am Surg | 2020 |
| Process mapping of the urgent red cell exchange procedure for patients with severe complications of sickle cell disease at a centralized hemapheresis service. | Smith JA, Seheult JN, Sevcik J, Kiss JE, Kaplan A | J Clin Apher | 2020 |
| Drug Therapies for the Management of Sickle Cell Disease. | Rai P, Ataga KI | F1000Res | 2020 |
| Evaluation of a clinical protocol using intranasal fentanyl for treatment of vaso-occlusive crisis in sickle cell patients in the emergency department. | Paquin H, Trottier ED, Pastore Y, Robitaille N, Dore Bergeron MJ, Bailey B | Paediatr Child Health | 2020 |
| Author Correction: Baseline and Disease-Induced Transcriptional Profiles in Children with Sickle Cell Disease. | Creary S, Shrestha CL, Kotha K, Minta A, Fitch J, Jaramillo L, Zhang S, Pinto S, Thompson R, Ramilo O, White P, Mejias A, Kopp BT | Sci Rep | 2020 |
| Nitric oxide donors offer protection to RBC from storage lesion. | Sengupta P, Mahalakshmi V, Stebin JJ, Ganesh S, Suganya N, Chatterjee S | Transfus Clin Biol | 2020 |
| Menstrual Type, Pain and Psychological Distress in Adult Women with Sickle Cell Disease (SCD). | Sollers JJ, Leach-Beale B, Barker CS, Wood M, Burford T, Bell K, Muhammad M, Lands JR, Smith N, Miller J, Jones B, Murrill AN, Killough A, Robinson E, Whitfield KE, Byrd GS, Edwards CL | J Natl Med Assoc | 2020 |
| Psychosocial and Clinical Risk Factors Associated with Substance Use in Observational Cohort of Patients with Sickle Cell Disease. | Wilson JD, Lanzkron S, Pecker LH, Bediako SM, Han D, Beach MC | Subst Use Misuse | 2020 |
| Assessment of cardiac and liver iron overload by magnetic resonance imaging in patients with thalassemia major: short-term follow-up. | Bayav M, Isiksalan Ozbulbul N, Bor O | J Int Med Res | 2020 |
| Unmasking hypertension in children and adolescents with sickle/beta-thalassemia. | Stabouli S, Antza C, Papadopoulou E, Teli A, Kotsis V, Economou M | J Clin Hypertens (Greenwich) | 2020 |
| Blood management during the COVID-19 pandemic. | Tolich D, Auron M, McCoy K, Dargis M, Quraishy N | Cleve Clin J Med | 2020 |
| Viral metagenomics in Brazilian multiply transfused patients with sickle cell disease as an indicator for blood transfusion safety. | Nunes Valença I, Silva-Pinto AC, Araújo da Silva Júnior W, Tadeu Covas D, Kashima S, Nanev Slavov S | Transfus Clin Biol | 2020 |
| Assessment of ventricular dysfunction in Egyptian children with Beta-thalassemia major. | Deraz SE, Abd El Naby SA, Mahmoud AA | Hematol Oncol Stem Cell Ther | 2020 |
| Ocular Manifestations of Sickle Cell Disease in Different Genotypes. | AlRyalat SA, Jaber BAM, Alzarea AA, Alzarea AA, Alosaimi WA, Al Saad M | Ophthalmic Epidemiol | 2020 |
| Existential analysis of mothers in the care of their children with Sickle Cell Disease. | Ramos CM, Pacheco ZML, Vargas IMÁ, Araújo PA | Rev Bras Enferm | 2020 |
| ATF4 Regulates MYB to Increase γ-Globin in Response to Loss of β-Globin. | Boontanrart MY, Schröder MS, Stehli GM, Banović M, Wyman SK, Lew RJ, Bordi M, Gowen BG, DeWitt MA, Corn JE | Cell Rep | 2020 |
| Elevated levels of circulating monocytic myeloid derived suppressor cells in splenectomised β-thalassaemia/HbE patients. | Siriworadetkun S, Thubthed R, Thiengtavor C, Paiboonsukwong K, Khuhapinant A, Fucharoen S, Pattanapanyasat K, Vadolas J, Svasti S, Chaichompoo P | Br J Haematol | 2020 |
| Has the time come to implement gene therapy for sickle cell disease? | Ginsberg N, Shulman LP | Arch Gynecol Obstet | 2020 |
| Patient-Reported Outcomes and Economic Burden of Adults with Sickle Cell Disease in the United States: A Systematic Review. | Lee S, Vania DK, Bhor M, Revicki D, Abogunrin S, Sarri G | Int J Gen Med | 2020 |
| Effect of Mutations on mRNA and Globin Stability: The Cases of Hb Bernalda/Groene Hart and Hb Southern Italy. | Cardiero G, Musollino G, Friscia MG, Testa R, Virruso L, Di Girgenti C, Caldora M, Colella Bisogno R, Gaudiano C, Manco G, Lacerra G | Genes (Basel) | 2020 |
| Automated Semantic Segmentation of Red Blood Cells for Sickle Cell Disease. | Zhang M, Li X, Xu M, Li Q | IEEE J Biomed Health Inform | 2020 |
| Cardiorenal syndrome in thalassemia patients. | Makmettakul S, Tantiworawit A, Phrommintikul A, Piriyakhuntorn P, Rattanathammethee T, Hantrakool S, Chai-Adisaksopha C, Rattarittamrong E, Norasetthada L, Fanhchaksai K, Charoenkwan P, Lekawanvijit S | BMC Nephrol | 2020 |
| Hepatocellular carcinoma in adult thalassemia patients: an expert opinion based on current evidence. | Mangia A, Bellini D, Cillo U, Laghi A, Pelle G, Valori VM, Caturelli E | BMC Gastroenterol | 2020 |
| Heparanase Level and Procoagulant Activity Are Increased in Thalassemia and Attenuated by Janus Kinase 2 Inhibition. | Ghoti H, Ackerman S, Rivella S, Casu C, Nadir Y | Am J Pathol | 2020 |
| Communicating and understanding pain: Limitations of pain scales for patients with sickle cell disorder and other painful conditions. | Collins PJ, Renedo A, Marston CA | J Health Psychol | 2020 |
| Accidental hydroxyurea overdosage in a child with sickle cell anemia: An African experience. | Nnebe-Agumadu U, Adebayo IA, Nnodu O, Adekile A | Pediatr Blood Cancer | 2020 |
| The effects of selective beta-adrenergic blockade on bone marrow dysfunction following severe trauma and chronic stress. | Miller ES, Apple CG, Kannan KB, Funk ZM, Efron PA, Mohr AM | Am J Surg | 2020 |
| Characterization of Sensorineural Hearing Loss in Adult Patients With Sickle Cell Disease: A Systematic Review and Meta-analysis. | Kapoor E, Strum D, Shim T, Kim S, Sabetrasekh P, Monfared A | Otol Neurotol | 2020 |
| The Liver in Sickle Cell Disease. | Lacaille F, Allali S, de Montalembert M | J Pediatr Gastroenterol Nutr | 2020 |
| COVID-19 Infection in a Child With Thalassemia Major After Hematopoietic Stem Cell Transplant. | Sarbay H, Atay A, Malbora B | J Pediatr Hematol Oncol | 2020 |
| Corrigendum to | Isa H, Adegoke S, Madu A, Hassan AA, Ohiaeri C, Chianumba R, Brown B, Okocha E, Ugwu N, Diaku-Akinwumi I, Adeyemo T, Kuliya-Gwarzo A, Dogara L, Lawal H, Tanko Y, Ladu A, Kangiwa U, Ekwem L, Oniyangi S, Wakama T, Umoru D, Olanrewaju O, Akinola N, Nnebe-Agumadu U, Asala S, Adekile A, Olaniyi J, Sangeda R, , Nnodu O | Blood Cells Mol Dis | 2020 |
| Combined chelation with high-dose deferiprone and deferoxamine to improve survival and restore cardiac function effectively in patients with transfusion-dependent thalassemia presenting severe cardiac complications. | Chuang TY, Li JP, Weng TF, Wu KH, Chao YH | Ann Hematol | 2020 |
| Vaso-occlusive crisis in a sickle cell patient after transfusion-transmitted dengue infection. | Santos FLS, Slavov SN, Bezerra RS, Santos EV, Silva-Pinto AC, Morais ALL, Sá MB, Ubiali EMA, De Santis GC, Covas DT, Kashima S | Transfusion | 2020 |
| Imaging review of sickle cell disease for the emergency radiologist. | Gilyard SN, Hamlin SL, Johnson JO, Herr KD | Emerg Radiol | 2020 |
| Effect of HBB genotype on survival in a cohort of transfusion-dependent thalassemia patients in Cyprus. | Kountouris P, Michailidou K, Christou S, Hadjigavriel M, Sitarou M, Kolnagou A, Kleanthous M, Telfer P | Haematologica | 2020 |
| Eculizumab for complement mediated thrombotic microangiopathy in sickle cell disease. | Chonat S, Graciaa S, Shin HS, Newton JG, Quarmyne MO, Boudreaux J, Tang A, Zerra PE, Rollins MR, Josephson CD, Brown C, Joiner CH, Fasano RM, Stowell SR | Haematologica | 2020 |
| Targeting the bone marrow niche in hemoglobinopathies. | Carlesso N | Blood | 2020 |
| Characterization of kidney complications in patients with sickle cell anemia. | Isaza-López MC, Rojas-Rosas LF, Echavarría-Ospina L, Serna-Higuita LM | Rev Chil Pediatr | 2020 |
| Smartphone-based sickle cell disease detection and monitoring for point-of-care settings. | Ilyas S, Sher M, Du E, Asghar W | Biosens Bioelectron | 2020 |
| Iron overload as a risk factor for poor graft function following allogeneic hematopoietic stem cell transplantation. | Wu XQ, Lin KN, Chen MM, Jiang PF, Zhang YX, Chen YQ, Chen QR, Xiao M, Zhu HJ, Issa HA, Chen SZ, Luo XF, Ren JH, Li Q, Zeng YL, Xu JJ, Lin YF, Zheng R, Zheng ZH, Chen ZZ, Hu JD, Yang T | Kaohsiung J Med Sci | 2020 |
| Early detection of ventricular dysfunction by tissue Doppler echocardiography related to cardiac iron overload in patients with thalassemia. | Silvilairat S, Charoenkwan P, Saekho S, Tantiworawit A, Srichairatanakool S | Int J Cardiovasc Imaging | 2020 |
| Analysis of Hb levels and degree of anemia in relation to genotype in 615 patients with hemoglobin H disease. | Luo S, Chen X, Chen L, Zhong Q, Wang Q, Xu Z, Huang J, Yan T, Tang N | Expert Rev Hematol | 2020 |
| α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser ( or c.96G>T or C)] with the α-Thalassemia-1 [- - (Southeast Asian)] Deletion in Thailand. | Panyasai S, Phasit A | Hemoglobin | 2020 |
| A Report on the Education, Employment and Marital Status of Thalassemia Patients from a Tertiary Care Center in the Middle East. | Bou-Fakhredin R, Ghanem NN, Kreidieh F, Tabbikha R, Daadaa H, Ajouz J, Koussa S, Taher AT | Hemoglobin | 2020 |
| Cellular and Molecular Aspects of Blood Cell-Endothelium Interactions in Vascular Disorders. | Wautier JL, Wautier MP | Int J Mol Sci | 2020 |
| Complications and Challenges in the Management of Iraqi Patients with β-Thalassemia Major: A Single-center Experience. | Sadullah RK, Atroshi SD, Al-Allawi NA | Oman Med J | 2020 |
| Time to apply a social determinants of health lens to addressing sickle cell disorders in sub-Saharan Africa. | Berghs M, Ola B, Cronin De Chavez A, Ebenso B | BMJ Glob Health | 2020 |
| Molecular spectrum of Hb H disease and characterization of rare deletional α-thalassemia found in Thailand. | Jomoui W, Tepakhan W, Satthakarn S, Panyasai S | Scand J Clin Lab Invest | 2020 |
| Novel α-Thalassemia Deletion Identified in an Indian Infant with Hb H Disease. | Moore JA, Pullon BM, Drake KM, Brennan SO | Hemoglobin | 2020 |
| Impact of COVID-19 Infection on 24 Patients with Sickle Cell Disease. One Center Urban Experience, Detroit, MI, USA. | Balanchivadze N, Kudirka AA, Askar S, Almadhoun K, Kuriakose P, Fadel R, Dabak V | Hemoglobin | 2020 |
| Sickle Cell Disease: A Paradigm for Venous Thrombosis Pathophysiology. | Lizarralde-Iragorri MA, Shet AS | Int J Mol Sci | 2020 |
| Analysis of rare thalassemia caused by HS-40 regulatory site deletion. | Luo S, Chen X, Zhong Q, Wang Q, Xu Z, Qin L, Wang J, Yuan D, Yan T, Tang N | Hematology | 2020 |
| Hydroxycarbamide decreases the free alpha-hemoglobin pool in red blood cells of adult patients with sickle cell anemia. | Domingues-Hamdi E, Vasseur C, Pakdaman S, Moutereau S, Habibi A, Bartolucci P, Galactéros F, Baudin-Creuza V | Am J Hematol | 2020 |
| Sickle cell disease: Progress made & challenges ahead. | Odame I, Jain D | Indian J Med Res | 2020 |
| Mutation spectrum and erythrocyte indices characterisation of α-thalassaemia and β-thalassaemia in Sichuan women in China: a thalassaemia screening survey of 42 155 women. | Li B, Han X, Ma J, Yang D | J Clin Pathol | 2020 |
| Evaluation of Erythroferrone, Hepcidin, and Iron Overload Status in Iraqi Transfusion-Dependent β-Thalassemia Major Patients. | Smesam HNK, Albuthabhak HAQ, Arjmand S, Al-Hakeim HK, R Siadat SO | Hemoglobin | 2020 |
| Design, synthesis, and optimization of a series of 2-azaspiro[3.3]heptane derivatives as orally bioavailable fetal hemoglobin inducers. | Katayama K, Tsunemi T, Miyazaki K, Uoto K, Yoshioka R, Terashima H, Terakawa M, Yamashiro K, Haruyama M, Maeda H, Makino T | Bioorg Med Chem Lett | 2020 |
| Blood transfusion for preventing primary and secondary stroke in people with sickle cell disease. | Estcourt LJ, Kohli R, Hopewell S, Trivella M, Wang WC | Cochrane Database Syst Rev | 2020 |
| Household material hardships impact emergency department reliance in pediatric patients with sickle cell disease. | Power-Hays A, Patterson A, Sobota A | Pediatr Blood Cancer | 2020 |
| NRF2 mediates γ-globin gene regulation through epigenetic modifications in a β-YAC transgenic mouse model. | Zhu X, Xi C, Ward A, Takezaki M, Shi H, Peterson KR, Pace BS | Exp Biol Med (Maywood) | 2020 |
| Hydroxycarbamide exposure and ovarian reserve in women with sickle cell disease in the Multicenter Study of Hydroxycarbamide. | Pecker LH, Hussain S, Christianson MS, Lanzkron S | Br J Haematol | 2020 |
| Molecular spectrum of α-thalassemia mutations in Erbil province of Iraqi Kurdistan. | Shamoon RP | Mol Biol Rep | 2020 |
| Biochemical and therapeutic effects of Omega-3 fatty acids in sickle cell disease. | Daak AA, Lopez-Toledano MA, Heeney MM | Complement Ther Med | 2020 |
| Randomized phase 2 trial of Intravenous Gamma Globulin (IVIG) for the treatment of acute vaso-occlusive crisis in patients with sickle cell disease: Lessons learned from the midpoint analysis. | Manwani D, Xu C, Lee SK, Amatuni G, Cohen HW, Carullo V, Morrone K, Davila J, Shi PA, Ireland K, Keenan J, Frenette PS | Complement Ther Med | 2020 |
| Moyamoya Syndrome in a 32-Year-Old Male With Sickle Cell Anemia. | Yamani M, Obaid EF, Hemida AH | Cureus | 2020 |
| Neurologic recovery in systemic nontraumatic fat embolism syndrome in an elderly patient with hemoglobin SC disease: A case report. | Ositelu A, Urrutia-Argueta S, Kapoor R | Clin Case Rep | 2020 |
| TLR4 Signaling by Heme and the Role of Heme-Binding Blood Proteins. | Janciauskiene S, Vijayan V, Immenschuh S | Front Immunol | 2020 |
| Nucleic Acid Therapy for β-Thalassemia. | d'Arqom A | Biologics | 2020 |
| 3 cases of variant hemoglobin Hb A2-Niigata detected by falsely high HbA1c values. | Ito M, Sano K, Koga M | Clin Chim Acta | 2020 |
| Cognitive functioning, patient health communication, and worry mediate pain predictive effects on health-related quality of life in youth with sickle cell disease. | Varni JW, Panepinto JA | Pediatr Blood Cancer | 2020 |
| Haemoglobin Constant Spring (HbA2: c.427T>C) and Haemoglobin Adana (HbA2: c.179G>A) in jaundiced Malaysian term neonates with clinically significant hyperbilirubinemia. | Shwe S, Boo NY, Ong HK, Chee SC, Maslina M, Ling MMM, Ahluwalia AK | Malays J Pathol | 2020 |
| Microcytic to hypochromic ratio as a discriminant index of thalassaemia trait in subjects with hypochromic anaemia. | Wee SY, Muhamed Said SS, Raja Sabudin RZA, Alauddin H, Ithnin A | Malays J Pathol | 2020 |
| Assessment of the Martín-Sánchez indices for distinguishing beta thalassemia trait from iron deficiency anemia. | Hoffmann JJML, Urrechaga E | Clin Chim Acta | 2020 |
| Prevalence of Sickle Cell Trait and Rare Hemoglobin Variants in the Metropolitan Washington DC Area. | Niu X, Parry CS, Mason A, Harrison B, Nouraie SM, Ammosova T, Salomon-Andonie J, Oneal PA, Gordeuk VR, Taylor JG, Nekhai S | J Hematol | 2020 |
| How to implement endurance exercise training in sickle cell disease. | Messonnier LA, Riccetti M, Chatel B, Galactéros F, Gellen B, Rupp T, Féasson L, Bartolucci P | Haematologica | 2020 |
| Fetal hemoglobin rescues ineffective erythropoiesis in sickle cell disease. | El Hoss S, Cochet S, Godard A, Yan H, Dussiot M, Frati G, Boutonnat-Faucher B, Laurance S, Renaud O, Joseph L, Miccio A, Brousse V, Mohandas N, El Nemer W | Haematologica | 2020 |
| Oxidative stress activates red cell adhesion to laminin in sickle cell disease. | Lizarralde-Iragorri MA, Lefevre SD, Cochet S, El Hoss S, Brousse V, Filipe A, Dussiot M, Azouzi S, Le Van Kim C, Rodrigues-Lima F, Français O, Le Pioufle B, Klei T, van Bruggen R, El Nemer W | Haematologica | 2020 |
| Evidence-based dental management in the new era of sickle cell disease: A scoping review. | Hsu LL, Fan-Hsu J | J Am Dent Assoc | 2020 |
| Association of HIV infection with clinical and laboratory characteristics of sickle cell disease. | Belisário AR, Blatyta PF, Vivanco D, Oliveira CDL, Carneiro-Proietti AB, Sabino EC, de Almeida-Neto C, Loureiro P, Máximo C, de Oliveira Garcia Mateos S, Flor-Park MV, de Oliveira Werneck Rodrigues D, Afonso Mota R, Gonçalez TT, Hoffmann TJ, Kelly S, Custer B, | BMC Infect Dis | 2020 |
| Sickle Cell-Related Complications in Patients Undergoing Cardiopulmonary Bypass. | Chacon-Portillo MA, Mossad EB, Zea-Vera R, Beckerman Z, Binsalamah ZM, Adachi I, Mery CM, Imamura M, Heinle JS, Fraser CD | World J Pediatr Congenit Heart Surg | 2020 |
| Peripartum hyperhemolysis prophylaxis and management in sickle cell disease: A case report and narrative review. | Vasanthamohan L, Choo S, Marshall T, Symons YT, Matsui D, Eastabrook G, Solh Z | Transfusion | 2020 |
| Epidemiology and treatment of beta thalassemia major in China. | Xu X, Wu X | Pediatr Investig | 2020 |
| An Innovative Multilevel Test for Hemoglobinopathies: TGA/Chemometrics Simultaneously Identifies and Classifies Sickle Cell Disease From Thalassemia. | Risoluti R, Caprari P, Gullifa G, Massimi S, Maffei L, Sorrentino F, Carcassi E, Materazzi S | Front Mol Biosci | 2020 |
| Chronic Thromboembolic Pulmonary Hypertension in a Child With Sickle Cell Disease. | Spencer R, Valencia Villeda G, Takeda K, Rosenzweig EB | Front Pediatr | 2020 |
| Post-translational modification as a response to cellular stress induced by hemoglobin oxidation in sickle cell disease. | Strader MB, Jana S, Meng F, Heaven MR, Shet AS, Thein SL, Alayash AI | Sci Rep | 2020 |
| Critical illness-associated cerebral microbleed in a patient with sickle cell disease: A case report and review of the literature. | Shafaat O, Sotoudeh H, Zandifar A, Chapman PR, Roberson GH, Sotoudeh E, Singhal A | Clin Imaging | 2020 |
| Acute lymphoblastic leukemia in a β-thalassemia intermedia child: A case report. | Sherief LM, Goneim E, Kamal NM, Ibraheim A, Alsofiani F, Alawur A | World J Clin Pediatr | 2020 |
| Diagnosis of Kikuchi-Fujimoto disease in an 11-year-old girl with fever and sickle cell disease. | Cannon L, Wang E, Becker M | BMJ Case Rep | 2020 |
| Multiple sclerosis in a young woman with sickle cell disease. | Kerpen K, Baptiste A, Yeshokumar AK | Mult Scler Relat Disord | 2020 |
| Age-dependent characterization of carotid and cerebral artery geometries in a transgenic mouse model of sickle cell anemia using ultrasound and microcomputed tomography. | Rivera CP, Li L, Cai S, Pei N, McAlear GE, Bollavaram K, Ariyo OV, Omojola VO, Song H, Alfonso AL, Tan W, Huo Y, Platt MO | Blood Cells Mol Dis | 2020 |
| Efficacy and safety of recently approved drugs for sickle cell disease: a review of clinical trials. | Ali MA, Ahmad A, Chaudry H, Aiman W, Aamir S, Anwar MY, Khan A | Exp Hematol | 2020 |
| Sickle cell disease and COVID-19: Atypical presentations and favorable outcomes. | Azerad MA, Bayoudh F, Weber T, Minon JM, Ketelslegers O, Hoyoux M, Ren X, Kaye O, De Marneffe N, Fraipont V, Masset C, Bouillon AS, Jaspers A, Tebache M, D'Hoen G, Habibi A, Efira A, Thachil J, Deckmyn H, Beguin Y | EJHaem | 2020 |
| Clinical management of a Nigerian patient affected by sickle cell disease with rare blood group and persistent SARS-CoV-2 positivity. | Quaresima M, Quaresima V, Naldini MM, Cirillo DM, Ferrari A, Mazzi A, Tesini EMC, Leone MC, Merli F | EJHaem | 2020 |
| Early Detection of Renal Injury in Children with Sickle Cell Anaemia using Microalbuminuria in a Tertiary Health Institution in Southern Nigeria. | Ekpenyong EE, Ikpeme EE, Bassey EG, Dixon-Umo OT | West Afr J Med | 2020 |
| Detection of Early Renal Disease In Children With Sickle Cell Anaemia Using Microalbuminuria As A Surrogate Marker. | Arogundade FA | West Afr J Med | 2020 |
| The Burden of Obstructive Sleep Apnea in Pediatric Sickle Cell Disease: a Kids' Inpatient Database Study. | Tsou PY, Cielo CM, Xanthopoulos MS, Wang YH, Kuo PL, Tapia IE | Sleep | 2020 |
| Alpha thalassemia genotypes in Kuwait. | Adekile A, Sukumaran J, Thomas D, D'Souza T, Haider M | BMC Med Genet | 2020 |
| Editorial for | Pattira B | J Magn Reson Imaging | 2020 |
| An Interrupted Time Series Analysis of the Dissemination of a Sickle Cell Vaso-Occlusive Episode Treatment Algorithm and a Case Management Referral Form for Individuals With Sickle Cell Disease in the Emergency Department. | Bulgin D, Bonnabeau E, Alexander A, Frederick E, Rains G, Shah N, Young M, Tanabe P | J Emerg Nurs | 2020 |
| Vulnerable Child Syndrome and Newborn Screening Carrier Results for Cystic Fibrosis or Sickle Cell. | Farrell MH, Sims AM, La Pean Kirschner A, Farrell PM, Tarini BA | J Pediatr | 2020 |
| Splenic Infarct Secondary to High Altitude Exposure in Sickle Cell Trait Patients: A Case Series. | Gonzalez L, Shapiro AF, Tafur A, Plaza-Meneses C, Sabando B | Cureus | 2020 |
| Mixed Bullous-Eczematous Contact Dermatitis From a Black Henna Tattoo in an African American Female With Sickle Cell Disease With Post-Dermatitis Pain. | Persaud-Sharma D, Govea M, Hernandez R | Cureus | 2020 |
| The Prevalence of Uterine Fibroids in African American Women with Hemoglobin SS Sickle Cell Disease as Determined by Pelvic Magnetic Resonance Imaging. | Jones DC, Ronald J, Pabon-Ramos W, Prescott J, Martin JG | Acad Radiol | 2020 |
| Screening for Obstructive Sleep Apnea in Children With Sickle Cell Disease: A Pilot Study. | Maroda AJ, Spence MN, Larson SR, Estepp JH, Gillespie MB, Harris AJ, Mamidala MP, Sheyn AM | Laryngoscope | 2020 |
| Long-term results of the NF-08-TM protocol in stem cell transplant for patients with thalassemia major: A multi-center large-sample study. | He Y, Jiang H, Li C, Zhu Y, Wu X, Liu S, Qu Y, Liao J, Feng X, Liu H, Peng Z, He L, Pu C, Gautam M, Leung W, Li C | Am J Hematol | 2020 |
| Severe delayed hemolytic transfusion reaction due to anti-Fy3 in a patient with sickle cell disease undergoing red cell exchange prior to hematopoietic progenitor cell collection for gene therapy. | Stone EF, Avecilla ST, Wuest DL, Lomas-Francis C, Westhoff CM, Diuguid DL, Sadelain M, Boulad F, Shi PA | Haematologica | 2020 |
| The molecular basis for the prothrombotic state in sickle cell disease. | Shet AS, Lizarralde-Iragorri MA, Naik RP | Haematologica | 2020 |
| Interleukin-1 receptor inhibition reduces stroke size in a murine model of sickle cell disease. | Venugopal J, Wang J, Mawri J, Guo C, Eitzman D | Haematologica | 2020 |
| De novo heterozygous Hb G-Waimanalo (α64(E13)Asp>Asn, CTG>CCG; HBA1:c.193G>A) variant in a sickle cell disease patient of an Indian tribe. | Kumar R, Mishra S, Uikey RS, Gwal A, Mun A, Bharti PK, Shanmugam R | J Clin Pathol | 2020 |
| Management of chronic respiratory complications in children and adolescents with sickle cell disease. | Arigliani M, Gupta A | Eur Respir Rev | 2020 |
| Retinal ultra-wide-field colour imaging versus dilated fundus examination to screen for sickle cell retinopathy. | Alabduljalil T, Cheung CS, VandenHoven C, Mackeen LD, Kirby-Allen M, Kertes PJ, Lam WC | Br J Ophthalmol | 2020 |
| Southeast Asian Ovalocytosis and Hemoglobinopathies in Newborns: Prevalence, Molecular, and Hematological Analyses. | Yamsri S, Kawon W, Duereh A, Fucharoen G, Fucharoen S | J Pediatr Hematol Oncol | 2020 |
| Assessment of Bone Metabolism Alterations in Transfusion-dependent Beta-thalassemia Major: An Observational Study. | Murtas A, Zanza C, Vacca N, Saderi L, Sotgiu G, Fozza C, Antonucci R | J Pediatr Hematol Oncol | 2020 |
| Physical Therapy in Pediatric and Young Adult Patients With Sickle Cell Disease: Assessing Potential Benefits and Barriers. | Callaway D, Chawla A, Sprinz P | J Pediatr Hematol Oncol | 2020 |
| Vaso-occlusive crises and costs of sickle cell disease in patients with commercial, Medicaid, and Medicare insurance - the perspective of private and public payers. | Shah NR, Bhor M, Latremouille-Viau D, Kumar Sharma V, Puckrein GA, Gagnon-Sanschagrin P, Khare A, Kumar Singh M, Serra E, Davidson M, Xu L, Guerin A | J Med Econ | 2020 |
| Assay for | Davis BH | Am J Hematol | 2020 |
| Ultrasound Features of Fetal Anemia Lessons From Hemoglobin Bart Disease. | Thammavong K, Luewan S, Wanapirak C, Tongsong T | J Ultrasound Med | 2020 |
| Sickle cell anemia and COVID-19: Use of voxelotor to avoid transfusion. | Ershler WB, Holbrook ME | Transfusion | 2020 |
| Adherence to a selective antenatal haemoglobinopathy screening policy within a tertiary level obstetric unit in Australia. | Borbolla Foster A, Smith E, Ross B | Aust N Z J Obstet Gynaecol | 2020 |
| Curative in vivo hematopoietic stem cell gene therapy of murine thalassemia using large regulatory elements. | Wang H, Georgakopoulou A, Li C, Liu Z, Gil S, Bashyam A, Yannaki E, Anagnostopoulos A, Pande A, Izsvák Z, Papayannopoulou T, Lieber A | JCI Insight | 2020 |
| Characterising demographics, knowledge, practices and clinical care among patients attending sickle cell disease clinics in Eastern Uganda. | Olupot-Olupot P, Wabwire H, Ndila C, Adong R, Ochen L, Amorut D, Abongo G, Okalebo CB, Akello SR, Oketcho JB, Okiror W, Asio S, Odiit A, Alaroker F, Nyutu G, Maitland K, Williams TN | Wellcome Open Res | 2020 |
| Abatacept is effective as GVHD prophylaxis in unrelated donor stem cell transplantation for children with severe sickle cell disease. | Ngwube A, Shah N, Godder K, Jacobsohn D, Hulbert ML, Shenoy S | Blood Adv | 2020 |
| Appropriate thresholds for accurate screening for β-thalassemias in the newborn period: results from a French center for newborn screening. | Allaf B, Pondarre C, Allali S, De Montalembert M, Arnaud C, Barrey C, Benkerrou M, Benhaim P, Bensaid P, Brousse V, Dollfus C, Eyssette-Guerreau S, Galacteros F, Gajdos V, Garrec N, Guillaumat C, Guitton C, Monfort-Gouraud M, Gouraud F, Holvoet L, Ithier G, Kamdem A, Koehl B, Malric A, Missud F, Monier B, Odièvre MH, Joly P, Renoux C, Patin F, Pissard S, Couque N | Clin Chem Lab Med | 2020 |
| Pica behaviors in pediatric patients with sickle cell disease: a scoping review protocol. | Clark OM, Williams R | JBI Evid Synth | 2020 |
| Automated exchange compared to manual and simple blood transfusion attenuates rise in ferritin level after 1 year of regular blood transfusion therapy in chronically transfused children with sickle cell disease. | Kelly S, Rodeghier M, DeBaun MR | Transfusion | 2020 |
| Pedigree Analysis of Nonhomologous Sequence Recombination of and Genes. | Luo SQ, Chen XY, Tang N, Huang J, Zhong QY, Cai R, Yan TZ | Hemoglobin | 2020 |
| Consanguinity, the driving force behind inheritance of HbS-β thalassemia in Southern Districts of KP. | Khan J, Muhammad D, Ismail M, Khan I, , Niaz S | J Pak Med Assoc | 2020 |
| Fetal Hemoglobin in Sickle Cell Anemia. | Steinberg MH | Blood | 2020 |
| Germline Gene Editing for Sickle Cell Disease. | Sharma A, Bhakta N, Johnson LM | Am J Bioeth | 2020 |
| Extremely high birth prevalence of sickle cell disease in rural Tanzania. | Eastburg L, Peckham A, Kawira E, Chirangi B, Adler D, Akungo BD, Smart LR, Ambrose EE | Pediatr Blood Cancer | 2020 |
| Phenotypical and functional abnormalities of circulating neutrophils in patients with β-thalassemia. | Buttari B, Profumo E, Caprari P, Massimi S, Sorrentino F, Maffei L, Gabbianelli M, Riganò R | Ann Hematol | 2020 |
| Prediction, management, and prognosis of mixed chimerism after hematopoietic stem cell transplantation in transfusion-dependent pediatric thalassemia patients. | Chen H, Li XY, Zhan LP, Fang JP, Huang K, Li Y, Weng WJ, Xu LH, Xu HG, Zhou DH | Pediatr Transplant | 2020 |
| Allogeneic hematopoietic stem cell transplantation from sibling and unrelated donors in pediatric patients with sickle cell disease-A single center experience. | Kogel F, Hakimeh D, Sodani P, Lang P, Kühl JS, Hundsdoerfer P, Künkele A, Eggert A, Oevermann L, Schulte JH | Pediatr Transplant | 2020 |
| Supramolecular nanosubstrate-mediated delivery system enables CRISPR-Cas9 knockin of hemoglobin beta gene for hemoglobinopathies. | Yang P, Chou SJ, Li J, Hui W, Liu W, Sun N, Zhang RY, Zhu Y, Tsai ML, Lai HI, Smalley M, Zhang X, Chen J, Romero Z, Liu D, Ke Z, Zou C, Lee CF, Jonas SJ, Ban Q, Weiss PS, Kohn DB, Chen K, Chiou SH, Tseng HR | Sci Adv | 2020 |
| Characterization of HIV risks in a Brazilian sickle cell disease population. | Blatyta PF, Kelly S, Goncalez TT, Carneiro-Proietti AB, Salomon T, Miranda C, Sabino E, Preiss L, Maximo C, Loureiro P, Custer B, de Almeida-Neto C, | BMC Public Health | 2020 |
| Liver complications of haemoglobin H disease in adults. | Chan LKL, Mak VWM, Chan SCH, Yu ELM, Chan NCN, Leung KFS, Ng CKM, Ng MHL, Chan JCW, Lee HKK | Br J Haematol | 2020 |
| Oxygen gradient ektacytometry-derived biomarkers are associated with vaso-occlusive crises and correlate with treatment response in sickle cell disease. | Rab MAE, Kanne CK, Bos J, van Oirschot BA, Boisson C, Houwing ME, Gerritsma J, Teske E, Renoux C, Riedl J, Schutgens REG, Bartels M, Nur E, Joly P, Fort R, Cnossen MH, van Wijk R, Connes P, van Beers EJ, Sheehan VA | Am J Hematol | 2020 |
| Diaphragm ultrasonography in adults with sickle cell anemia: evaluation of morphological and functional aspects. | Zeitoune R, Mogami R, Koifman ACB, Lopes AJ, Soares AR, Martins RAG, Maioli MCP | Hematology | 2020 |
| Co-morbidities and mortality associated with transfusion-dependent beta-thalassaemia in patients in England: a 10-year retrospective cohort analysis. | Jobanputra M, Paramore C, Laird SG, McGahan M, Telfer P | Br J Haematol | 2020 |
| Investigating the missing heritability of foetal haemoglobin level in Africa. | Wonkam A | Br J Haematol | 2020 |
| The evolution of clinical research in thalassaemia: where has all the funding gone? | Rund D | Br J Haematol | 2020 |
| Complications of Central Venous Access Devices in Patients With Sickle Cell Disease and Thalassemia Major. | Ordóñez J, Del Cañizo A, Beléndez C, García-Morín M, Pérez-Egido L, Fanjul M, García-Casillas MA, Cerdá J, Peláez D, Bardón E, de Agustín JC, Cela E | J Pediatr Hematol Oncol | 2020 |
| Pain in Youth with Sickle Cell Disease: A Report from the Sickle Cell Clinical Research and Intervention Program. | Alberts NM, Kang G, Li C, Richardson PA, Hodges J, Hankins JS, Klosky JL | Clin J Pain | 2020 |
| Surgical and Medical Perioperative Management of Sickle Cell Retinopathy: A Literature Review. | Nithianandan H, Sridhar J | Int Ophthalmol Clin | 2020 |
| Unannotated single nucleotide polymorphisms in the TATA box of erythropoiesis genes show in vitro positive involvements in cognitive and mental disorders. | Ponomarenko M, Sharypova E, Drachkova I, Chadaeva I, Arkova O, Podkolodnaya O, Ponomarenko P, Kolchanov N, Savinkova L | BMC Med Genet | 2020 |
| Conformational changes of β-thalassemia major hemoglobin and oxidative status of plasma after in vitro exposure to extremely low-frequency electromagnetic fields: An artificial neural network analysis. | Rahmani S, Ansarihadipour H, Bayatiani MR, Khosrowbeygi A, Babaei S, Rasmi Y | Electromagn Biol Med | 2020 |
| Prenatal Diagnosis and Screening of Thalassemia Mutations in Bangladesh: Presence of Rare Mutations. | Aziz MA, Khan WA, Banu B, Das SA, Sadiya S, Begum S | Hemoglobin | 2020 |
| The impact of COVID-19 on transfusion-dependent thalassemia patients of Karachi, Pakistan: A single-center experience. | Arshad Ali S, Azim D, Hassan HM, Iqbal A, Ahmed N, Kumar S, Nasim S | Transfus Clin Biol | 2020 |
| Sophie Uyoga-reducing sickle cell stigma in Africa. | Kirby T | Lancet Haematol | 2020 |
| Prevalence of Sensorineural Hearing Loss in Pediatric Patients with Sickle Cell Disease: A Meta-analysis. | Strum D, Kapoor E, Shim T, Kim S, Sabetrasekh P, Monfared A | Laryngoscope | 2020 |
| Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study. | Barbanera Y, Arcioni F, Lancioni H, La Starza R, Cardinali I, Matteucci C, Nofrini V, Roetto A, Piga A, Grammatico P, Caniglia M, Mecucci C, Gorello P | PLoS One | 2020 |
| Spontaneous splenic rupture, mesenteric ischemia and spinal infarction after aortic repair for acute type A dissection in a patient with sickle cell trait. | Toyoda M, Kitamura T, Nakashima K, Matsunaga Y, Nie M, Miyaji K | Gen Thorac Cardiovasc Surg | 2020 |
| Distinguishing iron deficiency from beta-thalassemia trait by new generation ektacytometry. | Krishnevskaya E, Payán-Pernía S, Hernández-Rodríguez I, Remacha Sevilla ÁF, Ancochea Serra Á, Morales-Indiano C, Serra Ferrer M, Vives-Corrons JL | Int J Lab Hematol | 2020 |
| The Sickle Cell Pro-Inflammatory Response to Interval Testing Study (SPRINTS) in children and young adults with sickle cell anemia - Study design and methodological strategies. | Liem RI, Baynard T, Hsu LL, Garofano R, Green NS, Hankins JS, Ness KK, Rodeghier M, Radom-Aizik S | Contemp Clin Trials Commun | 2020 |
| Effects of Aquatic Exercise on Dimensions of Quality of Life and Blood Indicators in Patients with Beta-Thalassemia Major. | Hasanpour Dehkordi A, Hasani T, Fekri K, Deris F, Etemadifar S | Int J Prev Med | 2020 |
| Complete RH and Kell matching related to low alloimmunisation risk in sickle cell disease: prevalence and risk factors of alloimmunisation in a Spanish Tertiary Care National Reference Centre. | Regalado-Artamendi I, Pérez-Corral AM, García-Morín M, Cela E, Beléndez C, Bardón-Cancho EJ, Pérez-Rus G, Pérez-Sánchez I, Pascual C, Monsalvo S, Falero C, Díez-Martín JL, Anguita J | Blood Transfus | 2020 |
| Mechanisms of enhanced vascular smooth muscle contraction induced by sickle erythrocyte constituents. | Azubuike-Osu S, Uche OK, Ajayi IO, Ebeigbe AB | Niger J Physiol Sci | 2020 |
| Acute Soft Head Syndrome (Subgaleal Haematoma) with Periorbital Oedema as a Rare Presentation in Sickle Cell Disease. | Al-Ansari RY, Al Harbi M, Al-Jubair N, Abdalla L | Eur J Case Rep Intern Med | 2020 |
| Significance of variant annotation for molecular diagnosis of thalassaemia. | Poon KS, Koay ES, Tan KM | J Clin Pathol | 2020 |
| High prevalence of thalassemia with a novel α-thalassemia mutationin in Baoan populations in Guangdong province, China. | Yu Y, Yang Z, Yu H, Sun R, Zhu Y, Guo F | Eur J Obstet Gynecol Reprod Biol | 2020 |
| Using cyproterone acetate to treat recurrent ischemic priapism in a patient with sickle cell anemia as a comorbidity: a case report. | Alshahrani A | J Med Case Rep | 2020 |
| Femur Fracture in a Premature Infant: An Unusual Association of Sickle Cell Disease with Osteogenesis Imperfecta. | Gozum G, Bogdan M, Sundaram R, Kulpa J, Narula P, Agdere L | Am J Case Rep | 2020 |
| Manipulation of developmental gamma-globin gene expression: an approach for healing hemoglobinopathies. | Venkatesan V, Srinivasan S, Babu P, Thangavel S | Mol Cell Biol | 2020 |
| Codanin-1 mutations engineered in human erythroid cells demonstrate role of CDAN1 in terminal erythroid maturation. | Murphy ZC, Getman MR, Myers JA, Burgos Villar KN, Leshen E, Kurita R, Nakamura Y, Steiner LA | Exp Hematol | 2020 |
| Randomized Control Trial of Oral Arginine Therapy for Children with Sickle Cell Anemia Hospitalized for Pain in Nigeria. | Onalo R, Cooper P, Cilliers A, Vorster BC, Uche NA, Oluseyi OO, Onalo VD, Zubairu Y, Ayodele-Kehinde AU, Damilare OM, Figueroa J, Morris CR | Am J Hematol | 2020 |
| F cell numbers are associated with an X-linked genetic polymorphism and correlate with haematological parameters in patients with sickle cell disease. | Urio F, Nkya S, Rooks H, Mgaya JA, Masamu U, Zozimus Sangeda R, Mmbando BP, Brumat M, Mselle T, Menzel S, Luzzatto L, Makani J | Br J Haematol | 2020 |
| Generation of nine iPSC lines (HNMUi002-A, HNMUi003-A, HNMUi004-A, HNMUi005-A, HNMUi006-A, HNMUi007-A, HNMUi008-A, HNMUi009-A, HNMUi010-A) from three Chinese families with thalassemia. | Long P, Wang Z, Yang H, Liu Z, Wu B, Zhong G, Chen J, Sun C, Wang F, Zhou Y, Sun F, Li Q, Ma Y | Stem Cell Res | 2020 |
| Nanoscale adhesion profiling and membrane characterisation in sickle cell disease using hybrid atomic force microscopy-IR spectroscopy. | Fellows AP, Casford MTL, Davies PB, Gibson JS, Brewin JN, Rees DC | Colloids Surf B Biointerfaces | 2020 |
| A broad diversity in oxygen affinity to haemoglobin. | Balcerek B, Steinach M, Lichti J, Maggioni MA, Becker PN, Labes R, Gunga HC, Persson PB, Fähling M | Sci Rep | 2020 |
| Effective Recruitment Strategies for a Sickle Cell Patient Registry Across Sites from the Sickle Cell Disease Implementation Consortium (SCDIC). | Masese RV, DeMartino T, Bonnabeau E, Burns EN, Preiss L, Varughese T, Nocek JM, Lasley P, Chen Y, Davila C, Nwosu C, Scott S, Bowman L, Gordon L, Clesca C, Peters-Lawrence M, Melvin C, Shah N, Tanabe P, | J Immigr Minor Health | 2020 |
| What is the future of patient-reported outcomes in sickle-cell disease? | Singh SA, Bakshi N, Mahajan P, Morris CR | Expert Rev Hematol | 2020 |
| The burden of respiratory syncytial virus infections among children with sickle cell disease. | Rostad CA, Maillis AN, Lai K, Bakshi N, Jerris RC, Lane PA, Yee ME, Yildirim I | Pediatr Blood Cancer | 2020 |
| Primary caregiver decision-making in hematopoietic cell transplantation and gene therapy for sickle cell disease. | Sinha CB, Bakshi N, Ross D, Loewenstein G, Krishnamurti L | Pediatr Blood Cancer | 2020 |
| Neuropathic pain is associated with poor health-related quality of life in adolescents with sickle cell disease: A preliminary report. | Román ME, Highland J, Retherford D, Pan AY, Panepinto JA, Brandow AM | Pediatr Blood Cancer | 2020 |
| Analysis of determinant factors of liver fibrosis progression in ex-thalassemic patients. | Rostami T, Monzavi SM, Poustchi H, Khoshdel AR, Behfar M, Hamidieh AA | Int J Hematol | 2020 |
| Generation of an immortalised erythroid cell line from haematopoietic stem cells of a haemoglobin E/β-thalassemia patient. | Trakarnsanga K, Tipgomut C, Metheetrairut C, Wattanapanitch M, Khuhapinant A, Poldee S, Kurita R, Nakamura Y, Srisawat C, Frayne J | Sci Rep | 2020 |
| Physical exercise in sickle cell anemia: a systematic review. | Pinto DMR, do Sacramento MS, Santos PHS, Silva WS, de Oliveira EC, Gardenghi G, Ladeia AMT, Petto J | Hematol Transfus Cell Ther | 2020 |
| Evaluation of sleep quality and restless legs syndrome in adult patients with sickle cell anemia. | Erdem NŞ, Erdem R, Oktay G, Kurtoğlu E | Sleep Breath | 2020 |
| Quality assessment of evidence-based clinical practice guidelines for the management of pregnant women with sickle cell disease using the AGREE II instrument: a systematic review. | Amer YS, Sabr Y, ElGohary GM, Altaki AM, Khojah OT, El-Malky A, Alzahrani MF | BMC Pregnancy Childbirth | 2020 |
| Discriminant indexes to simplify the differential diagnosis between iron deficiency anemia and thalassemia minor in individuals with microcytic anemia. | Reis FMP, Andrade RR, Rodrigues CFS, Barbosa FT | Rev Assoc Med Bras (1992) | 2020 |
| Outcomes of multidisciplinary team interventions in the management of sickle cell disease patients with opioid use disorders. A retrospective cohort study. | Al Zahrani O, Hanafy E, Mukhtar O, Sanad A, Yassin W | Saudi Med J | 2020 |
| Does Intravenous Acetaminophen Reduce Opioid Requirement in Pediatric Emergency Department Patients With Acute Sickle Cell Crises? | Dhebaria T, Sivitz A, Tejani C | Acad Emerg Med | 2020 |
| Standardized microfluidic assessment of red blood cell mediated microcapillary occlusion: association with clinical phenotype and hydroxyurea responsiveness in sickle cell disease. | Man Y, Kucukal E, An R, Bode A, Little JA, Gurkan UA | Microcirculation | 2020 |
| In vitro assessment of the anti-sickling properties of Buchholzia coriacea and Mucuna pruriens seed extracts. | Ikechukwu EL, Okafor PN, Egba SI | In Vitro Cell Dev Biol Anim | 2020 |
| Green tea influence on iron overload in thalassemia intermedia patients: a randomized controlled trial. | Al-Momen H, Hussein HK, Al-Attar Z, Hussein MJ | F1000Res | 2020 |
| Twelve-lead and signal-averaged electrocardiographic parameters among beta-thalassemia major patients. | Patsourakos D, Gatzoulis KA, Aggeli C, Delicou S, Dimitroglou Y, Xydaki K, Toutouzas K, Androulakis A, Tousoulis D | J Arrhythm | 2020 |
| Molecular Characterization of β- and α-Globin Gene Mutations in Individuals with Borderline Hb A Levels. | Satthakarn S, Panyasai S, Pornprasert S | Hemoglobin | 2020 |
| Association of Hb Shenyang [α26(B7)Ala→Glu, GG>GG, : c.80C>A (or )] with Several Types of α-Thalassemia in Thailand. | Panyasai S, Kongthai K, Phasit A | Hemoglobin | 2020 |
| Computational and drug target analysis of functional single nucleotide polymorphisms associated with Haemoglobin Subunit Beta (HBB) gene. | Soremekun OS, Ezenwa C, Isewon I, Soliman M, Idowu O, Nashiru O, Fatumo S | Comput Biol Med | 2020 |
