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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| Prenatal diagnosis of α- and β-thalassemias in southern Thailand. | Nopparatana C, Nopparatana C, Saechan V, Karnchanaopas S, Srewaradachpisal K | Int. J. Hematol. | 2020 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
