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| Comparison of efficacy and safety of thalidomide vs hydroxyurea in patients with Hb E-β thalassemia - a pilot study from a tertiary care Centre of India. | Jain M, Chakrabarti P, Dolai TK, Ghosh P, Mandal PK, Baul SN, De R | Blood Cells Mol Dis | 2021 |
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| Chronic osteo-articular changes in patients with sickle cell disease. | Ferreira TFA, Dos Santos APT, Leal AS, de Araújo Pereira G, Silva SS, Moraes-Souza H | Adv Rheumatol | 2021 |
| Evaluation of the Significance of Tear Ferning Patterns in beta-Thalassemia Patients. | Fagehi R, Abbadi IM, Abusharha A, Alanazi MA, Malhan H, El-Hiti GA, Masmali AM | Klin Monbl Augenheilkd | 2021 |
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| Evaluation of the High Resolution Melting Approach for Detection of β-Thalassemia Gene Mutations. | Tariq A, Khurshid S, Sajjad M | Hemoglobin | 2021 |
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| Emotion regulation, pain interference and affective symptoms in children and adolescents with sickle cell disease. | Miller M, Balsamo L, Pashankar F, Bailey CS | J Affect Disord | 2021 |
| Integrative holistic approaches for children, adolescents, and young adults with sickle cell disease: A single center experience. | Mahmood LA, Thaniel L, Martin B, Marguiles S, Reece-Stremtan S, Idiokitas R, Bettini E, Hardy SJ, Cohen I, Connolly M, Darbari DS | Complement Ther Med | 2021 |
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| Clinical presentations and outcomes of COVID-19 infection in sickle cell disease patients: Case series from Komfo Anokye teaching hospital, Ghana. | Hardy YO, Amenuke DAY, Abukari Y, Oti-Acheampong A, Hutton-Mensah K, Amoah-Dankwah J, Amoabeng Kontoh S, Danso KA, Berchie PO, Otu-Ansah C | Clin Case Rep | 2021 |
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| Characterisation of two unusual cases of haemoglobin Bart's hydrops foetalis caused by - and large novel α-globin gene cluster deletions. | Wang Y, Xiong Y, Liu C, Lu J, Wang J, Qin D, Liu L, Wu J, Zhao X, Fang L, Du L, Yin A | J Int Med Res | 2021 |
| Evidence-based interventions implemented in low-and middle-income countries for sickle cell disease management: A systematic review of randomized controlled trials. | Gyamfi J, Ojo T, Epou S, Diawara A, Dike L, Adenikinju D, Enechukwu S, Vieira D, Nnodu O, Ogedegbe G, Peprah E | PLoS One | 2021 |
| Patient Perspectives of Sickle Cell Management in the Emergency Department. | Crego N, Masese R, Bonnabeau E, Douglas C, Rains G, Shah N, Tanabe P | Crit Care Nurs Q | 2021 |
| Management of sickle cell disease: current practices and challenges in a northeastern region of the Democratic Republic of the Congo. | Kambale-Kombi P, Marini Djang'eing'a R, Alworong'a Opara JP, Minon JM, Boemer F, Bours V, Tonen-Wolyec S, Kayembe Tshilumba C, Batina-Agasa S | Hematology | 2021 |
| A Rare Case of Hb H Disease and Systemic Lupus Erythematosus. | Lin QY, Chen DY, Kong S, Liu WQ, Sun XF, Li DZ | Hemoglobin | 2021 |
| Prevalence and distribution of major β-thalassemia mutations and HbE/β-thalassemia variant in Nepalese ethnic groups. | Lama R, Yusof W, Shrestha TR, Hanafi S, Bhattarai M, Hassan R, Zilfalil BA | Hematol Oncol Stem Cell Ther | 2021 |
| CRISPR/Cas9-mediated β-globin gene knockout in rabbits recapitulates human β-thalassemia. | Yang Y, Kang X, Hu S, Chen B, Xie Y, Song B, Zhang Q, Wu H, Ou Z, Xian Y, Fan Y, Li X, Lai L, Sun X | J Biol Chem | 2021 |
| Correction of β-thalassemia by CRISPR/Cas9 editing of the α-globin locus in human hematopoietic stem cells. | Pavani G, Fabiano A, Laurent M, Amor F, Cantelli E, Chalumeau A, Maule G, Tachtsidi A, Concordet JP, Cereseto A, Mavilio F, Ferrari G, Miccio A, Amendola M | Blood Adv | 2021 |