| The Sickle Cell Disease Ontology: Enabling Collaborative Research and Co-Designing of New Planetary Health Applications. | Nembaware V, Mazandu GK, Hotchkiss J, Safari Serufuri JM, Kent J, Kengne AP, Anie K, Munung NS, Bukini D, Bitoungui VJN, Munube D, Chirwa U, Chunda-Liyoka C, Jonathan A, Flor-Park MV, Esoh KK, Jonas M, Mnika K, Oosterwyk C, Masamu U, Morrice J, Uwineza A, Nguweneza A, Banda K, Nyanor I, Adjei DN, Siebu NE, Nkanyemka M, Kuona P, Tayo BO, Campbell A, Oron AP, Nnodu OE, Painstil V, Makani J, Mulder N, Wonkam A | OMICS | 2020 |
| Non-hematopoietic deficiency of proprotein convertase subtilisin/kexin type 9 deficiency leads to more severe anemia in a murine model of sickle cell disease. | Venugopal J, Wang J, Guo C, Lu H, Chen YE, Eitzman DT | Sci Rep | 2020 |
| Successful Hematopoietic Stem Cell Transplantation from a Matched Related Donor with Beta-Thalassemia Minor for Severe Aplastic Anemia. | Jung MY, Lim YT, Lim H, Hah JO, Lee JM | Children (Basel) | 2020 |
| Measuring Pain in Sickle Cell Disease using Clinical Text. | Alambo A, Andrew R, Gollarahalli S, Vaughn J, Banerjee T, Thirunarayan K, Abrams D, Shah N | Annu Int Conf IEEE Eng Med Biol Soc | 2020 |
| Pregnancy Outcomes among Patients with Sickle Cell Disease in Brazzaville. | Galiba Atipo Tsiba FO, Itoua C, Ehourossika C, Ngakegni NY, Buambo G, Potokoue Mpia NSB, Elira Dokekias A | Anemia | 2020 |
| Polymorphisms in Inflammatory Genes Modulate Clinical Complications in Patients With Sickle Cell Disease. | Tozatto-Maio K, Girot R, Ly ID, Silva Pinto AC, Rocha V, Fernandes F, Diagne I, Benzerara Y, Dinardo CL, Soler JP, Kashima S, Araujo IL, Kenzey C, Fonseca GHH, Rodrigues ES, Volt F, Jarduli L, Ruggeri A, Mariaselvam C, Gualandro SFM, Rafii H, Cappelli B, Nogueira FM, Scigliuolo GM, Guerino-Cunha RL, Malmegrim KCR, Simões BP, Gluckman E, Tamouza R | Front Immunol | 2020 |
| Circulating Extracellular Vesicles and Endothelial Damage in Sickle Cell Disease. | Lapping-Carr G, Gemel J, Mao Y, Beyer EC | Front Physiol | 2020 |
| Sickle Cell Anemia: Variants in the , , and Genes Are Associated With Improved Hydroxyurea Response. | Yahouédéhou SCMA, Neres JSDS, da Guarda CC, Carvalho SP, Santiago RP, Figueiredo CVB, Fiuza LM, Ndidi US, de Oliveira RM, Fonseca CA, Nascimento VML, Rocha LC, Adanho CSA, da Rocha TSC, Adorno EV, Goncalves MS | Front Pharmacol | 2020 |
| CXCR4 effector neutrophils in sickle cell anemia: potential role for elevated circulating serotonin (5-HT) in CXCR4 neutrophil polarization. | Garcia F, Mendonça R, Miguel LI, Dominical VM, Saad STO, Costa FF, Conran N | Sci Rep | 2020 |
| Daily Cannabis Users with Sickle Cell Disease Show Fewer Admissions than Others with Similar Pain Complaints. | Curtis SA, Brandow AM, DeVeaux M, Zeltermam D, Devine L, Roberts JD | Cannabis Cannabinoid Res | 2020 |
| Management of Acute Pulmonary Embolism in a Patient with Sickle Cell Anemia Using Catheter-Directed Thrombolysis. | Bowers E, Mohapatra AA, Ali AA, Singh MJ | Ann Vasc Surg | 2020 |
| In Vivo HSC Gene Therapy Using a Bi-modular HDAd5/35++ Vector Cures Sickle Cell Disease in a Mouse Model. | Li C, Wang H, Georgakopoulou A, Gil S, Yannaki E, Lieber A | Mol Ther | 2020 |
| Crizanlizumab and comparators for adults with sickle cell disease: a systematic review and network meta-analysis. | Thom H, Jansen J, Shafrin J, Zhao L, Joseph G, Cheng HY, Gupta S, Shah N | BMJ Open | 2020 |
| Accelerated erythrocyte destruction mimicking post-transfusion hyperhaemolysis in the course of uncomplicated vaso-occlusive crisis associated with sickle cell disease. | Conrado MCAV, Fonseca GSVC, Dezan MR, Mendes FR, Hamasaki DT, Chinoca KZ, Fonseca GH, Gualandro SFM, Rocha V, Mendrone-Júnior A, Dinardo CL | Transfus Med | 2020 |
| A 15-years follow-up of deferasirox in beta-thalassaemia major patients with iron overload. | Wei Z, Yang G, Huang Y, Peng P, Long L, Long Y, Huang X, Zhou X, Lai Y, Liu R | Br J Haematol | 2020 |
| Microcytosis in patients with haemoglobin C trait: is α-thalassaemia trait to blame? | Forté S, Eng B, Verhovsek M, Soulières D, Waye JS | Br J Haematol | 2020 |
| Severe infusion-related reaction to crizanlizumab in an adolescent with sickle cell disease. | Karkoska K, Quinn CT, Clapp K, McGann PT | Am J Hematol | 2020 |
| Tricuspid regurgitant jet velocity and myocardial tissue Doppler parameters predict mortality in a cohort of patients with sickle cell disease spanning from pediatric to adult age groups - revisiting this controversial concept after 16 years of additional evidence. | Shah P, Suriany S, Kato R, Bush AM, Chalacheva P, Veluswamy S, Denton CC, Russell K, Khaleel M, Forman HJ, Khoo MCK, Sposto R, Coates TD, Wood JC, Detterich J | Am J Hematol | 2020 |
| Intentional and unintentional nonadherence to hydroxyurea among people with sickle cell disease: a qualitative study. | Hodges JR, Phillips SM, Norell S, Nwosu C, Khan H, Luo L, Badawy SM, King A, Tanabe P, Treadwell M, Rojas Smith L, Calhoun C, Hankins JS, Porter J | Blood Adv | 2020 |
| Managing patients with sickle cell disease in primary care. | Hehre RJ | JAAPA | 2020 |
| Administrative data identify sickle cell disease: A critical review of approaches in U.S. health services research. | Grosse SD, Green NS, Reeves SL | Pediatr Blood Cancer | 2020 |
| Relative and Absolute Quantification of Aberrant and Normal Splice Variants in β-Thalassemia. | Patsali P, Papasavva P, Christou S, Sitarou M, Antoniou MN, Lederer CW, Kleanthous M | Int J Mol Sci | 2020 |
| Genetic research and clinical analysis of deletional Chinese γ(γδβ) -thalassemia and Southeast Asian HPFH in South China. | Wu Y, Yao Q, Zhong M, Wu J, Xie L, Su L, Yu F | Ann Hematol | 2020 |
| A stable version of capillary electrophoresis for determining human hemoglobin chains aiming at the screening and diagnosis of thalassemia. | Guo C, Zhang Q, Bao L, Li H, Zheng Q, Guo Z, Chen Y | Anal Methods | 2020 |
| Impact of iron overload on bone remodeling in thalassemia. | Piriyakhuntorn P, Tantiworawit A, Phimphilai M, Shinlapawittayatorn K, Chattipakorn SC, Chattipakorn N | Arch Osteoporos | 2020 |
| EDSC: Working to Improve Emergency Department Care of Individuals With Sickle Cell Disease. | Kavanagh PL, Hirshon JM | Ann Emerg Med | 2020 |
| A Caregiver's Perspective: Internist, Active Duty Service Member, and Mother of a Child Living With Sickle Cell Disease. | McGann S | Ann Emerg Med | 2020 |
| A Survey-Based Needs Assessment of Barriers to Optimal Sickle Cell Disease Care in the Emergency Department. | Linton EA, Goodin DA, Hankins JS, Kanter J, Preiss L, Simon J, Souffront K, Tanabe P, Gibson R, Hsu LL, King A, Richardsona LD, Glassberg JA, | Ann Emerg Med | 2020 |
| A Multiyear Cross-sectional Study of Guideline Adherence for the Timeliness of Opioid Administration in Children With Sickle Cell Pain Crisis. | Brousseau DC, Alpern ER, Chamberlain JM, Ellison AM, Bajaj L, Cohen DM, Hariharan S, Cook LJ, Harding M, Panepinto J, | Ann Emerg Med | 2020 |
| Emergency Department Utilization for Patients Living With Sickle Cell Disease: Psychosocial Predictors of Health Care Behaviors. | Abdallah K, Buscetta A, Cooper K, Byeon J, Crouch A, Pink S, Minniti C, Bonham VL | Ann Emerg Med | 2020 |
| Utility of Point-of-Care Lung Ultrasonography for Evaluating Acute Chest Syndrome in Young Patients With Sickle Cell Disease. | Cohen SG, Malik ZM, Friedman S, Russell S, Hagbom R, Alazraki A, McCracken CE, Figueroa J, Adisa OA, Mendis RD, Manoranjithan S, Simon HK, Morris CR | Ann Emerg Med | 2020 |
| Inconsistent Emergency Department Care: The Hidden Cost for Patients With Sickle Cell Disease. | Williams AF | Ann Emerg Med | 2020 |
| Association of Antibiotic Choice With Hospital Length of Stay and Risk Factors for Readmission in Patients With Sickle Cell Disease and Acute Chest Syndrome: An Observational Cohort Study. | Badaki-Makun O, Casella JF, Tackett S, Tao X, Chamberlain JM | Ann Emerg Med | 2020 |
| Trends in Sickle Cell Disease-Related Mortality in the United States, 1979 to 2017. | Payne AB, Mehal JM, Chapman C, Haberling DL, Richardson LC, Bean CJ, Hooper WC | Ann Emerg Med | 2020 |
| The Effect of Use of Individualized Pain Plans in Sickle Cell Patients Presenting to the Emergency Department. | Della-Moretta S, Delatore L, Purcell M, Huang Y, Heinlein M, Adkins E, Desai P | Ann Emerg Med | 2020 |
| Outcomes of an Emergency Department Observation Unit-Based Pathway for the Treatment of Uncomplicated Vaso-occlusive Events in Sickle Cell Disease. | Lyon M, Sturgis L, Lottenberg R, Gibson ME, Eck J, Kutlar A, Gibson RW | Ann Emerg Med | 2020 |
| The State of Sickle Cell Disease Care in the United States: How Can Emergency Medicine Contribute? | Giroir BP, Collins F | Ann Emerg Med | 2020 |
| Rapid Molecular Detection for Differentiation of Homozygous HbE and ß0-Thalassemia/HbE in Samples Related With HbE >80% and Variable HbF Levels. | Tepakhan W, Jomoui W | Lab Med | 2020 |
| Coinherited Hemoglobin H/Constant Spring Disease and Heterozygous Hemoglobin Tak Causing Severe Hemolytic Anemia in a Thai Boy. | Choed-Amphai C, Phusua A, Ittiwut C, Charoenkwan P, Suphapeetiporn K, Shotelersuk V | J Pediatr Hematol Oncol | 2020 |
| Association of HFE Gene Mutations With Serum Ferritin Level and Heart and Liver Iron Overload in Patients With Transfusion-dependent Beta-Thalassemia. | Zekavat OR, Zareian Jahromi M, Haghpanah S, Kargar Jahromi Z, Cohan N | J Pediatr Hematol Oncol | 2020 |
| Pain in Children and Adolescents With Sickle Cell Disease: Multidimensional Assessment. | Abadesso C, Pacheco S, Machado MC, Finley GA | J Pediatr Hematol Oncol | 2020 |
| Fifteen Cases of Hb J-Meerut: The Rare Association with Hb E and/or : c.-24C>G (or ) Variants. | Khalil MSM, Timbs AT, Henderson SJ, Schuh A, Old JM | Hemoglobin | 2020 |
| Genetic Analysis of Patients With Sickle Cell Anemia and Stroke Before 4 Years of Age Suggest an Important Role for Apoliprotein E. | Brewin JN, Smith AE, Cook R, Tewari S, Brent J, Wilkinson S, Brousse V, Inusa B, Menzel S, Rees DC | Circ Genom Precis Med | 2020 |
| Initial Dosage Optimization of Tacrolimus in Pediatric Patients With Thalassemia Major Undergoing Hematopoietic Stem Cell Transplantation Based on Population Pharmacokinetics. | Zhou S, Zhang R, Lv C, Lu J, Wei Y, Li C, Chen M, Li Q, Liu T | Ann Pharmacother | 2020 |
| [Analysis of thalassemia-related mutations in Pingxiang area of Jiangxi]. | Gan J, Ding F, Liu H | Zhonghua Yi Xue Yi Chuan Xue Za Zhi | 2020 |
| Spirometry use in Patients with Sickle Cell Disease with and without asthma and acute chest syndrome: A Multicenter Study. | Duckworth L, Black LV, Ezmigna D, Green J, Yao Y, Grannis S, Klann J, Applegate R, Lipori G, Wallace T, Wilkie DJ | EJHaem | 2020 |
| Challenging the Erythropoiesis Paradigm in β-Thalassemia. | Vinchi F, Vance SZ | Hemasphere | 2020 |
| Cognitive Correlates of Math Performance in School-Aged Children with Sickle Cell Disease and Silent Cerebral Infarcts. | Peterson RK, Williams S, Janzen L | Arch Clin Neuropsychol | 2020 |
| Management of Osteomyelitis in Sickle Cell Disease: Review Article. | Al Farii H, Zhou S, Albers A | J Am Acad Orthop Surg Glob Res Rev | 2020 |
| "Pain is Subjective": A Mixed-Method Study of Provider Attitudes and Practices Regarding Pain Management in Sickle Cell Disease across Three Countries | Stewart KA, Parshad-Asnani M, Wonkam A, Bollinger J, Ngo Bitoungui V, Wonkam-Tingang E, Powell J, Desronvil K, Benson K, Clark A, Katz M, Martin B, Peterseim C, Williams C, Young N, Shah N, Babyak M, Tanabe P, Royal CD | J Pain Symptom Manage | 2020 |
| Innovative screening test for the early detection of sickle cell anemia. | Risoluti R, Caprari P, Gullifa G, Massimi S, Sorrentino F, Maffei L, Materazzi S | Talanta | 2020 |
| Changing patterns in the epidemiology of β-thalassemia. | Kattamis A, Forni GL, Aydinok Y, Viprakasit V | Eur J Haematol | 2020 |
| Feasibility and preliminary outcomes of an integrated pediatric sickle cell disease and pulmonary care clinic for children with sickle cell disease. | Black LV, Ezmigna D, Wallace-Farquharson T, Wilkie DJ, Duckworth L | Pediatr Blood Cancer | 2020 |
| Adjuvant interventions with opioids for vaso-occlusive crisis in sickle cell disease: A mixed treatment network meta-analysis of randomized controlled clinical trials. | Sridharan K, Sivaramakrishnan G | J Opioid Manag | 2020 |
| Prenatal diagnosis of a rare β-thalassemia gene －90 (C>T) (HBB: c.-140 C>T) mutation associated with deletional Hb H disease (-- /-α ). | Qian H, Huang J, Xu J, Zhao W, Ye X, Liu W | Mol Genet Genomic Med | 2020 |
| MEMSID: Results From a Phase 2 Pilot Study on Memantine Treatment for Sickle Cell Disease. | Hegemann I, Sasselli C, Valeri F, Makhro A, Müller R, Bogdanova A, Manz MG, Gassmann M, Goede JS | Hemasphere | 2020 |
| Recommendations for Pregnancy in Rare Inherited Anemias. | Taher AT, Iolascon A, Matar CF, Bou-Fakhredin R, de Franceschi L, Cappellini MD, Barcellini W, Russo R, Andolfo I, Tyan P, Gulbis B, Aydinok Y, Anagnou NP, Bencaiova GA, Tamary H, Martinez PA, Forni G, Vindigni R | Hemasphere | 2020 |
| Spinal cord compression by extramedullary hematopoiesis in beta-thalassemia major. | Ben Ammar L, Ferjani H, Maatallah K, Bouallegue S, Riahi H, Kaffel D, Hamdi W | Clin Case Rep | 2020 |
| Soluble transferrin receptor level, inflammation markers, malaria, alpha-thalassemia and selenium status are the major predictors of hemoglobin in children 6-23 months in Malawi. | Gebremedhin S | Food Sci Nutr | 2020 |
| Investigation of Lipid Profile and Clinical Manifestations in SCA Children. | da Guarda CC, Yahouédéhou SCMA, Santiago RP, Fernandes CFL, Neres JSDS, Oliveira AMJ, Aleluia MM, Figueiredo CVB, Fonseca CA, Fiuza LM, Carvalho SP, de Oliveira RM, Nascimento VML, Rocha LC, Gonçalves MS | Dis Markers | 2020 |
| Pure Erythroid Leukemia in a Sickle Cell Patient Treated with Hydroxyurea. | Yadav DK, Paul T, Alhamar M, Inamdar K, Guo Y | Case Rep Oncol | 2020 |
| The Use of Music by Adolescents and Young Adults With Sickle Cell Disease. | Solodiuk JC, Jantz B, Fuller M, Osterling D, Foxman H, Grafft N, Hanser S | Creat Nurs | 2020 |
| Evaluation of electrocardiographic markers of cardiac arrhythmic events and their correlation with cardiac iron overload in patients with β-thalassemia major. | Demircan T, Onder Sivis Z, Tatlı Güneş B, Karadeniz C | Cardiol Young | 2020 |
| Integrin VLA-4 as a PET imaging biomarker of hyper-adhesion in transgenic sickle mice. | Perkins LA, Nyiranshuti L, Little-Ihrig L, Latoche JD, Day KE, Zhu Q, Tavakoli S, Sundd P, Novelli EM, Anderson CJ | Blood Adv | 2020 |
| Influence of beta-cluster haplotypes, alpha-gene status and UGTA1 polymorphism on clinical and hematological data in sickle-cell disease children from French Guiana. | Elenga N, Cuadro-Alvarez E, Martin E, Njuieyon F, Defo A, Maniassom C | PLoS One | 2020 |
| Weight Loss as an Effective Strategy to Decrease Opioid Use and Frequency of Vaso-Occlusive Crises in Patients with Sickle Cell Disease. | Babroudi S, Vesel T | J Palliat Med | 2020 |
| [Prevalence of Chronic Complications of Sickle Cell Disease at the Bobo-Dioulasso Teaching Hospital, Burkina Faso]. | Traoré C, Kyelem CG, Semdé A, Koulidiati J, Sanou AF, Bokoum S, Kafando E | Bull Soc Pathol Exot | 2020 |
| Presumed Sickle Cell Retinopathy in an Elderly Woman. | Starr MR, Patel LG, Ho AC | JAMA Ophthalmol | 2020 |
| Association Between Genetic Polymorphisms and Hb F Levels in Heterozygous β-Thalassemia 3.5 kb Deletions. | Tepakhan W, Kanjanaopas S, Srewaradachpisal K | Hemoglobin | 2020 |
| Prevalence of Transfusion Transmissible Infections in Beta-Thalassemia Major Patients in Pakistan: A Systematic Review. | Ehsan H, Wahab A, Anwer F, Iftikhar R, Yousaf MN | Cureus | 2020 |
| Effectiveness of Deferasirox in Pediatric Thalassemia Patients: Experience from a Tertiary Care Hospital of Odisha. | Panigrahi M, Swain TR, Jena RK, Panigrahi A, Debta N | Indian J Pharmacol | 2020 |
| Precise and error-prone CRISPR-directed gene editing activity in human CD34+ cells varies widely among patient samples. | Modarai SR, Kanda S, Bloh K, Opdenaker LM, Kmiec EB | Gene Ther | 2020 |
| Receptor Activator of Nuclear Factor κ-Β Ligand/Osteoprotegerin Axis in Adults with Hb S/β-Thalassemia and β-Thalassemia Trait. | Tombak A, Boztepe B, Akbayir S, Dogru G, Sungur MA | Hemoglobin | 2020 |
| Challenges in the Management of Sickle Cell Disease During SARS-CoV-2 Pandemic. | Alsayegh F, Mousa SA | Clin Appl Thromb Hemost | 2020 |
| Preserved efficiency of sickle cell disease placentas despite altered morphology and function. | Cordier AG, Bouvier AS, Vibert F, Martinovic J, Couturier-Tarrade A, Lai-Kuen R, Curis E, Fournier T, Benachi A, Peoc'H K, Gil S | Placenta | 2020 |
| When Actions Speak Louder Than Words - Racism and Sickle Cell Disease. | Power-Hays A, McGann PT | N Engl J Med | 2020 |
| The opposing roles of the mTOR signaling pathway in different phases of human umbilical cord blood-derived CD34 cell erythropoiesis. | Liu Q, Luo L, Ren C, Zou M, Yang S, Cai B, Wu L, Wang Y, Fu S, Hua X, Tang N, Huang S, Huang X, Xin W, Chen F, Zhang X | Stem Cells | 2020 |
| A | Colby JM, Shajani-Yi Z | Clin Chem | 2020 |
| An assessment of the continuing medical education needs of US physicians in the management of patients with beta thalassemia. | Stacy S, Sheth S, Coleman B, Cerenzia W | Ann Hematol | 2020 |
| Distribution of Gene Mutations in the Kurdish Population of Ilam Province, West Iran. | Moradi K, Aznab M, Tahmasebi S, Omidniakan L, Bijari N, Alibakhshi R | Hemoglobin | 2020 |
| Functional Connectivity Decreases with Metabolic Stress in Sickle Cell Disease. | Fields ME, Mirro AE, Guilliams KP, Binkley MM, Gil Diaz L, Tan J, Fellah S, Eldeniz C, Chen Y, Ford AL, Shimony JS, King AA, An H, Smyser CD, Lee JM | Ann Neurol | 2020 |
| Changing the Clinical Paradigm of Hydroxyurea Treatment for Sickle Cell Anemia Through Precision Medicine. | Dong M, McGann PT | Clin Pharmacol Ther | 2020 |
| Clinical outcomes and healthcare utilization in patients with sickle cell disease: a nationwide cohort study of Medicaid beneficiaries. | Desai RJ, Mahesri M, Globe D, Mutebi A, Bohn R, Achebe M, Levin R, Schneeweiss S | Ann Hematol | 2020 |
| The Relationship Between Sickle Cell Disease and Sudden Onset Sensorineural Deafness. | Abdelmahmuod E, Yassin MA, Ahmed M, Ali E | Cureus | 2020 |
| Gender-specific transcriptional profiles identified in β-thalassemia patients. | Nanou A, Toumpeki C, Fanis P, Bianchi N, Cosenza LC, Zuccato C, Sentis G, Giagkas G, Stephanou C, Phylactides M, Christou S, Hadjigavriel M, Sitarou M, Lederer CW, Gambari R, Kleanthous M, Katsantoni E | Haematologica | 2020 |
| Visual cortex changes in children with sickle cell disease and normal visual acuity: a multimodal magnetic resonance imaging study. | Manara R, Dalla Torre A, Lucchetta M, Ermani M, Favaro A, Baracchini C, Favaretto S, Viaro F, Munaretto V, Sartori S, Ponticorvo S, Russo AG, Biffi A, Sainati L, Colombatti R | Br J Haematol | 2020 |
| Medical marijuana certification for patients with sickle cell disease: a report of a single center experience. | Curtis SA, Lew D, Spodick J, Hendrickson JE, Minniti CP, Roberts JD | Blood Adv | 2020 |
| Outcomes following kidney transplantation in patients with sickle cell disease: The impact of automated exchange blood transfusion. | Willis JC, Awogbade M, Howard J, Breen C, Abbas A, Harber M, Shendi AM, Andrews PA, Galliford J, Thuraisingham R, Gage A, Shah S, Sharpe CC | PLoS One | 2020 |
| Fetal Heart Diameter as a Predictor of Hemoglobin Bart Disease at Midpregnancy. | Nattawongsiri C, Tongprasert F, Tongsong T | J Ultrasound Med | 2020 |
| Patient-controlled analgesia and morphine consumption in sickle cell anemia painful crises: A new protocol. | Bakır M, Rumeli Atıcı Ş, Yıldırım HU, Tiftik EN, Ünal S | Agri | 2020 |
| Influence of gender norms in relation to child's quality of care: follow-up of families of children with SCD identified through NBS in Tanzania. | Bukini D, Mbekenga C, Nkya S, Malasa L, McCurdy S, Manji K, Makani J, Parker M | J Community Genet | 2020 |
| Cell-Derived Microparticles in Blood Products from Thalassemic Blood Donors. | Noulsri E, Lerdwana S, Palasuwan D, Palasuwan A | Lab Med | 2020 |
| Physicians' and nurses' perceptions and attitudes toward sickle cell disease patients in Jazan, Saudi Arabia. | Hazzazi AA, Ageeli MH, Sharahili KA, Hamaly HM, Aqeeli MH, Altherwi TI, Bakkar M, Malhan H | Saudi Med J | 2020 |
| Incidence of sickle cell disease patients with pulmonary embolism admitted to the intensive care unit in Bahrain. | Mandeel FH, Saeed HM, Alsadah AH, Ahmed SA, Alhammam RA | Saudi Med J | 2020 |
| A Child Lost to Follow Up Carrying Beta Thalassemia Major: A Case Report. | Banjade P, Bhandari J | JNMA J Nepal Med Assoc | 2020 |
| Comparative study of nutritional status of children and adolescents with sickle cell anemia in Enugu, Southeast Nigeria. | Ukoha OM, Emodi IJ, Ikefuna AN, Obidike EO, Izuka MO, Eke CB | Niger J Clin Pract | 2020 |
| Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects. | Kanter J, Smith WR, Desai PC, Treadwell M, Andemariam B, Little J, Nugent D, Claster S, Manwani DG, Baker J, Strouse JJ, Osunkwo I, Stewart RW, King A, Shook LM, Roberts JD, Lanzkron S | Blood Adv | 2020 |
| The participation of cohabitants with sickle cell disease in health care: a bibliographic study. | Lopes WSL, Gomes R | Cien Saude Colet | 2020 |
| Association between sickle cell disease and dental caries: a systematic review and meta-analysis. | Yue H, Xu X, Liu Q, Li X, Jiang W, Hu B | Hematology | 2020 |
| Using surveillance to determine the number of individuals with sickle cell disease in California and Georgia, 2005-2016. | Aluc A, Zhou M, Paulukonis ST, Snyder AB, Wong D, Hulihan MM | Pediatr Hematol Oncol | 2020 |
| Hb broomhill [α1 or α2 114(GH2) pro > ala; or :c.343C > G]: a rare Hb variant found in a diabetic chinese individual. | Yuan Y, Zhou X, Ren Q, Ji L | Scand J Clin Lab Invest | 2020 |
| Transient Second-Degree Atrioventricular Block: A Rare Finding in Sickle Cell Crisis. | Riaz S, Sampat PJ, Dhungana R, Bhatta L | Cureus | 2020 |
| Sickle Cell Trait and Risk of Ischemic Stroke in Young Adults. | Zhang RV, Ryan KA, Lopez H, Wozniak MA, Phipps MS, Cronin CA, Cole JW, Dutta TM, Mehndiratta P, Motta M, Merino JG, Kittner SJ | Stroke | 2020 |
| Using LIBS as a diagnostic tool in pediatrics beta-thalassemia. | Alsharnoubi J, Nassef Y, Fahmy RF, Gamal M | Lasers Med Sci | 2020 |
| Acute compartment syndrome in a patient with sickle cell disease. | Cochrane E, Young S, Shariff Z | Ann R Coll Surg Engl | 2020 |
| Pain Experience, Physical Function, Pain Coping, and Catastrophizing in Children With Sickle Cell Disease Who Had Normal and Abnormal Sensory Patterns. | Hyacinth O, Machado Silva-Rodrigues F, Darezzo Rodrigues Nunes M, Carlos Lopes L, Fernandes A, Castanheira Nascimento L, Jacob E | J Pain Symptom Manage | 2020 |
| Reduction in transcranial doppler ultrasound (TCD) velocity after regular blood transfusion therapy is associated with a change in hemoglobin S fraction in sickle cell anemia. | Jordan LC, Rodeghier M, Donahue MJ, DeBaun MR | Am J Hematol | 2020 |
| Red blood cell adhesion to ICAM-1 is mediated by fibrinogen and is associated with right-to-left shunts in sickle cell disease. | Kucukal E, Man Y, Quinn E, Tewari N, An R, Ilich A, Key NS, Little JA, Gurkan UA | Blood Adv | 2020 |
| Serum albumin is independently associated with higher mortality in adult sickle cell patients: Results of three independent cohorts. | Nouraie M, Ashley-Koch AE, Garrett ME, Sritharan N, Zhang Y, Little J, Gordeuk VR, Gladwin MT, Telen MJ, Kato GJ | PLoS One | 2020 |
| SARS-CoV-2 infection in pediatric patient with hemoglobin SC disease. | Dagalakis U, Hammershaimb E, McArthur MA, Macatangay RA | Pediatr Blood Cancer | 2020 |
| A pediatric patient with sickle cell disease presenting with severe anemia and splenic sequestration in the setting of COVID-19. | Jacob S, Dworkin A, Romanos-Sirakis E | Pediatr Blood Cancer | 2020 |
| The Trabecular Bone Score as a Predictor for Thalassemia-Induced Vertebral Fractures in Northeastern Thailand. | Teawtrakul N, Chukanhom S, Charoensri S, Somboonporn C, Pongchaiyakul C | Anemia | 2020 |
| Implications of COVID-19 infections in sickle cell disease. | John NA, John JE | Pan Afr Med J | 2020 |
| Prevalence of β thalassaemia trait and Haemoglobin E disorders among students aged between 14-17yrs in Kurunegala district, Sri Lanka. | Warushahennadi R, Wanasundara DH, Priyadarshani W, Abeysekara AM, Jiffry MN | Ceylon Med J | 2020 |
| Association between BCL11A, HSB1L-MYB, and XmnI γG-158 (C/T) gene polymorphism and hemoglobin F level in Egyptian sickle cell disease patients. | El-Ghamrawy M, Yassa ME, Tousson AMS, El-Hady MA, Mikhaeil E, Mohamed NB, Khorshied MM | Ann Hematol | 2020 |
| The risk of acute events among patients with sickle cell disease in relation to early or late initiation of care at a specialist center: evidence from a retrospective cohort study. | Rankine-Mullings AE, Logan TM, King LG, Cunningham-Myrie CA, Scott CR, Knight-Madden JM | BMC Pediatr | 2020 |
| [Effects of a standardized musical intervention on the management of pain and anxiety-state of sickle-cell adolescents]. | Martin J, Le Faucheur L, Pondarré C, Carlier-Gonod A, Baeza-Velasco C | Soins Pediatr Pueric | 2020 |
| Detection of a Hb A -Melbourne (HBD: c.130G>A) combined with β-thalassemia in a Chinese individual. | Li Y, Huang T, Mao T, Zhang X, Liang L, Meng M | J Clin Lab Anal | 2020 |
| Screening for Iron Deficiency Anemia in Infants in a Thalassemia-endemic Region. | Nanta N, Natesirinilkul R, Kittisakmontri K, Chimnuan K, Manowong S, Suanta S, Charoenkwan P | J Pediatr Hematol Oncol | 2020 |
| A microfluidic computational fluid dynamics model for cellular interaction studies of sickle cell disease vaso-occlusions. | Blakely IP, Horton RE | Microvasc Res | 2020 |
| Assessment of mandibular characteristics in patients affected with β-thalassaemia major: A retrospective case-control study. | Movahhedian N, Akbarizadeh F, Khojastepour L, Sardarian AR, Pakshir HR, Ahrari F | Int Orthod | 2020 |
| [Sickle cell trait complications: A case series of 6 patients]. | Marcombes C, Lafont E, Jullien V, Flamarion E, Dion J, Costedoat-Chalumeau N, Pouchot J, Arlet JB | Rev Med Interne | 2020 |
| Impact of relative systemic hypertension on the heart in sickle cell anaemia. | Oni OO, Adebiyi AA, Aje A, Akingbola TS | Indian Heart J | 2020 |
| Intracranial and Extracranial Vascular Stenosis as Risk Factors for Stroke in Sickle Cell Disease. | Schlotman AA, Donahue MJ, Kassim AA, Lee CA, Waddle SL, Pruthi S, Davis LT, Rodeghier M, DeBaun MR, Jordan LC | Pediatr Neurol | 2020 |
| Red blood cell exchange in an emergency in sickle cell disease. | Hequet O, Fort R, Driss F | Transfus Apher Sci | 2020 |
| Bone infarct transformation into undifferentiated pleomorphic sarcoma in sickle cell disease: A case report. | Alhamdan HA, Alrifai OI, Shaheen MF, Pant R, Altayeb MA | Int J Surg Case Rep | 2020 |
| Autoimmune Liver Disease in Patients With Sickle Cell Disease. | Waisbourd-Zinman O, Frenklak R, Hakakian O, Hilmara D, Lin H | J Pediatr Hematol Oncol | 2020 |
| The carriage rates of ααα, ααα, and HKαα in the population of Guangxi, China measured using a rapid detection qPCR system to determine CNV in the α-globin gene cluster. | Long J, Liu E | Gene | 2020 |
| A roadmap for the standardization of hemoglobin A. | Mosca A, Paleari R, Harteveld CL, | Clin Chim Acta | 2020 |
| Assessment of Complement Regulatory Proteins CD55 and CD59 on Erythrocytes in Beta-Thalassemia Major Patients. | Zahran AM, Shaltout AS, Hamada IH, Mohammed AM, Abo Elgheet AM, Elsayh KI | Egypt J Immunol | 2020 |
| Global loss of Tfr2 with concomitant induced iron deficiency greatly ameliorates the phenotype of a murine thalassemia intermedia model. | Schmidt PJ, Fitzgerald K, Butler JS, Fleming MD | Am J Hematol | 2020 |
| Rapid decline in estimated glomerular filtration rate in sickle cell anemia: results of a multicenter pooled analysis. | Ataga KI, Zhou Q, Derebail VK, Saraf SL, Hankins JS, Loehr LR, Garrett ME, Ashley-Koch AE, Cai J, Telen MJ | Haematologica | 2020 |
| Co-transplantation of bone marrow-derived mesenchymal stem cells with hematopoietic stem cells does not improve transplantation outcome in class III beta-thalassemia major: A prospective cohort study with long-term follow-up. | Rostami T, Maleki N, Kasaeian A, Nikbakht M, Kiumarsi A, Asadollah Mousavi S, Ghavamzadeh A | Pediatr Transplant | 2020 |
| Evaluation of Adipokines Concentration in Iraqi Patients with Major and Minor Beta Thalassemia. | Harbi NS, Jawad AH, Alsalman FK | Rep Biochem Mol Biol | 2020 |
| Epidemiology of Thalassemia in Gulf Cooperation Council Countries: A Systematic Review. | Abu-Shaheen A, Heena H, Nofal A, Abdelmoety DA, Almatary A, Alsheef M, AlFayyad I | Biomed Res Int | 2020 |
| EF Bart's Disease with Coinheritance of G-XmnI and A-Globin Polymorphisms: A Case of Nontransfusion-Dependant Thalassemia. | Laks KM, Hirner C, Gruner B, Coberly J, Laziuk K, Sathi BK | Case Rep Hematol | 2020 |
| Spatiotemporal Alterations in Gait in Humanized Transgenic Sickle Mice. | Kiven S, Wang Y, Aich A, Argueta DA, Lei J, Sagi V, Tennakoon M, Bedros SJ, Lambrecht N, Gupta K | Front Immunol | 2020 |
| Plasma Folate Levels in Acutely Ill and Steady State Pediatric Sickle Cell Disease Patients in Ghana. | Adjei GO, Sulley AM, Goka BQ, Enweronu-Laryea C, Amponsah SK, Alifrangis M, Kurtzhals JAL | J Blood Med | 2020 |
| Clinical management of sickle cell liver disease in children and young adults. | Kyrana E, Rees D, Lacaille F, Fitzpatrick E, Davenport M, Heaton N, Height S, Samyn M, Mavilio F, Brousse V, Suddle A, Chakravorty S, Verma A, Gupte G, Velangi M, Inusa B, Drasar E, Hadzic N, Grammatikopoulos T, Hind J, Deheragoda M, Sellars M, Dhawan A | Arch Dis Child | 2020 |
| Hyperhaemolytic Syndrome in Sickle cell disease: clearing the cobwebs. | Madu AJ, Ugwu AO, Efobi C | Med Princ Pract | 2020 |
| Abnormal Ambulatory Blood Pressure and Early Renal Dysfunction in Sickle Cell Disease. | Dubey SRK, Shrivastava N, Sharma T, Bhatt GC, Dhingra B, Pakhare AP, Goel SK, Joshi D | Indian J Pediatr | 2020 |
| GBT440 Increases Hematocrit and Improves Biventricular Function in Berkeley Sickle Cell Disease Mice. | Gassner R, Schreier DA, Hacker T, Tabima DM, Chesler N | J Biomech Eng | 2020 |
| Parental stress in the relationship with children affected by chronic hematological disease. | Ribilotta A, Sergio M, Scarponi D | Minerva Pediatr | 2020 |
| COVID-19 pneumonia and pulmonary microembolism in a patient with B-thalassemia major. | Marziali M, Ribersani M, Losardo AA, Taglietti F, Pugliese P, Micozzi A, Gentile G, Angeloni A | Clin Case Rep | 2020 |
| Fat Embolism Syndrome in Sickle Cell Disease. | Tsitsikas DA, Vize J, Abukar J | J Clin Med | 2020 |
| Comparison of two vitamin D supplementation strategies in children with sickle cell disease: a randomized controlled trial. | Grégoire-Pelchat P, Pastore Y, Robitaille N, LeMay S, Khamessan A, Kleiber N, Nyalendo C, Gagné N, Alos N, Mailhot G | Br J Haematol | 2020 |
| Machine-learning algorithms for predicting hospital re-admissions in sickle cell disease. | Patel A, Gan K, Li AA, Weiss J, Nouraie M, Tayur S, Novelli EM | Br J Haematol | 2020 |
| Multimodality Treatment for Nonhealing Wound With Osteomyelitis in Sickle Cell Disease. | Kakar J | Int J Low Extrem Wounds | 2020 |
| Implementation of the therapeutic use of hydroxyurea for sickle cell disease management in resource-constrained settings: a systematic review of adoption, cost and acceptability. | Ryan N, Dike L, Ojo T, Vieira D, Nnodu O, Gyamfi J, Peprah E | BMJ Open | 2020 |
| Multiple Enlarging Masses and Failure to Thrive in Infant With Sickle Cell Trait. | Jabbour AJ, Warrier R, Kretschmar P | Clin Pediatr (Phila) | 2020 |
| GDF-15 negatively regulates excess erythropoiesis and its overexpression is involved in erythroid hyperplasia. | Ranjbaran R, Abbasi M, Rahimian E, Dehbidi GR, Seyyedi N, Zare F, Behzad-Behbahani A | Exp Cell Res | 2020 |
| Association of Exon 14 of the Gene Sequence Variations with Response to Hydroxyurea Therapy in Patients Carrying Non Transfusion-Dependent Thalassemia. | Mohammadi Z, Mohammadi R, Haghpanah S, Moghadam M, Pazhoomand R, Karimi M | Hemoglobin | 2020 |
| Transcranial Doppler Velocities among Sickle Cell Disease Patients in Steady State. | Salama K, Rady R, Hashem RH, El-Ghamrawy M | Hemoglobin | 2020 |
| Inner Ear Complications in Children and Adolescents with Sickle Cell Disease. | Tantawy AAG, Ibrahim SW, Abdel-Aziz TT, Rabie AN, Makkeyah SM, Ragab IA | Hemoglobin | 2020 |
| Cytomegalovirus and Epstein-Barr Infections: Prevalence and Impact on Patients with Hematological Diseases. | de Melo Silva J, Pinheiro-Silva R, Dhyani A, Pontes GS | Biomed Res Int | 2020 |
| Fetal heterozygosity for both Hb G-Hsi-Tsou and beta thalassemia: A case report. | Alhazidou E, Androulaki M, Panagiotopoulos M, Boudouvas D, Lampropoulou D, Yfanti E, Delaki EE, Repa K, Petrakos G | Case Rep Womens Health | 2020 |
| Red blood cell exchange in sickle cell disease patient with multiple alloantibodies. | Aggarwal G, Tiwari AK, Dhiman P, Arora D, Pabbi SM, Setya D | Asian J Transfus Sci | 2020 |
| Generation of a human iPSC line CIBi008-A from amniotic fluid-derived cells of a fetus with β-thalassemia carrying variants of -28A > G and IVS-II-654C > T in HBB. | Wu S, Wei H, Chu M, Weng Z | Stem Cell Res | 2020 |
| Editorial for: | Carr JC | J Magn Reson Imaging | 2020 |
| Clinical outcomes following bone marrow transplantation in patients with sickle cell disease: A cohort study of US Medicaid enrollees. | Mahesri M, Schneeweiss S, Globe D, Mutebi A, Bohn R, Achebe M, Levin R, Desai RJ | Eur J Haematol | 2020 |
| Delayed repair of aortic dissection in sickle cell anaemia as a combined cardiac and vascular surgical approach. | Capoccia M, Mireskandari M, Cheshire NJ, Rosendahl UP | J Saudi Heart Assoc | 2020 |
| Right ventricular functions in subphenotypes of sickle cell disease. | Youssry I, Shaltout MF, AbdelMassih AF, Ghobrial C, Nabih M, Doss R, Fouda R, El-Sisi A | J Saudi Heart Assoc | 2020 |
| Hemolysis Inhibits Humoral B Cell Responses and Modulates Alloimmunization Risk in Patients with Sickle Cell Disease. | Pal M, Bao W, Wang R, Liu Y, An X, Mitchell WB, Lobo C, Minniti CP, Shi P, Manwani D, Yazdanbakhsh K, Zhong H | Blood | 2020 |
| Trends in Sickle Cell Trait and Disease Screening in the Republic of Uganda, 2014-2019. | Hernandez AG, Kiyaga C, Howard TA, Ssewanyana I, Ndeezi G, Aceng JR, Ware RE | Trop Med Int Health | 2020 |
| NT-proBNP Levels and Cardiopulmonary Function in Children with Sickle Cell Disease. | Feld L, Fiorino EK, Aygun B, Appiah-Kubi A, Mitchell EC, Jackson S, Mehran R, Fishbein J, Santiago MT | Pediatr Pulmonol | 2020 |
| Weight status and health behaviors of adolescents and young adults with sickle cell disease: The emerging risk for obesity. | Strong H, Harry O, Westcott E, Kidwell KM, Couch SC, Peairs A, Britto MT, Crosby LE | Pediatr Hematol Oncol | 2020 |
| MTHFR C677T, Prothrombin G20210A, and Factor V Leiden (G1691A) Polymorphism and Beta-Thalassemia Risk: A Meta-Analysis. | Nigam N, Singh PK, Agrawal M, Nigam S, Gupta H, Saxena S | Cureus | 2020 |
| Development of a Severity Classification System for Sickle Cell Disease. | Shah N, Beenhouwer D, Broder MS, Bronte-Hall L, De Castro LM, Gibbs SN, Gordeuk VR, Kanter J, Klings ES, Lipato T, Manwani D, Scullin B, Yermilov I, Smith WR | Clinicoecon Outcomes Res | 2020 |
| Hydroxyurea treatment is associated with reduced degree of oxidative perturbation in children and adolescents with sickle cell anemia. | Vinhaes CL, Teixeira RS, Monteiro-Júnior JAS, Tibúrcio R, Cubillos-Angulo JM, Arriaga MB, Sabarin AG, de Souza AJ, Silva JJ, Lyra IM, Ladeia AM, Andrade BB | Sci Rep | 2020 |
| Detection of an α-Globin Fusion Gene Using Real-Time Polymerase Chain Reaction-Based Multicolor Melting Curve. | Ju AP, Jiang F, Li J, Tang XW, Li DZ | Hemoglobin | 2020 |
| Randomized controlled trial of effect of N-acetylcysteine as an antioxidant on iron overload in children with thalassemia major. | Mohamed YA, Meabed MH, Ashraf A, Morgan DS, Abdul Latif MG, Abd-Elkareem RM, Ahmed HM | Clin Exp Pediatr | 2020 |
| An Investigation of Structure-Activity Relationships of Azolylacryloyl Derivatives Yielded Potent and Long-Acting Hemoglobin Modulators for Reversing Erythrocyte Sickling. | Omar AM, Abdulmalik O, Ghatge MS, Muhammad YA, Paredes SD, El-Araby ME, Safo MK | Biomolecules | 2020 |
| Unusual Presentation of Renal Medullary Carcinoma With Undiagnosed Sickle Cell Trait. | Basher F, Dutcher G, England JS, Lopes G | Cureus | 2020 |
| DXA and pQCT derived parameters in Indian children with beta thalassemia major - A case controlled study. | Shah N, Khadilkar A, Ekbote V, Mughal Z, Gondhalekar K, Khadilkar S, Ramanan V, Khadilkar V, Padidela R | Bone | 2020 |
| Monoterpenes as therapeutic candidates to induce fetal hemoglobin synthesis and up-regulation of gamma-globin gene: An in vitro and in vivo investigation. | Iftikhar F, Khan MBN, Musharraf SG | Eur J Pharmacol | 2020 |
| Priapism in Sickle Cell Trait With High Sensitivity to Multiple Psychotropic Medications. | Satodiya R, Yacoub A | J Clin Psychopharmacol | 2020 |
| Adherence to Quality of Care Indicators and Location of Sickle Cell Care Within Indiana. | Meier ER, Janson IA, Hampton K, Bloom E, Duncan N, Roberson C, Rampersad A | J Community Health | 2020 |
| Keys to Recruiting and Retaining Seriously Ill African Americans With Sickle Cell Disease in Longitudinal Studies: Respectful Engagement and Persistence. | Suarez ML, Schlaeger JM, Angulo V, Shuey DA, Carrasco J, Roach KL, Ezenwa MO, Yao Y, Wang ZJ, Molokie RE, Wilkie DJ | Am J Hosp Palliat Care | 2020 |
| Acute Care Utilization at End of Life in Sickle Cell Disease: Highlighting the Need for a Palliative Approach. | Johnston EE, Adesina OO, Alvarez E, Amato H, Paulukonis S, Nichols A, Chamberlain LJ, Bhatia S | J Palliat Med | 2020 |
| GDF11 contributes to hepatic hepcidin (HAMP) inhibition through SMURF1-mediated BMP-SMAD signalling suppression. | Fang Z, Zhu Z, Zhang H, Peng Y, Liu J, Lu H, Li J, Liang L, Xia S, Wang Q, Fu B, Wu K, Zhang L, Ginzburg Y, Liu J, Chen H | Br. J. Haematol. | 2020 |
| Retinal Thickness and Microvascular Changes in Children With Sickle Cell Disease Evaluated by Optical Coherence Tomography (OCT) and OCT Angiography. | Ong SS, Linz MO, Li X, Liu TYA, Han IC, Scott AW | Am. J. Ophthalmol. | 2020 |
| Perioperative care of children with sickle cell disease: A systematic review and clinical recommendations. | Schyrr F, Dolci M, Nydegger M, Canellini G, Andreu-Ullrich H, Joseph JM, Diezi M, Cachat F, Rizzi M, Renella R | Am. J. Hematol. | 2020 |
| Neuropathic pain in individuals with sickle cell disease. | Sharma D, Brandow AM | Neurosci. Lett. | 2020 |
| Delta beta thalassemia. | Bain BJ | Am. J. Hematol. | 2020 |
| Evidence for interactions between inflammatory markers and renin-angiotensin system molecules in the occurrence of albuminuria in children with sickle cell anemia. | Belisário AR, Vieira ÉLM, de Almeida JA, Mendes FG, Miranda AS, Rezende PV, Viana MB, Simões E Silva AC | Cytokine | 2020 |
| Multicenter Evaluation of HemoTypeSC as a Point-of-Care Sickle Cell Disease Rapid Diagnostic Test for Newborns and Adults Across India. | Mukherjee MB, Colah RB, Mehta PR, Shinde N, Jain D, Desai S, Dave K, Italia Y, Raicha B, Serrao E | Am. J. Clin. Pathol. | 2020 |
| Recent advances in screening and diagnosis of hemoglobinopathy. | Ghosh K, Ghosh K, Agrawal R, Nadkarni AH | Expert Rev Hematol | 2020 |
| Quantification of whole-brain oxygenation extraction fraction and cerebral metabolic rate of oxygen consumption in adults with sickle cell anemia using individual T -based oxygenation calibrations. | Li W, Xu X, Liu P, Strouse JJ, Casella JF, Lu H, van Zijl PCM, Qin Q | Magn Reson Med | 2020 |
| Sickle Cell Intrahepatic Cholestasis with Acute Liver Failure and Acute Kidney Injury: Favourable Outcome with Exchange Transfusion. | Maji P, Malik R, Lodha R, Bagga A | Indian J Pediatr | 2020 |
| Platelet Extracellular Vesicles Drive Inflammasome-IL-1β-Dependent Lung Injury in Sickle Cell Disease. | Vats R, Brzoska T, Bennewitz MF, Jimenez MA, Pradhan-Sundd T, Tutuncuoglu E, Jonassaint J, Gutierrez E, Watkins SC, Shiva S, Scott MJ, Morelli AE, Neal MD, Kato GJ, Gladwin MT, Sundd P | Am. J. Respir. Crit. Care Med. | 2020 |