| Ineffective erythropoiesis in sickle cell disease: new insights and future implications. | El Nemer W, Godard A, El Hoss S | Curr Opin Hematol | 2021 |
| Heterogeneity of fetal hemoglobin production in adult red blood cells. | Khandros E, Blobel GA | Curr Opin Hematol | 2021 |
| A Unique Monocyte Transcriptome Discriminates Sickle Cell Disease From Other Hereditary Hemolytic Anemias and Shows the Particular Importance of Lipid and Interferon Signaling. | van Vuren AJ, van Straaten S, Mokry M, van Wijk R, van Beers EJ | Hemasphere | 2021 |
| Pharmacokinetics and safety of ticagrelor in infants and toddlers with sickle cell disease aged <24 months. | Duniva Inusa BP, Inati A, Maes P, Githanga J, Ogutu B, Abboud MR, Miano M, Cela E, Nduba V, Niazi M, Åstrand M, Persson K, Berggren A, Carlson G | Pediatr Blood Cancer | 2021 |
| Oxidative stress, inflammation, blood rheology, and microcirculation in adults with sickle cell disease: Effects of hydroxyurea treatment and impact of sickle cell syndrome. | Connes P, Möckesch B, Tudor Ngo Sock E, Hardy-Dessources MD, Reminy K, Skinner S, Billaud M, Nader E, Tressieres B, Etienne-Julan M, Guillot N, Lemonne N, Hue O, Romana M, Antoine-Jonville S | Eur J Haematol | 2021 |
| Varied Age of First Presentation of Sickle Cell Disease: Case Presentations and Review. | Claeys A, Van Steijn S, Van Kesteren L, Damen E, Van Den Akker M | Case Rep Med | 2021 |
| Efficacy and Tolerance of Vascular Electrical Stimulation Therapy in the Management of Vaso-Occlusive Crises in Patients with Sickle Cell Disease: A Phase II Single-Centre Randomized Study in Ivory Coast. | Botti RP, Bokoum SS, L'Hermite E, Silue DA, Kouakou B, Bognini SA, Agoua SA, Mandeng Ma Linwa E, Ayemou R, Koffi KG | Adv Hematol | 2021 |
| Erythrocytes 3D genome organization in vertebrates. | Ryzhkova A, Taskina A, Khabarova A, Fishman V, Battulin N | Sci Rep | 2021 |
| Chronic organ injuries in children with sickle cell disease. | Allali S, Taylor M, Brice J, Montalembert M | Haematologica | 2021 |
| Transcranial Doppler Screening in a Current Cohort of Children With Sickle Cell Anemia: Results From the DISPLACE Study. | Kanter J, Phillips S, Schlenz AM, Mueller M, Dooley M, Sirline L, Nickel R, Brown RC, Hilliard L, Melvin CL, Adams RJ | J Pediatr Hematol Oncol | 2021 |
| Cognitive Functioning and Educational Support Plans in Youth With Sickle Cell Disease. | Connolly ME, Bills SE, Hardy SJ | J Pediatr Hematol Oncol | 2021 |
| First Observation of HbM-Saskatoon at the Origin of Neonatal Cyanosis in a Tunisian Baby. | Bouatrous E, Nouira S, Ben Khaled M, Ouederni M, Abbes S, Menif S, Ouragini H | J Pediatr Hematol Oncol | 2021 |
| Erythropoietin Concentration in Boys With p.His63Asp Polymorphism of the HFE Gene. | Kaczorowska-Hac B, Luszczyk M, Wasilewska E, Antosiewicz J, Kaczor JJ | J Pediatr Hematol Oncol | 2021 |
| Association of Anemia and Blood Pressure With Novel Markers of Diastolic Function in Pediatric Sickle Cell Disease. | Jhaveri S, Choueiter N, Manwani D, Ranabothu S, Morrone K, Hafeman M, Reidy K, Kaskel F, Mahgerefteh J | J Pediatr Hematol Oncol | 2021 |
| Hydroxyurea improves nitric oxide bioavailability in humanized sickle cell mice. | Taylor CM, Kasztan M, Sedaka R, Molina PA, Dunaway LS, Pollock JS, Pollock DM | Am J Physiol Regul Integr Comp Physiol | 2021 |
| Re 'Liver transplantation for sickle cell disease: a systematic' Feli et al. | Azoulay D, Habibi A, Galacteros F, Bartolucci P, Feray C | HPB (Oxford) | 2021 |
| Determinants of the Outcome of the Transition of Children with Sickle Cell Disease to Adult Programs. | Ballas SK, Riddick-Burden G, Congdon-Martin E | Hemoglobin | 2021 |