| Shedding New Light on Platelet Extracellular Vesicles in Sickle Cell Disease. | Middleton EA, Ware LB, Rondina MT | Am. J. Respir. Crit. Care Med. | 2020 |
| Retinal oximetry and fractal analysis of capillary maps in sickle cell disease patients and matched healthy volunteers. | Birkhoff WAJ, van Manen L, Dijkstra J, De Kam ML, van Meurs JC, Cohen AF | Graefes Arch. Clin. Exp. Ophthalmol. | 2020 |
| A QST-based Pain Phenotype in Adults With Sickle Cell Disease: Sensitivity and Specificity of Quality Descriptors. | Dyal BW, Ezenwa MO, Yoon SL, Fillingim RB, Yao Y, Schlaeger JM, Suarez ML, Wang ZJ, Molokie RE, Wilkie DJ | Pain Pract | 2020 |
| Curating the gnomAD database: Report of novel variants in the globin-coding genes and bioinformatics analysis. | Scheps KG, Hasenahuer MA, Parisi G, Targovnik HM, Fornasari MS | Hum. Mutat. | 2020 |
| Dengue in hospitalized children with sickle cell disease: A retrospective cohort study in the French departments of America. | Elenga N, Celicourt D, Muanza B, Elana G, Hocquelet S, Tarer V, Maillard F, Sibille G, Divialle Doumdo L, Petras M, Tressières B, Etienne-Julan M | J Infect Public Health | 2020 |
| Induction of Translational Readthrough across the Thalassemia-Causing Premature Stop Codon in β-Globin-Encoding mRNA. | Kar D, Sellamuthu K, Kumar SD, Eswarappa SM | Biochemistry | 2020 |
| Universal screening for social determinants of health in pediatric sickle cell disease: A quality-improvement initiative. | Power-Hays A, Li S, Mensah A, Sobota A | Pediatr Blood Cancer | 2020 |
| Erythrocyte Indices as Differential Diagnostic Biomarkers of Iron Deficiency Anemia and Thalassemia. | Düzenli Kar Y, Özdemir ZC, Emir B, Bör Ö | J. Pediatr. Hematol. Oncol. | 2020 |
| Evaluation of Efficacy, Safety, and Satisfaction Taking Deferasirox Twice Daily Versus Once Daily in Patients With Transfusion-Dependent Thalassemia. | Karimi M, Haghpanah S, Bahoush G, Ansari S, Azarkeivan A, Shahsavani A, Bazrafshan A, Jangjou A | J. Pediatr. Hematol. Oncol. | 2020 |
| Improved Titer and Gene Transfer by Lentiviral Vectors Using Novel, Small β-Globin Locus Control Region Elements. | Morgan RA, Unti MJ, Aleshe B, Brown D, Osborne KS, Koziol C, Ayoub PG, Smith OB, O'Brien R, Tam C, Miyahira E, Ruiz M, Quintos JP, Senadheera S, Hollis RP, Kohn DB | Mol. Ther. | 2020 |
| Thalassemia: Common Clinical Queries in Management. | Lal A, Bansal D | Indian J Pediatr | 2020 |
| Innovations in Targeted Anti-Adhesion Treatment for Sickle Cell Disease. | Kanter J, Lanzkron S | Clin. Pharmacol. Ther. | 2020 |
| Management of cesarean delivery in a parturient with sickle cell disease. | Romano D, Craig H, Katz D | Int J Obstet Anesth | 2020 |
| Generation of an in vitro model of β-thalassemia using the CRISPR/Cas9 genome editing system. | Ajami M, Atashi A, Kaviani S, Kiani J, Soleimani M | J. Cell. Biochem. | 2020 |
| Improvement in processing speed following haploidentical bone marrow transplant with posttransplant cytoxan in children and adolescents with sickle cell disease. | Prussien KV, Patel DA, Wilkerson K, Armstrong B, Karnik L, de la Fuente J, Kassim AA | Pediatr Blood Cancer | 2020 |
| Opioid treatment for acute and chronic pain in patients with sickle cell disease. | Carroll CP | Neurosci. Lett. | 2020 |
| Methodological aspects of the oxygenscan in sickle cell disease: A need for standardization. | Rab MAE, Kanne CK, Bos J, Boisson C, van Oirschot BA, Nader E, Renoux C, Joly P, Fort R, van Beers EJ, Sheehan VA, van Wijk R, Connes P | Am. J. Hematol. | 2020 |
| Intima-media thickness of the common carotid arteries as a marker of retinopathy and nephropathy in sickle cell disease. | Ayoola OO, Bolarinwa RA, Onakpoya OH, Onigbinde SO, Asaleye CM, Odedeyi AA | Ultrasonography | 2020 |
| Hereditary xerocytosis - spectrum and clinical manifestations of variants in the PIEZO1 gene, including co-occurrence with a novel β-globin mutation. | Maciak K, Adamowicz-Salach A, Siwicka A, Poznanski J, Urasinski T, Plochocka D, Gora M, Burzynska B | Blood Cells Mol. Dis. | 2020 |
| Polymorphisms in genes that affect the variation of lipid levels in a Brazilian pediatric population with sickle cell disease: rs662799 APOA5 and rs964184 ZPR1. | Valente-Frossard TNS, Cruz NRC, Ferreira FO, Belisario AR, Pereira BM, Gomides AFF, Resende GAD, Carlos AM, Moraes-Souza H, Velloso-Rodrigues C | Blood Cells Mol. Dis. | 2020 |
| Prevalence and predictive factors of splenic sequestration crisis among 423 pediatric patients with sickle cell disease in Tunisia. | Ben Khaled M, Ouederni M, Mankai Y, Rekaya S, Ben Fraj I, Dhouib N, Kouki R, Mellouli F, Bejaoui M | Blood Cells Mol. Dis. | 2020 |
| Pattern of Renal Blood Flow and Renovascular Parameters in Adult Patients With Sickle Cell Disease. | Asbeutah AM, Adekile A, AlMajran AA, Asbeutah AAA, Naief AA, Al-Jafar H | J Ultrasound Med | 2020 |
| Management of age-associated medical complications in patients with β-thalassemia. | Motta I, Mancarella M, Marcon A, Vicenzi M, Cappellini MD | Expert Rev Hematol | 2020 |
| Prenatal diagnosis of α- and β-thalassemias in southern Thailand. | Nopparatana C, Nopparatana C, Saechan V, Karnchanaopas S, Srewaradachpisal K | Int. J. Hematol. | 2020 |
| Mouse models in hematopoietic stem cell gene therapy and genome editing. | Radtke S, Humbert O, Kiem HP | Biochem. Pharmacol. | 2020 |
| Regulators' Advice Can Make a Difference: European Medicines Agency Approval of Zynteglo for Beta Thalassemia. | Schuessler-Lenz M, Enzmann H, Vamvakas S | Clin. Pharmacol. Ther. | 2020 |
| Co-inheritance of alpha globin gene deletion lowering serum iron level in female beta thalassemia patients. | AbdulAzeez S, Almandil NB, Naserullah ZA, Al-Jarrash S, Al-Suliman AM, ElFakharay HI, Borgio JF | Mol. Biol. Rep. | 2020 |
| Effect of photodynamic therapy on gingival inflammation in patients with thalassemia. | Al Asmari D, Khan MK | Photodiagnosis Photodyn Ther | 2020 |
| Improving the justice-based argument for conducting human gene editing research to cure sickle cell disease. | Chan B | Bioethics | 2020 |
| Molecular basis of Hb H and AEBart's diseases in the Lao People's Democratic Republic. | Singha K, Srivorakun H, Fucharoen G, Fucharoen S | Int J Lab Hematol | 2020 |
| Intestinal pathophysiological and microbial changes in sickle cell disease: Potential targets for therapeutic intervention. | Dutta D, Aujla A, Knoll BM, Lim SH | Br. J. Haematol. | 2020 |
| Sickle cell disease subjects and mouse models have elevated nitrite and cGMP levels in blood compartments. | Almeida LEF, Kamimura S, de Souza Batista CM, Spornick N, Nettleton MY, Walek E, Smith ML, Finkel JC, Darbari DS, Wakim P, Quezado ZMN | Nitric Oxide | 2020 |
| Cold External Temperatures and Sickle Cell Morbidity in Children: A Retrospective Analysis. | Wachnian C, Tompkins N, Corriveau-Bourque C, Belletrutti M, Bruce AAK | J. Pediatr. Hematol. Oncol. | 2020 |
| New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level. | Chaouch L, Sellami H, Kalai M, Darragi I, Boudrigua I, Chaouachi D, Abbes S, Mnif S | J. Pediatr. Hematol. Oncol. | 2020 |
| The Adolescent and Caregiver Sickle Cell Disease Self-management Skills Checklist: Preliminary Reliability and Validity. | Loew M, Williams JL, Russell K, Rupff R, Hankins JS, Porter J | J. Pediatr. Hematol. Oncol. | 2020 |
| Inpatient Ordering of Home Hydroxyurea by Residents for Hospitalized Patients With Sickle Cell Disease. | Shaw R, Kappa S, Nickel RS | J. Pediatr. Hematol. Oncol. | 2020 |
| HbE-Beta Thalassemia with Moyamoya Syndrome: A Rare Association. | Agrawal A, Bhinder OS, Mishra D, Juneja M | Indian J Pediatr | 2020 |
| Craniofacial Deformities in Patients With Beta-Thalassemia: Orthodontic Versus Surgical Correction-A Systematic Review. | Einy S, Ben-Barak A, Kridin K, Aizenbud D | J. Pediatr. Hematol. Oncol. | 2020 |
| Evaluation of Ocular Complications by Using Optical Coherence Tomography in Children With Sickle Cell Disease Eye Findings in Children With Sickle Cell Disease. | Vatansever E, Vatansever M, Dinç E, Temel GÖ, Ünal S | J. Pediatr. Hematol. Oncol. | 2020 |
| Emerging drugs in randomized controlled trials for sickle cell disease: are we on the brink of a new era in research and treatment? | Matte A, Cappellini MD, Iolascon A, Enrica F, De Franceschi L | Expert Opin Investig Drugs | 2020 |
| 50 Years Ago in TheJournal ofPediatrics: A New Diagnostic Test for Hemoglobin S. | Ross LF | J. Pediatr. | 2020 |
| Electrophoresis features and genotypes of Hb bart's hydrops fetalis. | Li Y, Liang L, Tian M, Qing T, Wu X | Scand. J. Clin. Lab. Invest. | 2020 |
| A Sickle Cell Crisis in a Blood Culture Bottle. | Kamada K, Matsuda T, Konno S, Oka H | Intern. Med. | 2020 |
| Practice patterns for stroke prevention using transcranial Doppler in sickle cell anemia: DISPLACE Consortium. | Schlenz AM, Phillips S, Mueller M, Melvin C, Adams RJ, Kanter J, | Pediatr Blood Cancer | 2020 |
| Sex differences in the trajectory of glomerular filtration rate in pediatric and murine sickle cell anemia. | Kasztan M, Aban I, Hande SP, Pollock DM, Lebensburger JD | Blood Adv | 2020 |
| Consumption of a green tea extract-curcumin drink decreases blood urea nitrogen and redox iron in β-thalassemia patients. | Koonyosying P, Tantiworawit A, Hantrakool S, Utama-Ang N, Cresswell M, Fucharoen S, Porter JB, Srichairatanakool S | Food Funct | 2020 |
| [Research advances in transplantation for thalassemia major]. | Huang CW, Jiang H | Zhongguo Dang Dai Er Ke Za Zhi | 2020 |
| Blood rheology biomarkers in sickle cell disease. | Lu M, Rab MA, Shevkoplyas SS, Sheehan VA | Exp. Biol. Med. (Maywood) | 2020 |
| Proteomic Studies for the Investigation of γ-Globin Induction by Decitabine in Human Primary Erythroid Progenitor Cultures. | Theodorou A, Phylactides M, Katsantoni E, Vougas K, Garbis SD, Fanis P, Sitarou M, Thein SL, Kleanthous M | J Clin Med | 2020 |
| One-Fifth of Children with Sickle Cell Anemia Show Exercise-Induced Hemoglobin Desaturation: Rate of Perceived Exertion and Role of Blood Rheology. | Brousse V, Pondarre C, Arnaud C, Kamden A, de Montalembert M, Boutonnat-Faucher B, Bourdeau H, Charlot K, Grévent D, Verlhac S, da Costa L, Connes P | J Clin Med | 2020 |
| Correction: Determining Glomerular Filtration Rate in Homozygous Sickle Cell Disease: Utility of Serum Creatinine Based Estimating Equations. | | PLoS ONE | 2020 |
| Characterization and identification of Hb Bart's hydrops fetalis caused by a compound heterozygous mutation -- /-- , a novel α -thalassemia deletion. | Ruengdit C, Panyasai S, Kunyanone N, Phornsiricharoenphant W, Ngamphiw C, Tongsima S, Sripichai O, Pissard S, Pornprasert S | Int J Lab Hematol | 2020 |
| Effect of Hydroxyurea Treatment on the Inflammatory Markers Among Children With Sickle Cell Disease. | Zahran AM, Nafady A, Saad K, Hetta HF, Abdallah AM, Abdel-Aziz SM, Embaby MM, Abo Elgheet AM, Darwish SF, Abo-Elela MGM, Elhoufey A, Elsayh KI | Clin. Appl. Thromb. Hemost. | 2020 |
| Blood transfusions for treating acute chest syndrome in people with sickle cell disease. | Dolatkhah R, Dastgiri S | Cochrane Database Syst Rev | 2020 |
| The HLA-DRB1*11 group-specific allele is a predictor for alloantibody production in the transfusion-dependent thalassemia patients. | Ebrahimi M, Maleknia M, Parav N, Mohammadi MB, Mortazavi Y, Saki N, Rahim F | Transfus. Apher. Sci. | 2020 |
| Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population. | Noor FA, Sultana N, Bhuyan GS, Islam MT, Hossain M, Sarker SK, Islam K, Khan WA, Rahman M, Qadri SK, Shekhar HU, Qadri F, Qadri SS, Mannoor K | Orphanet J Rare Dis | 2020 |
| A Novel β-Thalassemia Mutation [IVS-I-6 (T>G), : c.92+6T>G] in a Chinese Family. | Luo H, Zou Y, Liu Y | Hemoglobin | 2020 |
| Luspatercept: First Approval. | Markham A | Drugs | 2020 |
| Alpha-Thalassemia Carrier due to -α3.7 Deletion: Not So Silent. | Gilad O, Steinberg-Shemer O, Dgany O, Krasnov T, Noy-Lotan S, Tamary H, Yacobovich J | Acta Haematol. | 2020 |
| The History of Deferiprone (L1) and the Paradigm of the Complete Treatment of Iron Overload in Thalassaemia. | Kontoghiorghes GJ, Kleanthous M, Kontoghiorghe CN | Mediterr J Hematol Infect Dis | 2020 |
| The Evolving Pharmacotherapeutic Landscape for the Treatment of Sickle Cell Disease. | Ballas SK | Mediterr J Hematol Infect Dis | 2020 |
| A Concise Review on the Frequency, Major Risk Factors and Surveillance of Hepatocellular Carcinoma (HCC) in β-Thalassemias: Past, Present and Future Perspectives and the ICET-A Experience. | De Sanctis V, Soliman AT, Daar S, Alansary N, Kattamis A, Skafida M, Galati MC, Christou S, Campisi S, Messina G, Yassin MA, Canatan D, Di Maio S, Al Jaouni S, Raiola G, Karimi M, Kaleva V, Kakkar S, Mariannis D, Kattamis C | Mediterr J Hematol Infect Dis | 2020 |
| Diagnosis and Prenatal Diagnosis in a Chinese Family Carrying the Rare α-Thalassemia Gene : c.1A>G Mutation. | Chen X, Luo S, Huang J, Yuan D, Yan T, Cai R, Tang N | Hemoglobin | 2020 |
| Variable Phenotypic Presentation of Two Siblings with Hemoglobin SD Disease. | Aggarwal P, Jain A, Mishra OP, Gupta V | Indian J Pediatr | 2020 |
| The relationship between frequency and severity of vaso-occlusive crises and health-related quality of life and work productivity in adults with sickle cell disease. | Rizio AA, Bhor M, Lin X, McCausland KL, White MK, Paulose J, Nandal S, Halloway RI, Bronté-Hall L | Qual Life Res | 2020 |
| Corrigendum to | Shmukler BE, Rivera A, Bhargava P, Nishimura K, Hsu A, Kim EH, Trudel M, Rust MB, Hubner CA, Brugnara C, Alper SL | Blood Cells Mol. Dis. | 2020 |
| Comparison Between Three Molecular Diagnostics for the Identification of Heterozygous Hemoglobin E. | Arif AA, An-Nizamiya AD, Putri C, Nashrurrokhman M, Husna N, Mulyati , Hadisusanto S, Handayani NSN | Pak. J. Biol. Sci. | 2020 |
| Compound heterozygosity of a silent beta-thalassemia mutation at the 3'-untranslated region (HBB: c.*132 C>T) and beta-zero thalassemia results in thalassemia intermedia. | Sripusanapan A, Phusua A, Fanhchaksai K, Charoenkwan P | Pediatr Blood Cancer | 2020 |
| Sickle Cell Disease: A Primer for Primary Care Providers. | Kimrey S, Saving KL | Pediatr Ann | 2020 |
| Body Composition in Egyptian Children With Transfusion-dependent Thalassemia: The Impact of Nutrition and Metabolic Profile. | Elalfy MS, Ebeid FSE, El Gendy YG, Zaki MM, Kalifa ASA | J. Pediatr. Hematol. Oncol. | 2020 |
| Hydroxyurea for ALL children with sickle cell anemia: What can we learn from Africa? | Aygun B | Pediatr Blood Cancer | 2020 |
| Treating sickle cell anemia: A new era dawns. | Steinberg MH | Am. J. Hematol. | 2020 |
| Rifaximin on intestinally-related pathologic changes in sickle cell disease. | Dutta D, Li K, Methe B, Lim SH | Am. J. Hematol. | 2020 |
| [Hematological and genotypic features of 100 patients with hemoglobin E disorders from Yunnan Province]. | Yang J, Wang H, Zhang Z, Qian Y, Zhang L, Lu L, Wang K | Zhonghua Yi Xue Yi Chuan Xue Za Zhi | 2020 |
| Haptoglobin genotype predicts severe acute vaso-occlusive pain episodes in children with sickle cell anemia. | Willen SM, McNeil JB, Rodeghier M, Kerchberger VE, Shaver CM, Bastarache JA, Steinberg MH, DeBaun MR, Ware LB | Am. J. Hematol. | 2020 |
| Innate immune cells, major protagonists of sickle cell disease pathophysiology. | Allali S, Maciel TT, Hermine O, de Montalembert M | Haematologica | 2020 |
| Mortality in children with sickle cell disease in mainland France from 2000 to 2015. | Desselas E, Thuret I, Kaguelidou F, Benkerrou M, de Montalembert M, Odièvre MH, Lesprit E, Rumpler E, Fontanet A, Pondarre C, Brousse V | Haematologica | 2020 |
| Headache in beta-thalassemia: An Italian multicenter clinical, conventional MRI and MR-angiography case-control study. | Tartaglione I, Caiazza M, Di Concilio R, Ciancio A, De Michele E, Maietta C, Valentino MS, Russo C, Roberti D, Casale M, Elefante A, Femina G, Esposito F, Ponticorvo S, Russo AG, Canna A, Ermani M, Cirillo M, Perrotta S, Manara R | Blood Cells Mol. Dis. | 2020 |
| Transfusion-transmitted hepatitis C: A cluster of cases in transfusion-dependent thalassaemia patients in Sri Lanka. | Perera S, Bonsall D, Niriella MA, Allen A, Peries AC, Nelumdeniya UB, Dissanayake R, Silva I, de Cesare M, Klenerman P, Weatherall DJ, Roberts DJ, Premawardhena AP | Transfus Med | 2020 |
| Performance of ICD-10-CM diagnosis codes for identifying children with Sickle Cell Anemia. | Reeves SL, Madden B, Wu M, Miller LS, Anders D, Caggana M, Cogan LW, Kleyn M, Hurden I, Freed GL, Dombkowski KJ | Health Serv Res | 2020 |
| The role of hydroxyurea in decreasing the occurrence of vasso-occulusive crisis in pediatric patients with sickle cell disease at King Saud Medical City in Riyadh, Saudi Arabia. | Azmet FR, Al-Kasim F, Alashram WM, Siddique K | Saudi Med J | 2020 |
| A Japanese Family with the Unstable Hb Sydney (: c.203T>C) Variant and Persistent Low Hemoglobin Oxygen Saturation. | Sakamoto A, Nakadate H, Tada K, Yamashiro Y, Ishiguro A | Hemoglobin | 2020 |
| Reactivation of γ-globin expression through Cas9 or base editor to treat β-hemoglobinopathies. | Wang L, Li L, Ma Y, Hu H, Li Q, Yang Y, Liu W, Yin S, Li W, Fu B, Kurita R, Nakamura Y, Liu M, Lai Y, Li D | Cell Res. | 2020 |
| New Option for Sickle Cell Disease. | Voelker R | JAMA | 2020 |
| Web-Based Technology to Improve Disease Knowledge Among Adolescents With Sickle Cell Disease: Pilot Study. | Saulsberry AC, Hodges JR, Cole A, Porter JS, Hankins J | JMIR Pediatr Parent | 2020 |
| Iron Overload Associated Endocrine Dysfunction Leading to Lower Bone Mineral Density in Thalassemia Major. | Yang WP, Chang HH, Li HY, Lai YC, Huang TY, Tsai KS, Lin KH, Lin DT, Jou ST, Lu MY, Yang YL, Chou SW, Shih SR | J. Clin. Endocrinol. Metab. | 2020 |
| Sickle cell disease celebration. | Mullard A | Nat Rev Drug Discov | 2020 |
| Sickle-Cell Disease Co-Management, Health Care Utilization, and Hydroxyurea Use. | Crego N, Douglas C, Bonnabeau E, Earls M, Eason K, Merwin E, Rains G, Tanabe P, Shah N | J Am Board Fam Med | 2020 |
| Alpha and beta-Thalassemia mutations in Hubei area of China. | Zhu Y, Shen N, Wang X, Xiao J, Lu Y | BMC Med. Genet. | 2020 |
| World Health Organization's Growth Reference Overestimates the Prevalence of Severe Malnutrition in Children with Sickle Cell Anemia in Africa. | Ghafuri DL, Abdullahi SU, Jibir BW, Gambo S, Bello-Manga H, Haliru L, Bulama K, Usman FM, Gambo A, Aliyu MH, Greene BC, Kassim AA, Slaughter C, Rodeghier M, DeBaun MR | J Clin Med | 2020 |
| Sickle cell disease in Germany: Early insights from a national registry. | Odame I | Pediatr Blood Cancer | 2020 |
| Genotype/Phenotype Correlation of β-Thalassemia in Syrian Patients: A Cross-Sectional Study. | Shoujaa A, Moasses F, Mukhalalaty Y, Murad H, Al-Quobaili F | Hemoglobin | 2020 |
| Optical coherence tomography angiography findings in young β-thalassemia patients. | Güler Kazancı E, Korkmaz MF, Can ME | Eur J Ophthalmol | 2020 |
| Decreased erythrocyte binding of Siglec-9 increases neutrophil activation in sickle cell disease. | Kiser ZM, Lizcano A, Nguyen J, Becker GL, Belcher JD, Varki AP, Vercellotti GM | Blood Cells Mol. Dis. | 2020 |
| Sharpening the Molecular Scissors: Advances in Gene-Editing Technology. | Broeders M, Herrero-Hernandez P, Ernst MPT, van der Ploeg AT, Pijnappel WWMP | iScience | 2020 |
| Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central Iran. | Sajadpour Z, Amini-Farsani Z, Motovali-Bashi M, Yadollahi M, Khosravi-Farsani N | Hemoglobin | 2020 |
| Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α-thalassemia by targeted next-generation sequencing. | Li Z, Shang X, Luo S, Zhu F, Wei X, Zhou W, Ye Y, Yan T, Cai R, Xu X | Mol. Genet. Genomics | 2020 |
| Immunization Adherence in Children With Sickle Cell Disease: A Single-Institution Experience. | Infanti LM, Elder JJ, Franco K, Simms S, Statler VA, Raj A | J Pediatr Pharmacol Ther | 2020 |
| Alpha-hemoglobin-stabilizing protein (AHSP): a modulatory factor in β-thalassemia. | Che Yaacob NS, Islam MA, Alsaleh H, Ibrahim IK, Hassan R | Int. J. Hematol. | 2020 |
| Assessment of health-related quality of life among adults hospitalized with sickle cell disease vaso-occlusive crisis. | Esham KS, Rodday AM, Smith HP, Noubary F, Weidner RA, Buchsbaum RJ, Parsons SK | Blood Adv | 2020 |
| Expression analysis data of BCL11A and γ-globin genes in KU812 and KG-1 cell lines after CRISPR/Cas9-mediated BCL11A enhancer deletion. | Khosravi MA, Abbasalipour M, Concordet JP, Berg JV, Zeinali S, Arashkia A, Buch T, Karimipoor M | Data Brief | 2020 |
| Cd60 (GTG > GAG)/Hb Cagliari mutation was found in scanning of β-thalassemia alleles from patients of East Kalimantan, Indonesia. | Susanto Z, Siswandari W, Rujito L | Mol Genet Metab Rep | 2020 |
| 5-(Hydroxymethyl)furfural restores low-oxygen rheology of sickle trait blood in vitro. | Hansen S, Wood DK, Higgins JM | Br. J. Haematol. | 2020 |
| Increased ferritin levels in non-transfusion-dependent β°-thalassaemia/HbE are associated with reduced CXCR2 expression and neutrophil migration. | Thiengtavor C, Siriworadetkun S, Paiboonsukwong K, Fucharoen S, Pattanapanyasat K, Vadolas J, Svasti S, Chaichompoo P | Br. J. Haematol. | 2020 |
| Derivation of human embryonic stem cell line MUSIe001-A from an embryo with homozygous α-thalassemia (SEA deletion). | Laowtammathron C, Chingsuwanrote P, Choavaratana R, Phornwilardsiri S, Sitthirit K, Kaewjunun C, Makemaharn O, Terbto P, Waeteekul S, Lorthongpanich C, U-Pratya Y, Srisook P, Kheolamai P, Issaragrisil S | Stem Cell Res | 2020 |
| Emerging point-of-care technologies for sickle cell disease diagnostics. | Ilyas S, Simonson AE, Asghar W | Clin. Chim. Acta | 2020 |
| Urinary cross-linked carboxyterminal telopeptide, a bone resorption marker, decreases after vaso-occlusive crises in adults with sickle cell disease. | Adesina OO, Jenkins IC, Wu QV, Fung EB, Narla RR, Lipkin EW, Mahajan K, Konkle BA, Kruse-Jarres R | Blood Cells Mol. Dis. | 2020 |
| Renal Functional Decline in Sickle Cell Disease and Trait. | Nath KA, Vercellotti GM | J. Am. Soc. Nephrol. | 2020 |
| Combined use of gap-PCR and next-generation sequencing improves thalassaemia carrier screening among premarital adults in China. | Zhao J, Li J, Lai Q, Yu Y | J. Clin. Pathol. | 2020 |
| Study of Iron Status in Sickle cell disorder. | Varshney P | J Assoc Physicians India | 2020 |
| Sickle cell disease (SCD) causing cirrhosis presenting as Acute on Chronic Liver Failure(ACLF) due to viral hepatitis. | Yellapu V, Mohanty AP, Mohanty L, Yellapu V | J Assoc Physicians India | 2020 |
| Insulin resistance in transfusion dependent adult beta thalassemia major subjects with metabolic syndrome. | Pasricha N, Aggarwal R, Jain SK, Prakash A, Jain A | J Assoc Physicians India | 2020 |
| Primary Hyperparathyroidism in Sickle Cell Disease: An Unknown Complication of the Disease in Adulthood. | Denoix E, Bomahou C, Clavier L, Ribeil JA, Lionnet F, Bartolucci P, Courbebaisse M, Pouchot J, Arlet JB | J Clin Med | 2020 |
| Thrombin activation of PAR-1 contributes to microvascular stasis in mouse models of sickle cell disease. | Sparkenbaugh EM, Chen C, Brzoska T, Nguyen J, Wang S, Vercellotti GM, Key NS, Sundd P, Belcher JD, Pawlinski R | Blood | 2020 |
| Incidental Findings of Sickle Cell Trait From an Everyday Diabetes Test: Should General Health Care Providers and Testing Centers Report, Retest, or Refer? | Cronin de Chavez A, Atkin KM, Babbington F, Berghs MJ, Dyson SM, Miller A, Whitelaw DC | Clin Diabetes | 2020 |
| Splenic function is not maintained long-term after partial splenectomy in children with sickle cell disease. | El-Gohary Y, Khan S, Hodgman E, Wynn L, Kimble A, Abdelhafeez A, Talbot L, Wang W, Davidoff AM, Murphy AJ | J. Pediatr. Surg. | 2020 |
| Cardiovascular changes in children with sickle cell crisis. | Onalo R, Cooper P, Cilliers A, Nnebe-Agumadu U | Cardiol Young | 2020 |
| An Unusual Compound Heterozygosity for Hb O-Arab (: c.364G>A) and Hb D-Los Angeles (: c.364G>C). | van Gammeren AJ, Pelkmans L, Endschot CCWV, Roelofsen-de Beer RJAC, Harteveld CL | Hemoglobin | 2020 |
| Screening Readthrough Compounds to Suppress Nonsense Mutations: Possible Application to β-Thalassemia. | Borgatti M, Altamura E, Salvatori F, D'Aversa E, Altamura N | J Clin Med | 2020 |
| Evaluation of the effectiveness of prophylactic oral vitamin D (cholecalciferol) in children with sickle cell disease. | Garrido C, Bardón-Cancho EJ, Fajardo-Sánchez VLÁ, Cascón-Pérez-Teijón ME, García-Morín M, Cela E, | Bone | 2020 |
| Comparison of liver MRI R2(FerriScan®) VS liver MRI T2* as a measure of body iron load in a cohort of beta thalassaemia major patients. | Padeniya P, Siriwardana S, Ediriweera D, Samarasinghe N, Silva S, Silva I, Ahamed N, Niriella M, Premawardhena A | Orphanet J Rare Dis | 2020 |
| Correlates of Cognitive Function in Sickle Cell Disease: A Meta-Analysis. | Prussien KV, Siciliano RE, Ciriegio AE, Anderson AS, Sathanayagam R, DeBaun MR, Jordan LC, Compas BE | J Pediatr Psychol | 2020 |
| P-selectin-deficient mice to study pathophysiology of sickle cell disease. | Bennewitz MF, Tutuncuoglu E, Gudapati S, Brzoska T, Watkins SC, Monga SP, Pradhan-Sundd T, Sundd P | Blood Adv | 2020 |
| Prevalence and Risk Factors for Microalbuminuria in Children with Sickle Cell Disease at King Abdulaziz University Hospital: A Retrospective Cross-sectional Study. | Alzahrani YA, Algarni MA, Alnashri MM, AlSayyad HM, Aljahdali KM, Alead JE, Alhjrsy YA, Alzahrani F, Safdar O | Cureus | 2020 |
| Pharmacy hydroxyurea education materials for patients with sickle cell disease: An environmental scan and assessment of accuracy. | Cervi A, Diamantouros A, Azzam M, Lane SJ, Sapru H, Verhovsek M | Pediatr Blood Cancer | 2020 |
| Hyperuricemia is associated with a lower glomerular filtration rate in pediatric sickle cell disease patients. | Kaspar CDW, Beach I, Newlin J, Sisler I, Feig D, Smith W | Pediatr. Nephrol. | 2020 |
| Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation. | Basak A, Munschauer M, Lareau CA, Montbleau KE, Ulirsch JC, Hartigan CR, Schenone M, Lian J, Wang Y, Huang Y, Wu X, Gehrke L, Rice CM, An X, Christou HA, Mohandas N, Carr SA, Chen JJ, Orkin SH, Lander ES, Sankaran VG | Nat. Genet. | 2020 |
| Asymptomatic intracranial aneurysms in beta-thalassemia: a three-year follow-up report. | Manara R, Caiazza M, Di Concilio R, Ciancio A, De Michele E, Maietta C, Capalbo D, Russo C, Roberti D, Casale M, Elefante A, Esposito F, Ponticorvo S, Russo AG, Canna A, Cirillo M, Perrotta S, Tartaglione I | Orphanet J Rare Dis | 2020 |
| Aura and mental stress are associated with reports of pain in sickle cell disease-a pilot study using a mobile application. | Espinoza J, Shah P, Veluswamy S, Zeltzer L, Khoo MCK, Coates TD, Baskin J | Am. J. Hematol. | 2020 |
| Now I Am The Voice: | Hadjidemetriou M | Am. J. Hematol. | 2020 |
| Malnutrition, Its Attributes, and Impact on Quality of Life: An Epidemiological Study among β-Thalassemia Major Children. | Biswas B, Naskar NN, Basu K, Dasgupta A, Basu R, Paul B | Korean J Fam Med | 2020 |
| Prevalence of endocrine complications in transfusion dependent thalassemia in Hospital Pulau Pinang: A pilot study. | Lee KT, Lim SL, Goh AS | Med. J. Malaysia | 2020 |
| Zinc supplementation improves glucose homeostasis in patients with β-thalassemia major complicated with diabetes mellitus: A randomized controlled trial. | Matter RM, Elbarbary NS, Ismail EAR, Darwish YW, Nada AS, Banoub VP | Nutrition | 2020 |
| Goal-Oriented Monitoring of Cyclosporine Is Effective for Graft-versus-Host Disease Prevention after Hematopoietic Stem Cell Transplantation in Sickle Cell Disease and Thalassemia Major. | Gauthier A, Bleyzac N, Garnier N, Kebaili K, Joly P, Goutagny MP, Mollet I, Goutelle S, Renard C, Bertrand Y | Biol. Blood Marrow Transplant. | 2020 |
| Usefulness of azacitidine therapy in a sickle cell disease patient with myelodysplastic syndrome. | De Luna G, Darnige L, Roueff S, Peyrard T, Pouchot J, Arlet JB | Ann. Hematol. | 2020 |
| Pulmonary dysfunction among adolescents and adults with sickle cell disease in Nigeria: Implications for monitoring. | Al-Mendalawi MD | Ann Thorac Med | 2020 |
| Whole genome sequence-based haplotypes reveal a single origin of the 1393 bp deletion. | Wang X, Xu JZ, Conrey A, Mendelsohn L, Shriner D, Pirooznia M, Thein SL | J. Med. Genet. | 2020 |
| Nondeletional α-Thalassemia: Two New Mutations on the α2 Gene. | Ropero P, Arbeteta J, Nieto JM, González FA, González B, Villegas A, Benavente C | Hemoglobin | 2020 |
| Reproductive health issues in female patients with beta-thalassaemia major: a narrative literature review. | Nourollahpour Shiadeh M, Cassinerio E, Modarres M, Zareiyan A, Hamzehgardeshi Z, Behboodi Moghadam Z | J Obstet Gynaecol | 2020 |
| Sickle cell disease: A distinction of two most frequent genotypes (HbSS and HbSC). | da Guarda CC, Yahouédéhou SCMA, Santiago RP, Neres JSDS, Fernandes CFL, Aleluia MM, Figueiredo CVB, Fiuza LM, Carvalho SP, Oliveira RM, Fonseca CA, Ndidi US, Nascimento VML, Rocha LC, Goncalves MS | PLoS ONE | 2020 |
| Perinatal Management of Bart's Hemoglobinopathy: Paradoxical Effects of Intrauterine, Transplacental, and Partial Exchange Transfusions. | Curran M, Mikhael M, Sun WD, Lim J, Leung A, Morchi G, Chmait RH | AJP Rep | 2020 |
| Patients With Sickle Cell Disease Between Ages 0 and 20 Years Presenting With Acute Chest Syndrome in the United States. | Ramphul K, Mejias SG, Joynauth J | J. Pediatr. Hematol. Oncol. | 2020 |
| Gene therapy in sickle cell disease: Possible utility and impact. | Curtis SA, Shah NC | Cleve Clin J Med | 2020 |
| Sickle cell disease: A primary care update. | Onimoe G, Rotz S | Cleve Clin J Med | 2020 |
| Complement activation in sickle cell disease: Dependence on cell density, hemolysis and modulation by hydroxyurea therapy. | Roumenina LT, Chadebech P, Bodivit G, Vieira-Martins P, Grunenwald A, Boudhabhay I, Poillerat V, Pakdaman S, Kiger L, Jouard A, Audureau E, Pirenne F, Galactéros F, Frémeaux-Bacchi V, Bartolucci P | Am. J. Hematol. | 2020 |
| Development of gene editing strategies for human β-globin (HBB) gene mutations. | Kalkan BM, Kala EY, Yuce M, Karadag Alpaslan M, Kocabas F | Gene | 2020 |
| American Society of Hematology 2020 guidelines for sickle cell disease: transfusion support | Chou ST, Alsawas M, Fasano RM, Field JJ, Hendrickson JE, Howard J, Kameka M, Kwiatkowski JL, Pirenne F, Shi PA, Stowell SR, Thein SL, Westhoff CM, Wong TE, Akl EA. | Blood Adv | 2020 |
| First Detection of Hb Cenxi [β46(CD5)Gly→Arg (GG>GG), : c.139G>C] by Capillary Electrophoresis. | Li YQ, Li YW, Liang L, Meng MH, Zhang XQ | Hemoglobin | 2020 |
| Hb F-Wentzville [γ24(B6)Gly→Glu; : c.74G>A, p.Gly25Glu]: An Unstable γ-Globin Variant Associated with Neonatal Hemolytic Anemia. | Semkiu KM, Oliveira JL, Nguyen PL, Porter TR, Wilson DB | Hemoglobin | 2020 |
| L-glutamine for sickle cell disease: Knight or pawn? | Sadaf A, Quinn CT | Exp. Biol. Med. (Maywood) | 2020 |
| Evaluation of regulatory T cells frequency and FoxP3/GDF-15 gene expression in β-thalassemia major patients with and without alloantibody; correlation with serum ferritin and folate levels. | Shokrgozar N, Amirian N, Ranjbaran R, Bazrafshan A, Sharifzadeh S | Ann. Hematol. | 2020 |
| False positive testing for sickle hemoglobin in a blood donor with mild erythrocytosis and hemoglobin Geldrop St. Anna. | Dunseth CD, Schlueter AJ, Knudson CM | Transfus. Apher. Sci. | 2020 |
| Distribution of sickle cell disease and assessment of risk factors based on transcranial Doppler values in the Gulf region. | Wali Y, Kini V, Yassin MA | Hematology | 2020 |
| Systemo-pulmonary shunting and acute chest syndrome in a patient with SC sickle-cell disease. | Schlemmer F, Gellen-Dautremer J, Carette MF, de Prost N, Spagnolo S, Deux JF, Fartoukh M, Naccache JM, Habibi A, Mahevas M, Bartolucci P, Mekontso Dessap A, Maitre B | Respir Med Res | 2020 |
| Discrimination of β-thalassemia and iron deficiency anemia through extreme learning machine and regularized extreme learning machine based decision support system. | Çil B, Ayyıldız H, Tuncer T | Med. Hypotheses | 2020 |
| Ghana takes on sickle-cell disease. | Adepoju P | Lancet | 2020 |
| Biallelic correction of sickle cell disease-derived induced pluripotent stem cells (iPSCs) confirmed at the protein level through serum-free iPS-sac/erythroid differentiation. | Haro-Mora JJ, Uchida N, Demirci S, Wang Q, Zou J, Tisdale JF | Stem Cells Transl Med | 2020 |
| Curative options for sickle cell disease: haploidentical stem cell transplantation or gene therapy? | Leonard A, Tisdale J, Abraham A | Br. J. Haematol. | 2020 |
| Epidemiology and Predictors of all-cause 30-Day readmission in patients with sickle cell crisis. | Kumar V, Chaudhary N, Achebe MM | Sci Rep | 2020 |
| haemoglobin sabine masquerading as double heterozygosity for HbQ-India and β-thalassemia trait: first report from South Asia. | Jamwal M, Kaur J, Chhabra S, Trehan A, Sharma P, Das R | J. Clin. Pathol. | 2020 |
| Relation Between Cardiac T2* Values and Electrocardiographic Parameters in Children With Transfusion-dependent Thalassemia. | Aggarwal P, Kumar I, Jain A, Verma A, Gupta V | J. Pediatr. Hematol. Oncol. | 2020 |
| Liver Stiffness Measurement by Vibration Controlled Transient Elastography Does Not Correlate to Hepatic Iron Overload in Children With Sickle Cell Disease. | Costa P, Rudolph B, Kogan-Liberman D, Manwani D, Silver EJ, Ovchinsky N | J. Pediatr. Hematol. Oncol. | 2020 |
| Coinheritance of Triplicated Alpha-Globin Gene and Beta-Thalassemia Mutations in Adulthood: Ten Years of Referrals in Northern Greece. | Theodoridou S, Balassopoulou A, Boutou E, Delaki EE, Yfanti E, Vyzantiadis TA, Vetsiou E, Voskaridou E, Vlachaki E | J. Pediatr. Hematol. Oncol. | 2020 |
| The effect of Islamic semanticism on self-reporting and lifestyles of mothers of adolescents with thalassemia. | Yolme ABS, Hojjati H, Akhoundzadeh G | Int J Adolesc Med Health | 2020 |
| Investigating the suitability of high-resolution mass spectrometry for newborn screening: identification of hemoglobinopathies and β-thalassemias in dried blood spots. | Wiesinger T, Mechtler T, Schwarz M, Xie X, Grosse R, Nieves Cobos P, Kasper D, Lukacs Z | Clin. Chem. Lab. Med. | 2020 |
| Correlates of hopelessness in clinically stable nigerian adults with sickle cell disease. | Aloba O, Eyiolawi D | Niger J Clin Pract | 2020 |
| [Coexistence of sickle cell disease and systemic lupus erythematosus]. | Christiaens C, Florkin B, Philippet P | Rev Med Liege | 2020 |
| Regulation of iron homeostasis through the erythroferrone-hepcidin axis in sickle cell disease. | Mangaonkar AA, Thawer F, Son J, Ajebo G, Xu H, Barrett NJ, Wells LG, Bowman L, Clair B, Patel N, Bora P, Jung G, Nemeth E, Kutlar A | Br. J. Haematol. | 2020 |
| Acute kidney injury in paediatric patients with sickle cell disease is associated with increased morbidity and resource utilization. | McCormick M, Richardson T, Warady BA, Novelli EM, Kalpatthi R | Br. J. Haematol. | 2020 |
| Knowledge, Experiences and Coping Mechanisms for Priapism among Persons with Sickle Cell Disease in Ibadan, Nigeria. | Raji OH, Shokunbi WA, Ajuwon AJ | West Afr J Med | 2020 |
| Hemolytic transfusion reactions in sickle cell disease: underappreciated and potentially fatal. | Thein SL, Pirenne F, Fasano RM, Habibi A, Bartolucci P, Chonat S, Hendrickson JE, Stowell SR | Haematologica | 2020 |
| Hemolytic anemia due to the unstable hemoglobin Wien: manifestations and long-term course in the largest pedigree identified to date. | Hilbert S, Voill-Glaninger A, Höller B, Minkov M | Haematologica | 2020 |
| Understanding sickle cell disease: impact of surveillance and gaps in knowledge. | Kaur M, Brown M, Love TW, Thompson A, Treadwell M, Smith-Whitley K | Blood Adv | 2020 |
| [Application Value of Capillary Electrophoresis in Screeningβ-Thalassemia of Children]. | Ren ZM, Li CG, Xu G, Huang J, Lin ZH, Luo MZ, Chen SY, Chen YS | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2020 |
| Can PROMIS domains of pain and physical functioning detect changes in health over time for children with sickle cell disease? | Singh A, Dasgupta M, Simpson PM, Brousseau DC, Panepinto JA | Pediatr Blood Cancer | 2020 |
| Two novel polymorphic forms of iron-chelating agent deferiprone. | Rajendrakumar S, Durga ASVS, Nanubolu JB, Balasubramanian S | Acta Crystallogr C Struct Chem | 2020 |
| Total hip arthroplasty: Concerns and precautions in sickle-cell trait. | Pisanu F, Pes M, Caggiari G, Ortu S, Satta ML, Amorese V, Doria C | J Orthop | 2020 |
| Level of agreement between adolescents' self-assessment and parent proxy report of health-related quality of life in adolescents with sickle cell disease. | Blake A, Guthrie-Dixon N, Grindley M, Barton-Gooden A, Knight-Madden J, Asnani M | Pediatr Blood Cancer | 2020 |
| Endocrinopathies complicating transfusion-dependent hemoglobinopathy. | Al-Agha AE, Bawahab NS, Nagadi SA, Alghamdi SA, Felemban DA, Milyani AA | Saudi Med J | 2020 |
| Comparison of efficacy of packed red blood cell transfusion based on its hemoglobin content versus the standard transfusion practice in thalassemia major patients (HEMOCON study). | Raja A, Jain A, Marwaha N, Trehan A | Transfus. Apher. Sci. | 2020 |
| α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region. | Al-Riyami AZ, Daar S, Kindi SA, Madhani AA, Wali Y, Rawahi MA, Zadjali SA | Hemoglobin | 2020 |
| Atypical Retro Internal Limiting Membrane Haemorrhage in Homozygous Sickle Cell Disease. | Voide N, Mantel I, Ambresin A | Klin Monbl Augenheilkd | 2020 |
| Cerebral Revascularization for Moyamoya Syndrome Associated with Sickle Cell Disease: A Systematic Review of the Literature on the Role of Extracranial-Intracranial Bypass in Treating Neurologic Manifestations of Pediatric Patients with Sickle Cell Disease. | Terrell D, Savardekar AR, Whipple SG, Dossani RH, Spetzler RF, Sun H | World Neurosurg | 2020 |
| Reticulocyte hemoglobin content. | Ogawa C, Tsuchiya K, Maeda K | Clin. Chim. Acta | 2020 |
| Prevalence of spp. Infection in Patients with Sickle Cell Disease. | Soares TCB, Isaias GAB, Almeida AR, Drummond MR, da Silva MN, Lania BG, Vieira-Damiani G, Saad STO, Ericson ME, Gupta K, Velho PENF | Vector Borne Zoonotic Dis. | 2020 |
| Ocular Manifestations of Sickle Cell Disease: Signs, Symptoms and Complications. | AlRyalat SA, Nawaiseh M, Aladwan B, Roto A, Alessa Z, Al-Omar A | Ophthalmic Epidemiol | 2020 |
| An Evaluation of Bone Health Parameters in Regularly Transfused Beta-Thalassemia Major Patients. | Kothimira VK, Kumar A, Richhele LR, Sood N, Gulati A | J. Pediatr. Hematol. Oncol. | 2020 |
| The Adverse Impact of Thalassemia Major on Adolescents' Oral Health-related Quality of Life. | Ebeid FSE, Khan NIH | J. Pediatr. Hematol. Oncol. | 2020 |
| Wrist Joint Skeletal Changes in Children With Transfusion-Dependent Thalassemia. | Dhawan P, Kanojia RK, Chandra J, Kumar A, Anand R, Gupta S | J Pediatr Orthop | 2020 |
| Hemolysis and Fetal Fraction in Cell-Free DNA Blood Collection Tubes for Noninvasive Prenatal Testing. | Stokowski R, White K, Hacker C, Doshi J, Schmid M | Mol Diagn Ther | 2020 |
| Safe and efficient peripheral blood stem cell collection in patients with sickle cell disease using plerixafor. | Uchida N, Leonard A, Stroncek D, Panch SR, West K, Molloy E, Hughes TE, Hauffe S, Taylor T, Fitzhugh C, Hankins JS, Wilson M, Sharma A, Tsai SQ, Weiss MJ, Hsieh M, Tisdale JF | Haematologica | 2020 |
| A New Indicator Derived From Reticulocyte Hemoglobin Content for Screening Iron Deficiency in an Area Prevalent for Thalassemia. | Jamnok J, Sanchaisuriya K, Chaitriphop C, Sanchaisuriya P, Fucharoen G, Fucharoen S | Lab Med | 2020 |
| Hemoglobins F, A , and E levels in Laotian children aged 6-23 months with Hb E disorders: Effect of age, sex, and thalassemia types. | Kingchaiyaphum B, Sanchaisuriya K, Fucharoen G, Chaibunruang A, Hess SY, Hinnouho GM, Barffour MA, Wessells KR, Kounnavong S, Fucharoen S | Int J Lab Hematol | 2020 |
| Laparoscopic cholecystectomy in children with sickle cell disease: A simple modified technique. | Al Hindi S, Al Aradi H, Mubarak M | Asian J Endosc Surg | 2020 |
| Peptide Nucleic Acids and Gene Editing: Perspectives on Structure and Repair. | Economos NG, Oyaghire S, Quijano E, Ricciardi AS, Saltzman WM, Glazer PM | Molecules | 2020 |
| Psychological morbidity among children with transfusion dependent β-thalassaemia and their parents in Sri Lanka. | Mettananda S, Peiris R, Pathiraja H, Chandradasa M, Bandara D, de Silva U, Mettananda C, Premawardhena A | PLoS ONE | 2020 |