| Hb S (: c.20A>T) Characteristics by High Performance Liquid Chromatography in Patients with Sickle Cell Disease Receiving the Novel Agent Voxelotor. | Tsitsikas DA, Kamal M, Braimoh A, Benson S, Abukar J | Hemoglobin | 2021 |
| In vivo HSPC gene therapy with base editors allows for efficient reactivation of fetal γ-globin in β-YAC mice. | Li C, Georgakopoulou A, Mishra A, Gil S, Hawkins RD, Yannaki E, Lieber A | Blood Adv | 2021 |
| Major Thalassemia, Screening or Treatment: An Economic Evaluation Study in Iran. | Esmaeilzadeh F, Ahmadi B, Vahedi S, Barzegari S, Rajabi A | Int J Health Policy Manag | 2021 |
| Assertiveness in the patients with thalassaemia major: A qualitative study. | Valizadeh L, Zamanzadeh V, Ghahramanian A, Hasani Narenjbaghi S | Nurs Open | 2021 |
| P-selectin deficiency promotes liver senescence in sickle cell disease mice. | Vats R, Kaminski TW, Ju EM, Brozska T, Tutuncuoglu E, Tejero J, Novelli EM, Sundd P, Pradhan-Sundd T | Blood | 2021 |
| The potential hepatoprotective effect of metformin in hepatitis C virus-infected adolescent patients with beta thalassemia major: Randomised clinical trial. | Abdel Monem MS, Farid SF, Abbassi MM, Youssry I, Andraues NG, Hassany M, Selim YMM, El-Sayed MH | Int J Clin Pract | 2021 |
| Characteristics of sickle cell patients with frequent emergency department visits and hospitalizations. | Kidwell K, Albo C, Pope M, Bowman L, Xu H, Wells L, Barrett N, Patel N, Allison A, Kutlar A | PLoS One | 2021 |
| Adherence to hydroxyurea, health-related quality of life domains and attitudes towards a smartphone app among Irish adolescents and young adults with sickle cell disease. | Fogarty H, Gaul A, Syed S, Aleksejenko N, Geoghegan R, Conroy H, Crampton E, Ngwenya N, Tuohy E, McMahon C | Ir J Med Sci | 2021 |
| Long noncoding RNA HBBP1 enhances γ-globin expression through the ETS transcription factor ELK1. | Ma SP, Xi HR, Gao XX, Yang JM, Kurita R, Nakamura Y, Song XM, Chen HY, Lu DR | Biochem Biophys Res Commun | 2021 |
| Benserazide racemate and enantiomers induce fetal globin gene expression in vivo: Studies to guide clinical development for beta thalassemia and sickle cell disease. | Pace BS, Perrine S, Li B, Makala L, Xu H, Takezaki M, Wolf RF, Wang A, Xu X, Huang J, Alimardanov A, Tawa GJ, Sangerman J, Faller A, Zheng W, Toney L, Haugabook SJ | Blood Cells Mol Dis | 2021 |
| A pause in gene therapy: Reflecting on the unique challenges of sickle cell disease. | Leonard A, Tisdale JF | Mol Ther | 2021 |
| The Crisis of Sickle Cell Disease in Africa from Insights into Primary Prevention in Ghana and Nigeria: Notes from the Field. | Ezenwa MO, Dennis-Antwi JA, Dallas CM, Amarachukwu C, Ezema CI, Yao Y, Gallo AM, Wilkie DJ | J Immigr Minor Health | 2021 |
| The comfort ability program for adolescents with sickle cell pain: Evaluating feasibility and acceptability of an inpatient group-based clinical implementation. | Sil S, Lee JL, Klosky J, Vaz A, Mee L, Cochran S, Thompson B, Coakley R | Pediatr Blood Cancer | 2021 |
| Implementation of near-universal hydroxyurea uptake among children with sickle cell anemia: A single-center experience. | Karkoska K, Todd K, Niss O, Clapp K, Fenchel L, Kalfa TA, Malik P, Quinn CT, Ware RE, McGann PT | Pediatr Blood Cancer | 2021 |
| Sickle cell disease and ventricular myocardial strain: A systematic review. | Whipple NS, Joshi VM, Naik RJ, Mentnech T, McFarland MM, Nolan VG, Hankins JS | Pediatr Blood Cancer | 2021 |
| Red blood cell mannoses as phagocytic ligands mediating both sickle cell anaemia and malaria resistance. | Cao H, Antonopoulos A, Henderson S, Wassall H, Brewin J, Masson A, Shepherd J, Konieczny G, Patel B, Williams ML, Davie A, Forrester MA, Hall L, Minter B, Tampakis D, Moss M, Lennon C, Pickford W, Erwig L, Robertson B, Dell A, Brown GD, Wilson HM, Rees DC, Haslam SM, Alexandra Rowe J, Barker RN, Vickers MA | Nat Commun | 2021 |