| Dapagliflozin Suppresses Hepcidin And Increases Erythropoiesis. | Ghanim H, Abuaysheh S, Hejna J, Green K, Batra M, Makdissi A, Chaudhuri A, Dandona P | J. Clin. Endocrinol. Metab. | 2020 |
| The problems in evaluation of sleep disordered breathing in adults with sickle cell disease. | Roizenblatt S, Togeiro SMGP, Cabanas-Pedro AC, Figueredo MS | Sleep Med. | 2020 |
| Fever Management in Sickle Cell Disease in Low- and Middle-Income Countries: A Survey of SCD Management Programs. | Coria AL, Taylor CM, Tubman VN | Am. J. Trop. Med. Hyg. | 2020 |
| Hemopexin deficiency promotes acute kidney injury in sickle cell disease. | Ofori-Acquah SF, Hazra R, Orikogbo OO, Crosby D, Flage B, Ackah EB, Lenhart D, Tan RJ, Vitturi DA, Paintsil V, Owusu-Dabo E, Ghosh S, | Blood | 2020 |
| Prevalence of 3.7 and 4.2 deletions in Sudanese patients with red cells hypochromia and microcytosis. | Osman HA, Hamid MMA, Ahmad RB, Saleem M, Abdallah SA | BMC Res Notes | 2020 |
| Clinical Impact of Warmed Intravenous Saline in Sickle Cell Patients With Vasoocclusive Episodes. | Quarrie RP, Stoner MJ, Choueiki JM, Bonsu BK, Cohen DM | Pediatr Emerg Care | 2020 |
| Use of deferoxamine (DFO) in transfusion-dependent β-thalassemia during pregnancy: A retrospective study. | Piccioni MG, Capone C, Vena F, Del Negro V, Schiavi MC, D'Ambrosio V, Giancotti A, Smacchia MP, Brunelli R | Taiwan J Obstet Gynecol | 2020 |
| Impact of a paediatric-adult care transition programme on the health status of patients with sickle cell disease: study protocol for a randomised controlled trial (the DREPADO trial). | Hoegy D, Bleyzac N, Gauthier-Vasserot A, Cannas G, Denis A, Hot A, Bertrand Y, Occelli P, Touzet S, Dussart C, Janoly-Dumenil A, | Trials | 2020 |
| Addressing social determinants of health in sickle cell disease: The role of Medicaid policy. | Raphael JL | Pediatr Blood Cancer | 2020 |
| Pediatric Hematologists Report Infrequent Prognosis Discussions in the Routine Care of Children with Sickle Cell Disease. | Pecker LH, Silver EJ, Roth M, Manwani D | J Health Care Poor Underserved | 2020 |
| Engaging Individuals with Sickle Cell Disease in Patient-Centered Outcomes Research: A Community Health Ambassador Training Model. | Mayo-Gamble TL, Murry VM, Cunningham-Erves J, Cronin RM, Lari N, Gorden A, Scott L, DeBaun MR, Thompson T | J Health Care Poor Underserved | 2020 |
| The planimetric Grothoff's criteria by cardiac magnetic resonance can improve the specificity of left ventricular non-compaction diagnosis in thalassemia intermedia. | Macaione F, Meloni A, Positano V, Pistoia L, Barison A, Di Lisi D, Spasiano A, Campisi S, Spiga A, Righi R, Novo G, Novo S, Pepe A | Int J Cardiovasc Imaging | 2020 |
| Less 'reds' more 'blues': hemoglobin level and depression in non-transfusion-dependent thalassemia. | Mihailescu AM, Musallam KM, Cappellini MD, Taher AT | Ann. Hematol. | 2020 |
| Lack of knowledge and misperceptions about thalassaemia among college students in Bangladesh: a cross-sectional baseline study. | Hossain MS, Hasan MM, Raheem E, Islam MS, Al Mosabbir A, Petrou M, Telfer P, Siddiqee MH | Orphanet J Rare Dis | 2020 |
| A pilot study to screen for poor academic performance in children with sickle cell disease in the outpatient setting. | Karkoska K, Zaheer S, Chen V, Fishbein J, Appiah-Kubi A, Aygun B | Pediatr Blood Cancer | 2020 |
| Prevalence and risk factors for albuminuria and glomerular hyperfiltration in a large cohort of children with sickle cell anemia. | Belisário AR, de Almeida JA, Mendes FG, da Silva DMM, Planes W, Rezende PV, Silva CM, Brito AC, Sales RR, Viana MB, Simões E Silva AC | Am. J. Hematol. | 2020 |
| Two New Drugs for Sickle Cell Disease. | Aschenbrenner DS | Am J Nurs | 2020 |
| Molecular Heterogeneity of β-Thalassemia in the Kohat Region, Khyber Pakhtunkhwa Province, Pakistan. | Naz S, Rehman SU, Shakeel M, Rehman H, Hussain M, Haider A | Hemoglobin | 2020 |
| Increased Bone Marrow F-Choline Uptake in a Patient with Hepatocellular Carcinoma and Thalassemia Intermedia | Filippi L | Mol Imaging Radionucl Ther | 2020 |
| Corrigendum to | Valente-Frossard TNS, Cruz NRC, Ferreira FO, Belisario AR, Pereira BM, de Freitas Gomides AF, Resende GAD, Carlos AM, Moraes-Souza H, Velloso-Rodrigues C | Blood Cells Mol. Dis. | 2020 |
| Genetic polymorphisms of HbE/beta thalassemia related to clinical presentation: implications for clinical diversity. | Azman NF, Abdullah WZ, Hanafi S, Diana R, Bahar R, Johan MF, Zilfalil BA, Hassan R | Ann. Hematol. | 2020 |
| α-Thalassemia Mutations in Ilam Province, West Iran. | Moradi K, Aznab M, Azimi A, Biglari M, Shafieenia S, Alibakhshi R | Hemoglobin | 2020 |
| Microcytic anemia in children: parallel screening for iron deficiency and thalassemia provides a useful opportunity for thalassemia prevention in low- and middle-income countries. | Mettananda S, Paranamana S, Fernando R, Suranjan M, Rodrigo R, Perera L, Vipulaguna T, Fernando P, Fernando M, Dayanath BKTP, Costa Y, Premawardhena A | Pediatr Hematol Oncol | 2020 |
| Hemoglobin F mitigation of sickle cell complications decreases with aging. | Tolu SS, Reyes-Gil M, Ogu UO, Thomas M, Bouhassira EE, Minniti CP | Am. J. Hematol. | 2020 |
| The association of psychiatric comorbidities with emergency visits and hospitalisations in adult sickle-cell patients: a cohort study. | Fayand A, Dzierzynski N, Georgin-Lavialle S, Bachmeyer C, Mattioni S, Stankovic-Stojanovic K, Lionnet F, Steichen O | Br. J. Haematol. | 2020 |
| Students' knowledge on sickle cell disease in Kisangani, Democratic Republic of the Congo. | Kambale-Kombi P, Marini Djang'eing'a R, Alworong'a Opara JP, Tonen-Wolyec S, Kayembe Tshilumba C, Batina-Agasa S | Hematology | 2020 |
| Two Rare Pathogenic Variants in a Patient with β-Thalassemia Intermedia | Hançer VS, Fışgın T, Büyükdoğan M | Turk J Haematol | 2020 |
| Association of polymorphisms in the HBG1-HBD intergenic region with HbF levels. | Hu L, Huang L, Han Y, Jin T, Liu J, Jiang M, Liu X, Li Y, Han W, An B, Huang S | J. Clin. Lab. Anal. | 2020 |
| Effects of the dual sodium-glucose linked transporter inhibitor, licogliflozin vs placebo or empagliflozin in patients with type 2 diabetes and heart failure. | de Boer RA, Núñez J, Kozlovski P, Wang Y, Proot P, Keefe D | Br J Clin Pharmacol | 2020 |
| Recent insight on improving the iron chelation efficacy of deferasirox by adjuvant therapy in transfusion dependent beta thalassemia children with sluggish response. | Hamed EM, Meabed MH, Hussein RRS, Aly UF | Expert Opin Drug Metab Toxicol | 2020 |
| Characteristics and outcomes of osteomyelitis in children with sickle cell disease: A 10-year single-center experience. | Weisman JK, Nickel RS, Darbari DS, Hanisch BR, Diab YA | Pediatr Blood Cancer | 2020 |
| Reproductive intentions in mothers of young children with sickle cell disease. | Schultz CL, Tchume-Johnson T, Jackson T, Enninful-Eghan H, Schapira MM, Smith-Whitley K | Pediatr Blood Cancer | 2020 |
| Antioxidant Activity and Oxidative Stress Status in Maternal Serum of β-thalassemic Mothers Carrying β-thalassemic Major and Normal Fetuses. | Fazal Y, Zohaib M, Hashim Z, Ansari SH, Zarina S | Fetal Pediatr Pathol | 2020 |
| Pregnancy in sickle cell trait: what we do and don't know. | Wilson S, Ellsworth P, Key NS | Br. J. Haematol. | 2020 |
| Clinical Utility of Confirmatory Genetic Testing to Differentiate Sickle Cell Trait from Sickle-β-Thalassemia by Newborn Screening. | Shook LM, Haygood D, Quinn CT | Int J Neonatal Screen | 2020 |
| Prospective CMR Survey in Children With Thalassemia Major: Insights From a National Network. | Pepe A, Meloni A, Filosa A, Pistoia L, Borsellino Z, D'Ascola DG, Lisi R, Putti MC, Allò M, Gamberini MR, Quarta A, Fidone C, Casini T, Restaino G, Midiri M, Mangione M, Positano V, Casale M | JACC Cardiovasc Imaging | 2020 |
| Beta thalassemia major and Noonan syndrome - Two genetic disorders manifest in the blood film. | Tseu B, Siow W, Pushkaran B, Cheesebrough B, Bain BJ | Am. J. Hematol. | 2020 |
| Cerebral Infarcts and Vasculopathy in Tanzanian Children With Sickle Cell Anemia. | Jacob M, Saunders DE, Sangeda RZ, Ahmed M, Tutuba H, Kussaga F, Musa B, Mmbando B, Slee AE, Kawadler JM, Makani J, Kirkham FJ | Pediatr. Neurol. | 2020 |
| Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China. | Jiang F, Zuo L, Li D, Li J, Tang X, Chen G, Zhou J, Lu H, Liao C | BMC Med. Genet. | 2020 |
| Clinical and hematological features among β-thalassemia major patients in Jazan region: A hospital-based study. | Khawaji MM, Hazzazi AA, Ageeli MH, Mawkili YH, Darbashi AH, Abo Kathiyah AMA, Humedi RA | J Family Med Prim Care | 2020 |
| Association of hemoglobinosis D-Punjab and β-thalassemia in a Moroccan family. | Saoud MZ, Biaz A, Rachid A, El Amin G, Dami A, Ouzzif Z | Ann. Biol. Clin. (Paris) | 2020 |
| Bleeding in patients with sickle cell disease: a population-based study. | Hariharan N, Brunson A, Mahajan A, Keegan THM, Wun T | Blood Adv | 2020 |
| High bias and low precision for estimated versus measured glomerular filtration rate in pediatric sickle cell anemia. | Lebensburger JD, Gossett J, Zahr R, Wang WC, Ataga KI, Estepp JH, Kang G, Hankins JS | Haematologica | 2020 |
| The Coup-TFII orphan nuclear receptor is an activator of the γ-globin gene. | Fugazza C, Barbarani G, Elangovan S, Marini MG, Giolitto S, Font-Monclus I, Marongiu MF, Manunza L, Strouboulis J, Cantù C, Gasparri F, Barabino SML, Nakamura Y, Ottolenghi S, Moi P, Ronchi AE | Haematologica | 2020 |
| Response to | Ayache M, Strohl KP | Sleep Med. | 2020 |
| Association between hydroxycarbamide exposure and neurocognitive function in adolescents with sickle cell disease. | Partanen M, Kang G, Wang WC, Krull K, King AA, Schreiber JE, Porter JS, Hodges J, Hankins JS, Jacola LM | Br. J. Haematol. | 2020 |
| Attention difficulties are associated with lower engagement in adult care amongst youth with sickle cell disease. | Ali JS, Andrasik F, Berlin KS, Porter J, Hankins J, Anderson S, Schreiber JE | Br. J. Haematol. | 2020 |
| Changes in Mean Corpuscular Volume and RBC Distribution Width Predict Erythrocyte Engraftment Following ABO-Incompatible Hematopoietic Stem Cell Transplantation. | Sanford K, Case N, Blake B, Michaud T, McPherson RA, Roseff SD | Am. J. Clin. Pathol. | 2020 |
| Preimplantation genetic testing with HLA matching: from counseling to birth and beyond. | De Rycke M, De Vos A, Belva F, Berckmoes V, Bonduelle M, Buysse A, Keymolen K, Liebaers I, Nekkebroeck J, Verdyck P, Verpoest W | J. Hum. Genet. | 2020 |
| Improved health care utilization and costs in transplanted versus non-transplanted adults with sickle cell disease. | Saraf SL, Ghimire K, Patel P, Sweiss K, Gowhari M, Molokie RE, Gordeuk VR, Rondelli D | PLoS ONE | 2020 |
| A novel non-invasive prenatal sickle cell disease test for all at-risk pregnancies. | van Campen J, Silcock L, Yau S, Daniel Y, Ahn JW, Ogilvie C, Mann K, Oteng-Ntim E | Br. J. Haematol. | 2020 |
| Cognitive deficit in sickle cell disease: Is hydroxyurea part of the story? | Hyacinth HI, Idris IM | Br. J. Haematol. | 2020 |
| Editing a γ-globin repressor binding site restores fetal hemoglobin synthesis and corrects the sickle cell disease phenotype. | Weber L, Frati G, Felix T, Hardouin G, Casini A, Wollenschlaeger C, Meneghini V, Masson C, De Cian A, Chalumeau A, Mavilio F, Amendola M, Andre-Schmutz I, Cereseto A, El Nemer W, Concordet JP, Giovannangeli C, Cavazzana M, Miccio A | Sci Adv | 2020 |
| Profound Presentation of Retinopathy in a Patient with Sickle Cell Trait and Diabetes Mellitus. | Vangipuarm G, Saraf SS, Zhang Q, Wang R, Rezaei KA | J Ophthalmic Vis Res | 2020 |
| The Effect of Serum Ferritin Level on Gonadal, Prolactin, Thyroid Hormones, and Thyroid Stimulating Hormone in Adult Males with Sickle Cell Anemia. | Mostafa GG, Zahran FE, Omer SA, Ibrahim A, Elhakeem H | J Blood Med | 2020 |
| [Sickle cell retinopathy in children: Report of 42 cases]. | Saadouli D, Yahyaoui S, Ben Issa S, Ben Mansour K, Alaya N, Loukil I, Sammoud A, El Afrit MA | J Fr Ophtalmol | 2020 |
| Atypical presentation of acute post-infectious glomerulonephritis in patients with sickle cell disease: report of two cases. | de Menezes Neves PDM, Reichert BV, Bridi RA, Yu L, Dias CB, Pinheiro RBB, de Abreu Testagrossa L, Cavalcante LB, Malheiros DMAC, Jorge LB, Woronik V | BMC Nephrol | 2020 |
| ERFE regulation in sickle cell disease: complex but promising. | Girelli D, Busti F | Br. J. Haematol. | 2020 |
| Prevalence of Hemoglobinopathies (β-Thalassemia and Sickle Cell Trait) in the Adult Population of Al Majma'ah, Saudi Arabia. | Mir SA, Alshehri BM, Alaidarous M, Banawas SS, Dukhyil AAAB, Alturki MK | Hemoglobin | 2020 |
| Sickle Cell Disease is Associated with Increased Morbidity, Resource Utilization, and Readmissions after Common Abdominal Surgeries: A Multistate Analysis, 2007-2014. | Brumm J, White RS, Arroyo NS, Gaber-Baylis LK, Gupta S, Turnbull ZA, Mehta N | J Natl Med Assoc | 2020 |
| Correlation of lipid peroxidation and nitric oxide metabolites, trace elements, and antioxidant enzymes in patients with sickle cell disease. | Antwi-Boasiako C, Dankwah GB, Aryee R, Hayfron-Benjamin C, Aboagye G, Campbell AD | J. Clin. Lab. Anal. | 2020 |
| The association between vitamin D deficiency and hospitalization outcomes in pediatric patients with sickle cell disease. | Brown B, Long K, Agdere L, Kulpa J, Zarzoso-Fernandez S, Choudhary D, Sundarum R | Blood Cells Mol. Dis. | 2020 |
| When basic science reaches into rational therapeutic design: from historical to novel leads for the treatment of β-globinopathies. | Andrieu-Soler C, Soler E | Curr. Opin. Hematol. | 2020 |
| Small molecule therapeutics to treat the β-globinopathies. | Yu L, Myers G, Engel JD | Curr. Opin. Hematol. | 2020 |
| Oxidative stress assessment in sickle cell anemia patients treated with hydroxyurea. | Renó CO, Barbosa AR, de Carvalho SS, Pinheiro MB, Rios DR, Cortes VF, Barbosa LA, Santos HL | Ann. Hematol. | 2020 |
| Treating sickle cell anemia. | Tisdale JF, Thein SL, Eaton WA | Science | 2020 |
| Genetic epidemiology of beta-thalassemia in the Maldives: 23 years of a beta-thalassemia screening program. | Mustafa I, Firdous N, Shebl FM, Shi Z, Saeed M, Zahir Z, Zayed H | Gene | 2020 |
| Phenylethanolamine -methyltransferase gene polymorphisms associate with crisis pain in sickle cell disease patients. | Sadhu N, Jhun EH, Posen A, Yao Y, He Y, Molokie RE, Wilkie DJ, Wang ZJ | Pharmacogenomics | 2020 |
| Indicators of male fertility potential in adult patients with beta-thalassemia major: a comparative study between patients undergone allogeneic stem cell transplantation and transfusion-dependent patients. | Rostami T, Mohammadifard MA, Ansari S, Kiumarsi A, Maleki N, Kasaeian A, Aghamahdi F, Rad S, Ghavamzadeh A | Fertil Res Pract | 2020 |
| Validation of the breathmobile case identification survey for asthma screening in children with sickle cell disease. | Patel AP, Krupani S, Stark JM, Mosquera RA, Waller DK, Gonzales T, Brown DL, Nguyen TT, Jon CK, Yadav A | J Asthma | 2020 |
| SPATIAL DISTRIBUTION OF NEWBORNS WITH SICKLE CELL TRAIT IN SERGIPE, BRAZIL. | Leite DCF, Cipolotti R, Gurgel RQ, Martins Filho PRS, Lopes GD | Rev Paul Pediatr | 2020 |
| Laboratory Biomarkers, Cerebral Blood Flow Velocity, and Intellectual Function in Children with Sickle Cell Disease. | Apollonsky N, Lerner NB, Zhang F, Raybagkar D, Eng J, Tarazi R | Adv Hematol | 2020 |
| Parental Knowledge on Thalassaemia and Factors Associated with Refusal to Screen Their Children. | Mat MAC, Yaacob LH, Zakaria R | Malays J Med Sci | 2020 |
| A Case of Hemoglobin Sickle-D Punjab. | Ali W, Jain M, Agarwal S, Kumar A | Indian J Hematol Blood Transfus | 2020 |
| Hemoglobin Henri Mondor [β26(B8) Glu → Val, GAG > GTG], A First Case Report in South-East Asia. | Panyasai S, Jaiping K, Khantarag P, Pornprasert S | Indian J Hematol Blood Transfus | 2020 |
| Key Determinants of Phenotypic Heterogeneity of Hb E/β Thalassemia: A Comparative Study from Eastern India. | Kalantri SA, Ray R, Choudhuri S, Roy S, Bhattacharyya M | Indian J Hematol Blood Transfus | 2020 |
| Phenotypic Diversity and Clinico-Hematological Profile of Hb E-Beta Thalassemic Children. | Baruah A, Baruah MK | Indian J Hematol Blood Transfus | 2020 |
| Pathophysiology and recent therapeutic insights of sickle cell disease. | Shah F, Dwivedi M | Ann. Hematol. | 2020 |
| The role of HLA matching in unrelated donor hematopoietic stem cell transplantation for sickle cell disease in Europe. | Gluckman E, Fuente J, Cappelli B, Scigliuolo GM, Volt F, Tozatto-Maio K, Rocha V, Tommaso M, O'Boyle F, Smiers F, Cunha-Riehm CBD, Calore E, Bonanomi S, Graphakos S, Paisiou A, Albert MH, Ruggeri A, Zecca M, Lankester AC, Corbacioglu S, | Bone Marrow Transplant. | 2020 |
| Cardiomyopathy in Thalassemia: Quick Review from Cellular Aspects to Diagnosis and Current Treatments. | Ghanavat M, Haybar H, Pezeshki SMS, Shahjahani M, Jodat H, Elyasi M, Saki N | Lab Med | 2020 |
| The mRNA-Binding Protein IGF2BP1 Restores Fetal Hemoglobin in Cultured Erythroid Cells from Patients with β-Hemoglobin Disorders. | Chambers CB, Gross J, Pratt K, Guo X, Byrnes C, Lee YT, Lavelle D, Dean A, Miller JL, Wilber A | Mol Ther Methods Clin Dev | 2020 |
| Life-Threatening Infectious Complications in Sickle Cell Disease: A Concise Narrative Review. | Ochocinski D, Dalal M, Black LV, Carr S, Lew J, Sullivan K, Kissoon N | Front Pediatr | 2020 |
| Fetal subdural hematoma, sickle cell disease and storage pool disease: A case report. | Iannaccone A, Darkwah Oppong M, Dammann P, Kimmig R, Köninger A | Case Rep Womens Health | 2020 |
| Eleven healthy live births: a result of simultaneous preimplantation genetic testing of α- and β-double thalassemia and aneuploidy screening. | Chen D, Shen X, Wu C, Xu Y, Ding C, Zhang G, Xu Y, Zhou C | J. Assist. Reprod. Genet. | 2020 |
| Novel High Oxygen Affinity Hemoglobin Variant in a Patient with Polycythemia: Hb Kennisis [β85(F1)Phe→Leu (TT>TT); : c.258T>G]. | Nabhani IA, Aneke JC, Verhovsek M, Eng B, Kuo KHM, Rudinskas LC, Waye JS | Hemoglobin | 2020 |
| Osteoarticular infections in paediatric sickle cell disease: in the era of multidrugresistant bacteria. | Gouveia C, Duarte M, Norte S, Alves P, Kjöllerström P, Brito M, Tavares D | Br. J. Haematol. | 2020 |
| Impact of Medicaid expansion on access and healthcare among individuals with sickle cell disease. | Kayle M, Valle J, Paulukonis S, Holl JL, Tanabe P, French DD, Garg R, Liem RI, Badawy SM, Treadwell MJ | Pediatr Blood Cancer | 2020 |
| MINOCA in a Patient with Sickle Cell Disease. | Lee S, Kaplin S, Tamis-Holland J, Talebi S | Am. J. Med. | 2020 |
| Vitamin D supplementation and pain-related emergency department visits in children with sickle cell disease. | Hood AM, Quinn CT, King CD, Shook LM, Peugh JL, Crosby LE | Complement Ther Med | 2020 |
| Review/overview of pain in sickle cell disease. | Ballas SK, Darbari DS | Complement Ther Med | 2020 |
| Incorporating integrative medicine and patient preferences into a pilot interdisciplinary sickle cell wellness clinic. | Junghans-Rutelonis AN, Moquist KL, Blaylark RM, Anderson N, Brown ML | Complement Ther Med | 2020 |
| Preliminary evaluation of the clinical implementation of cognitive-behavioral therapy for chronic pain management in pediatric sickle cell disease. | Sil S, Lai K, Lee JL, Gilleland Marchak J, Thompson B, Cohen L, Lane P, Dampier C | Complement Ther Med | 2020 |
| Autonomically-mediated decrease in microvascular blood flow due to mental stress and pain in sickle cell disease: A target for neuromodulatory interventions. | Martin SR, Shah P, Denton C, Zeltzer LK, Veluswamy S, Khoo MCK, Coates TD | Complement Ther Med | 2020 |
| A Comprehensive Review of the Treatment and Management of Pain in Sickle Cell Disease. | Fiocchi J, Urits I, Orhurhu V, Orhurhu MS, Giacomazzi S, Hoyt B, Kaye AD, Kaye RJ, Viswanath O | Curr Pain Headache Rep | 2020 |
| Matched Family versus Alternative Donor Hematopoietic Stem Cell Transplantation for Patients with Thalassemia Major: Experience from a Tertiary Referral Center in South India. | Swaminathan VV, Uppuluri R, Patel S, Ravichandran N, Ramanan KM, Vaidhyanathan L, Ramakrishnan B, Jayakumar I, Raj R | Biol. Blood Marrow Transplant. | 2020 |
| Motivations and Decision-Making of Adult Sickle Cell Patients in High-Risk Clinical Research. | Cho HL, Kim SYH, Fitzhugh C, Hsieh M, Tisdale J, Grady C | Biol. Blood Marrow Transplant. | 2020 |
| Hb Sun Prairie: A rare cause of chronic hemolysis in an Indian patient. | Jain A, Prasad P, Chaudhry S, Gupta DK, Saluja S | Hematol Oncol Stem Cell Ther | 2020 |
| Prognostic Value of Hyponatremia During Acute Painful Episodes in Sickle Cell Disease. | Rech JS, Yao K, Bachmeyer C, Bailleul S, Javier O, Grateau G, Lionnet F, Steichen O | Am. J. Med. | 2020 |
| Platelet and megakaryocyte CD40L expression in β-Thalassemic patients. | Morsilli O, Guerriero R, Lulli V, Maffei L, Pasquini L, Pulcinelli FM, Sorrentino F, Gabbianelli M | Thromb. Res. | 2020 |
| The changing epidemiology of the ageing thalassaemia populations: A position statement of the Thalassaemia International Federation. | Farmakis D, Giakoumis A, Angastiniotis M, Eleftheriou A | Eur. J. Haematol. | 2020 |
| White matter volume changes in adult beta-thalassemia: Negligible and unrelated to anemia and cognitive performances. | Manara R, Canna A, Caiazza M, Ponticorvo S, Russo AG, Di Concilio R, Ciancio A, De Michele E, Carafa PA, Ammendola F, Roberti D, Casale M, Elefante A, Cirillo M, Di Salle F, Esposito F, Perrotta S, Tartaglione I | Am. J. Hematol. | 2020 |
| Nitrous oxide and vitamin B12 in sickle cell disease: Not a laughing situation. | Desprairies C, Imbard A, Koehl B, Lorrot M, Gaschignard J, Sommet J, Pichard S, Holvoet L, Faye A, Benkerrou M, Benoist JF, Schiff M | Mol Genet Metab Rep | 2020 |
| Using novel magnetic resonance imaging methods to predict stroke risk in individuals with sickle cell anemia. | Jordan LC, Kassim AA, Wilkerson KL, Lee CA, Waddle SL, Donahue MJ | Hematol Oncol Stem Cell Ther | 2020 |
| Editorial commentary: Sickle cell disease: Diagnosing the heart of the matter. | Caughey MC, Novelli EM | Trends Cardiovasc. Med. | 2020 |
| Amino acids and fatty acids in patients with beta thalassemia major. | Koca T, Canatan D, Örmeci AR, Koca YS, Duman H, Baykal A, Akcam M | Acta Biomed | 2020 |
| Mechanisms underlying priapism in sickle cell disease: targeting and key innovations on the preclinical landscape. | Musicki B, Burnett AL | Expert Opin. Ther. Targets | 2020 |
| Impaired bile secretion promotes hepatobiliary injury in Sickle Cell Disease. | Vats R, Liu S, Zhu J, Mukhi D, Tutuncuoglu E, Cardenes N, Singh S, Brzoska T, Kosar K, Bamne M, Jonassaint J, Adebayo Michael A, Watkins SC, Hillery C, Ma X, Nejak-Bowen K, Rojas M, Gladwin MT, Kato GJ, Ramakrishnan S, Sundd P, Monga SP, Pradhan-Sundd T | Hepatology | 2020 |
| A Quality Initiative to Decrease Time to Antibiotics in Children with Sickle Cell Disease and Fever. | McKinney C, Caruso-Brown A, Montgomery K, Gillespie A, Coughlin R, Law D, Brouwer A, Tytler L, Hilden J, Nuss R | Pediatr Qual Saf | 2020 |
| Beta-Thalassemia Intermedia: A Single Thalassemia Center Experience from Northeastern Iraq. | Amin SS, Jalal SD, Ali KM, Mohammed AI, Rasool LK, Osman TJ | Biomed Res Int | 2020 |
| Identification of seven novel variants in the β-globin gene in transfusion-dependent and normal patients. | Aldakeel SA, Ghanem NZ, Al-Amodi AM, Osman AK, Al Asoom LI, Ahmed NR, Almandil NB, Akhtar MS, Azeez SA, Borgio JF | Arch Med Sci | 2020 |
| Sickle cell disease presenting in the third trimester of pregnancy: Delayed detection heralding a public health problem? | Sharma A, Gaur K, Tiwari VP, Shukla S | Indian J Public Health | 2020 |
| Iron overload and periodontal status in patients with sickle cell anaemia: A case series. | Costa SA, Moreira ARO, Costa CPS, Carvalho Souza SF | J. Clin. Periodontol. | 2020 |
| Hemoglobin: Structure, Function and Allostery. | Ahmed MH, Ghatge MS, Safo MK | Subcell. Biochem. | 2020 |
| Sickle Cell Hemoglobin. | Mandal AK, Mitra A, Das R | Subcell. Biochem. | 2020 |
| Embryonic and Fetal Human Hemoglobins: Structures, Oxygen Binding, and Physiological Roles. | Manning JM, Manning LR, Dumoulin A, Padovan JC, Chait B | Subcell. Biochem. | 2020 |
| Potential Contribution of Pulmonary Thromboembolic Disease in Pulmonary Hypertension in Sickle Cell Disease. | Nouraie M, Zhang X, Srisuwananukorn A, Machado RF, Gordeuk VR, Gladwin MT, Saraf S | Ann Am Thorac Soc | 2020 |
| Failure of response to combination therapy of adalimumab and infliximab in a recalcitrant patient of severe psoriasis and major thalassemia: A case report. | Goldust M, Rahmatpour Rokni G, Gupta M, Lotti T, Bathaei M | Clin Case Rep | 2020 |
| Outcome of short-term emergency department observation care of children with sickle cell disease and vaso-occlusive crises: initial experience from south-western Nigeria. | Adegoke SA, Oladimeji OI, Ologun BG, Aladekomo TA, Oyelami OA | Trans. R. Soc. Trop. Med. Hyg. | 2020 |
| Characteristics and Prognosis of Hepatocellular Carcinoma in Multi-Transfused Patients with β-Thalassemia. Experience of a Single Tertiary Center. | Papadopoulos N, Kountouras D, Malagari K, Tampaki M, Theochari M, Koskinas J | Mediterr J Hematol Infect Dis | 2020 |
| Lower white matter volume in beta-thalassemia associated with anemia and cognitive performance. | Choi S, Leahy RM, Wood JC | Am. J. Hematol. | 2020 |
| Re: Abnormally Low Hemoglobin A1c as Harbinger of Hemoglobinopathy. | Mungmungpuntipantip R, Wiwanitkit V, Bitencourt SE, Rodrigues de Aguiar D, Baggio A, Marcon CEM | J Am Board Fam Med | 2020 |
| Ambient air pollution and sickle cell disease-related emergency department visits in Atlanta, GA. | Blumberg AH, Ebelt ST, Liang D, Morris CR, Sarnat JA | Environ. Res. | 2020 |
| Salbutamol Worsens the Autonomic Nervous System Dysfunction of Children With Sickle Cell Disease. | Bokov P, El Jurdi H, Denjoy I, Peiffer C, Medjahdi N, Holvoet L, Benkerrou M, Delclaux C | Front Physiol | 2020 |
| Hb S/-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics. | Belisário AR, Carneiro-Proietti AB, Sabino EC, Araújo A, Loureiro P, Máximo C, Flor-Park MV, Rodrigues DDOW, Ozahata MC, McClure C, Mota RA, Gomes Moura IC, Custer B, Kelly S, | Hemoglobin | 2020 |
| Paediatric to adult transition care for patients with sickle cell disease: a global perspective. | Inusa BPD, Stewart CE, Mathurin-Charles S, Porter J, Hsu LL, Atoyebi W, De Montalembert M, Diaku-Akinwumi I, Akinola NO, Andemariam B, Abboud MR, Treadwell M | Lancet Haematol | 2020 |
| [Analysis of beta-globin gene variants in Liuzhou area of Guangxi]. | Chen L, Luo S, Tang N, Wang Q, Xu Z, Qin L, Wang J, Zhong Q, Ya J, Liu X, Cai R, Huang J | Zhonghua Yi Xue Yi Chuan Xue Za Zhi | 2020 |
| Comparison of US Federal and Foundation Funding of Research for Sickle Cell Disease and Cystic Fibrosis and Factors Associated With Research Productivity. | Farooq F, Mogayzel PJ, Lanzkron S, Haywood C, Strouse JJ | JAMA Netw Open | 2020 |
| Heme A1M'ed at the kidney in sickle cell disease. | Saraf SL | Blood | 2020 |
| Iron homeostasis in a mouse model of thalassemia intermedia is altered between adolescence and adulthood. | Sanyear C, Butthep P, Eamsaard W, Fucharoen S, Svasti S, Masaratana P | PeerJ | 2020 |
| Renal medullary carcinoma and its association with sickle cell trait: a case report and literature review. | Holland P, Merrimen J, Pringle C, Wood LA | Curr Oncol | 2020 |
| Fibroblast Growth Factor 23 (FGF23) and Klotho Protein in Beta-Thalassemia. | Stefanopoulos D, Nasiri-Ansari N, Dontas I, Vryonidou A, Galanos A, Psaridi L, Fatouros IG, Mastorakos G, Papavassiliou AG, Kassi E, Tournis S | Horm. Metab. Res. | 2020 |
| Iron and Heart Failure: Diagnosis, Therapies, and Future Directions. | Ghafourian K, Shapiro JS, Goodman L, Ardehali H | JACC Basic Transl Sci | 2020 |
| A Phase 3 Trial of Luspatercept in Patients with Transfusion-Dependent β-Thalassemia. | Cappellini MD, Viprakasit V, Taher AT, Georgiev P, Kuo KHM, Coates T, Voskaridou E, Liew HK, Pazgal-Kobrowski I, Forni GL, Perrotta S, Khelif A, Lal A, Kattamis A, Vlachaki E, Origa R, Aydinok Y, Bejaoui M, Ho PJ, Chew LP, Bee PC, Lim SM, Lu MY, Tantiworawit A, Ganeva P, Gercheva L, Shah F, Neufeld EJ, Thompson A, Laadem A, Shetty JK, Zou J, Zhang J, Miteva D, Zinger T, Linde PG, Sherman ML, Hermine O, Porter J, Piga A, | N. Engl. J. Med. | 2020 |
| Quantifying Areas of Vascular Leakage in Sickle Cell Retinopathy Using Standard and Widefield Fluorescein Angiography. | Barbosa J, Malbin B, Le K, Lin X | Ophthalmic Surg Lasers Imaging Retina | 2020 |
| Phase 2 trial of montelukast for prevention of pain in sickle cell disease. | Field JJ, Kassim A, Brandow A, Embury SH, Matsui N, Wilkerson K, Bryant V, Zhang L, Simpson P, DeBaun MR | Blood Adv | 2020 |
| Leukocyte adhesion to P-selectin and the inhibitory role of Crizanlizumab in sickle cell disease: A standardized microfluidic assessment. | Man Y, Goreke U, Kucukal E, Hill A, An R, Liu S, Bode A, Solis-Fuentes A, Nayak LV, Little JA, Gurkan UA | Blood Cells Mol. Dis. | 2020 |
| Gene editing and CRISPR in the clinic: current and future perspectives. | Hirakawa MP, Krishnakumar R, Timlin JA, Carney JP, Butler KS | Biosci. Rep. | 2020 |
| Catheter associated thromboses in patients with sickle cell anaemia and dual lumen Vortex apheresis ports are common and can be clinically asymptomatic. | Brewin JN, Crowley MP, Kesse-Adu R, Stuart-Smith S, Awogbade M, Howard J | Br. J. Haematol. | 2020 |
| Longitudinal Description of Gonadal Function in Sickle-Cell Patients Treated With Hematopoietic Stem Cell Transplant Using Alkylator-based Conditioning Regimens. | Elchuri SV, Williamson Lewis R, Quarmyne MO, Haight AE, Cottrell HN, Meacham LR | J. Pediatr. Hematol. Oncol. | 2020 |
| Effective use of hydroxyurea for sickle cell anemia in low-resource countries. | Power-Hays A, Ware RE | Curr. Opin. Hematol. | 2020 |
| Current and future gene therapies for hemoglobinopathies. | Brendel C, Williams DA | Curr. Opin. Hematol. | 2020 |
| Haploidentical bone marrow transplant with posttransplant cyclophosphamide for sickle cell disease: An update. | Patel DA, Akinsete AM, de la Fuente J, Kassim AA | Hematol Oncol Stem Cell Ther | 2020 |
| Hematopoietic stem cell transplantation for patients with sickle cell disease in the Eastern Mediterranean. | Alahmari AD, Aljurf M, Alseraihy A, Hamidieh AA, Alkindi S, Rihani R, Satti T, Jastaniah W, Alsaedi H, Almohareb F, Al-Jefri A, Rasheed W | Hematol Oncol Stem Cell Ther | 2020 |
| Is sickle cell disease-related neurotoxicity a systemic endotheliopathy? | Palomo M, Diaz-Ricart M, Carreras E | Hematol Oncol Stem Cell Ther | 2020 |
| Alternative donor: αß/CD19 T-cell-depleted haploidentical hematopoietic stem cell transplantation for sickle cell disease. | Foell J, Kleinschmidt K, Jakob M, Troeger A, Corbacioglu S | Hematol Oncol Stem Cell Ther | 2020 |
| Standard management of sickle cell disease complications. | Abboud MR | Hematol Oncol Stem Cell Ther | 2020 |
| Status quo of allogeneic stem cell transplantation for patients with sickle cell disease using matched unrelated donors. | Oevermann L, Sodani P | Hematol Oncol Stem Cell Ther | 2020 |
| What is the place of hematopoietic stem cell transplantation in the management of cerebral vasculopathy in children with sickle cell anemia? | Bernaudin F | Hematol Oncol Stem Cell Ther | 2020 |
| Proceeding of the European Group for Blood and Marrow Transplantation (EBMT) congress on sickle cell disease, 16-17 may 2019, Regensburg, Germany: What is the impact of antithymocyte globulin pharmacokinetics on haploidentical hematopoietic stem cell transplantation? | Oostenbrink LVE, Jol-van der Zijde CM, Jansen-Hoogendijk AM, Pool ES, van Halteren AGS, Moes DJAR, Bredius RGM, Mohseny AB, Smiers FJW, van Tol MJD, Schilham MW, Lankester AC | Hematol Oncol Stem Cell Ther | 2020 |
| Alternative donor hematopoietic stem cell transplantation for sickle cell disease in Europe. | Gluckman E, Cappelli B, Scigliuolo GM, De la Fuente J, Corbacioglu S | Hematol Oncol Stem Cell Ther | 2020 |
| How to setup a successful transplant program for hemoglobinopathies in developing countries: The Cure2Children approach. | Faulkner L | Hematol Oncol Stem Cell Ther | 2020 |
| Curative options for sickle cell disease in Africa: Approach in Tanzania. | Makani J, | Hematol Oncol Stem Cell Ther | 2020 |
| The effect of transfusion on immune responses in thalassemia. | Politou M, Komninaka V, Valsami S, Kapsimali V, Pouliakis A, Koutsouri T, Panayiotakopoulos G, Kotsianidis I, Voskaridou E | Blood Cells Mol. Dis. | 2020 |
| Tandem P-selectin glycoprotein ligand immunoglobulin prevents lung vaso-occlusion in sickle cell disease mice. | Vats R, Tutuncuoglu E, Pradhan-Sundd T, Tejero J, Shaw GD, Sundd P | Exp. Hematol. | 2020 |
| COVID-19 pneumonia as a cause of acute chest syndrome in an adult sickle cell patient. | Beerkens F, John M, Puliafito B, Corbett V, Edwards C, Tremblay D | Am. J. Hematol. | 2020 |
| Tricuspid regurgitation velocity and other biomarkers of mortality in children, adolescents and young adults with sickle cell disease in the United States: The PUSH study. | Nouraie M, Darbari DS, Rana S, Minniti CP, Castro OL, Luchtman-Jones L, Sable C, Dham N, Kato GJ, Gladwin MT, Ensing G, Arteta M, Campbell A, Taylor JG, Nekhai S, Gordeuk VR | Am. J. Hematol. | 2020 |
| Clinicopathologic consequences following discontinuation of rifaximin in patients with sickle cell disease. | Lim SH, Dutta D | Am. J. Hematol. | 2020 |
| Rate of Food Insecurity Among Households with Children with Sickle Cell Disease is Above the National Average. | Ghafuri DL, Rodeghier M, DeBaun MR | South. Med. J. | 2020 |
| Pulmonary thromboendarterectomy in patients with chronic thromboembolic pulmonary hypertension and hemoglobinopathies. | Sousa ACC, Campos FTAF, Bernardes RC, Ivo MB, Corrêa RA | J Bras Pneumol | 2020 |
| The Sickle Cell Disease Multidisciplinary Clinic at the Lifespan Cancer Institute. | Sokolic R | R I Med J (2013) | 2020 |
| Outcome of pregnancies among women with sickle cell disease. | Nkwabong E, Ngoundjou Dongmo P, Tayou C, Nana Njamen T | J. Matern. Fetal. Neonatal. Med. | 2020 |
| Increased iron stores influence glucose metabolism in sickle cell anaemia. | Shah BN, Hassan TO, Zhang X, McClain DA, Gordeuk VR | Br. J. Haematol. | 2020 |
| Stress and the Home Environment in Caregivers of Children with Sickle Cell. | Varughese TE, Hoyt CR, L'Hotta AJ, Ikemenogo PA, Howdeshell SG, Housten AJ, Abel RA, King AA | J Pediatr Psychol | 2020 |
| Hardy-Weinberg Equilibrium in the Large Scale Genomic Sequencing Era. | Abramovs N, Brass A, Tassabehji M | Front Genet | 2020 |
| The Red Blood Cell-Inflammation Vicious Circle in Sickle Cell Disease. | Nader E, Romana M, Connes P | Front Immunol | 2020 |
| Generation of hematopoietic stem/progenitor cells with sickle cell mutation from induced pluripotent stem cell in serum-free system. | Paes BCMF, Stabeli LCJR, Costa PNM, Orellana MD, Kashima S, Covas DT, Picanço-Castro V | Hematol Transfus Cell Ther | 2020 |
| Association between HLA-DRB1*01 and HLA-DRB1*15 with alloimmunisation in transfusion-dependent patients with thalassaemia. | Ebrahimi M, Dayer D, Jalalifar MA, Keikhaei B, Tahan Nejad Asadi Z | Transfus Med | 2020 |
| Prolonged Weakness and Paresthesia After Revision Total Hip Arthroplasty in a Patient with Sickle Cell Anemia Receiving Spinal Anesthesia: A Case Report. | Yancey HB, Langfitt MK | JBJS Case Connect | 2020 |
| The Effect of Progressive Muscle Relaxation Exercises on Pain on Patients with Sickle Cell Disease: Randomized Controlled Study. | Kazak A, Ozkaraman A | Pain Manag Nurs | 2020 |
| Diagnosis support of sickle cell anemia by classifying red blood cell shape in peripheral blood images. | Delgado-Font W, Escobedo-Nicot M, González-Hidalgo M, Herold-Garcia S, Jaume-I-Capó A, Mir A | Med Biol Eng Comput | 2020 |
| New haematologic score to discriminate beta thalassemia trait from iron deficiency anaemia in a Spanish Mediterranean region. | Carla MG, Rafael SP, Isabel FG, Cristina GF, Teresa SM | Clin. Chim. Acta | 2020 |
| Patient and family experience with chronic transfusion therapy for sickle cell disease: A qualitative study. | Hawkins LM, Sinha CB, Ross D, Yee MEM, Quarmyne MO, Krishnamurti L, Bakshi N | BMC Pediatr | 2020 |
| The vaso-occlusive pain crisis in sickle cell disease: Definition, pathophysiology, and management. | Darbari DS, Sheehan VA, Ballas SK | Eur. J. Haematol. | 2020 |
| Preclinical Evaluation of a Novel Lentiviral Vector Driving Lineage-Specific BCL11A Knockdown for Sickle Cell Gene Therapy. | Brendel C, Negre O, Rothe M, Guda S, Parsons G, Harris C, McGuinness M, Abriss D, Tsytsykova A, Klatt D, Bentler M, Pellin D, Christiansen L, Schambach A, Manis J, Trebeden-Negre H, Bonner M, Esrick E, Veres G, Armant M, Williams DA | Mol Ther Methods Clin Dev | 2020 |
| The HRI-regulated transcription factor ATF4 activates BCL11A transcription to silence fetal hemoglobin expression. | Huang P, Peslak SA, Lan X, Khandros E, Yano JA, Sharma M, Keller CA, Giardine B, Qin K, Abdulmalik O, Hardison RC, Shi J, Blobel GA | Blood | 2020 |
| American Society of Hematology 2020 guidelines for sickle cell disease: prevention, diagnosis, and treatment of cerebrovascular disease in children and adults. | DeBaun MR, Jordan LC, King AA, Schatz J, Vichinsky E, Fox CK, McKinstry RC, Telfer P, Kraut MA, Daraz L, Kirkham FJ, Murad MH | Blood Adv | 2020 |
| Development of a genomic DNA reference material panel for thalassemia genetic testing. | Yin Z, Qu S, Huang C, Chen F, Li J, Chen S, Ye J, Yang Y, Zheng Y, Zhang X, Yang X, Xie L, Wei J, Wei F, Guo J, Huang J | Int J Lab Hematol | 2020 |
| Biallelic rare 17 bp deletion mutation (HBB:c.380_396 del TGCAGGCTGCCTATCAG) in a transfusion depended form of thalassemia. | Tripathi P, Agarwal S, Gupta A, Mandal K | Ann. Hematol. | 2020 |
| Total hip arthroplasty in sickle cell disease: a systematic review. | Kenanidis E, Kapriniotis K, Anagnostis P, Potoupnis M, Christofilopoulos P, Tsiridis E | EFORT Open Rev | 2020 |
| Prenatal diagnosis of rare genetic conditions at a tertiary care hospital in Karachi. | Karim K, Dileep D, Munim S | J Pak Med Assoc | 2020 |
| Sickle Cell Disease: Metabolomic Profiles of Vaso-Occlusive Crisis in Plasma and Erythrocytes. | Dembélé KC, Veyrat-Durebex C, Aldiouma G, Chupin S, Tessier L, Goïta Y, Baraïka MA, Diallo M, Touré BA, Homedan C, Mirebeau-Prunier D, Simard G, Diallo D, Cissé BM, Reynier P, Chao de la Barca JM | J Clin Med | 2020 |
| Progression of albuminuria in patients with sickle cell anemia: a multicenter, longitudinal study. | Niss O, Lane A, Asnani MR, Yee ME, Raj A, Creary S, Fitzhugh C, Bodas P, Saraf SL, Sarnaik S, Devarajan P, Malik P | Blood Adv | 2020 |
| Changes in Pain and Psychosocial Functioning and Transition to Chronic Pain in Pediatric Sickle Cell Disease: A Cohort Follow-up Study. | Sil S, Cohen LL, Bakshi N, Watt A, Hathaway M, Abudulai F, Dampier C | Clin J Pain | 2020 |
| Tilt-table Echocardiography Unmasks Early Diastolic Dysfunction in Patients With Hemoglobinopathies. | Mah K, Bruce A, Zahari N, Venner MA, Chow K, Thompson RB, Khoo NS, Tham EB | J. Pediatr. Hematol. Oncol. | 2020 |
| Parental Notification Via Text Messaging for Infant Sickle Screening Programs: Exploration of Feasibility and Acceptability in Uganda. | Fashakin V, Mathur S, Kwagala P, Mupere E, Kiguli S, Kitaka SB, Henry MB, Van Ells L, Tusuubira S, Mulumba L, Duong J, Stockwell MS, LaRussa P, Green NS | J. Pediatr. Hematol. Oncol. | 2020 |
| Leg Ulcers in Sickle-Cell Disease: Treatment Update. | Monfort JB, Senet P | Adv Wound Care (New Rochelle) | 2020 |
| Therapeutic base editing of human hematopoietic stem cells. | Zeng J, Wu Y, Ren C, Bonanno J, Shen AH, Shea D, Gehrke JM, Clement K, Luk K, Yao Q, Kim R, Wolfe SA, Manis JP, Pinello L, Joung JK, Bauer DE | Nat. Med. | 2020 |
| Directed evolution of adenine base editors with increased activity and therapeutic application. | Gaudelli NM, Lam DK, Rees HA, Solá-Esteves NM, Barrera LA, Born DA, Edwards A, Gehrke JM, Lee SJ, Liquori AJ, Murray R, Packer MS, Rinaldi C, Slaymaker IM, Yen J, Young LE, Ciaramella G | Nat. Biotechnol. | 2020 |