| Impact of COVID-19 on vasooclusive crisis in patients with sickle cell anaemia. | Alkindi S, Elsadek RA, Al-Madhani A, Al-Musalhi M, AlKindi SY, Al-Khadouri G, Al Rawahi B, Al-Ruqeishi S, Al-Yazeedi J, Wali YA, Al Shamakhi S, Al Rawahi M, Pathare AV | Int J Infect Dis | 2021 |
| Novel retinal findings in β-thalassemia major: older age and higher ferritin level as the risk factors. | Kurnia KH, Elvioza , Sidik M, Sari TT, Prihartono J, Sitorus RS | Graefes Arch Clin Exp Ophthalmol | 2021 |
| Gene replacement of α-globin with β-globin restores hemoglobin balance in β-thalassemia-derived hematopoietic stem and progenitor cells. | Cromer MK, Camarena J, Martin RM, Lesch BJ, Vakulskas CA, Bode NM, Kurgan G, Collingwood MA, Rettig GR, Behlke MA, Lemgart VT, Zhang Y, Goyal A, Zhao F, Ponce E, Srifa W, Bak RO, Uchida N, Majeti R, Sheehan VA, Tisdale JF, Dever DP, Porteus MH | Nat Med | 2021 |
| The value of the red cell distribution width index versus other parameters in the differentiation between iron deficiency anemia and beta thalassemia trait among children in Mosul, Iraq. | Al-Numan AH, Al-Obeidi RA | Expert Rev Hematol | 2021 |
| Epigenetic inactivation of ERF reactivates γ-globin expression in β-thalassemia. | Bao X, Zhang X, Wang L, Wang Z, Huang J, Zhang Q, Ye Y, Liu Y, Chen D, Zuo Y, Liu Q, Xu P, Huang B, Fang J, Lao J, Feng X, Li Y, Kurita R, Nakamura Y, Yu W, Ju C, Huang C, Mohandas N, Li D, Zhao C, Xu X | Am J Hum Genet | 2021 |
| Descriptive analysis of sickle cell patients living in France: The PHEDRE cross-sectional study. | Gerardin M, Rousselet M, Couec ML, Masseau A, Guerlais M, Authier N, Deheul S, Roussin A, Micallef J, Djezzar S, , Feuillet F, Jolliet P, Victorri-Vigneau C | PLoS One | 2021 |
| Clinical Guideline Highlights for the Hospitalist: Management of Acute and Chronic Pain in Sickle Cell Disease. | Pham CD, Hua DT | J Hosp Med | 2021 |
| Molecular and Hematological Analysis of Alpha- and Beta-Thalassemia in a Cohort of Mexican Patients. | Rizo-de la Torre LDC, Rentería-López VM, Sánchez-López JY, Magaña-Torres MT, Ibarra-Cortés B, Perea-Díaz FJ | Genet Test Mol Biomarkers | 2021 |
| Characterization and identification of Prachinburi β -thalassemia: A novel-60 kb deletion in beta globin gene related to high levels of Hb F in heterozygous state. | Jomoui W, Tepakhan W | Int J Lab Hematol | 2021 |
| Relation of Serum Ferritin Level with Serum Hepcidin and Fucose Levels in Children with β-Thalassemia Major. | Al-Zuhairy SH, Darweesh MA, Othman MA | Hemoglobin | 2021 |
| Iatrogenic arteriovenous fistula in patient with sickle cell disease undergoing red blood cell exchange. | Guarente J, Palladino M, Babariya S, Hayes C, Blumhof B, Peedin AR, Karp JK | Transfusion | 2021 |
| Author Correction: Transcription factor competition at the γ-globin promoters controls hemoglobin switching. | Liu N, Xu S, Yao Q, Zhu Q, Kai Y, Hsu JY, Sakon P, Pinello L, Yuan GC, Bauer DE, Orkin SH | Nat Genet | 2021 |
| Gross and radiographic appearance of porotic hyperostosis and cribra orbitalia in thalassemia affected skulls. | Chaichun A, Yurasakpong L, Suwannakhan A, Iamsaard S, Arun S, Chaiyamoon A | Anat Cell Biol | 2021 |
| Nutritional perspectives on sickle cell disease in Africa: a systematic review. | Nartey EB, Spector J, Adu-Afarwuah S, Jones CL, Jackson A, Ohemeng A, Shah R, Koryo-Dabrah A, Kuma AB, Hyacinth HI, Steiner-Asiedu M | BMC Nutr | 2021 |
| Silent cerebral infarcts in sickle cell disease: Really silent? | Garnier-Crussard A, Cotton F, Desestret V, Krolak-Salmon P, Fort R | J Neuroradiol | 2021 |
| WALANT and sickle cell disease: A cautionary tale. | Thakkar M, Bednarz B | J Plast Reconstr Aesthet Surg | 2021 |
| Insight of fetal to adult hemoglobin switch: Genetic modulators and therapeutic targets. | Hariharan P, Nadkarni A | Blood Rev | 2021 |
| Effects of a positive thinking program on hope and sleep quality in Iranian patients with thalassemia: a randomized clinical trial. | Makaremnia S, Dehghan Manshadi M, Khademian Z | BMC Psychol | 2021 |
| Psychosocial risk factors for increased emergency hospital utilization by sickle cell disease patients: a systematic review protocol. | Rech JS, Getten P, Dzierzynski N, Lionnet F, Boëlle PY, Ranque B, Steichen O | JBI Evid Synth | 2021 |
| Mitochondrial reactive oxygen species scavenging attenuates thrombus formation in a murine model of sickle cell disease. | Annarapu G, Nolfi-Donegan D, Reynolds M, Wang Y, Shiva S | J Thromb Haemost | 2021 |
| Prophylactic antibiotics for preventing pneumococcal infection in children with sickle cell disease. | Rankine-Mullings AE, Owusu-Ofori S | Cochrane Database Syst Rev | 2021 |
| Assessment of cystatin C in pediatric sickle cell disease and β-thalassemia as a marker of subclinical cardiovascular dysfunction: a case-control study. | Hanna D, Beshir M, Khalifa N, Baz E, Elhewala A | Pediatr Hematol Oncol | 2021 |
| Vasculo-toxic and pro-inflammatory action of unbound haemoglobin, haem and iron in transfusion-dependent patients with haemolytic anaemias. | Vinchi F, Sparla R, Passos ST, Sharma R, Vance SZ, Zreid HS, Juaidi H, Manwani D, Yazdanbakhsh K, Nandi V, Silva AMN, Agarvas AR, Fibach E, Belcher JD, Vercellotti GM, Ghoti H, Muckenthaler MU | Br J Haematol | 2021 |
| Pain-Related Injustice Appraisals in Youth with Sickle Cell Disease: A Preliminary Investigation. | Miller MM, Rumble DD, Hirsh AT, Vervoort T, Crosby LE, Madan-Swain A, Lebensburger J, Hood AM, Trost Z | Pain Med | 2021 |
| Professionally responsible management of the ethical and social challenges of antenatal screening and diagnosis of β-thalassemia in a high-risk population. | Corda V, Murgia F, Dessolis F, Murru S, Chervenak FA, McCullough LB, Monni G | J Perinat Med | 2021 |
| Pseudothrombocytosis in a Case of Beta-thalassaemia Intermedia Masquerading as Myeloproliferative Neoplasm. | Purohit AHL, Bharti S, Kumar D, Bohra GK, Khichar S | Curr Med Imaging | 2021 |
| Calibration of T oximetry MRI for subjects with sickle cell disease. | Bush A, Vu C, Choi S, Borzage M, Miao X, Li W, Qin Q, Nederveen AJ, Coates TD, Wood JC | Magn Reson Med | 2021 |
| Cardiac pathophysiology in sickle cell disease. | Gbotosho OT, Taylor M, Malik P | J Thromb Thrombolysis | 2021 |
| The Impact of Environmental Factors on Monogenic Mendelian Diseases. | Tukker AM, Royal CD, Bowman AB, McAllister KA | Toxicol Sci | 2021 |
| Oxidative status in the β-thalassemia syndromes in Sri Lanka; a cross-sectional survey. | Allen A, Perera S, Mettananda S, Rodrigo R, Perera L, Darshana T, Moggach F, Jackson Crawford A, Heirene L, Fisher C, Olivieri N, Rees D, Premawardhena A, Allen S | Free Radic Biol Med | 2021 |
| Anti-sickling activities of two isolated compounds from the root of Combretum racemosum P. beauv. (Combretaceae). | Famojuro TI, Adeyemi AA, Ajayi TO, Fasola FA, Fukushi Y, Omotade OO, Moody JO | J Ethnopharmacol | 2021 |
| Hb Maruchi [α165 (E14) Ala>Pro; HBA1: c.196G>C]: A new thalassemia hemoglobinopathy related to the alpha1 globin gene. | Ropero P, M Nieto J, González Fernández FA, Villegas A, Benavente C | Clin Biochem | 2021 |
| Pituitary Volume and Iron Overload Evaluation by 3T MRI in Thalassemia. | Nayak AM, Choudhari A, Patkar DP, Merchant RH | Indian J Pediatr | 2021 |
| Pain Experiences of Adults With Sickle Cell Disease and Hematopoietic Stem Cell Transplantation: A Qualitative Study. | Abu Al Hamayel N, Waldfogel JM, Hannum SM, Brodsky RA, Bolaños-Meade J, Gamper CJ, Jones RJ, Dy SM | Pain Med | 2021 |
| Nephrotic syndrome on sickle cell disease: the impact of Hydroxyurea. | Cunha M, Simão C, Ferrão A, Palaré MJ | BMJ Case Rep | 2021 |