| Veno-Venous Extracorporeal Membrane Oxygenation in Adult Patients with Sickle Cell Disease and Acute Chest Syndrome: a Single-Center Experience. | Alashkar F, Herbstreit F, Carpinteiro A, Baum J, Tzalavras A, Aramayo-Singelmann C, Vance C, Lenz V, Gulbins E, Reinhardt D, Beelen DW, Dührsen U, Röth A, Koldehoff M, Liebregts T | Hemoglobin | 2020 |
| Rapid and severe Covid-19 pneumonia with severe acute chest syndrome in a sickle cell patient successfully treated with tocilizumab. | De Luna G, Habibi A, Deux JF, Colard M, Pham Hung d'Alexandry d'Orengiani AL, Schlemmer F, Joher N, Kassasseya C, Pawlotsky JM, Ourghanlian C, Michel M, Mekontso-Dessap A, Bartolucci P | Am. J. Hematol. | 2020 |
| A Chinese Male with Normal Hematological Indices and High Hb A Levels in β-Thalassemia Trait. | Chen YJ, Li YQ, Liu Q, Tang LY, Lv FT | Hemoglobin | 2020 |
| Distribution of Hemoglobinopathy in Nepalese Population. | Shrestha RM, Pandit R, Yadav UK, Das R, Yadav BK, Upreti HC | J Nepal Health Res Counc | 2020 |
| Mitigating the effect of the COVID-19 pandemic on sickle cell disease services in African countries. | Dexter D, Simons D, Kiyaga C, Kapata N, Ntoumi F, Kock R, Zumla A | Lancet Haematol | 2020 |
| Sickle cell disease and malaria: decreased exposure and asplenia can modulate the risk from Plasmodium falciparum. | Mwaiswelo RO, Mawala W, Iversen PO, de Montalembert M, Luzzatto L, Makani J | Malar. J. | 2020 |
| Impact of sickle cell disease on presentation and progression of paediatric HIV: a retrospective cohort study. | Ssenyondwa J, George PE, Carlos Bazo-Alvarez J, Mercedes R, Kanywa JB, Naturinda E, Wasswa PLM, Lubega J | Trop. Med. Int. Health | 2020 |
| Prevalence of priapism in individuals with sickle cell disease and implications on male sexual function. | Alvaia MA, Maia HAADS, Nelli AM, Guimarães COS, Carvalho ESS, Netto JMB, Miranda EP, Gomes CM, Bessa Júnior J | Einstein (Sao Paulo) | 2020 |
| [Gene Diagnosis and Phenotypic Analysis of β-Thalassemia Caused from a Rare Synonymous Mutation CD29 (C>T)]. | Qin DQ, DU L, Ding HK, Wang JC, Yuan TL, Yao CZ, Lan FF | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2020 |
| Multi-Locus Models to Address Hb F Variability in Portuguese β-Thalassemia Carriers. | Manco L, Bento C, Relvas L, Cunha E, Pereira J, Moreira V, Alvarez M, Maia T, Ribeiro ML | Hemoglobin | 2020 |
| Growth pattern in thalassemic children and their correlation with serum ferritin. | Rathaur VK, Imran A, Pathania M | J Family Med Prim Care | 2020 |
| Fertility Concerns and Access to Care for Stem Cell Transplantation Candidates with Sickle Cell Disease. | Mishkin AD, Mapara MY, Barhaghi M, Reshef R | Biol. Blood Marrow Transplant. | 2020 |
| COVID-19 infection in patients with sickle cell disease. | Hussain FA, Njoku FU, Saraf SL, Molokie RE, Gordeuk VR, Han J | Br. J. Haematol. | 2020 |
| Using arterial-venous oxygen difference to guide red blood cell transfusion strategy. | Fogagnolo A, Taccone FS, Vincent JL, Benetto G, Cavalcante E, Marangoni E, Ragazzi R, Creteur J, Volta CA, Spadaro S | Crit Care | 2020 |
| Biventricular Reference Values by Body Surface Area, Age, and Gender in a Large Cohort of Well-Treated Thalassemia Major Patients Without Heart Damage Using a Multiparametric CMR Approach. | Meloni A, Righi R, Missere M, Renne S, Schicchi N, Gamberini MR, Cuccia L, Lisi R, Spasiano A, Roberti MG, Zuccarelli A, Ait-Ali L, Festa P, Aquaro GD, Mangione M, Barra V, Positano V, Pepe A | J Magn Reson Imaging | 2020 |
| SARS-CoV-2 infection in beta thalassemia: Preliminary data from the Italian experience. | Motta I, Migone De Amicis M, Pinto VM, Balocco M, Longo F, Bonetti F, Gianesin B, Graziadei G, Cappellini MD, De Franceschi L, Piga A, Forni GL | Am. J. Hematol. | 2020 |
| L-Glutamine in sickle cell disease. | Cox SE, Hart E, Kirkham FJ, Stotesbury H | Drugs Today | 2020 |
| Establishment and Evaluation of a Novel Method Based on Loop-Mediated Isothermal Amplification for the Rapid Diagnosis of Thalassemia Genes. | Wang WH, Lin M, Li HL, Huang JY, Chen JT, Fang XS, Huang DM, Xi XX, Zhao QF, Song FL, Huang S, Zhong TY | Risk Manag Healthc Policy | 2020 |
| Depression and Anxiety as Moderators of the Pain-Social Functioning Relationship in Youth with Sickle Cell Disease. | Valrie C, Floyd A, Sisler I, Redding-Lallinger R, Fuh B | J Pain Res | 2020 |
| Effect of the Hydoxyurea in Yemeni Transfusion-Dependent β-Thalassemia Patients. | Al-Nood HA, Al-Nood RM, Ghanem NS, Al-Hadi AM | Hemoglobin | 2020 |
| Gut leakage enhances sepsis susceptibility in iron-overloaded β-thalassemia mice through macrophage hyperinflammatory responses. | Visitchanakun P, Saisorn W, Wongphoom J, Chatthanathon P, Somboonna N, Svasti S, Fucharoen S, Leelahavanichkul A | Am. J. Physiol. Gastrointest. Liver Physiol. | 2020 |
| Homocysteine is associated with severity of microvasculopathy in sickle cell disease patients. | Samarron SL, Miller JW, Cheung AT, Chen PC, Lin X, Zwerdling T, Wun T, Green R | Br. J. Haematol. | 2020 |
| High-level induction of fetal haemoglobin by pomalidomide in β-thalassaemia/HbE erythroid progenitor cells. | Khamphikham P, Nualkaew T, Pongpaksupasin P, Kaewsakulthong W, Songdej D, Paiboonsukwong K, Engel JD, Hongeng S, Fucharoen S, Sripichai O, Jearawiriyapaisarn N | Br. J. Haematol. | 2020 |
| Dramatic improvement after tocilizumab of severe COVID-19 in a child with sickle cell disease and acute chest syndrome. | Odièvre MH, de Marcellus C, Ducou Le Pointe H, Allali S, Romain AS, Youn J, Taytard J, Nathan N, Corvol H | Am. J. Hematol. | 2020 |
| A Novel Method to Identify Autoantibodies against Putative Target Proteins in Serum from beta-Thalassemia Major: A Pilot Study. | Sumera A, Anuar ND, Radhakrishnan AK, Ibrahim H, Rutt NH, Ismail NH, Tan TM, Baba AA | Biomedicines | 2020 |
| The Effects of Postprandial Resistance Exercise on Blood Glucose and Lipids in Prediabetic, Beta-Thalassemia Major Patients. | Georgakouli K, Stamperna A, Deli CK, Syrou N, Draganidis D, Fatouros IG, Jamurtas AZ | Sports (Basel) | 2020 |
| The Imperative of Dengue Vaccination for Children with Sickle Cell Disease. | Elenga N, Nacher M, Trehan I | J. Trop. Pediatr. | 2020 |
| Genetic testing costs and compliance with clinical best practices. | Montanez K, Berninger T, Willis M, Harding A, Lutgendorf MA | J Genet Couns | 2020 |
| Lessons learned from a prenatal diagnosis program for thalassemia in Thailand. | Wong P, Suannum P, Jermnim S, Charoenporn P, Chan-In M, Tapprom A, Deoisares R | Prenat. Diagn. | 2020 |
| Short-Term Outcome and MRI Changes in Three Adult Patients with Sickle Cell Disease and Aseptic Osteonecrosis after Treatment with Hyperbaric Oxygen Therapy: A Preliminary Report. | Shier A, Abdelrazek M, Soliman A, De Sanctis V, Elsayed A, Abdulla M, Mohamed S, Yassin K, Bilal I, Yassin M | Case Rep Oncol | 2020 |
| Advances in genome editing: the technology of choice for precise and efficient β-thalassemia treatment. | Ali G, Tariq MA, Shahid K, Ahmad FJ, Akram J | Gene Ther. | 2020 |
| Concomitant Existence of Paroxysmal Nocturnal Hemoglobinuria in a Patient with Hb E (: c.79G>A) Trait. | Halder R, Sundaram UKD, Veetil KK, Rath A, Seth T, Tyagi S, Pati HP | Hemoglobin | 2020 |
| Nasal Colonization among Children with Sickle Cell Disease at the Children's Hospital, Accra: Prevalence, Risk Factors, and Antibiotic Resistance. | Appiah VA, Pesewu GA, Kotey FCN, Boakye AN, Duodu S, Tette EMA, Nyarko MY, Donkor ES | Pathogens | 2020 |
| Gene expression of HIF-1α and VEGF in response to hypoxia in sickle cell anaemia: Influence of hydroxycarbamide. | Pedrosa AM, Lemes RPG | Br. J. Haematol. | 2020 |
| Microvasculopathy and biomarkers in sickle cell disease: the promise of non-invasive real-time in vivo tools. | Colombatti R, Andemariam B | Br. J. Haematol. | 2020 |
| Gene Mutation Spectrum of Thalassemia Among Children in Yunnan Province. | Huang TL, Zhang TY, Song CY, Lin YB, Sang BH, Lei QL, Lv Y, Yang CH, Li N, Tian X, Yang YH, Zhang XW | Front Pediatr | 2020 |
| Two Consecutive Episodes of Severe Delayed Hemolytic Transfusion Reaction in a Sickle Cell Disease Patient. | Mpinganzima C, Haaland A, Holm AGV, Thein SL, Tjønnfjord GE, Iversen PO | Case Rep Hematol | 2020 |
| Deletional Alpha-Thalassemia Alleles in Amazon Blood Donors. | Anselmo FC, Ferreira NS, da Mota AJ, Gonçalves MS, Albuquerque SRL, Fraiji NA, Ferreira ACD, de Moura Neto JP | Adv Hematol | 2020 |
| Rare Case of Diffuse Splenic Uptake on Methylene Diphosphonate Bone Scan in a Patient with Sickle Cell Disease. | Parida GK, Mitra S, Muthu GS, Suman A | Indian J Nucl Med | 2020 |
| Smad2/3-pathway ligand trap luspatercept enhances erythroid differentiation in murine β-thalassaemia by increasing GATA-1 availability. | Martinez PA, Li R, Ramanathan HN, Bhasin M, Pearsall RS, Kumar R, Suragani RNVS | J. Cell. Mol. Med. | 2020 |
| Systematic Review of Crizanlizumab: A New Parenteral Option to Reduce Vaso-occlusive Pain Crises in Patients with Sickle Cell Disease. | Han J, Saraf SL, Gordeuk VR | Pharmacotherapy | 2020 |
| The prevalence of hepatitis C virus infection in β-thalassemia patients in Pakistan: a systematic review and meta-analysis. | Akhtar S, Nasir JA, Hinde A | BMC Public Health | 2020 |
| Inhibition of Band 3 tyrosine phosphorylation: a new mechanism for treatment of sickle cell disease. | Noomuna P, Risinger M, Zhou S, Seu K, Man Y, An R, Sheik DA, Wan J, Little JA, Gurkan UA, Turrini FM, Kalfa T, Low PS | Br. J. Haematol. | 2020 |
| Comparison of global strain values of myocardium in beta-thalassemia major patients with iron load using specific feature tracking in cardiac magnetic resonance imaging. | Rezaeian N, Mohtasham MA, Khaleel AJ, Parnianfard N, Kasani K, Golshan R | Int J Cardiovasc Imaging | 2020 |
| New mutations of locus control region in Saudi sickle patients. | Alenzi FQ | Saudi J Biol Sci | 2020 |
| Pulmonary complications for women with sickle cell disease in pregnancy: systematic review and meta-analysis. | Inparaj S, Buckingham M, Oakley L, Seed PT, Lucas S, Oteng-Ntim E | Thorax | 2020 |
| Oxidation Impacts the Intracellular Signaling Machinery in Hematological Disorders. | Tibaldi E, Federti E, Matte A, Iatcenko I, Wilson AB, Riccardi V, Pagano MA, De Franceschi L | Antioxidants (Basel) | 2020 |
| Hematopoietic stem cell function in β-thalassemia is impaired and is rescued by targeting the bone marrow niche. | Aprile A, Gulino A, Storto M, Villa I, Beretta S, Merelli I, Rubinacci A, Ponzoni M, Marktel S, Tripodo C, Lidonnici MR, Ferrari G | Blood | 2020 |
| Systematic Review of Voxelotor: A First-in-Class Sickle Hemoglobin Polymerization Inhibitor for Management of Sickle Cell Disease. | Han J, Saraf SL, Gordeuk VR | Pharmacotherapy | 2020 |
| Sexual dysfunction in female subjects with beta-thalassemia minor. | Keşkek ŞÖ, Demirtaş D, Uysal G, Başaran E | Int. J. Impot. Res. | 2020 |
| Caring for Africa's sickle cell children: will we rise to the challenge? | Oron AP, Chao DL, Ezeanolue EE, Ezenwa LN, Piel FB, Ojogun OT, Uyoga S, Williams TN, Nnodu OE | BMC Med | 2020 |
| Celocentesis for early prenatal diagnosis of hemoglobinopathies. | Makrydimas G, Damiani G, Jakil C, Cigna V, Orlandi M, Picciotto F, Schillaci G, Cassarà F, Vinciguerra M, Leto F, Giambona A, Maggio A, Nicolaides KH | Ultrasound Obstet Gynecol | 2020 |
| Hematological Characteristics of Hb Constant Spring (: c.427T>C) Carriers in Mainland China. | Jiang F, Xu LL, Chen GL, Zhou JY, Li J, Tang XW, Zuo LD, Li DZ | Hemoglobin | 2020 |
| The Relation between Different Aspects of Quality of Life with Coping Style in Adolescents with Thalassemia in Comparison to a Healthy Group. | Abbasi S, Shahriari M, Ghanavat M, Talakoub S, Mosavi Asl FS, Hemati Z | Int J Hematol Oncol Stem Cell Res | 2020 |
| The association of HBG2, BCL11A, and HBS1L-MYB polymorphisms to thalidomide response in Chinese β-thalassemia patients. | Yang K, Wu Y, Ma Y, Xiao J, Zhou Y, Yin X | Blood Cells Mol. Dis. | 2020 |
| Biochemical and imaging markers in patients with thalassaemia. | Vlachou M, Kamperidis V, Giannakoulas G, Karamitsos T, Vlachaki E, Karvounis H | Hellenic J Cardiol | 2020 |
| Voxelotor for the Treatment of Sickle Cell Disease. | Fantasia HC, Morse BL | Nurs Womens Health | 2020 |
| Experience with Parent Follow-Up for Communication Outcomes after Newborn Screening Identifies Carrier Status. | Farrell MH, La Pean Kirschner A, Tluczek A, Farrell PM | J. Pediatr. | 2020 |
| Measuring hydroxyurea adherence by pharmacy and laboratory data compared with video observation in children with sickle cell disease. | Creary S, Chisolm D, Stanek J, Neville K, Garg U, Hankins JS, O'Brien SH | Pediatr Blood Cancer | 2020 |
| Nephrectomy Does not Exacerbate Cancellous Bone loss in Thalassemic Mice. | Lotinun S, Atjanasuppat K, Limsuvech J, Leelahavanichkul A, Svasti S, Krishnamra N | Sci Rep | 2020 |
| Clinical, laboratory, and genetic risk factors for thrombosis in sickle cell disease. | Srisuwananukorn A, Raslan R, Zhang X, Shah BN, Han J, Gowhari M, Molokie RE, Gordeuk VR, Saraf SL | Blood Adv | 2020 |
| Impact of Arginine Therapy on Mitochondrial Function in Children with Sickle Cell Disease during Vaso-occlusive Pain. | Morris CR, Brown LA, Reynolds M, Dampier CD, Lane P, Watt A, Kumari P, Harris F, Manoranjithan S, Mendis RD, Figueroa J, Shiva S | Blood | 2020 |
| Development of the InCharge Health Mobile App to Improve Adherence to Hydroxyurea in Patients With Sickle Cell Disease: User-Centered Design Approach. | Alberts NM, Badawy SM, Hodges J, Estepp JH, Nwosu C, Khan H, Smeltzer MP, Homayouni R, Norell S, Klesges L, Porter JS, Hankins JS | JMIR Mhealth Uhealth | 2020 |
| Detecting HbE Gene Using DNA Extracted from Urine Sediments by Chelex-plus-Heating Technique. | Pankham A, Tatu T | J Biomol Tech | 2020 |
| Microsurgery in the sickle cell trait population: is it actually safe? | Abraham PF, Allam O, Park KE, Alperovich M | BMJ Case Rep | 2020 |
| Hematologist and transplant physicians: How and where to meet for the best of sickle cell disease patients? | Dalle JH | Hematol Oncol Stem Cell Ther | 2020 |
| S100B single nucleotide polymorphisms exhibit sex-specific associations with chronic pain in sickle cell disease in a largely African-American cohort. | Jhun EH, Sadhu N, He Y, Yao Y, Wilkie DJ, Molokie RE, Wang ZJ | PLoS ONE | 2020 |
| A study of the geographic distribution and associated risk factors of leg ulcers within an international cohort of sickle cell disease patients: the CASiRe group analysis. | Antwi-Boasiako C, Andemariam B, Colombatti R, Asare EV, Strunk C, Piccone CM, Manwani D, Boruchov D, Farooq F, Urbonya R, Wilson S, Boatemaa GD, Perrotta S, Sainati L, Rivers A, Rao S, Zempsky W, Ekem I, Sey F, Segbefia C, Inusa B, Tartaglione I, Campbell AD | Ann. Hematol. | 2020 |
| Partial recovery of vegetative state after a massive ischaemic stroke in a child with sickle cell anaemia. | Machado C, Rodríguez-Rojas R, Leisman G | BMJ Case Rep | 2020 |
| Total Hip Arthroplasty in Patients With Sickle Cell Disease: A Comprehensive Systematic Review. | Fassihi SC, Lee R, Quan T, Tran AA, Stake SN, Unger AS | J Arthroplasty | 2020 |
| Psychosocial Burden of Childhood Sickle Cell Disease on Caregivers in Kenya. | Kuerten BG, Brotkin S, Bonner MJ, Ayuku DO, Njuguna F, Taylor SM, Puffer ES | J Pediatr Psychol | 2020 |
| Association between plasma and urinary orosomucoid and chronic kidney disease in adults with sickle cell disease. | Jerebtsova M, Taye A, Smith N, Afangbedji N, Stokes D, Niu X, Diaz S, Taylor JG, Nekhai S | Br. J. Haematol. | 2020 |
| Hb S (: c.20A>T) and α- and β-Thalassemia Coinheritance in Iranian Patients. | Azarkeivan A, Cohan N, Niazkar HR, Azizi A, Rad F | Hemoglobin | 2020 |
| COVID-19 infection and sickle cell disease: a UK centre experience. | McCloskey KA, Meenan J, Hall R, Tsitsikas DA | Br. J. Haematol. | 2020 |
| A decision support scheme for beta thalassemia and HbE carrier screening. | Das R, Datta S, Kaviraj A, Sanyal SN, Nielsen P, Nielsen I, Sharma P, Sanyal T, Dey K, Saha S | J Adv Res | 2020 |
| [Pain management in sickle cell disease]. | Rasche T, Emmert D, Seidel H, Sellin J, Conrad R, Mücke M | Schmerz | 2020 |
| Outcomes related to intravenous fluid administration in sickle cell patients during vaso-occlusive crisis. | Gaut D, Jones J, Chen C, Ghafouri S, Leng M, Quinn R | Ann. Hematol. | 2020 |
| Acetazolamide aggravated diabetic ketoacidosis severity in a boy post-transplantation thalassaemia with intracranial hypertension. | Sakornyutthadej N, Mahachoklertwattana P, Anantasit N, Hongeng S, Poomthavorn P | J Paediatr Child Health | 2020 |
| Shift of HbF to HbA under Influence of SKA2 Gene; A Possible Link between Cortisol and Hematopoietic Maturation in Term and Preterm Newborns. | Ijabi J, Afrisham R, Moradi-Sardareh H, Roozehdar P, Seifi F, Sahebkar A, Ijabi R | Endocr Metab Immune Disord Drug Targets | 2020 |
| Noninvasive prenatal diagnosis for pregnancies at risk for β-thalassaemia: a retrospective study. | Lv W, Linpeng S, Li Z, Liang D, Jia Z, Meng D, Cram DS, Zhu H, Teng Y, Yin A, Wu L | BJOG | 2020 |
| Red blood cell consumption in a large cohort of patients with thalassaemia: a retrospective analysis of main predictors. | Ricchi P, Meloni A, Costantini S, Spasiano A, Cinque P, Gargiulo B, Pepe A, Filosa A | Ann. Hematol. | 2020 |
| Sickle cell anemia in the state of Maranhão: a haplotype study. | Alves AC, da Silva VAL, Dos Santos A, Serra MB, Marques FA, Cruz SMP, Barroso WA, de Oliveira RAG | Ann. Hematol. | 2020 |
| Sickle cell disease as a vascular disorder. | Ofori-Acquah SF | Expert Rev Hematol | 2020 |
| The Use of Religion in the Management of Depression in Sickle Cell Disease: A Systematic Review. | Quasie-Woode DP, Cunningham-Erves J, Mayo-Gamble TL | J Relig Health | 2020 |
| Application of HbA levels and red cell indices-based new model in the differentiation of thalassemia traits from iron deficiency in hypochromic microcytic anemia Cases. | Zhou Y, Zhang J, Wang C, Zhou L, Zhou L, Ou D, Peng D | Int J Lab Hematol | 2020 |
| Placental transcriptome profile of women with sickle cell disease reveals differentially expressed genes involved in migration, trophoblast differentiation and inflammation. | Baptista LC, Costa ML, Surita FG, Rocha CS, Lopes-Cendes I, Souza BB, Costa FF, Melo MB | Blood Cells Mol. Dis. | 2020 |
| Functional polymorphisms of BCL11A and HBS1L-MYB genes affect both fetal hemoglobin level and clinical outcomes in a cohort of children with sickle cell anemia. | Sales RR, Belisário AR, Faria G, Mendes F, Luizon MR, Viana MB | Ann. Hematol. | 2020 |
| COVID-19: beta-thalassemia subjects immunised? | Lansiaux E, Pébaÿ PP, Picard JL, Son-Forget J | Med. Hypotheses | 2020 |
| Gene therapies for transfusion dependent β-Thalassemia: current status and critical criteria for success. | Soni S | Am. J. Hematol. | 2020 |
| SC411 treatment can enhance survival in a mouse model of sickle cell disease. | Wu CYC, Lopez-Toledano MA, Daak AA, Clemons GA, Citadin CT, Sancilio FD, Rabinowicz AL, Minagar A, Neumann JT, Lee RHC, Lin HW | Prostaglandins Leukot. Essent. Fatty Acids | 2020 |
| The Impact of Sickle Cell Anemia and Mental Health Diagnoses on Healthcare Use and Preventive Care among Children Enrolled in Medicaid, 2005-2012. | Gondhi JP, Dombkowski KJ, Scott EL, Reeves SL | J. Pediatr. | 2020 |
| Voxelotor Treatment Interferes With Quantitative and Qualitative Hemoglobin Variant Analysis in Multiple Sickle Cell Disease Genotypes. | Rutherford-Parker NJ, Campbell ST, Colby JM, Shajani-Yi Z | Am. J. Clin. Pathol. | 2020 |
| American Society of Hematology 2020 guidelines for sickle cell disease: management of acute and chronic pain. | Brandow AM, Carroll CP, Creary S, Edwards-Elliott R, Glassberg J, Hurley RW, Kutlar A, Seisa M, Stinson J, Strouse JJ, Yusuf F, Zempsky W, Lang E | Blood Adv | 2020 |
| Managing sickle cell patients with COVID-19 infection: the need to pool our collective experience. | Sahu KK, Siddiqui AD, Cerny J | Br. J. Haematol. | 2020 |
| Knowledge, awareness, and attitude of premarital screening with special focus on sickle cell disease: a study from Odisha. | Bindhani BK, Devi NK, Nayak JK | J Community Genet | 2020 |
| Beta Thalassemia: New Therapeutic Options Beyond Transfusion and Iron Chelation. | Motta I, Bou-Fakhredin R, Taher AT, Cappellini MD | Drugs | 2020 |
| Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Congenital Anemias. | Steinberg-Shemer O, Tamary H | Mol Diagn Ther | 2020 |
| Cardiac T2* MR in patients with thalassemia major: a 10-year long-term follow-up. | Daar S, Al Khabori M, Al Rahbi S, Hassan M, El Tigani A, Pennell DJ | Ann. Hematol. | 2020 |
| Correcting β-thalassemia by combined therapies that restrict iron and modulate erythropoietin activity. | Casu C, Pettinato M, Liu A, Aghajan M, Lo Presti V, Lidonnici MR, Munoz KA, O'Hara E, Olivari V, Di Modica SM, Booten S, Guo S, Neil G, Miari R, Shapir N, Zafir-Lavie I, Domev H, Ferrari G, Sitara D, Nai A, Rivella S | Blood | 2020 |
| Differential diagnosis of hereditary hemolytic anemias in a single multiscreening test by TGA/chemometrics. | Risoluti R, Caprari P, Gullifa G, Sorrentino F, Maffei L, Massimi S, Carcassi E, Materazzi S | Chem. Commun. (Camb.) | 2020 |
| The Effects of L-Carnitine on Echocardiographic Changes in Patients With β-Thalassemia Major and Intermedia. | Shahidi M, Hashemi SR, Fattahi N, Roshani D, Vahedi S, Sharifi P, Moradveisi B | J. Pediatr. Hematol. Oncol. | 2020 |
| Magnetic mechanism for the biological functioning of hemoglobin. | Mayda S, Kandemir Z, Bulut N, Maekawa S | Sci Rep | 2020 |
| [Prevalence and Genotypes Analysis of Thalassemia Among People of Reproductive Age in Yuzhong District of Chongqing Based on Next-Generation Sequencing]. | Qin M, Gu HY, Zhang HY, Ren J, Peng R, Zhu X | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2020 |
| [Analysis of the Types of Thalassemia Gene Mutations in Nanping Area of Fujian, China]. | Chen MF, Huang MZ, Lin Q, Huang J, Chen F, Zhang JY, Xue F | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2020 |
| Association between hospital admissions and healthcare provider communication for individuals with sickle cell disease. | Cronin RM, Yang M, Hankins JS, Byrd J, Pernell BM, Kassim A, Adams-Graves P, Thompson AA, Kalinyak K, DeBaun M, Treadwell M | Hematology | 2020 |
| Further Characterization of Hb Bronovo [α103(G10)His→Leu; : c.311A>T] and First Report of the Homozygous State. | Mehta N, Johnston JM, Hein M, Kipp BR, Coon L, Savedra ME, Hoyer JD, He R, Rangan A, Shi M, Oliveira JL | Hemoglobin | 2020 |
| COVID-19 in a Patient with β-Thalassemia Major and Severe Pulmonary Arterial Hypertension. | Pinto VM, Derchi GE, Bacigalupo L, Pontali E, Forni GL | Hemoglobin | 2020 |
| Correction to: The role of using different reference population in the prevalence of low BMD in the thalassemia patients. | Mohajeri-Tehrani MR, Darvishian N, Arab F, Salemkar S, Mohseni F, Larijani B, Hamidi Z | J Diabetes Metab Disord | 2020 |
| Perceptions and Practice of Early Diagnosis of Sickle Cell Disease by Parents and Physicians in a Southwestern State of Nigeria. | Olatunya OS, Babatola AO, Ogundare EO, Olofinbiyi BA, Lawal OA, Awoleke JO, Aduloju OP, Daramola AO, Emmanuel EE, Olajuyin OA, Komolafe AK, Olaleye AO | ScientificWorldJournal | 2020 |
| Frontal Bone Infarctions Masquerading as Bilateral Orbital Cellulitis in a Patient with Sickle Cell Disease. | Al Somali AI, Bin Helayel HS, Jubran SA, Hariri JT, Nassim Ali HM | Middle East Afr J Ophthalmol | 2020 |
| Knowledge and awareness of individual sickle cell genotype among adolescents in a unity school in Southeast, Nigeria: a cross-sectional study. | Ezenwosu OU, Chukwu BF, Ezenwosu IL, Ikefuna AN, Emodi IJ, Ezeanolue EE | Int J Adolesc Med Health | 2020 |
| [Sickle cell disease]. | Distelmaier L, Dührsen U, Dickerhoff R | Internist (Berl) | 2020 |
| Haplotype Analysis in Carriers of -Globin Gene Mutation Facilitates Genetic Counseling in -Thalassemia: A Cross-Sectional Study in Kerman Province, Iran. | Saleh-Gohari N, Saeidi K, Ziaadini-Dashtkhaki S | Iran. J. Public Health | 2020 |
| N-acetylcysteine Restored Heart Rate Variability and Prevented Serious Adverse Events in Transfusion-dependent Thalassemia Patients: a Double-blind Single Center Randomized Controlled Trial. | Pattanakuhar S, Phrommintikul A, Tantiworawit A, Srichairattanakool S, Chattipakorn SC, Chattipakorn N | Int J Med Sci | 2020 |
| Massive Transfusion Protocols for Pediatric Patients: Current Perspectives. | Evangelista ME, Gaffley M, Neff LP | J Blood Med | 2020 |
| Letter to the Editor Regarding | Yu J, Du Q, Chen J | World Neurosurg | 2020 |
| Polymorphisms of the receptor for advanced glycation end products as vasculopathy predictor in sickle cell disease. | Safwat NA, ELkhamisy MM, Abdel-Wahab SEA, Hamza MT, Boshnak NH, Kenny MA | Pediatr. Res. | 2020 |
| Macular Infarction in a Patient with Sickle Cell Trait. | Dow ER, Tsui I, Sarraf D | Retin Cases Brief Rep | 2020 |
| Liver Transplantation in Patients with Sickle Cell Disease in the United States. | Hogen R, Kim M, Lee Y, Lo M, Kaur N, Kahn J, Chopra S, Qazi Y, Sedra A, Kim J, O'Brien L, Genyk Y, Sher L, Emamaullee J | J. Surg. Res. | 2020 |
| -Induced Cellulitis in an Immunocompetent Patient With Sickle Cell Disease: A Case Report. | Samrah S, Sweidan A, Aleshawi A, Ayesh M | J Investig Med High Impact Case Rep | 2020 |
| Splenomegaly May Increase the Risk of Rejection in Low-Risk Matched Related Donor Transplant for Thalassemia, This Risk Can Be Partially Overcome by Additional Immunosuppression during Conditioning. | Ramprakash S, Raghuram CP, Marwah P, Soni R, Trivedi D, Khalid S, Yaqub N, Itrat F, Gilani SK, Zahra T, Dhanya R, Agarwal RK, Faulkner L | Biol Blood Marrow Transplant. | 2020 |
| Integration of Mobile Health Into Sickle Cell Disease Care to Increase Hydroxyurea Utilization: Protocol for an Efficacy and Implementation Study. | Hankins JS, Shah N, DiMartino L, Brambilla D, Fernandez ME, Gibson RW, Gordeuk VR, Lottenberg R, Kutlar A, Melvin C, Simon J, Wun T, Treadwell M, Calhoun C, Baumann A, Potter MB, Klesges L, Bosworth H, | JMIR Res Protoc | 2020 |
| Advances in Sickle Cell Disease Management. | Engel ER, Howard AL, Ankus EJ, Rico JF | Adv Pediatr. | 2020 |
| Implementing newborn screening for sickle cell disease as part of immunisation programmes in Nigeria: a feasibility study. | Nnodu OE, Sopekan A, Nnebe-Agumadu U, Ohiaeri C, Adeniran A, Shedul G, Isa HA, Owolabi O, Chianumba RI, Tanko Y, Iyobosa JH, Adekile AD, Olopade OI, Piel FB | Lancet Haematol | 2020 |
| β2-Microglobulin, Neutrophil Gelatinase-Associated Lipocalin, and Endocan Values in Evaluating Renal Functions in Patients with β-Thalassemia Major. | Cetinkaya PU, Azik FM, Karakus V, Huddam B, Yilmaz N | Hemoglobin | 2020 |
| Addressing bias towards patients with sickle cell disease. | DeLaune J, Close J, Murphy M | Lancet Haematol | 2020 |
| Screening infants for sickle cell disease in sub-Saharan Africa: starting the journey to a sustainable model in primary care. | Streetly A | Lancet Haematol | 2020 |
| Mirror aneurysms of extracranial internal carotid arteries in a patient with beta-thalassemia major. | Taydas O, Guven F, Ogul H, Ogul Y | Acta Neurol Belg | 2020 |
| Sickle cell trait and the potential risk of severe coronavirus disease 2019-A mini-review. | Kehinde TA, Osundiji MA | Eur J Haematol | 2020 |
| The Spectrum of α-Thalassemia Mutations in Kurdistan Province, West Iran. | Alibakhshi R, Moradi K, Aznab M, Dastafkan Z, Tahmasebi S, Ahmadi M, Omidniakan | Hemoglobin | 2020 |
| Emotional distress among parent caregivers of adolescents with sickle cell disease: Association with patients and caregivers variables. | Bioku AA, Ohaeri JU, Oluwaniyi SO, Olagunju TO, Chaimowitz GA, Olagunju AT | J Health Psychol | 2020 |
| Determination of mutations in iron regulating genes of beta thalassemia major patients of Khyber Pakhtunkhwa, Pakistan. | Shah M, Danish L, Khan NU, Zaman F, Ismail M, Hussain M, Pervaiz R, Iqbal A | Mol Genet Genomic Med | 2020 |
| Haptoglobin Gene Polymorphism in Patients with Sickle Cell Anemia: Findings from a Nigerian Cohort Study. | Olatunya OS, Albuquerque DM, Santos MNN, Kayode TS, Adekile A, Costa FF | Appl Clin Genet | 2020 |
| Combination of ferric ammonium citrate with cytokines involved in apoptosis and insulin secretion of human pancreatic beta cells related to diabetes in thalassemia. | Rattanaporn P, Tongsima S, Mandrup-Poulsen T, Svasti S, Tanyong D | PeerJ | 2020 |
| Author Correction: Origin of complexity in haemoglobin evolution. | Pillai AS, Chandler SA, Liu Y, Signore AV, Cortez-Romero CR, Benesch JLP, Laganowsky A, Storz JF, Hochberg GKA, Thornton JW | Nature | 2020 |
| Thromboinflammatory mechanisms in sickle cell disease - challenging the hemostatic balance. | Conran N, De Paula EV | Haematologica | 2020 |
| 2'-O-methoxyethyl splice-switching oligos correct splicing from IVS2-745 β-thalassemia patient cells restoring HbA production and chain rebalance. | Dong A, Ghiaccio V, Motta I, Guo S, Peralta R, Freier SM, Watt A, Damle S, Ikawa Y, Jarocha D, Chappell M, Stephanou C, Delbini P, Chen C, Christou S, Kleanthous M, Smith-Whitley K, Manwani D, Casu C, Abdulmalik O, Cappellini MD, Rivella S, Breda L | Haematologica | 2020 |
| Parents of Children with Sickle Cell Disease Are Interested in Preimplantation Genetic Testing. | Attia M, Kripalani S, Darbari I, Nickel RS | J Pediatr | 2020 |
| Vaso-occlusive crisis of the temporo-mandibular joint: An unusual finding in sickle cell disease. | Plantin S, Allali S, Khonsari RH, De Montalembert M, Segna E | J Stomatol Oral Maxillofac Surg | 2020 |
| Characterization of circulating and cultured Tfh-like cells in sickle cell disease in relation to red blood cell alloimmunization status. | Balbuena-Merle R, Santhanakrishnan M, Devine L, Gibb DR, Tormey CA, Siddon AJ, Curtis SA, Gallagher PG, Weinstein JS, Hendrickson JE | Transfus. Apher. Sci. | 2020 |
| Genotype-Phenotype Correlation of β-Thalassemia in Malaysian Population: Toward Effective Genetic Counseling. | Abdullah UYH, Ibrahim HM, Mahmud NB, Salleh MZ, Teh LK, Noorizhab MNFB, Zilfalil BA, Jassim HM, Wilairat P, Fucharoen S | Hemoglobin | 2020 |
| Micromapping of Thalassemia and Hemoglobinopathies Among Laos, Khmer, Suay and Yer Ethnic Groups Residing in Lower Northeastern Thailand. | Bunthupanich R, Karnpean R, Pinyachat A, Jiambunsri N, Prakobkaew N, Pakdee N, Fucharoen S, Fucharoen S | Hemoglobin | 2020 |
| Red cell exchange for patients with sickle cell disease: an international survey of current practices. | Karafin MS, Hendrickson JE, Kim HC, Kuliya-Gwarzo A, Pagano MB, Perumbeti A, Shi PA, Tanhehco YC, Webb J, Wong E, Eichbaum Q | Transfusion | 2020 |
| Anterior Chamber Angle, Intraocular Pressure, and Globe Biometric Parameters in the Children with β-Thalassemia Major. | El-Haddad NS | J Curr Glaucoma Pract | 2020 |
| Trans-Sternal Repair of Incidentally Diagnosed Morgagni Hernia during Ventricular Septal Defect Closure in a Sickle Cell Trait Infant. | Palanisamy V, Raman RK, Indrajith SD, Agarwal R | J Indian Assoc Pediatr Surg | 2020 |
| Hydroxyurea Dose Escalation for Sickle Cell Anemia in Sub-Saharan Africa. | John CC, Opoka RO, Latham TS, Hume HA, Nabaggala C, Kasirye P, Ndugwa CM, Lane A, Ware RE. | N Engl J Med. | 2020 |
| Blood utilization and characteristics of patients treated with chronic transfusion therapy in a large cohort of Brazilian patients with sickle cell disease. | Kelly S, Belisário AR, Werneck Rodrigues DO, Carneiro-Proietti ABF, Gonçalez TT, Loureiro P, Flor-Park MV, Maximo C, Mota RA, Dinardo C, Brambilla D, Preiss L, Sabino E, Custer B, | Transfusion | 2020 |
| Liver necrosis following cholecystectomy in sickle cell disease. | Muttillo EM, Felli E, Pessaux P | Clin Case Rep | 2020 |
| Right ventricular function among South East Nigeria children with sickle cell anaemia. | Chinawa JM, Chukwu BF, Chinawa AT, Ossai EN, Ikefuna AN, Aronu AE, Obidike EO | BMC Pediatr | 2020 |
| Urinary Tract Infection in Febrile Children with Sickle Cell Disease Who Present to the Emergency Room with Fever. | Patel N, Farooqi A, Callaghan M, Sethuraman U | J Clin Med | 2020 |
| Thalassemia Major and Intermedia Patients in East Java do not Show Fetal Hemoglobin Level Difference in Relation to XMNI Polymorphism. | Wulandari RD, Lyrawati D, Fatchiyah F, Fitri LE | Med Arch | 2020 |
| Comparative targeting analysis of KLF1, BCL11A, and HBG1/2 in CD34 HSPCs by CRISPR/Cas9 for the induction of fetal hemoglobin. | Lamsfus-Calle A, Daniel-Moreno A, Antony JS, Epting T, Heumos L, Baskaran P, Admard J, Casadei N, Latifi N, Siegmund DM, Kormann MSD, Handgretinger R, Mezger M | Sci Rep | 2020 |
| Thrombin generation in children with sickle cell Anemia is Higher in the presence of platelets. | Menon N, Journeycake J, Huang R, Riley P, Zia A | Transfus Apher Sci | 2020 |
| Impact of neuropathic pain on quality of life in adults with sickle cell disease: observational study. | Santos LFOD, Guimarães MW, Baptista AF, Sá KN | Hematol Transfus Cell Ther | 2020 |
| Asymptomatic carriage of Plasmodium falciparum by individuals with variant blood groups and haemoglobin genotypes in southern Ghana. | Acquah FK, Donu D, Bredu D, Eyia-Ampah S, Amponsah JA, Quartey J, Obboh EK, Mawuli BA, Amoah LE | Malar J | 2020 |
| High molecular weight kininogen contributes to early mortality and kidney dysfunction in a mouse model of sickle cell disease. | Sparkenbaugh EM, Kasztan M, Henderson MW, Ellsworth P, Davis PR, Wilson KJ, Reeves B, Key NS, Strickland S, McCrae K, Pollock DM, Pawlinski R | J Thromb Haemost | 2020 |
| COVID-19 and thalassaemia: A position statement of the Thalassaemia International Federation. | Farmakis D, Giakoumis A, Cannon L, Angastiniotis M, Eleftheriou A | Eur J Haematol | 2020 |
| Liver damage and sickle cell disease: genotype relationship. | Bortolotti M, D'Ambrosio R, Fraquelli M, Pedrotti P, Consonni D, Migone De Amicis M, Scaramellini N, Di Pierro E, Graziadei G | Ann Hematol | 2020 |
| A hypothesis about the role of fetal hemoglobin in COVID-19. | Sotoudeh E, Sotoudeh H | Med Hypotheses | 2020 |
| Immune mechanisms involved in sickle cell disease pathogenesis: current knowledge and perspectives. | de Azevedo JTC, Malmegrim KCR | Immunol. Lett. | 2020 |
| Impact of splenectomy on outcomes of hematopoietic stem cell transplantation in pediatric patients with transfusion-dependent thalassemia. | Sanpakit K, Narkbunnam N, Buaboonnam J, Takpradit C, Viprakasit V, Pongtanakul B | Pediatr Blood Cancer | 2020 |
| Interventions for treating intrahepatic cholestasis in people with sickle cell disease. | Martí-Carvajal AJ, Martí-Amarista CE | Cochrane Database Syst Rev | 2020 |
| UNC0638 induces high levels of fetal hemoglobin expression in β-thalassemia/HbE erythroid progenitor cells. | Nualkaew T, Khamphikham P, Pongpaksupasin P, Kaewsakulthong W, Songdej D, Paiboonsukwong K, Sripichai O, Engel JD, Hongeng S, Fucharoen S, Jearawiriyapaisarn N | Ann Hematol | 2020 |
| Hb Westmead (: c.369C>G): Hematological Characteristics in Heterozygotes with and without α-Thalassemia. | Jiang F, Ju AP, Li J, Chen GL, Zhou JY, Tang XW, Zuo LD, Li DZ | Hemoglobin | 2020 |
| Leucocytosis and Asymptomatic Urinary Tract Infections in Sickle Cell Patients at a Tertiary Hospital in Zambia. | Musonda T, Zulu M, Samutela M, Kalonda A, Mantina H, Okuku P, Sinkala M, Nkhoma P | Anemia | 2020 |
| Socioeconomic status dependent medical complexities in children with sickle cell disease in Saudi Arabia. | Khan SA, AlSiny F, Makki A, Ali A, AlAnsari I, Khan S | Saudi J Biol Sci | 2020 |
| Cumulative outcome of pre-implantation genetic diagnosis for sickle cell disease: a 5-year review. | Vali S, Mukhtar S, Nandi A, Wilson K, Oakley L, El-Toukhy T, Oteng-Ntim E | Br J Haematol | 2020 |
| Thalassemia in the emergency department: special considerations for a rare disease. | Saliba AN, Atoui A, Labban M, Hamade H, Bou-Fakhredin R, Mufarrij A, Taher AT | Ann Hematol | 2020 |
| Severity of heart failure and health-related quality of life in beta-thalassemia patients: a cross-sectional study. | Dimitroglou Y, Anagnostopoulos F, Aggeli C, Delicou S, Xydaki A, Patsourakos D, Tousoulis D | Ann. Hematol. | 2020 |
| Prognostic value of left ventricular longitudinal strain by speckle-tracking echocardiography in patients with sickle cell disease. | Resende MBS, Ferrari TCA, Araujo CG, Vasconcelos MCM, Tupinambás JT, Dias RCTM, Barros FC, Januário JN, Barbosa MM, Nunes MCP | Int J Cardiovasc Imaging | 2020 |
| Evaluation of Cardiac Function in Patients with Sickle Cell Disease with Left Ventricular Global Longitudinal Strain. | Morissens M, Besse-Hammer T, Azerad MA, Efira A, Rodriguez JC | J Transl Int Med | 2020 |
| The effect of anticoagulant choice on venous thromboembolism recurrence and bleeding in sickle cell disease. | Gupta VK, Strykowski R, Scarpato B, Lawrence R, Khan SL, Patel J, Nouraie SM, Cohen RT, Sloan JM, Klings ES | Am J Hematol | 2020 |
| Paracentral Acute Middle Maculopathy as a Presenting Sign of CRAO in Sickle Cell Disease Treated with Tissue Plasminogen Activator. | Chua MR, Giovinazzo JV, Kaplan RI, Connor T, Kellner C, Barash A, Rosen RB | Retin Cases Brief Rep | 2020 |
| Hematopoietic stem cell transplantation for people with sickle cell disease. | Oringanje C, Nemecek E, Oniyangi O | Cochrane Database Syst Rev | 2020 |
| Altered pulmonary capillary blood volume in childhood sickle cell disease. | Bokov P, Boizeau P, Pautrat J, Missud F, Ba A, Haouari Z, Denjean A, Delclaux C, Benkerrou M | Eur Respir J | 2020 |
| [Gene characteristics and changing trend of neonatal thalassemia in Dongguan, China]. | Zhong YH, Ye LX, Cai XJ, Xie CL, Chen JG | Zhongguo Dang Dai Er Ke Za Zhi | 2020 |
| Outcomes of haemoglobin Bart's hydrops fetalis following intrauterine transfusion in Ontario, Canada. | Zhang HJ, Amid A, Janzen LA, Segbefia CI, Chen S, Athale U, Charpentier K, Merelles-Pulcini M, Seaward G, Kelly EN, Odame I, Waye JS, Ryan G, Kirby-Allen M | Arch Dis Child Fetal Neonatal Ed | 2020 |
| Urinary Metabolic Profile of Patients with Transfusion-Dependent β-Thalassemia Major Undergoing Deferasirox Therapy. | Capolongo G, Zacchia M, Beneduci A, Costantini S, Cinque P, Spasiano A, De Luca G, Di Pietro ME, Ricchi P, Trepiccione F, Capasso G, Filosa A | Kidney Blood Press. Res. | 2020 |
| Biomarkers and genetic modulators of cerebral vasculopathy in sub-Saharan ancestry children with sickle cell anemia. | Silva M, Vargas S, Coelho A, Ferreira E, Mendonça J, Vieira L, Maia R, Dias A, Ferreira T, Morais A, Soares IM, Lavinha J, Silva R, Kjöllerström P, Faustino P | Blood Cells Mol. Dis. | 2020 |
| The Homozygous Hemoglobin EE Variant Is Associated with Poorer Riboflavin Status in Cambodian Women of Reproductive Age. | Williams BA, Cochrane KM, Fischer JAJ, Aljaadi AM, McAnena L, Ward M, McNulty H, Kroeun H, Green TJ, Whitfield KC, Karakochuk CD | J. Nutr. | 2020 |
| Anti-C5 antibody treatment for delayed hemolytic transfusion reactions in sickle cell disease. | Floch A, Morel A, Zanchetta-Balint F, Cordonnier-Jourdin C, Allali S, Grall M, Ithier G, Carpentier B, Pakdaman S, Merle JC, Goulabchand R, Khalifeh T, Berceanu A, Helmer C, Chantalat-Auger C, Frémeaux-Bacchi V, Michel M, de Montalembert M, Mekontso-Dessap A, Pirenne F, Habibi A, Bartolucci P | Haematologica | 2020 |
| Beta-thalassemia may protect against COVID 19. | Drouin E | Med Hypotheses | 2020 |
| Hereditary Hemorrhagic Telangiectasia in a Sickle Cell Trait Patient: A Report of a Rare Case with Use of Nuclear Medicine, and a Literature Review. | Kang HC, Martins Pereira MA, Silva LNL, Oliveira LC, Márvila IS | Am J Case Rep | 2020 |
| L-Selectin P213S and Integrin Alpha 2 C807T Genetic Polymorphisms in Pediatric Sickle Cell Disease Patients. | Shaheen I, Khorshied M, Abdel-Raouf R, Gouda H, Kamal D, Abulata N, Aboukhalil R, Meligy B | J. Pediatr. Hematol. Oncol. | 2020 |
| Fatal complication of sickle cell anemia in an immigrant patient rescued from the mediterranean sea. | Alongi A, Ventura Spagnolo E, Zerbo S, Aronica GL, Korte F, Maresi E, Argo A | Clin Ter | 2020 |
| The association between timely opioid administration and hospitalization in children with sickle cell disease presenting to the emergency department in acute pain. | Muslu CS, Kopetsky M, Nimmer M, Visotcky A, Fraser R, Brousseau DC | Pediatr Blood Cancer | 2020 |
| Genetic counselling in sickle cell disease: views of single young adults in Ghana. | Appiah S, Korsah KA, AmpongAdjei C, Appiah OE | J Community Genet | 2020 |