| Lysophosphatidic Acid-Activated Calcium Signaling Is Elevated in Red Cells from Sickle Cell Disease Patients. | Wang J, Hertz L, Ruppenthal S, El Nemer W, Connes P, Goede JS, Bogdanova A, Birnbaumer L, Kaestner L | Cells | 2021 |
| Automated Red Cell Exchange in the Management of Sickle Cell Disease. | Tsitsikas DA, Badle S, Hall R, Meenan J, Bello-Sanyaolu O, Orebayo F, Abukar J, Elmi M, Mulla A, Dave S, Lewis N, Sharma M, Chatterjee B, Amos RJ | J Clin Med | 2021 |
| and Its Virulence Factors HO and Pneumolysin Are Potent Mediators of the Acute Chest Syndrome in Sickle Cell Disease. | Gonzales J, Chakraborty T, Romero M, Mraheil MA, Kutlar A, Pace B, Lucas R | Toxins (Basel) | 2021 |
| Sickle Cell Disease: Role of Oxidative Stress and Antioxidant Therapy. | Vona R, Sposi NM, Mattia L, Gambardella L, Straface E, Pietraforte D | Antioxidants (Basel) | 2021 |
| Variability of Prognostic Results Based on Biological Parameters in Sickle Cell Disease Cohort Studies in Children: What Should Clinicians Know? | Sommet J, Roux EL, Koehl B, Haouari Z, Mohamed D, Baruchel A, Benkerrou M, Alberti C | Children (Basel) | 2021 |
| Mechanisms of Bone Impairment in Sickle Bone Disease. | Giordano P, Urbano F, Lassandro G, Faienza MF | Int J Environ Res Public Health | 2021 |
| Characterization and statistical modeling of glycosylation changes in sickle cell disease. | Ashwood HE, Ashwood C, Schmidt AP, Gundry RL, Hoffmeister KM, Anani WQ | Blood Adv | 2021 |
| Methylenetetrahydrofolate reductase polymorphisms as genetic markers to predict homocysteinemia and clinical severity in sickle cell disease. | Patel S, Nanda R, Hussain N, Mohapatra E, Patra PK | Biomark Med | 2021 |
| Persistence of CRISPR/Cas9 gene edited hematopoietic stem cells following transplantation: A systematic review and meta-analysis of preclinical studies. | Maganti HB, Bailey AJM, Kirkham AM, Shorr R, Pineault N, Allan DS | Stem Cells Transl Med | 2021 |
| Determinants of Care-Seeking Practices for Children with Sickle Cell Disease in Ekiti, Southwest Nigeria. | Olatunya OS, Babatola AO, Adeniyi AT, Lawal OA, Daramola AO, Agbesanwa TA, Olumuyiwa Ojo T, Ajayi PO, Ibijola AA, Komolafe AK, Adekile A | J Blood Med | 2021 |
| Distinct effects of V617F and exon12-mutated JAK2 expressions on erythropoiesis in a human induced pluripotent stem cell (iPSC)-based model. | Nilsri N, Jangprasert P, Pawinwongchai J, Israsena N, Rojnuckarin P | Sci Rep | 2021 |
| Hyperhemolysis Syndrome in a Patient With Sickle Cell Disease and Acute Chest Syndrome. | Shankar K, Shah D, Huffman DL, Peterson C, Bhagavatula R | Cureus | 2021 |
| Luspatercept: A Gigantic Step in the Treatment of Transfusion-Dependent β-Thalassemia Patients-a Quick Review. | Darvishi-Khezri H, Karami H | Adv Ther | 2021 |
| MetAP2 inhibition modifies hemoglobin S to delay polymerization and improves blood flow in sickle cell disease. | Demers M, Sturtevant S, Guertin KR, Gupta D, Desai K, Vieira BF, Li W, Hicks A, Ismail A, Gonçalves BP, Di Caprio G, Schonbrun E, Hansen S, Musayev FN, Safo MK, Wood DK, Higgins JM, Light DR | Blood Adv | 2021 |
| Sickle cell disease, interleukin-18, and arrhythmias. | Zhabyeyev P, Oudit GY | Blood | 2021 |
| Circulating mitochondrial DNA is a proinflammatory DAMP in sickle cell disease. | Tumburu L, Ghosh-Choudhary S, Seifuddin FT, Barbu EA, Yang S, Ahmad MM, Wilkins LHW, Tunc I, Sivakumar I, Nichols JS, Dagur PK, Yang S, Almeida LEF, Quezado ZMN, Combs CA, Lindberg E, Bleck CKE, Zhu J, Shet AS, Chung JH, Pirooznia M, Thein SL | Blood | 2021 |
| Is Busulfan Clearance Different in Patients With Sickle Cell Disease? Let's Clear Up That Case With Some Controls. | Remy A, Théorêt Y, Ansari M, Bittencourt H, Ducruet T, Nava T, Pastore Y, Rezgui MA, Krajinovic M, Kleiber N | J Pediatr Hematol Oncol | 2021 |
| A pilot study of the effect of rivaroxaban in sickle cell anemia. | Ataga KI, Elsherif L, Wichlan D, Wogu AF, Matsui N, Pawlinski R, Cai J, Key NS | Transfusion | 2021 |
| Therapeutic drug monitoring of intravenous busulfan in Thai children undergoing hematopoietic stem cell transplantation: A pilot study. | Jansing T, Sanpakit K, Tharnpanich T, Jiranantakan T, Niphandwongkorn V, Chindavijak B, Suansanae T | Pediatr Hematol Oncol | 2021 |
| Prevalence and association of malaria with ABO blood group and hemoglobin level in individuals visiting Mekaneeyesus Primary Hospital, Estie District, northwest Ethiopia: a cross-sectional study. | Tazebew B, Munshea A, Nibret E | Parasitol Res | 2021 |
| Perspectives on Building Sustainable Newborn Screening Programs for Sickle Cell Disease: Experience from Tanzania. | Bukini D, Nkya S, McCurdy S, Mbekenga C, Manji K, Parker M, Makani J | Int J Neonatal Screen | 2021 |
| A rare complex rearrangement in the β-globin gene cluster causing a novel homozygous γ( γδβ) -thalassemia. | Zhang X, Yang Y, Zhang H, Du Z, Liu H, Shen Y | Am J Hematol | 2021 |
| American Society of Hematology 2020 Podcast Collection: Sickle Cell Anaemia. | Russo G, Colombatti R | Adv Ther | 2021 |
| Whole-blood phenotyping to assess alloimmunization status in transfused sickle cell disease patients. | Tamagne M, Pakdaman S, Bartolucci P, Habibi A, Galactéros F, Pirenne F, Vingert B | Blood Adv | 2021 |
| Long-term tolerability of phosphodiesterase-5 inhibitors in pulmonary hypertension of sickle cell disease. | Cramer-Bour C, Ruhl AP, Nouraie SM, Emeh RO, Ruopp NF, Thein SL, Weir NA, Klings ES | Eur J Haematol | 2021 |
| Transcription factor competition at the γ-globin promoters controls hemoglobin switching. | Liu N, Xu S, Yao Q, Zhu Q, Kai Y, Hsu JY, Sakon P, Pinello L, Yuan GC, Bauer DE, Orkin SH | Nat Genet | 2021 |
| BEHAVIORAL CHARACTERISTICS OF CHILDREN WITH SICKLE CELL DISEASE. | Pereira FB, Pedroso GC, Resegue RM, Ribeiro MVV, Hokazono M, Braga JAP | Rev Paul Pediatr | 2021 |
| Correction of Hemoglobin E/Beta-Thalassemia Patient-Derived iPSCs Using CRISPR/Cas9. | Wattanapanitch M | Methods Mol Biol | 2021 |
| Adherence to Quality of Care Indicators and Location of Sickle Cell Care Within Indiana. | Meier ER, Janson IA, Hampton K, Bloom E, Duncan N, Roberson C, Rampersad A | J Community Health | 2020 |
| Keys to Recruiting and Retaining Seriously Ill African Americans With Sickle Cell Disease in Longitudinal Studies: Respectful Engagement and Persistence. | Suarez ML, Schlaeger JM, Angulo V, Shuey DA, Carrasco J, Roach KL, Ezenwa MO, Yao Y, Wang ZJ, Molokie RE, Wilkie DJ | Am J Hosp Palliat Care | 2020 |
| Acute Care Utilization at End of Life in Sickle Cell Disease: Highlighting the Need for a Palliative Approach. | Johnston EE, Adesina OO, Alvarez E, Amato H, Paulukonis S, Nichols A, Chamberlain LJ, Bhatia S | J Palliat Med | 2020 |
| GDF11 contributes to hepatic hepcidin (HAMP) inhibition through SMURF1-mediated BMP-SMAD signalling suppression. | Fang Z, Zhu Z, Zhang H, Peng Y, Liu J, Lu H, Li J, Liang L, Xia S, Wang Q, Fu B, Wu K, Zhang L, Ginzburg Y, Liu J, Chen H | Br. J. Haematol. | 2020 |
| Retinal Thickness and Microvascular Changes in Children With Sickle Cell Disease Evaluated by Optical Coherence Tomography (OCT) and OCT Angiography. | Ong SS, Linz MO, Li X, Liu TYA, Han IC, Scott AW | Am. J. Ophthalmol. | 2020 |
| Perioperative care of children with sickle cell disease: A systematic review and clinical recommendations. | Schyrr F, Dolci M, Nydegger M, Canellini G, Andreu-Ullrich H, Joseph JM, Diezi M, Cachat F, Rizzi M, Renella R | Am. J. Hematol. | 2020 |
| Neuropathic pain in individuals with sickle cell disease. | Sharma D, Brandow AM | Neurosci. Lett. | 2020 |