| In Vitro Lymphocyte Functions in Undernourished Children With Sickle Cell Anemia. | Kuvibidila SR, Gardner R, Velez MC, Yu L, Warrier RP | Ochsner J | 2020 |
| Replacing the suppressed hormone: toward a better treatment for iron overload in β-thalassemia major? | Girelli D, Busti F | Haematologica | 2020 |
| Necrobiosis Lipoidica in a Patient with β-Thalassemia Major: A Case Report and Review of the Literature. | Vetsiou E, Mpouras V, Nikolaidou C, Klonizakis P, Mandala E, Vamvakis K, Psarras K, Vlachaki E | Hemoglobin | 2020 |
| Utilising red cell antigen genotyping and serological phenotyping in sickle cell disease patients to risk-stratify patients for alloimmunisation risk. | Shih AW, Yan MTS, Elahie AL, Barty RL, Liu Y, Berardi P, Azzam M, Siddiqui R, Parvizian MK, Mcdougall T, Heddle NM, Al-Habsi KS, Goldman M, Cote J, Athale U, Verhovsek MM | Transfus Med | 2020 |
| A Woman with Missing Hb A Due to a Novel (εγ)δβ-Thalassemia and a Novel δ-Globin Variant Hb A-Gebenstorf (: c.209G>A). | Saller E, Knijnenburg J, Harteveld CL, Dutly F | Hemoglobin | 2020 |
| Umbilical Cord Blood Screening for the Detection of Common Deletional Mutations of α-Thalassemia in Bangladesh. | Anwar S, Taslem Mourosi J, Hasan MK, Hosen MJ, Miah MF | Hemoglobin | 2020 |
| Iconic Visualization of Sickle Cell Patients Current and Past Health Status. | Diallo AH, Camara G, Lo M, Diagne I, Lamy JB | Stud Health Technol Inform | 2020 |
| Potential Risk Factors Associated With Graft Failure of Haploidentical Hematopoietic Stem Cell Transplantation (HSCT) in Children With Sickle Cell Disease (SCD). | Yu J, Black V, Lamba J, Horn B | J Pediatr Hematol Oncol | 2020 |
| Observational study on the current status of thalassaemia in Malaysia: a report from the Malaysian Thalassaemia Registry. | Mohd Ibrahim H, Muda Z, Othman IS, Mohamed Unni MN, Teh KH, Thevarajah A, Gunasagaran K, Ong GB, Yeoh SL, Muhammad Rivai A, Che Mohd Razali CH, Din ND, Abdul Latiff Z, Jamal R, Mohamad N, Mohd Ariffin H, Alias H | BMJ Open | 2020 |
| Angioid streaks secondary to homozygous sickle cell disease. | Malek Y, Abdellaoui T, Khmamouche M, Zerrouk R, Reda K, Oubaaz A | J Fr Ophtalmol | 2020 |
| Non-deletional alpha thalassaemia: a review. | Kalle Kwaifa I, Lai MI, Md Noor S | Orphanet J Rare Dis | 2020 |
| Folic acid supplementation in children with sickle cell disease: study protocol for a double-blind randomized cross-over trial. | Williams BA, McCartney H, Adams E, Devlin AM, Singer J, Vercauteren S, Wu JK, Karakochuk CD | Trials | 2020 |
| Silent Cerebral Infarct in Sickle Cell Anemia Patients of South Turkey. | Nafİle Sayman E, Leblebİsatan G, Leblebİsatan Ş, BiÇakci YK, KilinÇ Y, BarutÇu A | Turk J Med Sci | 2020 |
| Validation of the fine motor subtest of the Bayley-III with children with sickle cell disease using Rasch analysis. | L'Hotta AJ, Hoyt CR, Lindsey T, Abel RA, Chang CH, King AA | Child Care Health Dev | 2020 |
| The Economic Burden of End-Organ Damage Among Medicaid Patients with Sickle Cell Disease in the United States: A Population-Based Longitudinal Claims Study. | Campbell A, Cong Z, Agodoa I, Song X, Martinez DJ, Black D, Lew CR, Varker H, Chan C, Lanzkron S | J Manag Care Spec Pharm | 2020 |
| A Wide Spectrum Study of α-Globin Chain Variants: Cases from the UK. | Khalil MSM, Timbs AT, Henderson SJ, Schuh A, El-Khawanky MM, Old JM | Hemoglobin | 2020 |
| Management of haemoglobin Barts hydrops fetalis syndrome with exchange transfusions. | Ong J, Bowden D, Kaplan Z | Intern Med J | 2020 |
| Identification of a new hemoglobin variant Hb Liuzhou [:C.182A→G] by MALDI-TOF mass spectrometry during HbA measurement. | Xu A, Chen W, Xie W, Ji L | Scand J Clin Lab Invest | 2020 |
| Red Blood Cell-Mediated S-Nitrosohemoglobin-Dependent Vasodilation: Lessons Learned from a β-Globin Cys93 Knock-in Mouse. | Premont RT, Reynolds JD, Zhang R, Stamler JS | Antioxid Redox Signal | 2020 |
| Epigenetic Reexpression of Hemoglobin F Using Reversible LSD1 Inhibitors: Potential Therapies for Sickle Cell Disease. | Holshouser S, Cafiero R, Robinson M, Kirkpatrick J, Casero RA, Hyacinth HI, Woster PM | ACS Omega | 2020 |
| Hemoglobin S/O: Retinal Manifestations of a Rare Hemoglobinopathy. | Sanders R, Ly V, Ahmad K, Swift J, Sallam A, Uwaydat S | Case Rep Ophthalmol | 2020 |
| Differences among hemoglobin thresholds for red blood cell transfusions in patients with hematological diseases in teaching hospitals: a real world data in Japan. | Yokohama A, Okuyama Y, Ueda Y, Itoh M, Fujiwara SI, Hasegawa Y, Nagai K, Arakawa K, Miyazaki K, Makita M, Watanabe M, Ikeda K, Tanaka A, Fujino K, Matsumoto M, Makino S, Kino S, Takeshita A, Muroi K | Int J Hematol | 2020 |
| Combating iron overload: a case for deferoxamine-based nanochelators. | Jones G, Goswami SK, Kang H, Choi HS, Kim J | Nanomedicine (Lond) | 2020 |
| LOVD-DASH: A comprehensive LOVD database coupled with diagnosis and an at-risk assessment system for hemoglobinopathies. | Zhang L, Zhang Q, Tang Y, Cong P, Ye Y, Chen S, Zhang X, Chen Y, Zhu B, Cai W, Chen S, Cai R, Guo X, Zhang C, Zhou Y, Zou J, Liu Y, Chen B, Yan S, Chen Y, Zhou Y, Ding H, Li X, Chen D, Zhong J, Shang X, Liu X, Qi M, Xu X | Hum. Mutat. | 2019 |
| Dual-energy X-ray absorptiometry pitfalls in Thalassemia Major. | Pellegrino F, Zatelli MC, Bondanelli M, Carnevale A, Cittanti C, Fortini M, Gamberini MR, Giganti M, Ambrosio MR | Endocrine | 2019 |
| Surface plasmon resonance based analysis of the binding of LYAR protein to the rs368698783 (G>A) polymorphic Aγ-globin gene sequences mutated in β-thalassemia. | Gemmo C, Breveglieri G, Marzaro G, Lampronti I, Cosenza LC, Gasparello J, Zuccato C, Fabbri E, Borgatti M, Chilin A, Finotti A, Gambari R | Anal Bioanal Chem | 2019 |
| Genotype-phenotype association analysis identifies the role of α globin genes in modulating disease severity of β thalassaemia intermedia in Sri Lanka. | Perera S, Allen A, Silva I, Hapugoda M, Wickramarathne MN, Wijesiriwardena I, Allen S, Rees D, Efremov DG, Fisher CA, Weatherall DJ, Premawardhena A | Sci Rep | 2019 |
| Gene therapy of hematological disorders: current challenges. | Al-Saif AM | Gene Ther. | 2019 |
| Transfusing children with hemoglobinopathies. | Allali S, Taylor M, Albinni S, Amiranoff D, de Montalembert M | Transfus Clin Biol | 2019 |
| Capillary electrophoresis and mutational images of hemoglobin sendagi [Β42 (CD1) PHE → VAL; HBB: C.127T→G]. | Recasens V, Ropero P, Lacalle L, Rodríguez-Vigil C, Montañés A, González FA, Pinzón S, Paúl P, Yus F, Rubio R, Díez R, Gómez A, Bustamante E | Clin. Biochem. | 2019 |
| Quadrupole-Time-of-Flight Mass Spectrometric Identification of Hemoglobin Subunits α, β, γ and δ in Unknown Peaks of High Performance Liquid Chromatography of Hemoglobin in β-Thalassemias. | Abdullah UYH, Ibrahim HM, Mahmud NB, Salleh MZ, Kek TL, Noorizhab MNFB, Jassim HM, Othman I, Zainal Abidin SA, Zilfalil BA, Wilairat P, Fucharoen S | Hemoglobin | 2019 |
| Sickling-preventive effects of rutin is associated with modulation of deoxygenated haemoglobin, 2,3-bisphosphoglycerate mutase, redox status and alteration of functional chemistry in sickle erythrocytes. | Muhammad A, Waziri AD, Forcados GE, Sanusi B, Sani H, Malami I, Abubakar IB, Oluwatoyin HY, Adinoyi OA, Mohammed HA | Heliyon | 2019 |
| T-cell deplete versus T-cell replete haploidentical hematopoietic stem cell transplantation for sickle cell disease: where are we? | Patel DA, Akinsete AM, Connelly JA, Kassim AA | Expert Rev Hematol | 2019 |
| Erythrocyte cAMP in Determining Frequency of Acute Pain Episodes in Sickle Cell Disease Patients from Odisha State, India. | Jit BP, Mohanty PK, Pradhan A, Purohit P, Das K, Patel S, Meher S, Sinha S, Mohanty JR, Behera RK, Das P | Hemoglobin | 2019 |
| Modelling the relationships between haemoglobin oxygen affinity and the oxygen cascade in humans. | Shepherd JRA, Dominelli PB, Roy TK, Secomb TW, Hoyer JD, Oliveira JL, Joyner MJ | J. Physiol. (Lond.) | 2019 |
| Multifocal electroretinogram findings in sickle cell maculopathy. | Beral L, Romana M, Lemonne N, Garnier Y, Billaud M, Acomat M, Zorobabel C, Etienne-Julan M, David T, Connes P | Eye (Lond) | 2019 |
| Severe oxidative stress in sickle cell disease patients with uncomplicated Plasmodium falciparum malaria in Kampala, Uganda. | Atiku SM, Louise N, Kasozi DM | BMC Infect. Dis. | 2019 |
| The experience of adults with sickle cell disease and their HLA-matched adult sibling donors after allogeneic hematopoietic stem cell transplantation. | Gallo AM, Patil CL, Knafl KA, Angst DA, Rondelli D, Saraf SL | J Adv Nurs | 2019 |
| The Inflammatory Response to Surgery in Sickle Cell Disease Patients Undergoing Cholecystectomy. | Adisa AO, Adedeji TA, Bolarinwa RA, Owojuyigbe TO, Jeje OA, Glasbey J, Akinola NO | JSLS | 2019 |
| Relationship of Pain Quality Descriptors and Quantitative Sensory Testing: Sickle Cell Disease. | Dyal BW, Ezenwa MO, Yoon SL, Fillingim RB, Yao Y, Schlaeger JM, Suarez ML, Wang ZJ, Molokie RE, Wilkie DJ | Nurs Res | 2019 |
| Use of 18F-Fluciclovine to Diagnose Recurrent Prostate Carcinoma in a Patient With Beta-Thalassemia. | Schmitt CR, Schmitt CT, Hinds PR, Sawyer KJ | Clin Nucl Med | 2019 |
| CRISPR/Cas9 Ribonucleoprotein-mediated Precise Gene Editing by Tube Electroporation. | Ma L, Jang L, Chen J, Song J, Yang D, Zhang J, Chen YE, Xu J | J Vis Exp | 2019 |
| MS-275 Chemical Analogues Promote Hemoglobin Production and Erythroid Differentiation of K562 Cells. | Voskou S, Phylactides M, Afantitis A, Melagraki G, Tsoumanis A, Koutentis PA, Mitsidi T, Mirallai SI, Kleanthous M | Hemoglobin | 2019 |
| Red blood cell alloimmunizations in beta-thalassemia patients in Casablanca/Morocco: Prevalence and risk factors. | El Kababi S, Benajiba M, El Khalfi B, Hachim J, Soukri A | Transfus Clin Biol | 2019 |
| In Vivo Outcome of Homology-Directed Repair at the HBB Gene in HSC Using Alternative Donor Template Delivery Methods. | Pattabhi S, Lotti SN, Berger MP, Singh S, Lux CT, Jacoby K, Lee C, Negre O, Scharenberg AM, Rawlings DJ | Mol Ther Nucleic Acids | 2019 |
| Erythrocyte and plasma oxidative stress appears to be compensated in patients with sickle cell disease during a period of relative health, despite the presence of known oxidative agents. | Detterich JA, Liu H, Suriany S, Kato RM, Chalacheva P, Tedla B, Shah PM, Khoo MC, Wood JC, Coates TD, Milne GL, Oh JY, Patel RP, Forman HJ | Free Radic. Biol. Med. | 2019 |
| Sickle cell disease complications: Prevalence and resource utilization. | Shah N, Bhor M, Xie L, Paulose J, Yuce H | PLoS ONE | 2019 |
| Contrast-enhanced ultrasound detects changes in microvascular blood flow in adults with sickle cell disease. | Lindner JR, Belcik T, Widlansky M, Harmann LM, Karafin MS, Wandersee NJ, Puligandla M, Neuberg D, Linden J, Field JJ | PLoS ONE | 2019 |
| Immune recovery after in vivo T-cell depletion myeloablative conditioning hematopoietic stem cell transplantation in severe beta-thalassemia children. | Qin F, Shi L, Li Q, Zhang Z, Liu L, Li J, Yang G, Lai YR | Eur. J. Haematol. | 2019 |
| Nrf2 controls iron homeostasis in haemochromatosis and thalassaemia via Bmp6 and hepcidin. | Lim PJ, Duarte TL, Arezes J, Garcia-Santos D, Hamdi A, Pasricha SR, Armitage AE, Mehta H, Wideman S, Santos AG, Santos-Gonçalves A, Morovat A, Hughes JR, Soilleux E, Wang CY, Bayer AL, Klenerman P, Willberg CB, Hartley RC, Murphy MP, Babitt JL, Ponka P, Porto G, Drakesmith H | Nat Metab | 2019 |
| Subperiosteal Orbital Hematoma: Imaging Findings of a Rare Complication of Sickle Cell Disease: Subperiosteal orbital hematoma is a rare entity mainly seen in pediatric patients with sickle cell disease and occurs secondary to local vascular disturbances following facial bone infarction. | Van de Voorde N, Parizel PM, Dekeyzer S | J Belg Soc Radiol | 2019 |
| Computational Analysis of Protein Structure Changes as a Result of Nondeletion Insertion Mutations in Human -Globin Gene Suggests Possible Cause of -Thalassemia. | Qadah T, Jamal MS | Biomed Res Int | 2019 |
| Doppler echocardiographic assessment of pulmonary artery pressure in children with sickle cell anaemia. | Lamina MO, Animasahun BA, Akinwumi IN, Njokanma OF | Cardiovasc Diagn Ther | 2019 |
| Interventions for treating neuropathic pain in people with sickle cell disease. | Asnani MR, Francis DK, Brandow AM, Hammond Gabbadon CE, Ali A | Cochrane Database Syst Rev | 2019 |
| The Impact of Perinatal Cobalt Chloride Exposure on Extramedullary Erythropoiesis, Tissue Iron Levels, and Transferrin Receptor Expression in Mice. | Gluhcheva Y, Pavlova E, Petrova E, Tinkov AA, Ajsuvakova OP, Skalnaya MG, Vladov I, Skalny AV | Biol Trace Elem Res | 2019 |
| Iranian patients with hemoglobin H disease: genotype-phenotype correlation. | Paridar M, Azizi E, Keikhaei B, Takhviji V, Baluchi I, Khosravi A | Mol. Biol. Rep. | 2019 |
| Development and characterization of cellular biosensors for HTS of erythroid differentiation inducers targeting the transcriptional activity of γ-globin and β-globin gene promoters. | Breveglieri G, Salvatori F, Finotti A, Cosenza LC, Zuccato C, Bianchi N, Breda L, Rivella S, Bresciani A, Bisbocci M, Borgatti M, Gambari R | Anal Bioanal Chem | 2019 |
| Impact of ET-1 and sex in glomerular hyperfiltration in humanized sickle cell mice. | Kasztan M, Pollock DM | Clin. Sci. | 2019 |
| β-Thalassemia in Iran: Things Everyone Needs to Know About This Disease. | Hadipour Dehshal M, Tabrizi Namini M, Hantoushzadeh R, Yousefi Darestani S | Hemoglobin | 2019 |
| Molecular prevalence of thalassemia and hemoglobinopathies among the Lao Loum Group in the Lao People's Democratic Republic. | Phanmany S, Chanprasert S, Munkongdee T, Svasti S, Leecharoenkiat K | Int J Lab Hematol | 2019 |
| Left ventricular non-compaction in patients with β-thalassemia: structural remodeling or cardiomyopathy? | Lazaros G, Vogiatzi G, Lazarou E, Vlachopoulos C, Tousoulis D | Intern Emerg Med | 2019 |
| Exon sequencing of the alpha-2-globin gene for the differential diagnosis of central cyanosis in newborns: a case report. | Shin C, Hong M, Kim M, Lee JH | BMC Pediatr | 2019 |
| Coinheritance of Hb City of Hope (: c.208G>A) and β-Thalassemia: Compromising the Molecular Diagnosis of the Codons 71/72 (+A) (: c.216_217insA) Mutation by Reverse Dot-Blot Hybridization. | Zhou JY, Jiang F, Li J, Chen GL, Li DZ | Hemoglobin | 2019 |
| Higher executive abilities following a blood transfusion in children and young adults with sickle cell disease. | Hood AM, King AA, Fields ME, Ford AL, Guilliams KP, Hulbert ML, Lee JM, White DA | Pediatr Blood Cancer | 2019 |
| Hereditary methemoglobinemia caused by Hb M-Hyde Park (Hb M-Akita) (HBB:c.277C > T; p.His93Tyr). | Schnedl WJ, Queissner R, Schenk M, Enko D, Mangge H | Wien. Klin. Wochenschr. | 2019 |
| Evaluation of maxillary sinus volume and surface area in children with β-thalassaemia using cone beam computed tomography. | Koparal M, Yalcın ED, Aksoy O, Ozcan-Kucuk A | Int. J. Pediatr. Otorhinolaryngol. | 2019 |
| Circadian period 2: a missing beneficial factor in sickle cell disease by lowering pulmonary inflammation, iron overload, and mortality. | Adebiyi MG, Zhao Z, Ye Y, Manalo J, Hong Y, Lee CC, Xian W, McKeon F, Culp-Hill R, D' Alessandro A, Kellems RE, Yoo SH, Han L, Xia Y | FASEB J. | 2019 |
| Klebsiella pneumoniae Multiple Liver Abscesses and Bacteremia in a Transfusion-dependent β Thalassemia Major Patient. | Rathnayake D, Somasuriyan K, Kumarasamy Thadsanamoorthy S, Maheshvaran U, Francis V | J. Pediatr. Hematol. Oncol. | 2019 |
| Anemia predicts lower white matter volume and cognitive performance in sickle and non-sickle cell anemia syndrome. | Choi S, O'Neil SH, Joshi AA, Li J, Bush AM, Coates TD, Leahy RM, Wood JC | Am. J. Hematol. | 2019 |
| Curative Therapies for Sickle Cell Disease. | Khemani K, Katoch D, Krishnamurti L | Ochsner J | 2019 |
| Increasing Educational Attainment in Adolescents with Sickle Cell Disease. | Harris KM, Dadekian JN, Abel RA, Jones B, Housten A, Ddamulira B, Chadwick-Mansker K, King AA | Soc Work Public Health | 2019 |
| Personalizing transfusion in sickle cell disease: where is the canary in the mine? | Fields ME | Transfusion | 2019 |
| Compliance with Deferoxamine Therapy and Thyroid Dysfunction of Patients with β-Thalassemia Major in Syria. | Yassouf MY, Alquobaili F, Kabalan Y, Mukhalalaty Y | Hemoglobin | 2019 |
| Investigation of RFLP Haplotypes β-Globin Gene Cluster in Beta-Thalassemia Patients in Central Iran. | Sajadpour Z, Amini-Farsani Z, Motovali-Bashi M, Yadollahi M, Yadollahi F | Int J Hematol Oncol Stem Cell Res | 2019 |
| Effective method of evaluating myocardial iron concentration in pediatric patients with thalassemia major. | Khaled A, Ezzat DA, Salem HA, Seif HM, Rabee H | J Blood Med | 2019 |
| Myeloid neoplasms in the setting of sickle cell disease: an intrinsic association with the underlying condition rather than a coincidence; report of 4 cases and review of the literature. | Li Y, Maule J, Neff JL, McCall CM, Rapisardo S, Lagoo AS, Yang LH, Crawford RD, Zhao Y, Wang E | Mod. Pathol. | 2019 |
| Air Drep-A Retrospective Study Evaluating the Influence of Weather Conditions and Viral Epidemics on Vaso-Occlusive Crises in Patients with Sickle Cell Disease Living in French Guiana. | Parriault MC, Cropet C, Fahrasmane A, Rogier S, Parisot M, Nacher M, Elenga N | Int J Environ Res Public Health | 2019 |
| Implementation of an Emergency Department Screening and Care Management Referral Process for Patients With Sickle Cell Disease. | Rushton S, Murray D, Talley C, Boyd S, Eason K, Earls M, Tanabe P | Prof Case Manag | 2019 |
| Providers' Perspectives on Treating Patients With Thalassemia. | Radke T, Paulukonis S, Hulihan MM, Feuchtbaum L | J. Pediatr. Hematol. Oncol. | 2019 |
| Treatment of post-transfusion hyperhaemolysis syndrome in Sickle Cell Disease with the anti-IL6R humanised monoclonal antibody Tocilizumab. | Sivapalaratnam S, Linpower L, Sirigireddy B, Agapidou A, Jain S, Win N, Tsitsikas DA | Br. J. Haematol. | 2019 |
| Therapeutically relevant engraftment of a CRISPR-Cas9-edited HSC-enriched population with HbF reactivation in nonhuman primates. | Humbert O, Radtke S, Samuelson C, Carrillo RR, Perez AM, Reddy SS, Lux C, Pattabhi S, Schefter LE, Negre O, Lee CM, Bao G, Adair JE, Peterson CW, Rawlings DJ, Scharenberg AM, Kiem HP | Sci Transl Med | 2019 |
| Paraoxonases (PON) 1, 2, and 3 Polymorphisms and PON-1 Activities in Patients with Sickle Cell Disease. | Reichert CO, de Macedo CG, Levy D, Sini BC, Monteiro AM, Gidlund M, Maselli LMF, Gualandro SFM, Bydlowski SP | Antioxidants (Basel) | 2019 |
| Management of Sickle Cell Disease Pain among Adolescent and Pediatric Patients. | Abdo S, Nuseir KQ, Altarifi AA, Barqawi M, Ayoub NM, Mukkatash TL | Brain Sci | 2019 |
| New and emerging treatments for vaso-occlusive pain in sickle cell disease. | Dampier C | Expert Rev Hematol | 2019 |
| Alloimmunization in Thalassemia Patients. | Joob B, Wiwanitkit V | Int J Prev Med | 2019 |
| Hydroxyurea: Pattern of Use, Patient Adherence, and Safety Profile in Patients with Sickle Cell Disease in Oman. | Jose J, Elsadek RA, Jimmy B, George P | Oman Med J | 2019 |
| Does Obstructive Sleep Apnea Increase Cognitive Deficits in Pediatric Sickle Cell Disease? | Bills SE, Katz T, McNeil J, Schatz J | J Int Neuropsychol Soc | 2019 |
| Improving the Care of Individuals With Sickle Cell Disease in the Emergency Department Using a Quality Improvement Framework: The Emergency Department Sickle Cell Assessment of Needs and Strengths (ED-SCANS). | Brennan-Cook J, Bonnabeau E, Harris-Bloom H, Tanabe P | Adv Emerg Nurs J | 2019 |
| Alpha Globin Gene Mutation: A Major Determinant of Hydroxyurea Response in Transfusion-Dependent HbE-β-Thalassaemia. | Biswas S, Ray R, Roy K, Bandyopadhyay A, Ghosh K, Bhattacharyya M | Acta Haematol. | 2019 |
| Combined genetic disruption of K-Cl cotransporters and Gardos channel KCNN4 rescues erythrocyte dehydration in the SAD mouse model of sickle cell disease. | Shmukler BE, Rivera A, Bhargava P, Nishimura K, Hsu A, Kim EH, Trudel M, Rust MB, Hubner CA, Brugnara C, Alper SL | Blood Cells Mol. Dis. | 2019 |
| Conjugate prodrug AN-233 induces fetal hemoglobin expression in sickle erythroid progenitors and β-YAC transgenic mice. | Oseghale AR, Zhu X, Li B, Peterson KR, Nudelman A, Rephaeli A, Xu H, Pace BS | Blood Cells Mol. Dis. | 2019 |
| Analgesic management of uncomplicated acute sickle-cell pain crisis in pediatrics: a systematic review and meta-analysis. | Saramba MI, Shakya S, Zhao D | J Pediatr (Rio J) | 2019 |
| Genetic comparison of sickle cell anaemia cohorts from Brazil and the United States reveals high levels of divergence. | Cruz PRS, Ananina G, Gil-da-Silva-Lopes VL, Simioni M, Menaa F, Bezerra MAC, Domingos IF, Araújo AS, Pellegrino R, Hakonarson H, Costa FF, de Melo MB | Sci Rep | 2019 |
| Zinc for Infection Prevention in Sickle Cell Anemia (ZIPS): study protocol for a randomized placebo-controlled trial in Ugandan children with sickle cell anemia. | Datta D, Namazzi R, Conroy AL, Cusick SE, Hume HA, Tagoola A, Ware RE, Opoka RO, John CC | Trials | 2019 |
| Survival and specific outcome of sickle cell disease patients after renal transplantation. | Gérardin C, Moktefi A, Couchoud C, Duquesne A, Ouali N, Gataut P, Karras A, Anglicheau D, Lefaucheur C, Figueres L, Albano L, Lionet A, Novion M, Ziliotis MJ, Louis M, Del Bello A, Matignon M, Dahan K, Habibi A, Galacteros F, Bartolucci P, Grimbert P, Audard V | Br. J. Haematol. | 2019 |
| Spontaneous Epidural Hemorrhage in Sickle Cell Disease, Are They All the Same? A Case Report and Comprehensive Review of the Literature. | Saha B, Saha A | Case Rep Hematol | 2019 |
| Clinical meaning of PROMIS pain domains for children with sickle cell disease. | Singh A, Panepinto JA | Blood Adv | 2019 |
| Red Blood Cell Alloimmunization in Transfused Patients With Sickle Cell Disease in Sub-Saharan Africa; a Systematic Review and Meta-Analysis. | Boateng LA, Ngoma AM, Bates I, Schonewille H | Transfus Med Rev | 2019 |
| Long-term sequential deferiprone and deferasirox therapy in transfusion-dependent thalassaemia patients: a prospective clinical trial. | Vitrano A, Ruffo GB, Pepe A, D'Ascola DG, Caruso V, Filosa A, Masera N, Pitrolo L, Rigano P, Cuccia L, Giangreco A, Di Maggio R, Maggio A | Br. J. Haematol. | 2019 |
| Sickle cell trait, estimated glomerular filtration rate, and risk of adverse outcomes in chronic kidney disease. | Sood R, Surapaneni A, Luo S, Appel LJ, Winkler C, Grams ME, Naik RP | Am. J. Hematol. | 2019 |
| A Novel Pathogenic β-Thalassemia Mutation Identified at Codon 8 (: c.27delG) in a Bangladeshi Family Acquired . | Hasan KN, Sufian A, Mazumder AK, Khaleque MA, Rahman M, Akhteruzzaman S | Hemoglobin | 2019 |
| Foveal avascular zone morphology and parafoveal capillary perfusion in sickle cell retinopathy. | Lynch G, Scott AW, Linz MO, Han I, Andrade Romo JS, Linderman RE, Carroll J, Rosen RB, Chui TY | Br J Ophthalmol | 2019 |
| Sickle Cell Education: A Survey of Antenatal Healthcare Givers. | Aboagye S, Torto M, Asah-Opoku K, Nuamah MA, Oppong SA, Samba A | Am. J. Trop. Med. Hyg. | 2019 |
| Ultrasound-guided recruitment maneuvers in pediatric acute chest syndrome due to sickle cell disease. | Bobillo-Perez S, Rodriguez-Fanjul J, Girona-Alarcon M, Cambra FJ, Jordan I, Balaguer M | Med Intensiva | 2019 |
| Germline mosaicism in an α-thalassemia family: Incidental identification by prenatal ultrasound. | Xu LL, Liu YN, Zhen L, Li DZ | Prenat. Diagn. | 2019 |
| National trends in hydroxyurea and opioid prescribing for sickle cell disease by office-based physicians in the United States, 1997-2017. | Su ZT, Segal JB, Lanzkron S, Ogunsile FJ | Pharmacoepidemiol Drug Saf | 2019 |
| Comparison of serology and molecular detection of common red cell antigens in multitransfused thalassemia major and sickle cell disease patients. | Shah A, Patel P, Patel K, Patel B, Jariwala K, Sharma P, Mishra K, Ghosh K | Transfus. Apher. Sci. | 2019 |
| Chronic pain persists in adults with sickle cell disease despite regular red cell transfusions. | Karafin MS, Mullins DE, Johnson ST, Nischik D, Feng M, Simpson P, Field JJ | Transfus. Apher. Sci. | 2019 |
| Challenges of blood transfusions in β-thalassemia. | Shah FT, Sayani F, Trompeter S, Drasar E, Piga A | Blood Rev. | 2019 |
| Splenectomy is not associated with a higher tricuspid regurgitant jet velocity in people with sickle cell anemia. | Sinha AA, Adusumilli T, Cohen HW, Nouraie M, Little J, Manwani D | Pediatr Blood Cancer | 2019 |
| Combined and differential effects of alpha-thalassemia and HbF-quantitative trait loci in Senegalese hydroxyurea-free children with sickle cell anemia. | Gueye Tall F, Martin C, Ndour EHM, Renoux C, Ly ID, Connes P, Gueye PM, Diallo RN, Diagne I, Diop PA, Cissé A, Lopez Sall P, Joly P | Pediatr Blood Cancer | 2019 |
| Gene therapy of hemoglobinopathies: progress and future challenges. | Ikawa Y, Miccio A, Magrin E, Kwiatkowski JL, Rivella S, Cavazzana M | Hum. Mol. Genet. | 2019 |
| Quality of life in patients with β-thalassemia: A prospective study of transfusion-dependent and non-transfusion-dependent patients in Greece, Italy, Lebanon, and Thailand. | Cappellini MD, Kattamis A, Viprakasit V, Sutcharitchan P, Pariseau J, Laadem A, Jessent-Ciaravino V, Taher A | Am. J. Hematol. | 2019 |
| Prevention of Morbidity in Sickle Cell Disease (POMS2a)-overnight auto-adjusting continuous positive airway pressure compared with nocturnal oxygen therapy: a randomised crossover pilot study examining patient preference and safety in adults and children. | Howard J, Lee SA, Inusa B, Cheng MYE, Bavenjit C, Reading IC, Wakeford SA, Gavlak JC, Murphy PB, Hart N, Gupta A, Sahota S, Jacob E, Chorozoglou M, Ossai C, Gwam M, Kirkham FJ, Wade AM, Liossi C | Trials | 2019 |
| Impact of Depression in Sickle Cell Disease Hospitalization-Related Outcomes: An Analysis of the National Inpatient Sample (NIS). | Onyeaka HK, Queeneth U, Rashid W, Ahmad N, Rajan SK, Jaladi PR, Patel RS | Medicina (Kaunas) | 2019 |
| Characterizing complication risk from multisite, intermittent transfusions for the treatment of sickle cell disease. | Tang A, Branscomb J, Zhou M, Snyder A, Eckman J | Pediatr Blood Cancer | 2019 |
| Beta-thalassemia major complicated by intracranial hemorrhage and critical illness polyneuropathy. | Sanju S, Tullu MS, Karande S, Muranjan MN, Parekh P | J Postgrad Med | 2019 |
| The Role of Cognitive Behavioral Therapy in Opioid Use Reduction in Pediatric Sickle Cell Disease: Protocol for a Systematic Review. | Anderson AT, Tran N, Smith K, Kelley-Quon LI | JMIR Res Protoc | 2019 |
| Case Report: Kryptonite-A Rare Case of Left-Sided Bilothorax in a Sickle Cell Patient. | Reddy VD, Al-Khateeb A, Hussain M, Patel V, Kadri M, Patel R, Maruboyina SP, Miller RA, DePasquale JR | Case Rep Pulmonol | 2019 |
| QT Prolongation and Associated Ventricular Tachycardia due to Cardiac Iron Load in a Patient with Thalassemia Major. | Demirtas D, Demirtas AO, Sumbul HE, Koc AS | Case Rep Hematol | 2019 |
| Acacia Senegal (Gum Arabic) Supplementation Modulate Lipid Profile and Ameliorated Dyslipidemia among Sickle Cell Anemia Patients. | Kaddam L, Fadl-Elmula I, Eisawi OA, Abdelrazig HA, Saeed AM | J Lipids | 2019 |
| [The History of Beta Thalassaemia in Sardinia: The Contribution of the Italian Schools of Pediatrics]. | Martini M, Tornali C, Bragazzi NL, Paluan F, Vardeu MF | Acta Med Hist Adriat | 2019 |
| Towards New Frontiers of Direct Oral Anticoagulants: Sickle Cell Disease. | Boccatonda A, Santilli F | Acta Haematol. | 2019 |
| The genetics of human hematopoiesis and its disruption in disease. | Bao EL, Cheng AN, Sankaran VG | EMBO Mol Med | 2019 |
| Sickle cell trait and risk of cognitive impairment in African-Americans: The REGARDS cohort. | Cahill CR, Leach JM, McClure LA, Irvin MR, Zakai NA, Naik R, Unverzagt F, Wadley VG, Hyacinth HI, Manly J, Judd SE, Winkler C, Cushman M | EClinicalMedicine | 2019 |
| Sickle cell trait: A sigh of relief? | Wood JC | EClinicalMedicine | 2019 |
| A pilot test of the Adult Sickle Cell Quality of Life Measurement Information System (ASCQ-Me) and the Jenerette Self-Care Assessment (J-SAT) Tools in adults with sickle cell disease. | Bulgin D, Douglas C, Tanabe P | Pilot Feasibility Stud | 2019 |
| Splenic sequestration crisis as an index manifestation of heterozygous hemoglobinopathy in an adult. | Edo-Osagie E, Enofe I, Hakeem H, Rai M, Adomako E, Tismenetsky M, Janosky M | Oxf Med Case Reports | 2019 |
| Sickle cell disease in anaemic children in a Sierra Leonean district hospital: a case series. | Italia MB, Kirolos S | Oxf Med Case Reports | 2019 |
| Fetal hemoglobin does not inhibit growth. | Archer NM, Petersen N, Duraisingh MT | Blood Adv | 2019 |
| Sickle Cell Disease and Infections in High- and Low-Income Countries. | Cannas G, Merazga S, Virot E | Mediterr J Hematol Infect Dis | 2019 |
| Prevalence of TEM, SHV, and CTX-M Genes among ESBL-Producing and Isolated from Thalassemia Patients in Erbil, Iraq. | Pishtiwan AH, Khadija KM | Mediterr J Hematol Infect Dis | 2019 |
| Sickle Cell Disease and Pregnancy. | Jain D, Atmapoojya P, Colah R, Lodha P | Mediterr J Hematol Infect Dis | 2019 |
| Homozygous Deletion Alpha-Thalassemia and Hereditary Persistence of Fetal Hemoglobin, Two Genetic Factors Predictive the Reduction of Morbidity and Mortality During Pregnancy in Sickle Cell Patients. A Report from the Democratic Republic of Congo. | Mikobi TM, Lukusa PT, Muamba JM, Rhama T | Mediterr J Hematol Infect Dis | 2019 |
| Molecular Analysis of Non-Transfusion Dependent Thalassemia Associated with Hemoglobin E-β-Thalassemia Disease without α-Thalassemia. | Phanrahan P, Yamsri S, Teawtrakul N, Fucharoen G, Sanchaisuriya K, Fucharoen S | Mediterr J Hematol Infect Dis | 2019 |
| Economic Evaluation of Chelation Regimens for β-Thalassemia Major: a Systematic Review. | Li J, Lin Y, Li X, Zhang J | Mediterr J Hematol Infect Dis | 2019 |
| On artherogenic index of plasma in sickle cell anaemia patients. | Akinbami AA, Uche EI, Suleiman AM, Ogbenna AA, Olowoselu FO, Augustine B, Badiru MA, Bamiro RA, Kamson OR | Pan Afr Med J | 2019 |
| Frequency of Alpha Thalassaemia in homozygous Beta Thalassaemia paediatric patients and its clinical impact at a blood disease centre in Karachi, Pakistan. | Hassan J, Nadeem M, Ansari SH, Ahmed S, Parveen S, Shamsi T | J Pak Med Assoc | 2019 |
| Pediatric to Adult Transition in Sickle Cell Disease: Survey Results from Young Adult Patients. | Travis K, Wood A, Yeh P, Allahabadi S, Chien LC, Curtis S, Hammond A, Kohn J, Ogugbuaja C, Rees M, Shumway J, Sheehan V | Acta Haematol. | 2019 |
| Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia. | Yahouédéhou SCMA, da Guarda CC, Figueiredo CVB, Santiago RP, Carvalho SP, Fiuza LM, Ndidi US, Oliveira RM, Carvalho MOS, Nascimento VML, Rocha LC, Lyra IM, Adorno EV, Goncalves MS | PLoS ONE | 2019 |
| Differential effects of adenylyl cyclase-protein kinase A cascade on shear-induced changes of sickle cell deformability. | Ugurel E, Connes P, Yavas G, Eglenen B, Turkay M, Aksu AC, Renoux C, Joly P, Gauthier A, Hot A, Bertrand Y, Cannas G, Yalcin O | Clin. Hemorheol. Microcirc. | 2019 |
| First Description of Hb San Diego (: c.328G>A) in a Chinese Family with Congenital Erythrocytosis. | Xiong H, Chen S | Hemoglobin | 2019 |
| The Spectrum of α-Thalassemia Mutations in the Lak Population of Iran. | Moradi K, Aznab M, Tahmasebi S, Dastafkan Z, Omidniakan L, Ahmadi M, Alibakhshi R | Hemoglobin | 2019 |
| Gallstone Pancreatitis and Extramedullary ArticleTitlespinal Hematopoiesis in Hb E/beta Thalassemia. | Goldie L, Kinzang W, Thangjam G, Konsam V | J Assoc Physicians India | 2019 |
| Iron status and inherited haemoglobin disorders modify the effects of micronutrient powders on linear growth and morbidity among young Lao children in a double-blind randomised trial. | Hess SY, Wessells KR, Hinnouho GM, Barffour MA, Sanchaisuriya K, Arnold CD, Brown KH, Larson CP, Fucharoen S, Kounnavong S | Br. J. Nutr. | 2019 |
| Fe enrichment in mice for β-thalassaemia studies via Mössbauer spectroscopy of blood samples. | Charitou G, Tsertos C, Parpottas Y, Kleanthous M, Lederer CW, Phylactides M | Eur. Biophys. J. | 2019 |
| [Analysis of hematological phenotype and genotype of Hb Q-Thailand in Fujian area]. | Chen L, Chen M, Zhang M, Wang Y, Huang H, Li Y, Xu L | Zhonghua Yi Xue Yi Chuan Xue Za Zhi | 2019 |
| Targeting sickle cell disease root-cause pathophysiology with small molecules. | Saunthararajah Y | Haematologica | 2019 |
| Epidemiology and risk factors of transfusion transmitted infections in thalassemia major: a multicenter study in Pakistan. | Yasmeen H, Hasnain S | Hematol Transfus Cell Ther | 2019 |
| Shine & Lal index as a predictor for early detection of β-thalassemia carriers in a limited resource area in Bandung, Indonesia. | Maskoen AM, Reniarti L, Sahiratmadja E, Sisca J, Effendi SH | BMC Med. Genet. | 2019 |
| Hb Alcorn County: A β-Globin Variant [β40(C6)Arg→Thr; : c.122G>C (p.Arg41Thr)] with Increased Oxygen Affinity. | Luu HS, McCavit TL, Park JY, Mitui M, Lopez DD, Timmons CF | Hemoglobin | 2019 |
| A Multidimensional Electronic Hydroxyurea Adherence Intervention for Children With Sickle Cell Disease: Single-Arm Before-After Study. | Creary S, Chisolm D, Stanek J, Hankins J, O'Brien SH | JMIR Mhealth Uhealth | 2019 |
| Real-world experience using hydroxyurea in children with sickle cell disease in Lilongwe, Malawi. | Mvalo T, Topazian HM, Kamthunzi P, Chen JS, Kambalame I, Mafunga P, Mumba N, Chiume M, Paseli K, Tegha G, Kumwenda W, Heimlich JB, Ellis G, Key N, Gopal S, Hoffman I, Ataga KI, Westmoreland KD | Pediatr Blood Cancer | 2019 |
| Antisickling Drugs Targeting βCys93 Reduce Iron Oxidation and Oxidative Changes in Sickle Cell Hemoglobin. | Kassa T, Wood F, Strader MB, Alayash AI | Front Physiol | 2019 |
| Receptor for Advanced Glycation End Products Antagonism Blunts Kidney Damage in Transgenic Townes Sickle Mice. | Charrin E, Faes C, Sotiaux A, Skinner S, Pialoux V, Joly P, Connes P, Martin C | Front Physiol | 2019 |
| Health related quality of life among children with transfusion dependent β-thalassaemia major and haemoglobin E β-thalassaemia in Sri Lanka: a case control study. | Mettananda S, Pathiraja H, Peiris R, Bandara D, de Silva U, Mettananda C, Premawardhena A | Health Qual Life Outcomes | 2019 |
| Unusual β-Globin Haplotype Distribution in Newborns from Bengo, Angola. | Borges E, Tchonhi C, Couto CSB, Gomes V, Amorim A, Prata MJ, Brito M | Hemoglobin | 2019 |
| Noninvasive prenatal detection of hemoglobin Bart hydrops fetalis via maternal plasma dispensed with parental haplotyping using the semiconductor sequencing platform. | Yang J, Peng CF, Qi Y, Rao XQ, Guo F, Hou Y, He W, Wu J, Chen YY, Zhao X, Wang YN, Peng H, Wang D, Du L, Luo MY, Huang QF, Liu HL, Yin A | Am. J. Obstet. Gynecol. | 2019 |
| Genomic variants in members of the Krüppel-like factor gene family are associated with disease severity and hydroxyurea treatment efficacy in β-hemoglobinopathies patients. | Stratopoulos A, Kolliopoulou A, Karamperis K, John A, Kydonopoulou K, Esftathiou G, Sgourou A, Kourakli A, Vlachaki E, Chalkia P, Theodoridou S, Papadakis MN, Gerou S, Symeonidis A, Katsila T, Ali BR, Papachatzopoulou A, Patrinos GP | Pharmacogenomics | 2019 |
| An approach to revising mHealth interventions for children and families: A case example in sickle cell disease. | Phillips S, Kanter J, Ruggiero KJ, Mueller M, Johnson MA, Kelechi TJ | Res Nurs Health | 2019 |
| An Hb-mediated circulating macrophage contributing to pulmonary vascular remodeling in sickle cell disease. | Redinus K, Baek JH, Yalamanoglu A, Shin HKH, Moldova R, Harral JW, Swindle D, Pak D, Ferguson SK, Nuss R, Hassell K, Nozik-Grayck E, Palmer AF, Fini MA, Karoor V, Stenmark KR, Buehler PW, Irwin DC | JCI Insight | 2019 |
| Insights into determinants of spleen injury in sickle cell anemia. | El Hoss S, Cochet S, Marin M, Lapouméroulie C, Dussiot M, Bouazza N, Elie C, de Montalembert M, Arnaud C, Guitton C, Pellegrino B, Odièvre MH, Moati F, Le Van Kim C, Aronovicz YC, El Nemer W, Brousse V | Blood Adv | 2019 |
| Sickle cell disease nephropathy: an update on risk factors and potential biomarkers in pediatric patients. | Belisário AR, da Silva AA, Silva CV, de Souza LM, Wakabayashi EA, Araújo SA, Simoes-E-Silva AC | Biomark Med | 2019 |
| Cardiac expression of HMOX1 and PGF in sickle cell mice and haem-treated wild type mice dominates organ expression profiles via Nrf2 (Nfe2l2). | Gbotosho OT, Ghosh S, Kapetanaki MG, Lin Y, Weidert F, Bullock GC, Ofori-Acquah SF, Kato GJ | Br. J. Haematol. | 2019 |
| Frequency of silent brain lesions and aspirin protection evaluation over 3 years follow-up in beta thalassemia patients. | Karimi M, Haghpanah S, Pishdad P, Zahedi Z, Parand S, Safaei S | Ann. Hematol. | 2019 |
| TTP-like syndrome associated with hemoglobin SC disease treated successfully with plasma and red cell exchange. | Kodali S, Ramachandran P, Richard IN, Wang JC | Leuk Res Rep | 2019 |
| Immunostick Test for Detecting ζ-Globin Chains and Screening of the Southeast Asian α-Thalassemia 1 Deletion. | Pata S, Pongpaiboon M, Laopajon W, Munkongdee T, Paiboonsukwong K, Pornpresert S, Fucharoen S, Kasinrerk W | Biol Proced Online | 2019 |
| An Uncommon Variant Hemoglobin: Hb Ty Gard Detected from Gujarat, India. | Wahengbam AKGS, Kumari K, Singh RK, Rao VR, Saraswathy KN, Dharajiya K, Das R, Murry B | Indian J Hematol Blood Transfus | 2019 |
| Clinico-Hematological Presentation of Rare Hemoglobin Variant (HB-O Indonesia) in 3 Families. | Kumar R, Patel P, Gwal A, Bharti PK, Colah R, Rajasubramaniam S | Indian J Hematol Blood Transfus | 2019 |
| Hemoglobin Titusville [α2 Codon 94 G>A]: A Rare Alpha Globin Chain Variant Causing Low Oxygen Saturation. | Das Gupta A, Hariharan P, Daruwalla M, Sidhwa K, Pawar R, Nadkarni A | Indian J Hematol Blood Transfus | 2019 |
| Polyneuropathy Associated with Severe Iron Overload and Oxidative Stress in β-Thalassemia Patients. | El-Tagui MH, Salama KM, El-Sabbagh MH, Youness ER, Ragaey M, Abdel-Salam A | Indian J Hematol Blood Transfus | 2019 |
| Spectrum of Hemoglobinopathies: A New Revelation in a Tertiary Care Hospital of Odisha. | Ray GK, Jena RK | Indian J Hematol Blood Transfus | 2019 |
| Hb Gibbon [β124(H2)Pro→Thr (: c.373C>A, p.P125T)], an Asymptomatic Novel Hemoglobin Variant Detected by Newborn Screening. | Wolf A, Rohr JM, Amador C, Starr LJ, Hoyer JD, Ford JB | Hemoglobin | 2019 |
| Metabolic impact of red blood cell exchange with rejuvenated red blood cells in sickle cell patients. | Gehrke S, Shah N, Gamboni F, Kamyszek R, Srinivasan AJ, Gray A, Landrigan M, Welsby I, D'Alessandro A | Transfusion | 2019 |
| Genetic variation influencing hemoglobin levels and risk for anemia across populations. | Barrera-Reyes PK, Tejero ME | Ann. N. Y. Acad. Sci. | 2019 |
| Sickle cell disease: a review for the internist. | Pinto VM, Balocco M, Quintino S, Forni GL | Intern Emerg Med | 2019 |
| Association of sickle cell trait with measures of cognitive function and dementia in African Americans. | Chen N, Caruso C, Alonso A, Derebail VK, Kshirsagar AV, Sharrett AR, Key NS, Gottesman RF, Grove ML, Bressler J, Boerwinkle E, Windham BG, Mosley TH, Hyacinth HI | eNeurologicalSci | 2019 |
| Candidemia complicating biliary atresia in an infant with hemoglobinopathy. | Kyriakidis I, Palabougiouki M, Vasileiou E, Tragiannidis A, Stamou M, Moudiou T, Vyzantiadis T, Gombakis N, Hatzistilianou M | Turk Pediatri Ars | 2019 |
| Association Between Periodic Limb Movements in Sleep and Cerebrovascular Changes in Children With Sickle Cell Disease. | Lin J, Morrone K, Manwani D, Chernin R, Silver EJ, Shifteh K, Sin S, Arens R, Graw-Panzer K | J Clin Sleep Med | 2019 |
| Shared Care for Adults with Sickle Cell Disease: An Analysis of Care from Eight Health Systems. | Mainous AG, Rooks B, Tanner RJ, Carek PJ, Black V, Coates TD | J Clin Med | 2019 |
| Anemia Severity in β-Thalassemia Correlates with Elevated Levels of microRNA-125b in Activated Phagocytic Monocytes. | Kuno S, Penglong T, Srinoun K | Hemoglobin | 2019 |
| Kidney ultrasound findings according to kidney function in sickle cell anemia. | Patel R, Kang S, Valeshabad AK, Shah BN, Han J, Gowhari M, Molokie RE, Xie K, Lash JP, Gordeuk VR, Saraf SL | Am. J. Hematol. | 2019 |
| Fat Embolism Syndrome in a Child with Sickle Cell Disease. | Maroni A, Dauger S, Chomton M | J. Pediatr. | 2019 |
| Resolution of Acute Priapism in Two Children With Sickle Cell Disease Who Received Nitrous Oxide. | Greenwald MH, Gutman CK, Morris CR | Acad Emerg Med | 2019 |
| [False positive Kleihauer test and hereditary persistence of fetal hemoglobin]. | Picard L, Delabaere A, Serre Sapin AF, Giansily Blaizot M, Gallot D | Gynecol Obstet Fertil Senol | 2019 |
| Prevalence of endocrine disorders and their associated factors in transfusion-dependent thalassemia patients: a historical cohort study in Southern Iran. | Bordbar M, Bozorgi H, Saki F, Haghpanah S, Karimi M, Bazrafshan A, Zekavat OR | J. Endocrinol. Invest. | 2019 |
| Hydroxyurea Use for Sickle Cell Disease Among Medicaid-Enrolled Children. | Brousseau DC, Richardson T, Hall M, Ellison AM, Shah SS, Raphael JL, Bundy DG, Arnold S | Pediatrics | 2019 |
| Sickle cell disease: a new era. | Simpson S | Lancet Haematol | 2019 |
| Knowledge, beliefs and practices regarding sickle cell eye disease of patients at the sickle cell unit, Jamaica. | Mowatt L, Ajanaku A, Knight-Madden J | Pan Afr Med J | 2019 |
| Sex differences in physical activity among Ghanaian patients with sickle cell disease. | Nyante GG, Oppong C, Bonney E | Pan Afr Med J | 2019 |
| An Electronic Teaching Module for Improving Knowledge of Self-Management of Vaso-Occlusive Pain Crises in Patients With Sickle Cell Disease: Pilot Questionnaire Study. | Tam T, Baer MR, Hsu LL, Law JY | JMIR Mhealth Uhealth | 2019 |
| Detection of a Large Novel α-Thalassemia Deletion in an Autochthonous Belgian Family. | Heireman L, Luyckx A, Schynkel K, Dheedene A, Delaunoy M, Adam AS, Gulbis B, Dierick J | Hemoglobin | 2019 |
| Invasive Yersiniosis in a Pediatric Patient With β-Thalassemia Major: Acute Decompensation After Rapid Blood Transfusion. | Hsu G, Jones A, Thornton B | Pediatr Emerg Care | 2019 |
| Longitudinal Trend in Emergency Department Reliance for Pain Among Sickle Cell Disease Patients in Wisconsin. | Singh A, Yan K, Brandow AM, Panepinto JA | J. Pediatr. Hematol. Oncol. | 2019 |
| A case of bone marrow necrosis and fat embolism in a sickle-cell disease patient. | Debus J, Dumont B, Le Breton C, Emery M, Peynaud-Debayle E, Affo L | Ann. Biol. Clin. (Paris) | 2019 |
| Global gene expression reveals an increase of HMGB1 and APEX1 proteins and their involvement in oxidative stress, apoptosis and inflammation pathways among beta-thalassaemia intermedia and major phenotypes. | Maia de Oliveira da Silva JP, Brugnerotto AF, S Romanello K, K L Teixeira K, Lanaro C, S Duarte A, G L Costa G, da Silva Araújo A, C Bezerra MA, de Farias Domingos I, Pereira Martins DA, Malavazi I, F Costa F, da Cunha AF | Br. J. Haematol. | 2019 |
| Urinary dysfunction in transgenic sickle cell mice: model of idiopathic overactive bladder syndrome. | Karakus S, Anele UA, Silva FH, Musicki B, Burnett AL | Am. J. Physiol. Renal Physiol. | 2019 |
| A Medication Adherence App for Children With Sickle Cell Disease: Qualitative Study. | Curtis K, Lebedev A, Aguirre E, Lobitz S | JMIR Mhealth Uhealth | 2019 |
| Hydroxycarbamide treatment in children with Sickle Cell Anaemia is associated with more intact white matter integrity: a quantitative MRI study. | Kapustin D, Leung J, Odame I, Williams S, Shroff M, Kassner A | Br. J. Haematol. | 2019 |
| International Comparison of Thalassemia Registries: Challenges and Opportunities. | Noori T, Ghazisaeedi M, Aliabad GM, Mehdipour Y, Mehraeen E, Conte R, Safdari R | Acta Inform Med | 2019 |
| The Relationship Between Psychological Distress and Religious Practices and Coping in Malaysian Parents of Children with Thalassemia. | Chong LT, Chong MC, Tang LY, Ramoo V, Chui PL, Hmwe NTT | J Pediatr Nurs | 2019 |
| [Study of - maximum systolic velocities and mean maximum velocities of skull base arteries recorded with transcranial Doppler in adult sickle cell patients without neurovascular complication]. | Desnos L, Allaert F, Etienne-Julan M, Blanchet-Deverly A | J Med Vasc | 2019 |
| Prevalence and factors associated with renal dysfunction among children with sickle cell disease attending the sickle cell disease clinic at a tertiary hospital in Northwestern Tanzania. | Kimaro FD, Jumanne S, Sindato EM, Kayange N, Chami N | PLoS ONE | 2019 |
| Oral aspects of sickle cell disease. | Grossman S, Bailey E, Makdissi J | Br Dent J | 2019 |
| Molecular characteristics of α-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnostics. | Charoenwijitkul T, Singha K, Fucharoen G, Sanchaisuriya K, Thepphitak P, Wintachai P, Karnpean R, Fucharoen S | Clin. Biochem. | 2019 |
| Detection of Hb H disease caused by a novel mutation and -- deletion using capillary electrophoresis. | Li Y, Liang L, Tian M, Qin T, Wu X | J. Clin. Lab. Anal. | 2019 |
| A Phase 3 Randomized Trial of Voxelotor in Sickle Cell Disease. | Vichinsky E, Hoppe CC, Ataga KI, Ware RE, Nduba V, El-Beshlawy A, Hassab H, Achebe MM, Alkindi S, Brown RC, Diuguid DL, Telfer P, Tsitsikas DA, Elghandour A, Gordeuk VR, Kanter J, Abboud MR, Lehrer-Graiwer J, Tonda M, Intondi A, Tong B, Howard J, | N. Engl. J. Med. | 2019 |
| Need for a universal thalassemia screening programme in India? A public health perspective. | Thiyagarajan A, Bhattacharya S, Sharma N, Srivastava A, Dhar DK | J Family Med Prim Care | 2019 |
| New Advances in Evaluation of Hearing in a Sample of Egyptian Children with β-Thalassemia Major. | Alzaree FA, Shehata MA, Atti MA, Elzaree GA, El-Kassas GM | Open Access Maced J Med Sci | 2019 |
| Cellular adaptation mediated through Nrf2-induced glutamate cysteine ligase up-regulation against oxidative stress caused by iron overload in β-thalassemia/HbE patients. | Somparn N, Prawan A, Senggunprai L, Kukongviriyapan U, Jetsrisuparb A, Lee MH, Kim DH, Kukongviriyapan V, Surh YJ | Free Radic. Res. | 2019 |
| Fertility in Patients with Thalassemia and Outcome of Pregnancies: A Turkish Experience | Akıncı B, Yaşar AŞ, Özdemir Karadaş N, Önder Siviş Z, Hekimci Özdemir H, Yılmaz Karapınar D, Balkan C, Kavaklı K, Aydınok Y | Turk J Haematol | 2019 |
| Transcranial Doppler and Magnetic Resonance in Tanzanian Children With Sickle Cell Disease. | Kija EN, Saunders DE, Munubhi E, Darekar A, Barker S, Cox TCS, Mango M, Soka D, Komba J, Nkya DA, Cox SE, Kirkham FJ, Newton CRJC | Stroke | 2019 |
| Current perspectives of sickle cell disease in Nigeria: changing the narratives. | Ojewunmi OO, Adeyemo TA, Ayinde OC, Iwalokun B, Adekile A | Expert Rev Hematol | 2019 |
| Considering the spleen in sickle cell disease. | El Hoss S, Brousse V | Expert Rev Hematol | 2019 |
| Metabolomic Investigation of β-Thalassemia in Chorionic Villi Samples. | Monni G, Murgia F, Corda V, Peddes C, Iuculano A, Tronci L, Balsamo A, Atzori L | J Clin Med | 2019 |
| Serum homocysteine and disease severity in sickle cell anemia patients in Lagos. | Uche E, Adelekan O, Akinbami A, Osunkalu V, Ismail K, Ogbenna AA, Badiru M, Dosunmu A, Oluwole E, Kamson O | J Blood Med | 2019 |
| Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India. | Dehury S, Meher S, Patel S, Das K, Jana A, Bhattacharya S, Sahoo S, Sarkar B, Mohanty PK | Hemoglobin | 2019 |
| A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia. | Klei TRL, Kheradmand Kia S, Veldthuis M, Dehbozorgian J, Karimi M, Geissler J, Sellink E, Thiel-Valkhof M, Burger P, van Alphen F, Meijer AB, van Bruggen R, van Zwieten R | Hemoglobin | 2019 |
| A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the Gene Misdiagnosed as β-Thalassemia Intermedia Due to a Gene Mutation. | Yang K, Ren Q, Wu Y, Zhou Y, Yin X | Hemoglobin | 2019 |
| Association of alpha hemoglobin-stabilizing protein (AHSP) gene mutation and disease severity among HbE-beta thalassemia patients. | Ray R, Kalantri SA, Bhattacharjee S, Biswas A, Shahab A, Biswas S, Bhattacharyya M | Ann. Hematol. | 2019 |
| Co-existing iron deficiency/overload in beta-thalassemia trait. | Yousafzai YM, Wahid QUA, Khan S, Mir A, Khan A, Raziq F | J Pak Med Assoc | 2019 |
| Antiplatelet agents for preventing vaso-occlusive events in people with sickle cell disease: a systematic review. | Martí-Carvajal A, Abd El Aziz MA, Martí-Amarista C, Solà I | Clin Adv Hematol Oncol | 2019 |
| The effect of the coinheritance of Glucose-6-phosphate dehydrogenase deficiency on the severity of sickle cell disease. | Fasola FA, Fowodu FO, Shokunbi WA, Kotila TR | Niger Postgrad Med J | 2019 |
| Oxysterol concentrations are associated with cholesterol concentrations and anemia in pediatric patients with sickle cell disease. | Yalcinkaya A, Samadi A, Lay I, Unal S, Sabuncuoglu S, Oztas Y | Scand. J. Clin. Lab. Invest. | 2019 |
| Quantifying the Levels of Knowledge, Attitude, and Practice Associated with Sickle Cell Disease and Premarital Genetic Counseling in 350 Saudi Adults. | Al-Qattan HM, Amlih DF, Sirajuddin FS, Alhuzaimi DI, Alageel MS, Bin Tuwaim RM, Al Qahtani FH | Adv Hematol | 2019 |
| Relationship of Omega-3 fatty acids DHA and EPA with the inflammatory biomarker hs-CRP in children with sickle cell anemia. | Setty BNY, Betal SG, Miller RE, Brown DS, Meier M, Cahill M, Lerner NB, Apollonsky N, Stuart MJ | Prostaglandins Leukot. Essent. Fatty Acids | 2019 |
| Electron paramagnetic resonance oximetry as a novel approach to monitor the effectiveness and quality of red blood cell transfusions. | Hou H, Baek JH, Zhang H, Wood F, Gao Y, Flood AB, Swartz HM, Buehler PW | Blood Transfus | 2019 |
| Laparoscopic Sleeve Gastrectomy in Sickle Cell Disease: a Case Series. | Han J, Gowhari M, Gordeuk VR, Saraf SL | Obes Surg | 2019 |
| Effect of whole body vibration training on bone mineral density and functional capacity in children with thalassemia. | Eid MA, Aly SM | Physiother Theory Pract | 2019 |
| Prevalence and Risk Factors for Cardiac and Liver Iron Overload in Adults with Thalassemia in Malaysia. | Ngim CF, Lee MY, Othman N, Lim SM, Ng CS, Ramadas A | Hemoglobin | 2019 |
| A Cell-free DNA Barcode-Enabled Single-Molecule Test for Noninvasive Prenatal Diagnosis of Monogenic Disorders: Application to β-Thalassemia. | Yang X, Zhou Q, Zhou W, Zhong M, Guo X, Wang X, Fan X, Yan S, Li L, Lai Y, Wang Y, Huang J, Ye Y, Zeng H, Chuan J, Du Y, Ma C, Li P, Song Z, Xu X | Adv Sci (Weinh) | 2019 |
| Early Kidney Damage Markers after Deferasirox Treatment in Patients with Thalassemia Major: A Case-Control Study. | Badeli H, Baghersalimi A, Eslami S, Saadat F, Rad AH, Basavand R, Papkiadeh SR, Darbandi B, Kooti W, Peluso I | Oxid Med Cell Longev | 2019 |
| Faster Sickling Kinetics and Sickle Cell Shape Evolution during Repeated Deoxygenation and Oxygenation Cycles. | Du E, Dao M | Exp Mech | 2019 |
| Editing the Sickle Cell Disease Mutation in Human Hematopoietic Stem Cells: Comparison of Endonucleases and Homologous Donor Templates. | Romero Z, Lomova A, Said S, Miggelbrink A, Kuo CY, Campo-Fernandez B, Hoban MD, Masiuk KE, Clark DN, Long J, Sanchez JM, Velez M, Miyahira E, Zhang R, Brown D, Wang X, Kurmangaliyev YZ, Hollis RP, Kohn DB | Mol. Ther. | 2019 |
| [Associations of parental thalassemia with preterm birth and low birth weight]. | Huang XC, Qiu XQ, Zeng XY, Liu S, Wei FL, Li YN, Liu T, Wu YN, Feng BY, Jiang QJ, Huang DP | Zhonghua Liu Xing Bing Xue Za Zhi | 2019 |
| A nationwide survey of hospital-based thalassemia patients and standards of care and a preliminary assessment of the national prevention program in Sri Lanka. | Premawardhana AP, Mudiyanse R, De Silva ST, Jiffry N, Nelumdeniya U, de Silva U, Lamabadusuriya SP, Pushpakumara K, Dissanayaka R, Jansz M, Rifaya I, Navarathne U, Thirukumaran V, Arambepola M, Dayanada Bandara W, Vaidyanatha U, Mendis D, Weerasekara K, De Silva N, Shantha Kumara DK, Amarasena SD, Hemantha KK, Refai MACM, Silva I, Hameed N, Rajiyah F, Mettananda S, Allen A, Weatherall DJ, Oliveri NF | PLoS ONE | 2019 |
| [Genotypic and Phenotypic Analysis of αβ-Thalassemia in Children]. | Ren ZM, Xiao WW, Liu SX, Liu YQ, Li B, Chen YS | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2019 |
| [Analysis of Genetic Screening in Couples of Reproductive Age for Thalassemia in Lingshui Li Autonomous County of Hainan Province]. | Tu ZH, Zhou Z, Wu WX, Wang XP, Zhou YZ, Huang CD, Ma N, Ruan HL, Zhao LQ, Wang J | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2019 |
| [Clinical Significance of Screening Thalassemia with High- Throughput Sequencing]. | Wang K, Dang YH, Li ZL, Pu YD, He SZ | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2019 |
| Management of the aging beta-thalassemia transfusion-dependent population - The Italian experience. | Pinto VM, Poggi M, Russo R, Giusti A, Forni GL | Blood Rev. | 2019 |
| A sickle cell disease patient with dural venous sinus thrombosis: a case report and literature review. | Wang MK, Shergill R, Jefkins M, Cheung J | Hemoglobin | 2019 |
| Systematic Review: Pain and Emotional Functioning in Pediatric Sickle Cell Disease. | Reader SK, Rockman LM, Okonak KM, Ruppe NM, Keeler CN, Kazak AE | J Clin Psychol Med Settings | 2019 |
| A randomized controlled trial evaluating the effects of amlodipine on myocardial iron deposition in pediatric patients with thalassemia major. | Khaled A, Salem HA, Ezzat DA, Seif HM, Rabee H | Drug Des Devel Ther | 2019 |
| Effect of acute exercise on RBC deformability and RBC nitric oxide synthase signalling pathway in young sickle cell anaemia patients. | Grau M, Jerke M, Nader E, Schenk A, Renoux C, Collins B, Dietz T, Bizjak DA, Joly P, Bloch W, Connes P, Prokop A | Sci Rep | 2019 |
| Emerging disease-modifying therapies for sickle cell disease. | Carden MA, Little J | Haematologica | 2019 |
| The Spectrum of β-Thalassemia Mutations in Siirt Province, Southeastern Turkey. | Yılmaz S | Hemoglobin | 2019 |
| The Role of Patient-Physician Communication on the Use of Hydroxyurea in Adult Patients with Sickle Cell Disease. | Jabour SM, Beachy S, Coburn S, Lanzkron S, Eakin MN | J Racial Ethn Health Disparities | 2019 |
| Multifactorial Painful Leg Ulcers Due to Hyperhomocysteinemia, Plasminogen Activator Inhibitor-1 4G/5G Heterozygote Gene Mutation, and Beta Thalassemia Minor: A Case Report. | Çaytemel C, Topaloğlu Demir F, Büyükbabani N, Türkoğlu Z, Uzuner EG | Int J Low Extrem Wounds | 2019 |
| Free heme regulates placenta growth factor through NRF2-antioxidant response signaling. | Kapetanaki MG, Gbotosho OT, Sharma D, Weidert F, Ofori-Acquah SF, Kato GJ | Free Radic. Biol. Med. | 2019 |
| Diversity of RH and transfusion support in Brazilian sickle cell disease patients with unexplained Rh antibodies. | Dinardo CL, Kelly S, Dezan MR, Ribeiro IH, Castilho SL, Schimidt LC, Valgueiro MDC, Preiss LR, Custer B, Sabino EC, Westhoff CM, | Transfusion | 2019 |
| Male sickle cell patients, compensated transpubertal hypogonadism and normal final growth. | Martins PRJ, De Vito FB, Resende GAD, Kerbauy J, Pereira GA, Moraes-Souza H, Figueiredo MS, Verreschi IT | Clin. Endocrinol. (Oxf) | 2019 |
| Related and unrelated donor transplantation for β-thalassemia major: results of an international survey. | Li C, Mathews V, Kim S, George B, Hebert K, Jiang H, Li C, Zhu Y, Keesler DA, Boelens JJ, Dvorak CC, Agarwal R, Auletta JJ, Goyal RK, Hanna R, Kasow K, Shenoy S, Smith AR, Walters MC, Eapen M | Blood Adv | 2019 |
| CRISPR-Cas9 gene editing for patients with haemoglobinopathies. | The Lancet Haematology | Lancet Haematol | 2019 |
| Total Serum Magnesium Levels and Calcium-To-Magnesium Ratio in Sickle Cell Disease. | Antwi-Boasiako C, Kusi-Mensah YA, Hayfron-Benjamin C, Aryee R, Dankwah GB, Kwawukume LA, Darkwa EO | Medicina (Kaunas) | 2019 |
| Cases of malaria in travellers with sickle cell disease - Chemoprophylaxis is important for this risk group. | Bachmeyer C, Steichen O, Moreno-Sabater A, Magne D, Valin N, Mattioni S, Santin A, Lionnet F | Travel Med Infect Dis | 2019 |
| Identifying Clinical and Research Priorities in Sickle Cell Lung Disease. An Official American Thoracic Society Workshop Report. | Ruhl AP, Sadreameli SC, Allen JL, Bennett DP, Campbell AD, Coates TD, Diallo DA, Field JJ, Fiorino EK, Gladwin MT, Glassberg JA, Gordeuk VR, Graham LM, Greenough A, Howard J, Kato GJ, Knight-Madden J, Kopp BT, Koumbourlis AC, Lanzkron SM, Liem RI, Machado RF, Mehari A, Morris CR, Ogunlesi FO, Rosen CL, Smith-Whitley K, Tauber D, Terry N, Thein SL, Vichinsky E, Weir NA, Cohen RT, Klings ES | Ann Am Thorac Soc | 2019 |
| Enhancing the care of patients with sickle cell disease. | De D, Blackmore A, Taylor H | Nurs Stand | 2019 |
| Lentiviral and genome-editing strategies for the treatment of β-hemoglobinopathies. | Magrin E, Miccio A, Cavazzana M | Blood | 2019 |
| Prevalence and correlates of microalbuminuria in Yemeni children with sickle cell disease. | Al-Musawa FE, Al-Saqladi AM | Saudi J Kidney Dis Transpl | 2019 |
| Brief Screening Measures Identify Risk for Psychological Difficulties Among Children with Sickle Cell Disease. | Hood AM, Reife I, King AA, White DA | J Clin Psychol Med Settings | 2019 |
| Family planning practices in couples with children affected by β-thalassemia major and its relationship with their education: An epidemiological study. | Biswas B, Basu K, Naskar NN, Dasgupta A, Paul B, Basu R | J Educ Health Promot | 2019 |
| Barriers to the use of hydroxyurea in the management of sickle cell disease in Nigeria. | Adeyemo TA, Diaku-Akinwunmi IN, Ojewunmi OO, Bolarinwa AB, Adekile AD | Hemoglobin | 2019 |
| Current and emerging treatments for sickle cell disease. | Monus T, Howell CM | JAAPA | 2019 |
| Quantitative prediction of erythrocyte sickling for the development of advanced sickle cell therapies. | Lu L, Li Z, Li H, Li X, Vekilov PG, Karniadakis GE | Sci Adv | 2019 |
| The Effect of Antioxidants on the Properties of Red Blood Cells From Patients With Sickle Cell Anemia. | Al Balushi H, Hannemann A, Rees D, Brewin J, Gibson JS | Front Physiol | 2019 |
| Double Heterozygosity for Hb Durham-N.C. (: c.344T>C) [β114(G16)Leu→Pro] and the IVS-I-110 (: c.93-21G>A) Causing a Severe β-Thalassemia Phenotype. | Cannata M, Cassarà F, Vinciguerra M, Licari P, Passarello C, Leto F, Lo Pinto C, Pitrolo L, Ganci R, Maggio A, Giambona A | Hemoglobin | 2019 |
| Cellular Iron Metabolism and Regulation. | Gao G, Li J, Zhang Y, Chang YZ | Adv. Exp. Med. Biol. | 2019 |
| Antioxidant properties and membrane stabilization effects of methanol extract of leaves on normal and sickle erythrocytes. | Anosike CA, Igboegwu ON, Nwodo OFC | J Tradit Complement Med | 2019 |
| Differential Diagnosis of Iron-Deficiency Anemia from β-Thalassemia Trait Using an Intelligent Model in Comparison with Discriminant Indexes. | Kabootarizadeh L, Jamshidnezhad A, Koohmareh Z | Acta Inform Med | 2019 |
| Improving Care for Patients with Sickle Cell Disease: a Qualitative Study of Hospitalized Sickle Cell Patients. | Del Pino-Jones A, Bowden K, Misky G, Jones CD | J Gen Intern Med | 2019 |
| Sickle cell disease in Africa: an urgent need for longitudinal cohort studies. | Wonkam A, Makani J | Lancet Glob Health | 2019 |
| The epidemiology of sickle cell disease in children recruited in infancy in Kilifi, Kenya: a prospective cohort study. | Uyoga S, Macharia AW, Mochamah G, Ndila CM, Nyutu G, Makale J, Tendwa M, Nyatichi E, Ojal J, Otiende M, Shebe M, Awuondo KO, Mturi N, Peshu N, Tsofa B, Maitland K, Scott JAG, Williams TN | Lancet Glob Health | 2019 |
| Clinical and molecular characterization of novel deletions causing epsilon gamma delta beta thalassemia: Report of two cases. | Repnikova E, Roberts J, Mc Dermott S, Farooqi MS, Iqbal NT, Silvey M, Nolen J, Taboada E, Li W | Pathol. Res. Pract. | 2019 |
| The Role of Family Functioning in the Development of Executive Functions in Preschool Children with Sickle Cell Anemia. | Downes M, de Haan M, Telfer PT, Kirkham FJ | Dev Neuropsychol | 2019 |
| Coinheritance of Hb A-Melbourne (: c.130G>A) and Hb E (: c.79G>A) in Laos and Simultaneous High Resolution Melt Detection of Hb A-Melbourne and Hb A-Lampang (: c.142G>A) in a Single Tube. | Jomoui W, Panichchob P, Rujirachaivej P, Panyasai S, Tepakhan W | Hemoglobin | 2019 |
| Pulmonary Artery Pseudoaneurysm in a Child With β-Thalassemia Major. | Qureshi TN, Haider SR, Al Rawas A, Al Sukaiti R, Al Kindi H, Al Senaidi KS, Elshinawy M, Wali Y | J. Pediatr. Hematol. Oncol. | 2019 |
| Frequency of Interleukins IL1ß/IL18 and Inflammasome NLRP1/NLRP3 Polymorphisms in Sickle Cell Anemia Patients and their Association with Severity Score. | de Almeida E, Frantz SR, Cesar P, Tarragô AM, de Amorim Xabregas L, Garcia NP, Costa AG, de Paula EV, Malheiro A | Curr. Mol. Med. | 2019 |
| Substance P modulates electroacupuncture analgesia in humanized mice with sickle cell disease. | Wang Y, Lei J, Jha RK, Kiven S, Gupta K | J Pain Res | 2019 |
| [Effect of genetic modifiers on the clinical severity of β-thalassemia]. | Zhang QQ, Shang X, Lin WY, Xu XM | Yi Chuan | 2019 |
| Posterior Reversible Encephalopathy Syndrome in adult sickle-cell patients: Case series and literature review. | Vargas A, Testai FD | J Clin Neurosci | 2019 |
| Ticagrelor versus placebo for the reduction of vaso-occlusive crises in pediatric sickle cell disease: Rationale and design of a randomized, double-blind, parallel-group, multicenter phase 3 study (HESTIA3). | Heeney MM, Abboud MR, Amilon C, Andersson M, Githanga J, Inusa B, Kanter J, Leonsson-Zachrisson M, Michelson AD, Berggren AR, | Contemp Clin Trials | 2019 |
| High erythropoietin may be associated with vascular complications in patients with secondary erythrocytosis caused by high oxygen affinity variant hemoglobin Coimbra. | Santos BC, Jorge SE, de Albuquerque DM, Gilli SCO, Sonati MF, Fertrin KY, Costa FF | Blood Cells Mol. Dis. | 2019 |
| Validation of a composite vascular high-risk profile for adult patients with sickle cell disease. | Nouraie M, Little JA, Hildesheim M, Gibbs JSR, Morris CR, Machado RF, Kato GJ, Gordeuk VR, Gladwin MT | Am. J. Hematol. | 2019 |
| Corrigendum to | Masilamani V, Al Salhi MS, Devanesan S, AlGahtani FH, Abu-Salah KM, Ahamad I, Agastian P | Photodiagnosis Photodyn Ther | 2019 |
| Association of plasma homocysteine level with vaso-occlusive crisis in sickle cell anemia patients of Odisha, India. | Meher S, Patel S, Das K, Dehury S, Jit BP, Maske MM, Das P, Dash BP, Mohanty PK | Ann. Hematol. | 2019 |
| Haemoglobinopathies from the cardiac point of view. | Romano MMD | Hematol Transfus Cell Ther | 2019 |
| SIMENS-LIS4SC, a Laboratory Information System for Biological Tests of Sickle Cell Screening and Healthcare. | Diallo AH, Camara G, Lamy JB, Lo M, Diagne I, Makalou D, Diop M, Doupa D | Stud Health Technol Inform | 2019 |
| Hb Guangxi [β65(E9)Lys→Glu (>AG); : c.196A>G]: A Novel β-Globin Variant. | Xu M, Chen WD, Wang YJ, Zhou Y, Li J, Xu AP, Ji L | Hemoglobin | 2019 |
| Cholelithiasis in patients with paediatric sickle cell anaemia in a Saudi hospital. | Alhawsawi ZM, Alshenqeti AM, Alqarafi AM, Alhussayen LK, Turkistani WA | J Taibah Univ Med Sci | 2019 |
| The autophagy-activating kinase ULK1 mediates clearance of free α-globin in β-thalassemia. | Lechauve C, Keith J, Khandros E, Fowler S, Mayberry K, Freiwan A, Thom CS, Delbini P, Romero EB, Zhang J, Motta I, Tillman H, Cappellini MD, Kundu M, Weiss MJ | Sci Transl Med | 2019 |
| The challenges of handling deferasirox in sickle cell disease patients older than 40 years. | Ribeiro LB, Soares EA, Costa FF, Gilli SCO, Olalla Saad ST, Benites BD | Hematology | 2019 |
| HLA-haploidentical hematopoietic stem cell transplantation in pediatric patients with hemoglobinopathies: current practice and new approaches. | Oevermann L, Schulte JH, Hundsdörfer P, Hakimeh D, Kogel F, Lang P, Corbacioglu S, Eggert A, Sodani P | Bone Marrow Transplant. | 2019 |
| Sickle Cell Trait, European Ancestry, and Longitudinal Tracking of HbA Among African Americans: The Jackson Heart Study. | Echouffo-Tcheugui JB, Mwasongwe SE, Sims M, Dagogo-Jack S, Golden SH, Correa A, Musani SK | Diabetes Care | 2019 |
| Correlates of successful transition in young adults with sickle cell disease. | Darbari I, Jacobs E, Gordon O, Weiss D, Winship K, Casella JF, Strouse JJ, Takemoto CM | Pediatr Blood Cancer | 2019 |
| Thirty-year risk of ischemic stroke in individuals with sickle cell trait and modification by chronic kidney disease: The atherosclerosis risk in communities (ARIC) study. | Caughey MC, Derebail VK, Key NS, Reiner AP, Gottesman RF, Kshirsagar AV, Heiss G | Am. J. Hematol. | 2019 |
| Hemoglobin S and C affect biomechanical membrane properties of -infected erythrocytes. | Fröhlich B, Jäger J, Lansche C, Sanchez CP, Cyrklaff M, Buchholz B, Soubeiga ST, Simpore J, Ito H, Schwarz US, Lanzer M, Tanaka M | Commun Biol | 2019 |
| Effect of Health Education Programme on the Knowledge of and Attitude about Sickle Cell Anaemia among Male Secondary School Students in the Jazan Region of Saudi Arabia: Health Policy Implications. | Kotb MM, Almalki MJ, Hassan Y, Al Sharif A, Khan M, Sheikh K | Biomed Res Int | 2019 |
| Asymptomatic actinomycosis in a girl with thalassemia major. | Yu U, Wang X | IDCases | 2019 |
| Effects of Individualized Treadmill Endurance Training on Oxidative Stress in Skeletal Muscles of Transgenic Sickle Mice. | Gouraud E, Charrin E, Dubé JJ, Ofori-Acquah SF, Martin C, Skinner S, Chatel B, Boreau A, Messonnier LA, Connes P, Pialoux V, Hautier C, Faes C | Oxid Med Cell Longev | 2019 |
| Treatment of dental and orthodontic complications in thalassaemia. | Mulimani P, Abas AB, Karanth L, Colombatti R, Kulkarni P | Cochrane Database Syst Rev | 2019 |
| A case of compound heterozygous hemoglobin Köln/hemoglobin E in an Indian family. | Mittal N, Garg A, Kashyap R, Agarwal S | Pediatr Hematol Oncol | 2019 |
| The Experience and Health-Related Quality of Life after Haploidentical Stem Cell Transplantation for Adults with Sickle Cell Disease. | Hastings B, Patil C, Gallo AM | West J Nurs Res | 2019 |
| Occurrence of acute myeloid leukemia in hydroxyurea-treated sickle cell disease patient. | Regan S, Yang X, Finnberg NK, El-Deiry WS, Pu JJ | Cancer Biol. Ther. | 2019 |
| Approximately 40 000 children with sickle cell anemia require screening with TCD and treating with hydroxyurea for stroke prevention in three states in northern Nigeria. | Galadanci AA, Galadanci NA, Jibir BW, Abdullahi SU, Idris N, Gambo S, Ali Abubakar SA, Kabo NA, Bello-Manga H, Haliru L, Bashir I, Aliyu MH, Galadanci JA, DeBaun MR | Am. J. Hematol. | 2019 |
| Evaluation of the Effect of Support-Training System of Peer Group on Promotion of Self-Care in β-Thalassemia Major Patients in Southern Iran. | Safaei S, Abedi H, Parand S, Karimi M | Hemoglobin | 2019 |
| Thalassemia and Moyamoya syndrome: unfurling an intriguing association. | Das S, Dubey S, Acharya M, Chatterjee S, Lahiri D, Das G, Ray BK, Kraemer M | J. Neurol. | 2019 |
| Dysfunction of the auditory system in sickle cell anaemia: a systematic review with meta-analysis. | Rissatto-Lago MR, Fernandes LDC, Alves AAG, de Oliveira ACG, de Andrade CLO, Salles C, Ladeia AMT | Trop. Med. Int. Health | 2019 |
| Red blood cells microparticles are associated with hemolysis markers and may contribute to clinical events among sickle cell disease patients. | Olatunya OS, Lanaro C, Longhini AL, Penteado CFF, Fertrin KY, Adekile A, Saad STO, Costa FF | Ann. Hematol. | 2019 |
| Allogenic hematopoietic stem cell transplantation in sickle cell disease. | Galal A, Asslan M | Curr. Opin. Hematol. | 2019 |
| Quality of life in pre-adolescent children with sickle cell disease in Brazil. | Oliveira CDL, Kelly S, de Almeida-Neto C, Carneiro-Proietti AB, Camargos Piassi FC, Salomon T, Flor-Park MV, Maximo C, Rodrigues DW, Mota RA, Teixeira CM, Loureiro P, Sabino EC, Custer B, | Pediatr Hematol Oncol | 2019 |
| Ischemic stroke in children and young adults with sickle cell disease in the post-STOP era. | Kwiatkowski JL, Voeks JH, Kanter J, Fullerton HJ, Debenham E, Brown L, Adams RJ, | Am. J. Hematol. | 2019 |
| Transfusion practices in the care of pregnant women with sickle cell disease in Ouagadougou. | Zamané H, Sanou F, Kiemtoré S, Kain DP, Sawadogo AK, Bonané-Thiéba B | Int J Gynaecol Obstet | 2019 |
| Effect of different iron chelation regimens on bone mass in transfusion-dependent thalassemia patients. | Bordbar M, Haghpanah S, Zekavat OR, Saki F, Bazrafshan A, Bozorgi H | Expert Rev Hematol | 2019 |
| Nitric oxide loading reduces sickle red cell adhesion and vaso-occlusion in vivo. | McMahon TJ, Shan S, Riccio DA, Batchvarova M, Zhu H, Telen MJ, Zennadi R | Blood Adv | 2019 |
| Hematopoietic stem cell transplantation and cellular therapy in sickle cell disease: where are we now? | Tanhehco YC, Bhatia M | Curr. Opin. Hematol. | 2019 |
| Mechanisms of alloimmunization in sickle cell disease. | Hudson KE, Fasano RM, Karafin MS, Hendrickson JE, Francis RO | Curr. Opin. Hematol. | 2019 |
| Single-Incision Pediatric Endosurgery Cholecystectomy Performed by Residents in Children with Sickle Cell Disease. | Raboe E, Owiwi Y, Al Nofeai Z, Ghallab A, Zainelabdeen AS, Alsaggaf AA, Zidan M, Fayez M, Atta A, Alofi T, Sindi OA, Almanea A, Alharbi IA, Madani H, Seet M, Sait A, Fallatah R | J Laparoendosc Adv Surg Tech A | 2019 |
| Noninvasive optical assessment of resting-state cerebral blood flow in children with sickle cell disease. | Lee SY, Cowdrick KR, Sanders B, Sathialingam E, McCracken CE, Lam WA, Joiner CH, Buckley EM | Neurophotonics | 2019 |
| Genetic modulators of fetal hemoglobin expression and ischemic stroke occurrence in African descendant children with sickle cell anemia. | Nicolau M, Vargas S, Silva M, Coelho A, Ferreira E, Mendonça J, Vieira L, Kjöllerström P, Maia R, Silva R, Dias A, Ferreira T, Morais A, Soares IM, Lavinha J, Faustino P | Ann. Hematol. | 2019 |
| A Novel Frameshift Mutation at Codon 2 (-T) (: c.9delT) and First Report of Three New β-Globin Mutations From Azerbaijan. | Bayramov B, Aliyeva G, Asadov C, Mammadova T, Karimova N, Eynullazadeh K, Gafarova S, Akbarov S, Farhadova S, Safarzadeh Z, Abbasov M | Hemoglobin | 2019 |
| Reticulocyte Hemoglobin Equivalent (Ret-He) Combined with Red Blood Cell Distribution Width Has a Differentially Diagnostic Value for Thalassemias. | Lian Y, Shi J, Nie N, Huang Z, Shao Y, Zhang J, Huang J, Li X, Ge M, Jin P, Wang M, Zheng Y | Hemoglobin | 2019 |
| Vascular Instability and Neurological Morbidity in Sickle Cell Disease: An Integrative Framework. | Stotesbury H, Kawadler JM, Hales PW, Saunders DE, Clark CA, Kirkham FJ | Front Neurol | 2019 |
| Genetic diversity of CD14, CD28, CTLA-4 and ICOS gene promoter polymorphism in African and American sickle cell disease. | Seamans BN, Pellechio SL, Capria AL, Agyingi SE, Morenikeji OB, Ojurongbe O, Thomas BN | Hum. Immunol. | 2019 |
| Association of frequency of hereditary hemochromatosis (HFE) gene mutations (H63D and C282Y) with iron overload in beta-thalassemia major patients in Pakistan. | Sharif Y, Irshad S, Tariq A, Rasheed S, Tariq MH | Saudi Med J | 2019 |
| Iron overload and malignancies in patients with haemoglobinopathies: A single center experience. | Rigoli L, Petrungaro A, Di Bella C, Caruso R | Transfus. Apher. Sci. | 2019 |
| The effect of quercetin on iron overload and inflammation in β-thalassemia major patients: A double-blind randomized clinical trial. | Sajadi Hezaveh Z, Azarkeivan A, Janani L, Hosseini S, Shidfar F | Complement Ther Med | 2019 |
| Pharmacokinetics and pharmacodynamics of single dose of inhaled nebulized sodium nitrite in healthy and hemoglobin E/β-thalassemia subjects. | Sirirat K, Sriwantana T, Kaewchuchuen J, Paiboonsukwong K, Fucharoen S, Ritthidej G, Parakaw T, Srihirun S, Vivithanaporn P, Sritara P, Sibmooh N | Nitric Oxide | 2019 |
| [Cephalometric evaluation of patients with β-thalassemia major living in Azerbaijan]. | Shadlinskaya RV, Gasymova ZV, Gasymov OF | Stomatologiia (Mosk) | 2019 |
| Hemoglobin-based Oxygen Carriers: Current State-of-the-art and Novel Molecules. | Sen Gupta A | Shock | 2019 |
| Hemoglobin-based Oxygen Carriers (HBOC)-What the Next Generation Holds: When Red Blood Cells are not an Option. | Hill-Pryor C, Pusateri AE, Weiskopf RB | Shock | 2019 |
| Rifaximin for sickle cell disease. | Lim SH, Dutta D, Moore J | Am. J. Hematol. | 2019 |
| Hemoglobin alters vitamin carrier uptake and vitamin D metabolism in proximal tubule cells: implications for sickle cell disease. | Gliozzi ML, Rbaibi Y, Long KR, Vitturi DA, Weisz OA | Am. J. Physiol., Cell Physiol. | 2019 |
| Antenatal screening for haemoglobinopathies: current status, barriers and ethics. | Chakravorty S, Dick MC | Br. J. Haematol. | 2019 |
| Evaluation of hydroxyurea genotoxicity in patients with sickle cell disease. | Oliveira EAM, Boy KA, Santos APP, Machado CDS, Velloso-Rodrigues C, Gerheim PSAS, Mendonça LM | Einstein (Sao Paulo) | 2019 |
| Profile of crizanlizumab and its potential in the prevention of pain crises in sickle cell disease: evidence to date. | Riley TR, Riley TT | J Blood Med | 2019 |
| Decoding the role of SOD2 in sickle cell disease. | Dosunmu-Ogunbi AM, Wood KC, Novelli EM, Straub AC | Blood Adv | 2019 |
| [Serum level of soluble transferrin receptor in children with hemoglobin H disease]. | Ren ZM, Huang LL, Huang BX, Li CG, Chen YS | Zhongguo Dang Dai Er Ke Za Zhi | 2019 |
| Prevalence and genetic analysis of thalassemia in neonates in Wuhan area: a national megacity in central China. | Cai W, Xiong Q, Tong J, Dai X, Zhou B, Shen S, Hu X | J. Matern. Fetal. Neonatal. Med. | 2019 |
| Updated mechanisms underlying sickle cell disease-associated pain. | Du S, Lin C, Tao YX | Neurosci. Lett. | 2019 |
| Systematic Review of l-glutamine for Prevention of Vaso-occlusive Pain Crisis in Patients with Sickle Cell Disease. | Cieri-Hutcherson NE, Hutcherson TC, Conway-Habes EE, Burns BN, White NA | Pharmacotherapy | 2019 |
| Animal Models of Normal and Disturbed Iron and Copper Metabolism. | Wang X, Garrick MD, Collins JF | J. Nutr. | 2019 |
| Iron stores in pregnant women with sickle cell disease: a protocol for a systematic review and meta-analysis. | Aroke D, Momo Kadia B, Njim T | BMJ Open | 2019 |
| Magnesium for treating sickle cell disease. | Than NN, Soe HHK, Palaniappan SK, Abas AB, De Franceschi L | Cochrane Database Syst Rev | 2019 |
| Treatment Status of Patients with B-Thalassemia Major in Northern Iran: Thalassemia Registry System. | Kosaryan M, Karami H, Darvishi-Khezri H, Akbarzadeh R, Aliasgharian A, Bromand K | Iran. J. Public Health | 2019 |
| Megestrol Acetate Induced Paradoxical Embolism in a Sickle Cell Disease Patient. | Dominguez L, Tatar F, Malakooti SK, Kulchinsky RP | Cureus | 2019 |
| Mini review: leg ulcers - a secondary complication of sickle cell disease. | AlDallal SM | Int J Gen Med | 2019 |
| Clinical Transformation in Care for Patients With Sickle Cell Disease at an Urban Academic Medical Center. | Rizk S, Axelrod D, Riddick-Burden G, Congdon-Martin E, McKenzie S, Haines C, Ward L, McAna J, Crawford AG | Am J Med Qual | 2019 |
| CRISPR/Cas9 gene correction of HbH-CS thalassemia-induced pluripotent stem cells. | Yingjun X, Yuhuan X, Yuchang C, Dongzhi L, Ding W, Bing S, Yi Y, Dian L, Yanting X, Zeyu X, Nengqing L, Diyu C, Xiaofang S | Ann. Hematol. | 2019 |
| Investigation of JAK2V617F Mutation Prevalence in Patients with Beta Thalassemia Major. | Tahannejad Asadi Z, Yarahmadi R, Saki N, Jalali MT, Amin Asnafi A, Tangestani R | Lab Med | 2019 |
| Stem cell transplantation in sickle-cell disease. | Sheth S | Lancet Haematol | 2019 |
| Echocardiographic Screening of Cardiovascular Status in Pediatric Sickle Cell Disease. | Allen KY, Jones S, Jackson T, DeCost G, Stephens P, Hanna BD, Cohen MS, Smith-Whitley K, Mercer-Rosa L, Natarajan SS | Pediatr Cardiol | 2019 |
| Construction and Analysis of a Long Non-Coding RNA (lncRNA)-Associated ceRNA Network in β-Thalassemia and Hereditary Persistence of Fetal Hemoglobin. | Jia W, Jia S, Chen P, He Y | Med. Sci. Monit. | 2019 |
| Hepatobiliary Complications in Children with Sickle Cell Disease: A Retrospective Review of Medical Records from 616 Patients. | Allali S, de Montalembert M, Brousse V, Heilbronner C, Taylor M, Brice J, Manzali E, Garcelon N, Lacaille F | J Clin Med | 2019 |
| Selenium Status and Hemolysis in Sickle Cell Disease Patients. | Delesderrier E, Cople-Rodrigues CS, Omena J, Kneip Fleury M, Barbosa Brito F, Costa Bacelo A, Correa Koury J, Citelli M | Nutrients | 2019 |
| Clinical phenotypes and outcomes of precapillary pulmonary hypertension of sickle cell disease. | Savale L, Habibi A, Lionnet F, Maitre B, Cottin V, Jais X, Chaouat A, Artaud-Macari E, Canuet M, Prevot G, Chantalat-Auger C, Montani D, Sitbon O, Galacteros F, Simonneau G, Parent F, Bartolucci P, Humbert M | Eur. Respir. J. | 2019 |
| Antibiotics for treating acute chest syndrome in people with sickle cell disease. | Martí-Carvajal AJ, Conterno LO, Knight-Madden JM | Cochrane Database Syst Rev | 2019 |
| Newborn Screening With Sickle Cell Point of Care: A Valuable Resource in Low-Income Settings. | Ware RE, Odame I | Pediatrics | 2019 |
| Newborn Screening for Sickle Cell Disease Using Point-of-Care Testing in Low-Income Setting. | Alvarez OA, Hustace T, Voltaire M, Mantero A, Liberus U, Saint Fleur R | Pediatrics | 2019 |
| A Heterozygous Variant (: c.379delG, p.Val127Cysfs*32) Associated with a Mild β-Thalassemia Intermedia Phenotype in a Turkish Child. | Gürlek-Gökçebay D, Akpinar-Tekgunduz S, Erdem HB, Yarali N | Hemoglobin | 2019 |
| Splenectomy for people with thalassaemia major or intermedia. | Sharma A, Easow Mathew M, Puri L | Cochrane Database Syst Rev | 2019 |
| Spectral domain optical coherence tomography findings in Turkish sickle-cell disease and beta thalassemia major patients. | Ulusoy MO, Türk H, Kıvanç SA | J Curr Ophthalmol | 2019 |
| Role of some members of chemokine/cytokine network in the pathogenesis of thalassemia and sickle cell hemoglobinopathies: a mini review. | Mousavi Z, Yazdani Z, Moradabadi A, Hoseinpourkasgari F, Hassanshahi G | Exp Hematol Oncol | 2019 |
| Prevalence and Factors Associated with Human Parvovirus B19 Infection in Sickle Cell Patients Hospitalized in Tanzania. | Urio F, George H, Tluway F, Nyambo TB, Mmbando BP, Makani J | Mediterr J Hematol Infect Dis | 2019 |
| Dengue with Normal Platelet Count and no Hemoconcentration: Automated Hematogram in Cases with Underlying Thalassemia. | Joob B, Wiwanitkit V | Iran J Pathol | 2019 |
| Insulin secretion-sensitivity index-2 could be a novel marker in the identification of the role of pancreatic iron deposition on beta-cell function in thalassemia major. | Karadas N, Yurekli B, Bayraktaroglu S, Aydinok Y | Endocr. J. | 2019 |
| The effect of positive thinking training on the quality of life of parents of adolescent with thalassemia. | Sadeghloo A, Shamsaee P, Hesari E, Akhondzadeh G, Hojjati H | Int J Adolesc Med Health | 2019 |
| Serum Potassium, Sodium, and Chloride Levels in Sickle Cell Disease Patients and Healthy Controls: A Case-Control Study at Korle-Bu Teaching Hospital, Accra. | Antwi-Boasiako C, Kusi-Mensah YA, Hayfron-Benjamin C, Aryee R, Dankwah GB, Abla KL, Owusu Darkwa E, Botchway FA, Sampene-Donkor E | Biomark Insights | 2019 |
| Prevalence of hemoglobin abnormalities in an apparently healthy population in Benin. | Zohoun A, Baglo Agbodande T, Zohoun L, Anani L | Hematol Transfus Cell Ther | 2019 |
| Extensive multilineage analysis in patients with mixed chimerism after allogeneic transplantation for sickle cell disease: insight into hematopoiesis and engraftment thresholds for gene therapy. | Magnani A, Pondarré C, Bouazza N, Magalon J, Miccio A, Six E, Roudaut C, Arnaud C, Kamdem A, Touzot F, Gabrion A, Magrin E, Couzin C, Fusaro M, André I, Vernant JP, Gluckman E, Bernaudin F, Bories D, Cavazzana M | Haematologica | 2019 |
| Airway Inflammation and Lung Function in Sickle Cell Disease. | De A, Agrawal S, Morrone K, Zhang J, Bjorklund NL, Manwani D, Rastogi D | Pediatr Allergy Immunol Pulmonol | 2019 |
| Relating retinal blood flow and vessel morphology in sickle cell retinopathy. | Cano J, Farzad S, Khansari MM, Tan O, Huang D, Lim JI, Shahidi M | Eye (Lond) | 2019 |
| The monoclonal antibody against γ-globin chain; , accurately measured F cells in SEA-α thalassemia 1 trait. | Tangpan L, Jansai T, Kerdpoo S, Kiewkarnkha T, Limweeraprajak E, Tatu T | J Immunoassay Immunochem | 2019 |
| Review of Sickle Cell Disease and Spinal Pathology. | Rudy HL, Yang D, Nam AD, Cho W | Global Spine J | 2019 |
| Why, Who, When, and How? Rationale for Considering Allogeneic Stem Cell Transplantation in Children with Sickle Cell Disease. | Bernaudin F | J Clin Med | 2019 |
| Awareness of Ocular Manifestations, Complications, and Treatment of Sickle Cell Disease in the Eastern Province of Saudi Arabia: A Cross-Sectional Study. | Alshehri AM, Feroze KB, Amir MK | Middle East Afr J Ophthalmol | 2019 |
| Hemoglobin S and Glucose-6-Phosphate Dehydrogenase Deficiency Coinheritance in AS and SS Individuals in Malaria-Endemic Region: A Study in Calabar, Nigeria. | Okafor IM, Okoroiwu HU, Ekechi CA | J Glob Infect Dis | 2019 |
| Low levels of coagulation inhibitors: A high-risk thrombotic factor in thalassemic patients. | Mousavi Z, Soleymani S, Hassanshahi G, Nikbakht R, Mirzaee Khalilabadi R | Rev Clin Esp | 2019 |
| Randomized Pilot Study: A Mobile Technology-based Self-management Intervention for Sickle Cell Pain. | Ezenwa MO, Yao Y, Nguyen MT, Mandernach MW, Hunter CT, Yoon SL, Fedele D, Lucero RJ, Lyon D, Wilkie DJ | West J Nurs Res | 2019 |
| Knowledge and attitude toward genetic diseases and genetic tests among pre-marriage individuals: A cross-sectional study in northern Iran. | Hashemi-Soteh MB, Nejad AV, Ataei G, Tafazoli A, Ghasemi D, Siamy R | Int J Reprod Biomed (Yazd) | 2019 |
| Minihepcidins improve ineffective erythropoiesis and splenomegaly in a new mouse model of adult beta-thalassemia major. | Casu C, Chessa R, Liu A, Gupta R, Drakesmith H, Fleming R, Ginzburg YZ, MacDonald B, Rivella S | Haematologica | 2019 |
| Thalassemia and Hemoglobinopathies in an Ethnic Minority Group in Northern Vietnam. | Anh TM, Sanchaisuriya K, Kieu GN, Tien DN, Thu HBT, Sanchaisuriya P, Fucharoen S, Fucharoen G, Schelp FP | Hemoglobin | 2019 |
| Evaluation of Outcomes and Quality of Care in Children with Sickle Cell Disease Diagnosed by Newborn Screening: A Real-World Nation-Wide Study in France. | Brousse V, Arnaud C, Lesprit E, Quinet B, Odièvre MH, Etienne-Julan M, Guillaumat C, Elana G, Belloy M, Garnier N, Chamouine A, Dumesnil C, Montalembert M, Pondarre C, Bernaudin F, Couque N, Boutin E, Bardakjian J, Djennaoui F, Ithier G, Benkerrou M, Thuret I | J Clin Med | 2019 |
| Attrition from Care and Clinical Outcomes in a Cohort of Sickle Cell Disease Patients in a Tribal Area of Western India. | Dave K, Chinnakali P, Thekkur P, Desai S, Vora C, Desai G | Trop Med Infect Dis | 2019 |
| Allogeneic Hematopoietic Stem Cell Transplantation for Adults with Sickle Cell Disease. | Saraf SL, Rondelli D | J Clin Med | 2019 |
| The emerging challenge of sickle cell nephropathy. | Baptista RB, Almeida E | Nephrol. Dial. Transplant. | 2019 |
| Marital status and paternity in patients with Transfusion- Dependent Thalassemia (TDT) and Non Transfusion-Dependent Thalassemia (NTDT): an ICET - A survey in different countries. | De Sanctis V, Soliman AT, El-Hakim I, Christou S, Mariannis D, Karimi M, Ladis V, Kattamis A, Daar S, Yassin M, Canatan D, Galati MC, Raiola G, Campisi S, Kakkar S, Kaleva V, Saki F, Ellinides A, Pikis G, Christodoulides C, Abdulla M, Di Maio S, Theodoridis C, Elsedfy H, Kattamis C | Acta Biomed | 2019 |
| Responsive Parenting Behaviors and Cognitive Function in Children With Sickle Cell Disease. | Yarboi J, Prussien KV, Bemis H, Williams E, Watson KH, McNally C, Henry L, King AA, DeBaun MR, Compas BE | J Pediatr Psychol | 2019 |
| Peripheral nerve pathology in sickle cell disease mice. | Sadler KE, Lewis TR, Waltz TB, Besharse JC, Stucky CL | Pain Rep | 2019 |
| Detection of Extramedullary Hematopoietic Tissue in a Patient with Beta-Thalassemia Major on Tc99m-Sestamibi Parathyroid Scintigraphy. | Valotassiou V, Angelidis G, Alexiou S, Psimadas D, Tsougos I, Georgoulias P | Indian J Nucl Med | 2019 |
| Noninvasive prenatal screening test for compound heterozygous beta thalassemia using an amplification refractory mutation system real-time polymerase chain reaction technique. | Suwannakhon N, Pangeson T, Seeratanachot T, Mahingsa K, Pingyod A, Bumrungpakdee W, Sanguansermsri T | Hematol Rep | 2019 |
| Rare double heterozygosity for poly A(A〉 G) and CD17(A〉 T) of beta thalassemia intermedia in a Chinese family. | Xie J, Zhou Y, Xiao Q, Long R, Li L, Li L | Hematol Rep | 2019 |
| Concurrent juvenile myelomonocytic leukemia with thalassemia in a case with infection from Sabah, Malaysian Borneo. | Abdullah MA, Abdullah SM, Kumar SV, Hoque MZ | Hematol Rep | 2019 |
| First gene therapy for β-thalassemia approved. | Harrison C | Nat. Biotechnol. | 2019 |
| Development of a forward-oriented therapeutic lentiviral vector for hemoglobin disorders. | Uchida N, Hsieh MM, Raines L, Haro-Mora JJ, Demirci S, Bonifacino AC, Krouse AE, Metzger ME, Donahue RE, Tisdale JF | Nat Commun | 2019 |
| Reversal of a rheologic cardiomyopathy following hematopoietic stem cell transplantation for sickle cell disease. | Sachdev V, Hsieh M, Jeffries N, Noreuil A, Li W, Sidenko S, Hannoush H, Limerick E, Wilson D, Tisdale J, Fitzhugh C | Blood Adv | 2019 |
| Knowledge and Beliefs Regarding Thalassemia in an Urban Population. | Ebrahim S, Raza AZ, Hussain M, Khan A, Kumari L, Rasheed R, Mahmood S, Khatri MA, Bijoora M, Zaheer R, Sattar N, Sohail W, Zakir H, Jafry FH, Memon A, Anwer S, Fatima K | Cureus | 2019 |
| Gene Therapy For Beta-Thalassemia: Updated Perspectives. | Karponi G, Zogas N | Appl Clin Genet | 2019 |
| Thalassaemia. | Barnett R | Lancet | 2019 |
| The impact of Host vs. Graft mismatches on rejection of haploidentical bone marrow transplants in thalassemia patients using posttransplant cyclophosphamide. | Marwah P, Soni R, Ramprakash S, Raghuram CP, Trivedi D, Kumar Agarwal R, Dhanya R, Sedai A, Kumari A, Parmar L, Faulkner L | Bone Marrow Transplant. | 2019 |
| Cas9 interrogates genomic DNA with very high specificity and can be used for mammalian genome editing. | Acharya S, Mishra A, Paul D, Ansari AH, Azhar M, Kumar M, Rauthan R, Sharma N, Aich M, Sinha D, Sharma S, Jain S, Ray A, Jain S, Ramalingam S, Maiti S, Chakraborty D | Proc. Natl. Acad. Sci. U.S.A. | 2019 |
| Parental Attitudes Towards Prenatal Genetic Testing For Sickle Cell Disease. | Stevens EM, Patterson CA, Tchume-Johnson T, Antiel RM, Flake A, Smith-Whitley K, Barakat LP | J. Pediatr. Hematol. Oncol. | 2019 |
| The controversial role of red cell transfusions for sickle cell pain. | Karafin MS, Field JJ | Curr. Opin. Hematol. | 2019 |
| Noninvasive prenatal diagnosis of β-thalassemia by relative haplotype dosage without analyzing proband. | Li H, Du B, Jiang F, Guo Y, Wang Y, Zhang C, Zeng X, Xie Y, Ouyang S, Xian Y, Chen M, Liu W, Sun X | Mol Genet Genomic Med | 2019 |
| Morpho-functional evaluation of lung aeration as a marker of sickle-cell acute chest syndrome severity in the ICU: a prospective cohort study. | Garnier M, Hafiani EM, Arbelot C, Blayau C, Labbe V, Stankovic-Stojanovic K, Lionnet F, Bonnet F, Fulgencio JP, Fartoukh M, Quesnel C | Ann Intensive Care | 2019 |
| Prevalence of enuresis and its impact in quality of life of patients with sickle cell disease. | Nelli AM, Mrad FCC, Alvaia MA, Maia HAADS, Guimarães COS, Carvalho ESS, Gomes CM, Bastos JM, de Bessa J | Int Braz J Urol | 2019 |
| [Newborn screening of sickle cell disease and management of care.] | Allaf B, Couque N, de Montalembert M | Rev Prat | 2019 |
| Craniofacial and occlusal features of children with sickle cell disease compared to normal standards: a clinical and radiographic study of 50 paediatric patients. | Pashine A, Shetty RM, Shetty SY, Gadekar T | Eur Arch Paediatr Dent | 2019 |
| Differences in lung function between children with sickle cell anaemia from West Africa and Europe. | Arigliani M, Castriotta L, Zubair R, Dogara LG, Zuiani C, Raywood E, Vecchiato K, Petoello E, Sunday AD, Ndoro S, Canciani MC, Gupta A, Cogo P, Inusa B | Thorax | 2019 |
| Optimizing Hydroxyurea Treatment for Sickle Cell Disease Patients: The Pharmacokinetic Approach. | Nazon C, Sabo AN, Becker G, Lessinger JM, Kemmel V, Paillard C | J Clin Med | 2019 |
| Pulmonary dysfunction among adolescents and adults with sickle cell disease in Nigeria: Implications for monitoring. | Ozoh OB, Kalejaiye OO, Eromesele OE, Adelabu YA, Dede SK, Ogunlesi FO | Ann Thorac Med | 2019 |
| Prevalence of sickle cell disease and sickle cell trait among children admitted to Al Fashir Teaching Hospital North Darfur State, Sudan. | Adam MA, Adam NK, Mohamed BA | BMC Res Notes | 2019 |
| Treatment patterns and economic burden of sickle-cell disease patients prescribed hydroxyurea: a retrospective claims-based study. | Shah N, Bhor M, Xie L, Halloway R, Arcona S, Paulose J, Yuce H | Health Qual Life Outcomes | 2019 |
| Uridine diphosphate glucuronosyl transferase 1A (UGT1A1) promoter polymorphism in young patients with sickle cell anaemia: report of the first cohort study from Nigeria. | Olatunya OS, Albuquerque DM, Akanbi GO, Aduayi OS, Taiwo AB, Faboya OA, Kayode TS, Leonardo DP, Adekile A, Costa FF | BMC Med. Genet. | 2019 |
| Vaso-Occlusion in Sickle Cell Disease: Is Autonomic Dysregulation of the Microvasculature the Trigger? | Veluswamy S, Shah P, Denton CC, Chalacheva P, Khoo MCK, Coates TD | J Clin Med | 2019 |
| Serum Immunoglobulin Levels in Children with Sickle Cell Disease: A Large Prospective Study. | Cherif-Alami S, Hau I, Arnaud C, Kamdem A, Coulon B, Idoux E, Bechet S, Creidy R, Bernaudin F, Epaud R, Pondarré C | J Clin Med | 2019 |
| Higher values of triglycerides:HDL-cholesterol ratio hallmark disease severity in children and adolescents with sickle cell anemia. | Teixeira RS, Arriaga MB, Terse-Ramos R, Ferreira TA, Machado VR, Rissatto-Lago MR, Silveira-Mattos PS, Boa-Sorte N, Ladeia AMT, Andrade BB | Braz. J. Med. Biol. Res. | 2019 |
| Effect of A Mobile-Phone Mediated Based Education on Self-Care Behaviors of Patients With Thalassemia Major. | Gharaati F, Aghamolaei T, Hosseini Z, Davoodi SH, Hassani L, Mohamadi R, Mohsseni S, Soleimani-Ahmadi M | J Caring Sci | 2019 |
| Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients. | Guarda CC, Silveira-Mattos PSM, Yahouédéhou SCMA, Santiago RP, Aleluia MM, Figueiredo CVB, Fiuza LM, Carvalho SP, Oliveira RM, Nascimento VML, Luz NF, Borges VM, Andrade BB, Gonçalves MS | Sci Rep | 2019 |
| HABIT efficacy and sustainability trial, a multi-center randomized controlled trial to improve hydroxyurea adherence in youth with sickle cell disease: a study protocol. | Smaldone A, Manwani D, Aygun B, Smith-Whitley K, Jia H, Bruzzese JM, Findley S, Massei J, Green NS | BMC Pediatr | 2019 |
| Sensitivity and Specificity of Ultrawide-Field Fundus Photography for the Staging of Sickle Cell Retinopathy in Real-Life Practice at Varying Expertise Level. | Bunod R, Mouallem-Beziere A, Amoroso F, Capuano V, Bitton K, Kamami-Levy C, Jung C, Souied EH, Miere A | J Clin Med | 2019 |
| Hematologic Conditions: Common Hemoglobinopathies. | Keber B, Lam L, Mumford J, Flanagan B | FP Essent | 2019 |
| IFCC-HbA1c May Be More Useful than NGSP-HbA1c in the Comparison between HbA1c Values in Variant Hemoglobin with a Mutation on α Chain and β Chain. | Koga M, Inada S, Yoshino K, Miyazaki A | Ann. Clin. Lab. Sci. | 2019 |
| Effectiveness and Safety of Hydroxyurea in the Treatment of Sickle Cell Anaemia Children in Jos, North Central Nigeria. | Ofakunrin AOD, Oguche S, Adekola K, Okpe ES, Afolaranmi TO, Diaku-Akinwumi IN, Zoakah AI, Sagay AS | J. Trop. Pediatr. | 2019 |
| Diffuse Ischemic Strokes and Sickle Cell Crisis Induced by Disseminated Anaplasmosis: A Case Report. | Herbst J, Crissinger T, Baldwin K | Case Rep Neurol | 2019 |
| [Genetic Screening of Thalassemia among the Couples of Childbearing Age in Ding'an County of Hainan Province and Its Analysis]. | Tu ZH, Wang J, Hu JJ, Zhao LQ, Ran HL, Wang AG, Li YJ, Ma N, Wu Z, Zhou Z | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2019 |
| [Genetic Analysis, Prenatal Diagnosis and Preimplantation Genetic Diagnosis of Taiwanese Deletion β-Thalassemia]. | DU L, Qin DQ, Liu L, Lu J, Yao CZ, Huang HJ, Wang JC | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2019 |
| [Phenotype Analysis of 78 Cases of Abnormal Hemoglobin E Homozygotes]. | Pan YH, Guo WX, Luo SL, Tan XR, Ge SJ, Yang BQ, Yang ZQ | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2019 |
| Inpatient pain management in sickle cell disease. | Zassman SM, Zamora FJ, Roberts JD | Am J Health Syst Pharm | 2019 |
| Sickle cell drug raises hopes and doubts. | Wadman M | Science | 2019 |
| Inhaled nitric oxide for treating pain crises in people with sickle cell disease. | Aboursheid T, Albaroudi O, Alahdab F | Cochrane Database Syst Rev | 2019 |
| Genetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β-Thalassemia Frameshift Mutation (: c.374dup; p.Pro126Thrfs*15). | Abdaoui W, Benouareth DE, Djenouni A, Renoux C, Grifi F, Gouri A, Athamnia F, Benalioua M, Joly P | Hemoglobin | 2019 |
| Reducing Health Care Disparities in Sickle Cell Disease: A Review. | Lee L, Smith-Whitley K, Banks S, Puckrein G | Public Health Rep | 2019 |
| Alteration of humoral, cellular and cytokine immune response to inactivated influenza vaccine in patients with Sickle Cell Disease. | Nagant C, Barbezange C, Dedeken L, Besse-Hammer T, Thomas I, Mahadeb B, Efira A, Ferster A, Corazza F | PLoS ONE | 2019 |
| Heritable Genome Editing: Who Speaks for | Knoppers BM, Kleiderman E | CRISPR J | 2019 |
| Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of α-Thalassemia. | Pyae AC, Srivorakun H, Chaibunruang A, Singha K, Tomanakarn K, Fucharoen G, Fucharoen S | Hemoglobin | 2019 |
| Hydroxycarbamide and white matter integrity in pediatric sickle cell disease: Commentary to accompany: Hydroxycarbamide treatment in children with sickle cell anaemia is associated with more intact white matter integrity: a quantitative MRI study. | Lance EI, Jordan LC | Br. J. Haematol. | 2019 |
| Hypoxia-inducible factor (HIF): how to improve osseointegration in hip arthroplasty secondary to avascular necrosis in sickle cell disease. | George A, Ellis M, Gill HS | EFORT Open Rev | 2019 |
| [Translational research for artificial red blood cells (hemoglobin vesicles)]. | Azuma H, Sakai H | Rinsho Ketsueki | 2019 |
| The use of rejuvenated red blood cells for transfusion in patients with sickle cell anemia. | Webb J | Transfusion | 2019 |
| Bitopertin, a selective oral GLYT1 inhibitor, improves anemia in a mouse model of β-thalassemia. | Matte A, Federti E, Winter M, Koerner A, Harmeier A, Mazer N, Tomka T, Di Paolo ML, De Falco L, Andolfo I, Beneduce E, Iolascon A, Macias-Garcia A, Chen JJ, Janin A, Lebouef C, Turrini F, Brugnara C, De Franceschi L | JCI Insight | 2019 |
| Dissecting the web of ischemic stroke, sickle cell trait, and chronic kidney disease. | Neuberg D | Am. J. Hematol. | 2019 |
| A novel high-throughput molecular counting method with single base-pair resolution enables accurate single-gene NIPT. | Tsao DS, Silas S, Landry BP, Itzep NP, Nguyen AB, Greenberg S, Kanne CK, Sheehan VA, Sharma R, Shukla R, Arora PN, Atay O | Sci Rep | 2019 |
| The cause and pathogenesis of hemolytic transfusion reactions in sickle-cell disease. | Pirenne F | Curr. Opin. Hematol. | 2019 |
| Antibiotics for treating osteomyelitis in people with sickle cell disease. | Martí-Carvajal AJ, Agreda-Pérez LH | Cochrane Database Syst Rev | 2019 |
| Repurposing pyridoxamine for therapeutic intervention of intravascular cell-cell interactions in mouse models of sickle cell disease. | Li J, Jeong SY, Xiong B, Tseng A, Mahon AB, Isaacman S, Gordeuk VR, Cho J | Haematologica | 2019 |
| Gates and NIH join forces on HIV and sickle cell diseases. | Cohen J, Kaiser J | Science | 2019 |
| Wide range of F cell levels in healthy Thai adults: Influence of Swiss-type hereditary persistence of foetal haemoglobin & β-haemoglobinopathy. | Tatu T | Indian J. Med. Res. | 2019 |
| Clinical and Genetic Predictors of Priapism in Sickle Cell Disease: Results from the Recipient Epidemiology and Donor Evaluation Study III Brazil Cohort Study. | Cintho Ozahata M, Page GP, Guo Y, Ferreira JE, Dinardo CL, Carneiro-Proietti ABF, Loureiro P, Mota RA, Rodrigues DOW, Belisario AR, Maximo C, Flor-Park MV, Custer B, Kelly S, Sabino EC, | J Sex Med | 2019 |
| Racial mixture, blood and nation in medical publications on sickle cell disease in 1950s Brazil. | Cavalcanti JM | Hist Philos Life Sci | 2019 |
| Investigating the potential of the secretome of mesenchymal stem cells derived from sickle cell disease patients. | Ribeiro TO, Silveira BM, Meira MC, Carreira ACO, Sogayar MC, Meyer R, Fortuna V | PLoS ONE | 2019 |
| The cost of blood: a study of the total cost of red blood cell transfusion in patients with β-thalassemia using time-driven activity-based costing. | McQuilten ZK, Higgins AM, Burns K, Chunilal S, Dunstan T, Haysom HE, Kaplan Z, Rushford K, Saxby K, Tahiri R, Waters N, Wood EM | Transfusion | 2019 |
| Assessing Knowledge of Sickle Cell Trait/Disease Inheritance in Metropolitan Detroit. | Orelaru F, Bolanle G, Tolulope I, Ishmael J | J Natl Med Assoc | 2019 |
| Impact of the detection of ζ-globin chains and hemoglobin Bart's using immunochromatographic strip tests for α0-thalassemia (--SEA) differential diagnosis. | Pata S, Laopajon W, Pongpaiboon M, Thongkum W, Polpong N, Munkongdee T, Paiboonsukwong K, Fucharoen S, Tayapiwatana C, Kasinrerk W | PLoS ONE | 2019 |
| Pica in Pediatric Sickle Cell Disease. | Rodrigues N, Shih S, Cohen LL | J Clin Psychol Med Settings | 2019 |
| Special care dentistry for patients diagnosed with sickle cell disease: an update for dentists. | Abed H, Sharma SP, Balkhoyor A, Aljohani K, Dickinson C | Gen Dent | 2019 |
| Association of the Δ Mutant Genotype with Sickle Cell Disease in Egyptian Patients. | El Sissy MH, Hafez AA, Moneim SEA, Eldemerdash DM | Hemoglobin | 2019 |
| A Kindred with a β-Globin Base Substitution [β89(F5)Ser→Arg (AG>AG); : c.270T>G] Resulting in Hemoglobin Vanderbilt. | Shomali W, Brar R, Arekapudi SR, Gotlib JR | Hemoglobin | 2019 |
| Role of the coagulation system in the pathogenesis of sickle cell disease. | Nasimuzzaman M, Malik P | Blood Adv | 2019 |
| BCL2L1 is associated with γ-globin gene expression. | Dai Y, Shaikho EM, Perez J, Wilson CA, Liu LY, White MR, Farrell JJ, Chui DHK, Sebastiani P, Steinberg MH | Blood Adv | 2019 |
| Evaluation of the vitamin D and biomedical statuses of young children with β-thalassemia major at a single center in southern China. | Yu U, Chen L, Wang X, Zhang X, Li Y, Wen F, Liu S | BMC Pediatr | 2019 |
| "Waiting for a Miracle": Spirituality/Religiosity in Coping With Sickle Cell Disease | Gomes MV, Xavier ADSG, Carvalho ESS, Cordeiro RC, Ferreira SL, Morbeck AD | Rev Bras Enferm | 2019 |
| Non-invasive urinary biomarkers of renal function in sickle cell disease: an overview. | Laurentino MR, Parente Filho SLA, Parente LLC, da Silva Júnior GB, Daher EF, Lemes RPG | Ann. Hematol. | 2019 |
| Sensorineural Hearing Loss and Its Relationship with Duration of Chelation Among Major β-Thalassemia Patients. | Khan MA, Khan MA, Seedat AM, Khan M, Khuwaja SF, Kumar R, Usama SM, Fareed S | Cureus | 2019 |
| Informing thresholds for paediatric transfusion in Africa: the need for a trial. | Maitland K, Ohuma EO, Mpoya A, Uyoga S, Hassall O, Williams TN | Wellcome Open Res | 2019 |
| Interference of Hemoglobin A Due to Hemoglobin Franklin Park. | Kim JT, Winter WE, Luo HY, Chui DHK, Harris NS | J Appl Lab Med | 2019 |
| Oral ferroportin inhibitor ameliorates ineffective erythropoiesis in a model of β-thalassemia. | Manolova V, Nyffenegger N, Flace A, Altermatt P, Varol A, Doucerain C, Sundstrom H, Dürrenberger F | J. Clin. Invest. | 2019 |
| Prescription Opioid Misuse Index in sickle cell patients: A brief questionnaire to assess at-risk for opioid abuse. | Smith WR, McClish DK, Roberts JD, Kandalaft O, Dahman B, Knisely J, Levenson J, Roseff S, Aisiku IP | J Opioid Manag | 2019 |
| Diagnosing sickle cell disease and iron deficiency anemia in human blood by Raman spectroscopy. | da Silva WR, Silveira L, Fernandes AB | Lasers Med Sci | 2019 |
| Deferasirox in thalassemia: a comparative study between an innovator drug and its copy among a sample of Iraqi patients. | Daher AM, Al-Momen H, Jasim SK | Ther Adv Drug Saf | 2019 |
| Effect of N(Epsilon)-(carboxymethyl)lysine on Laboratory Parameters and Its Association with Haplotype in Children with Sickle Cell Anemia. | Ndidi US, Adanho CSA, Santiago RP, Yahouédéhou SCMA, Santana SS, Mafili VV, Pitanga TN, Fonseca CA, Ferreira JRD, Adorno EV, Lyra IM, Adekile AD, Barbosa CG, Goncalves MS | Dis. Markers | 2019 |
| Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α-Thalassemia (- - deletion) Allele and Application for Double-Check Diagnosis of Hb Bart's Hydrops Fetalis Syndrome in Thailand. | Jomoui W, Tepakhan W, Karnpean R | Hemoglobin | 2019 |
| Evaluation of a Non-Parenteral Opioid Analgesia Protocol for Acute Sickle Cell Pain Episodes in Children. | Telfer P, Barroso F, Newell K, Challands J, Kaya B | J Clin Med | 2019 |
| Dysregulated NO/PDE5 signaling in the sickle cell mouse lower urinary tract: Reversal by oral nitrate therapy. | Musicki B, Anele UA, Campbell JD, Karakus S, Shiva S, Silva FH, Burnett AL | Life Sci. | 2019 |
| TGA/Chemometric Test Is Able to Detect the Presence of a Rare Hemoglobin Variant Hb Bibba. | Risoluti R, Caprari P, Gullifa G, Diana L, Luciani M, Amato A, Materazzi S | Front Mol Biosci | 2019 |
| To Join Or Not To Join? A Case Of Sickle Cell Clubs, Stigma And Discrimination In Secondary Schools In Butambala District, Uganda. | Tusuubira SK, Naggawa T, Nakamoga V | Adolesc Health Med Ther | 2019 |
| Efficient gene correction of an aberrant splice site in β-thalassaemia iPSCs by CRISPR/Cas9 and single-strand oligodeoxynucleotides. | Xiong Z, Xie Y, Yang Y, Xue Y, Wang D, Lin S, Chen D, Lu D, He L, Song B, Yang Y, Sun X | J. Cell. Mol. Med. | 2019 |
| Challenges in providing compatible blood with Rh genotype-matching in Brazilian patients with sickle cell disease. | Santos TD, Macedo MD, Menegati SFP, Gilli S, Castilho L | Transfus Med | 2019 |
| Severe hyperhomocysteinemia and peripheral neuropathy as side effects of nitrous oxide in two patients with sickle cell disease. | Neveu J, Perelman S, Suisse G, Monpoux F | Arch Pediatr | 2019 |
| Comment on: Hemochromatosis (HFE) gene mutations (H63D and C282Y) and iron overload in beta-thalassemia major. | Yasri S, Wiwanitkit V | Saudi Med J | 2019 |
| Adenovirus vectors in hematopoietic stem cell genome editing. | Li C, Lieber A | FEBS Lett. | 2019 |
| [Clinical and genetic analysis of a patient with Hb Ottawa in conjunction with β -thalassemia]. | Ma X, Cai Z, Peng Y, Ma J, Zheng J, Cai G | Zhonghua Yi Xue Yi Chuan Xue Za Zhi | 2019 |
| [Application of NGS-based SNP haplotyping for preimplantation genetic diagnosis for beta-thalassemia and HLA matching]. | Yang Y, Liu Y, Lu Q, Chen J, Luo H, Ma P | Zhonghua Yi Xue Yi Chuan Xue Za Zhi | 2019 |
| Severity of Salmonella infection among sickle cell diseases pediatric patients: Description of the infection pattern. | AlFawaz T, Alzumar O, AlShahrani D, Alshehri M | Int J Pediatr Adolesc Med | 2019 |
| Curing Hemoglobinopathies: Challenges and Advances of Conventional and New Gene Therapy Approaches. | Motta I, Ghiaccio V, Cosentino A, Breda L | Mediterr J Hematol Infect Dis | 2019 |
| Does Splenectomy Influence the Development of Hypothyroidism in Transfusion Dependent Thalassemia Patients? A Retrospective Study. | Skafida M, Sofocleous C, Kattamis A, Kattamis C | Mediterr J Hematol Infect Dis | 2019 |
| The Course of Hepatitis C Infection and Response to Anti-viral Therapy in Patients with Thalassemia major and Hepatitis C Infection: A Longitudinal, Prospective Study. | Kamal S, Abdelhakam S, Ghoraba D, Mohsen MA, Salam AA, Hassan H, Nabeigh L | Mediterr J Hematol Infect Dis | 2019 |
| Prevalence of Hepatitis B, Hepatitis C, and HIV in Multiply Transfused Sickle Cell Disease Patients from Oman. | Alkindi S, Al-Umairi N, Jaju S, Pathare A | Mediterr J Hematol Infect Dis | 2019 |
| ThalPred: a web-based prediction tool for discriminating thalassemia trait and iron deficiency anemia. | Laengsri V, Shoombuatong W, Adirojananon W, Nantasenamat C, Prachayasittikul V, Nuchnoi P | BMC Med Inform Decis Mak | 2019 |
| Genome editing of HBG1 and HBG2 to induce fetal hemoglobin. | Métais JY, Doerfler PA, Mayuranathan T, Bauer DE, Fowler SC, Hsieh MM, Katta V, Keriwala S, Lazzarotto CR, Luk K, Neel MD, Perry SS, Peters ST, Porter SN, Ryu BY, Sharma A, Shea D, Tisdale JF, Uchida N, Wolfe SA, Woodard KJ, Wu Y, Yao Y, Zeng J, Pruett-Miller S, Tsai SQ, Weiss MJ | Blood Adv | 2019 |
| Association between clinical outcomes and metformin use in adults with sickle cell disease and diabetes mellitus. | Badawy SM, Payne AB | Blood Adv | 2019 |
| How I treat sickle cell disease with hematopoietic cell transplantation. | Stenger EO, Shenoy S, Krishnamurti L | Blood | 2019 |
| Single-cell analysis of bone marrow-derived CD34+ cells from children with sickle cell disease and thalassemia. | Hua P, Roy N, de la Fuente J, Wang G, Thongjuea S, Clark K, Roy A, Psaila B, Ashley N, Harrington Y, Nerlov C, Watt SM, Roberts I, Davies JOJ | Blood | 2019 |
| A feasibility study of telemedicine for paediatric sickle cell patients living in a rural medically underserved area. | Jacob SA, Carroll AE, Bennett WE | J Telemed Telecare | 2019 |
| Psychotropic-Induced Priapism in a Treatment-Refractory Patient: A Case Report. | Burk BG, Nelson LA | J Pharm Pract | 2019 |
| and Liver Iron Content in Children with Sickle Cell Anemia and Iron Overload. | Puri L, Flanagan JM, Kang G, Ding J, Bi W, McCarville BM, Loeffler RB, Tipirneni-Sajja A, Villavicencio M, Crews KR, Hillenbrand CM, Hankins JS | J Clin Med | 2019 |
| [Digestives diseases associated to sickle cell anemia in Lubumbashi: epidemiological and clinical aspects]. | Banza MI, Mulefu JP, Lire LI, N'dwala YTB, Tshiamala IB, Cabala VPK | Pan Afr Med J | 2019 |
| Persistent hematuria among children with sickle cell anemia in steady state. | Akubuilo UC, Ayuk A, Ezenwosu OU, Okafor UH, Emodi IJ | Hematol Transfus Cell Ther | 2019 |
| A β-Thalassemia Trait with Two Mutations in in a Chinese Family. | Li J, Jiang F, Zhen L, Tang XW, Li DZ | Hemoglobin | 2019 |
| Molecular and Hematological Characterization of a Novel Translation Initiation Codon Mutation of the α2-Globin Gene (AT>AT or : c.3G>C). | Lei YL, Sui H, Liu YJ, Pan JJ, Liu YH, Lou JW | Hemoglobin | 2019 |
| A large intrathoracic extramedullary hematopoiesis in alpha-thalassemia: A case report. | Chen J, Liu YL, Lu MZ, Gao XL | Medicine (Baltimore) | 2019 |
| Noteworthy Points in the Management of Patients With β-Thalassemia Major. | Aoki Y | Pediatr Emerg Care | 2019 |
| Is Hemoglobin D Trait Hematologically Silent: Comparison With Healthy Controls and β-thalassemia Carriers. | Aslan D | J. Pediatr. Hematol. Oncol. | 2019 |
| Missed Diagnosis of β-Thalassemia Trait in Premarital Screening Due to Accompanying HbA2-Yialousa (HBD: c.82G>T). | Yilmaz Keskin E, Acar Ö, Özbas H | J. Pediatr. Hematol. Oncol. | 2019 |
| Analysis of Deletional Hb H Diseases in Samples with Hb A-Hb H and Hb A-Hb Bart's on Capillary Electrophoresis. | Khongthai K, Ruengdit C, Panyasai S, Pornprasert S | Hemoglobin | 2019 |
| Serum ferritin levels and irregular use of iron chelators predict liver iron load in patients with major beta thalassemia: a cross-sectional study. | Sobhani S, Rahmani F, Rahmani M, Askari M, Kompani F | Croat. Med. J. | 2019 |
| Targeted screening failures in neonates with sickle cell disease in metropolitan France from 2005 to 2017: Number of cases, failure circumstances and health at diagnosis. | Remion J, Pluchart C | Arch Pediatr | 2019 |
| Regular long-term red blood cell transfusions for managing chronic chest complications in sickle cell disease. | Estcourt LJ, Hopewell S, Trivella M, Hambleton IR, Cho G | Cochrane Database Syst Rev | 2019 |
| Identification of Clinical and Laboratory Parameters Associated with the Development of Acute Chest Syndrome during Vaso-Occlusive Episodes in Children with Sickle Cell Disease: A Preliminary Step before Assessing Specific and Early Treatment Strategies. | Madhi F, Kamdem A, Jung C, Carlier-Gonod A, Biscardi S, Busca J, Arnaud C, Hau I, Narbey D, Epaud R, Pondarre C | J Clin Med | 2019 |
| Altered HDL particle in sickle cell disease: decreased cholesterol content is associated with hemolysis, whereas decreased Apolipoprotein A1 is linked to inflammation. | Yalcinkaya A, Unal S, Oztas Y | Lipids Health Dis | 2019 |
| Severity of Anaemia Has Corresponding Effects on Coagulation Parameters of Sickle Cell Disease Patients. | Antwi-Baffour S, Kyeremeh R, Annison L | Diseases | 2019 |
| The role of hydroxyurea to prevent silent stroke in sickle cell disease: Systematic review and meta-analysis. | Hasson C, Veling L, Rico J, Mhaskar R | Medicine (Baltimore) | 2019 |
| Comparison of Outcomes for Adult Inpatients With Sickle Cell Disease Cared for by Hospitalists Versus Hematologists. | Slade J, Rohatgi N, Weng Y, Hom J, Ahuja N | Am J Med Qual | 2019 |
| Translating exercise benefits in sickle cell disease. | Cooper DM, Liem RI | Blood | 2019 |
| Evaluation of endocrine complications in beta-thalassemia intermedia (β-TI): a cross-sectional multicenter study. | Karimi M, Zarei T, Haghpanah S, Azarkeivan A, Kattamis C, Ladis V, Kattamis A, Kilinc Y, Daar S, Alyaarubi S, Khater D, Wali Y, Elshinawy M, Almadhani A, Yassin M, Soliman AT, Canatan D, Obiedat M, Al-Rimawi H, Mariannis D, Christodoulides C, Christou S, Tzoulis P, Campisi S, Di Maio S, De Sanctis V | Endocrine | 2019 |
| Self-care deficits in women with leg ulcers and sickle cell disease. | Lacerda FKL, Ferreira SL, Nascimento ERD, Costa DO, Cordeiro RC | Rev Bras Enferm | 2019 |
| Prevalence of Bacteremia in Febrile Patients With Sickle Cell Disease: Meta-Analysis of Observational Studies. | Bala N, Chao J, John D, Sinert R | Pediatr Emerg Care | 2019 |
| National comparative audit of blood transfusion: 2014 audit of transfusion services and practice in children and adults with sickle cell disease. | Trompeter S, Bolton-Maggs P, Ryan K, Shah F, Estcourt L, Cho G, Rees D, Lowe D, Davis B | Transfus Med | 2019 |
| Can RBC Indices be Used as Screening Test for Beta-Thalassemia in Indian Antenatal Women? | Baliyan M, Kumar M, Nangia A, Parakh N | J Obstet Gynaecol India | 2019 |
| Rational Drug Design of Peptide-Based Therapies for Sickle Cell Disease. | Olubiyi OO, Olagunju MO, Strodel B | Molecules | 2019 |
| Massive Splenic Infarction and Autosplencetomy: First Presentation of Homozygous Sickle Cell Disease in a Toddler. | Krepis P, Maritsi DN, Tsolia MN, Vakaki M, Kossiva L | J. Pediatr. Hematol. Oncol. | 2019 |
| Treatment of dental complications in sickle cell disease. | Mulimani P, Ballas SK, Abas AB, Karanth L | Cochrane Database Syst Rev | 2019 |
| [Analysis of Gene Mutation Types of Thalassemia in Quanzhou Area of Fujian Province in China]. | Jiang YC, Chen ZX, Chen YB, Zhang ZS | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2019 |
| [Analysis on the Genotype of 5018 Cases of Thalassemia in Hunan Area]. | Liu Q, Jia ZJ, Xi H, Liu J, Peng Y, Wang H | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2019 |
| [Serum Level of MiR-609 and Its Clinical Prognostic Value in Patients with Thalassemia]. | Wang MQ, Cheng LL, Gao JJ, Xie RW, Lin LP, Yang JZ, Xu RY | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2019 |
| [Genetic Analysis and Prenatal Diagnosis for Thalassemia of Pregnant Women in Wuhan Area of China]. | Cai WQ, Hu XJ, Dai X, Xiong Q | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2019 |
| Comparison of diastolic function in children with transfusion dependent beta thalassemia major by tissue and conventional doppler imaging indices and its correlation with serum ferritin levels. | Nanjegowda CK, Kamath SP, Kamath P, Shah TD, Kulkarni V, Lashkari HP, Baliga BS | Turk. J. Pediatr. | 2019 |
| Enhancing Pain Assessment in Pediatric Sickle Cell Disease by Applying Quality Improvement Science. | Sil S, Goldstein-Leever A, Travers C, Gilleland-Marchak J, Alexander A, Thompson B, Griffin A, McCracken C, New T | Clin Pract Pediatr Psychol | 2019 |
| Clinical and socio-demographic determinants of pentazocine misuse among patients with sickle cell disease, Benin City, Nigeria: a case-control study. | Adewoyin A, Adeyemi O, Davies N, Ojo M | Pan Afr Med J | 2019 |
| Identification of a novel pre-terminating mutation in human HBB gene as a cause of β-thalassemia phenotype. | Xu L, Chen M, Huang H, Lin N, Chen L, Wang Y, Zhang M, He D, Lin Y | Int J Clin Exp Pathol | 2019 |
| Frequencies and hematological manifestations of the HKαα allele in southern Chinese population. | Zhang M, Huang H, Chen M, Chen L, Wang Y, Lin N, Lin Y, Xu L | Int J Clin Exp Pathol | 2019 |
| The Effects of Hydroxyurea Therapy on the Six-Minute Walk Distance in Patients with Adult Sickle Cell Anemia: An Echocardiographic Study. | Garadah T, Mandeel F, Jaradat A, Bin Thani K | J Blood Med | 2019 |
| Cerebral oxygen metabolism in adults with sickle cell disease. | Václavů L, Petr J, Petersen ET, Mutsaerts HJMM, Majoie CBL, Wood JC, VanBavel E, Nederveen AJ, Biemond BJ | Am. J. Hematol. | 2019 |
| Vaso-occlusive crises in patients with sickle cell disease: Parents' perspectives and association with disease outcomes. | Zolaly M, Al-Mohammadi G, Al-Saadi G, Qasim D | J Taibah Univ Med Sci | 2019 |
| Subclinical nephrotoxicity in patients with beta-thalassemia: role of urinary kidney injury molecule. | Nafea OE, Zakaria M, Hassan T, El Gebaly SM, Salah HE | Drug Chem Toxicol | 2019 |
| Mutational analysis of thalassemia in transfusion-dependent beta-thalassemia patients from central India. | Shrivastava M, Bathri R, Chatterjee N | Asian J Transfus Sci | 2019 |
| A comparative study of temperamental, behavioral, and cognitive changes in thalassemia major, thalassemia minor, and normal population. | Bhattacharyya R, Chakraborty K, Sen A, Neogi R, Bhattacharyya S | Indian J Psychiatry | 2019 |
| Wide-field imaging of sickle retinopathy. | Linz MO, Scott AW | Int J Retina Vitreous | 2019 |
| Hemoglobin E, malaria and natural selection. | Ha J, Martinson R, Iwamoto SK, Nishi A | Evol Med Public Health | 2019 |
| Clinical method evaluation of hemoglobin S and C identification by top-down selected reaction monitoring and electron transfer dissociation. | Lassout O, Hartmer R, Jabs W, Clerici L, Tsybin YO, Samii K, Vuilleumier N, Hochstrasser D, Scherl A, Lescuyer P, Coelho Graça D | Clin Proteomics | 2019 |
| Social and Psychological Factors Associated With Health Care Transition for Young Adults Living With Sickle Cell Disease. | Clayton-Jones D, Matthie N, Treadwell M, Field JJ, Mager A, Sawdy R, George Dalmida S, Leonard C, Koch KL, Haglund K | J Transcult Nurs | 2019 |
| Comment on: Prevalence of growth and endocrine disorders in Malaysian children with transfusion-dependent thalassaemia. | Sookaromdee P, Wiwanitkit V | Singapore Med J | 2019 |
| A Meta-Analysis on the Seroprevalence of Parvovirus B19 among Patients with Sickle Cell Disease. | Obeid Mohamed SO, Osman Mohamed EM, Ahmed Osman AA, Abdellatif MohamedElmugadam FA, Abdalla Ibrahim GA | Biomed Res Int | 2019 |
| Prevalence of Transfusion Transmitted Infections and the Quality of Life in β-thalassemia Major Patients. | Al-Moshary M, Al-Mussaed E, Khan A | Cureus | 2019 |
| Arrhythmias and Sudden Cardiac Death in Beta-Thalassemia Major Patients: Noninvasive Diagnostic Tools and Early Markers. | Russo V, Melillo E, Papa AA, Rago A, Chamberland C, Nigro G | Cardiol Res Pract | 2019 |
| Malaria chemoprophylaxis in sickle cell disease. | Oniyangi O, Omari AA | Cochrane Database Syst Rev | 2019 |
| Investigation of correlation between H63D and C282Y mutations in HFE gene and serum Ferritin level in beta-thalassemia major patients. | Rahmani R, Naseri P, Safaroghli-Azar A, Tarighi S, Hosseini T, Hojjati MT | Transfus Clin Biol | 2019 |
| Comparison of gene mutation spectrum of thalassemia in different regions of China and Southeast Asia. | Cui Q, Zhou W, Qiu L, Han B | Mol Genet Genomic Med | 2019 |
| Craniofacial geometric morphometrics in the identification of patients with sickle cell anemia and sickle cell trait. | Ferreira WB, Nunes LA, Pithon MM, Maia LC, Casotti CA | Hematol Transfus Cell Ther | 2019 |
| Skin ulcers complicating sickle cell disease: an interlinked reparative model. | Morgante A, Li Destri A | G Chir | 2019 |
| Quality of life outcomes in thalassaemia patients in Saudi Arabia: a cross-sectional study. | Adam S | East. Mediterr. Health J. | 2019 |
| [Evaluation of the Follow-Up and State of Adolescents with Sickle-Cell Disease in Brazzaville (Congo)]. | Ikobo LCO, Mberi FDM, Nika ER, Mandilou SVM, Ngoulou BSA, Loufoua ABM, Mabiala-Babela JR | Bull Soc Pathol Exot | 2019 |
| [Homozygous Sickle Cell Children Treated with Hydroxyurea in Brazzaville (Congo)]. | Mabiala-Babela JR, Nika ER, Ikobo LCO, Gnakingue ANO, Ngoulou BPS, Mandilou SVM | Bull Soc Pathol Exot | 2019 |
| Hodgkin lymphoma with co-existing extramedullary haematopoiesis in a Thalasaemia Major patient: Killing two birds with one stone using PET-CT. | Ahad Aziz Qureshi PA, Razi M, Rehman A, Hassan A | J Pak Med Assoc | 2019 |
| Treatment of Chronic HCV Infection in Patients With Thalassemia. | Bou Daher H, Sharara AI | Clin Liver Dis (Hoboken) | 2019 |
| The interaction of valine and glucose and the influence on the spectrin-actin complex in sickle cell disease. | Purnell MC | Discov Med | 2019 |
| Rare Co-occurrence of Beta-Thalassemia and : Novel Biomolecular Findings. | Boraldi F, Lofaro FD, Costa S, Moscarelli P, Quaglino D | Front Med (Lausanne) | 2019 |
| Convergence of Inflammatory Pathways in Allergic Asthma and Sickle Cell Disease. | Samarasinghe AE, Rosch JW | Front Immunol | 2019 |
| India's First Child using PGT-M, PGT-A and HLA Matching for Helping a Sibling having β-Thalassemia Major. | Banker JM, Arora P, Khajuria R, Banker M | J Hum Reprod Sci | 2019 |
| The Incidence of Minor β-thalassemia Among Individuals Participated in Premarital Screening Program in Ardabil Province: North-west of Iran. | Fathi A, Amani F, Mazhari N | Mater Sociomed | 2019 |
| New Insights and Methods in the Approach to Thalassemia Major: The Lesson From the Case of Adrenal Insufficiency. | Poggi M, Samperi I, Mattia L, Di Rocco A, Iorio C, Monti S, Pugliese G, Toscano V | Front Mol Biosci | 2019 |
| . Hemoglobinopathies (Sickle Cell Disease and Thalassemia). | Cappelli B, Gluckman E, Ghanem K, Abboud MR. | The EBMT Handbook: | 2019 |
| Effectiveness of Nurse Led Intervention on Health Related Quality of Life among Children with Sickle Cell Disease in Oman: A Pilot Study. | Pandarakutty S, Murali K, Arulappan J, Thomas DS | Adv Hematol | 2019 |
| Exploring Potential Mechanisms Behind the Respiratory Burden of Sickle Cell Disease in Children. | Cataletto M | Pediatr Allergy Immunol Pulmonol | 2019 |
| Prevalence of hepatitis E virus in thalassemia patients with hepatitis C in Tehran, Iran. | Dalvand N, Dalvand A, Sharifi Z, Hosseini SM | Iran J Microbiol | 2019 |
| Short Tandem Repeats Used in Preimplantation Genetic Testing of Β-Thalassemia: Genetic Polymorphisms For 15 Linked Loci in the Vietnamese Population. | Truong DT, Minh NVN, Nhung DP, Luong HV, Quyet D, Anh TN, Son TT, Tung NT, Ha NTT, Anh DTP, Hoang L, Thuy NL, Hoa NT, Bac ND, Nga VT, Dinh TC | Open Access Maced J Med Sci | 2019 |
| Structural modification of azolylacryloyl derivatives yields a novel class of covalent modifiers of hemoglobin as potential antisickling agents. | Omar AM, David T, Pagare PP, Ghatge MS, Chen Q, Mehta A, Zhang Y, Abdulmalik O, Naghi AH, El-Araby ME, Safo MK | Medchemcomm | 2019 |
| Methylene tetrahydrofolate reductase gene mutation in sickle cell anaemia patients in Lagos, Nigeria. | Adelekan OO, Uche EI, Balogun TM, Osunkalu VO, Akinbami AA, Ismail KA, Badiru MA, Dosunmu AO, Kamson OR | Pan Afr Med J | 2019 |
| Trends in Hospitalizations for Sickle Cell Disease Related-Complications in USA 2004 - 2012. | Thi Nhat Ho A, Shmelev A, Joshi A, Ho N | J Hematol | 2019 |
| Sickle Cell Anemia in Cuba: Prevention and Management, 1982-2018. | Marcheco-Teruel B | MEDICC Rev | 2019 |
| KNOWLEDGE, ATTITUDE AND USE OF HYDROXUYREA AMONG ADULT SICKLE CELL DISEASE PATIENTS. | Sonubi O, Kotila TR | Ann Ib Postgrad Med | 2019 |
| High Healthcare Utilization in Adolescents with Sickle Cell Disease Prior to Transition to Adult Care: A Retrospective Study. | Kanter J, Bhor M, Li X, Li FY, Paulose J | J Health Econ Outcomes Res | 2019 |