| Delta beta thalassemia. | Bain BJ | Am. J. Hematol. | 2020 |
| Evidence for interactions between inflammatory markers and renin-angiotensin system molecules in the occurrence of albuminuria in children with sickle cell anemia. | Belisário AR, Vieira ÉLM, de Almeida JA, Mendes FG, Miranda AS, Rezende PV, Viana MB, Simões E Silva AC | Cytokine | 2020 |
| Multicenter Evaluation of HemoTypeSC as a Point-of-Care Sickle Cell Disease Rapid Diagnostic Test for Newborns and Adults Across India. | Mukherjee MB, Colah RB, Mehta PR, Shinde N, Jain D, Desai S, Dave K, Italia Y, Raicha B, Serrao E | Am. J. Clin. Pathol. | 2020 |
| Recent advances in screening and diagnosis of hemoglobinopathy. | Ghosh K, Ghosh K, Agrawal R, Nadkarni AH | Expert Rev Hematol | 2020 |
| Quantification of whole-brain oxygenation extraction fraction and cerebral metabolic rate of oxygen consumption in adults with sickle cell anemia using individual T -based oxygenation calibrations. | Li W, Xu X, Liu P, Strouse JJ, Casella JF, Lu H, van Zijl PCM, Qin Q | Magn Reson Med | 2020 |
| Sickle Cell Intrahepatic Cholestasis with Acute Liver Failure and Acute Kidney Injury: Favourable Outcome with Exchange Transfusion. | Maji P, Malik R, Lodha R, Bagga A | Indian J Pediatr | 2020 |
| Platelet Extracellular Vesicles Drive Inflammasome-IL-1β-Dependent Lung Injury in Sickle Cell Disease. | Vats R, Brzoska T, Bennewitz MF, Jimenez MA, Pradhan-Sundd T, Tutuncuoglu E, Jonassaint J, Gutierrez E, Watkins SC, Shiva S, Scott MJ, Morelli AE, Neal MD, Kato GJ, Gladwin MT, Sundd P | Am. J. Respir. Crit. Care Med. | 2020 |
| Shedding New Light on Platelet Extracellular Vesicles in Sickle Cell Disease. | Middleton EA, Ware LB, Rondina MT | Am. J. Respir. Crit. Care Med. | 2020 |
| Retinal oximetry and fractal analysis of capillary maps in sickle cell disease patients and matched healthy volunteers. | Birkhoff WAJ, van Manen L, Dijkstra J, De Kam ML, van Meurs JC, Cohen AF | Graefes Arch. Clin. Exp. Ophthalmol. | 2020 |
| A QST-based Pain Phenotype in Adults With Sickle Cell Disease: Sensitivity and Specificity of Quality Descriptors. | Dyal BW, Ezenwa MO, Yoon SL, Fillingim RB, Yao Y, Schlaeger JM, Suarez ML, Wang ZJ, Molokie RE, Wilkie DJ | Pain Pract | 2020 |
| Curating the gnomAD database: Report of novel variants in the globin-coding genes and bioinformatics analysis. | Scheps KG, Hasenahuer MA, Parisi G, Targovnik HM, Fornasari MS | Hum. Mutat. | 2020 |
| Dengue in hospitalized children with sickle cell disease: A retrospective cohort study in the French departments of America. | Elenga N, Celicourt D, Muanza B, Elana G, Hocquelet S, Tarer V, Maillard F, Sibille G, Divialle Doumdo L, Petras M, Tressières B, Etienne-Julan M | J Infect Public Health | 2020 |
| Induction of Translational Readthrough across the Thalassemia-Causing Premature Stop Codon in β-Globin-Encoding mRNA. | Kar D, Sellamuthu K, Kumar SD, Eswarappa SM | Biochemistry | 2020 |
| Universal screening for social determinants of health in pediatric sickle cell disease: A quality-improvement initiative. | Power-Hays A, Li S, Mensah A, Sobota A | Pediatr Blood Cancer | 2020 |
| Erythrocyte Indices as Differential Diagnostic Biomarkers of Iron Deficiency Anemia and Thalassemia. | Düzenli Kar Y, Özdemir ZC, Emir B, Bör Ö | J. Pediatr. Hematol. Oncol. | 2020 |
| Evaluation of Efficacy, Safety, and Satisfaction Taking Deferasirox Twice Daily Versus Once Daily in Patients With Transfusion-Dependent Thalassemia. | Karimi M, Haghpanah S, Bahoush G, Ansari S, Azarkeivan A, Shahsavani A, Bazrafshan A, Jangjou A | J. Pediatr. Hematol. Oncol. | 2020 |
| Improved Titer and Gene Transfer by Lentiviral Vectors Using Novel, Small β-Globin Locus Control Region Elements. | Morgan RA, Unti MJ, Aleshe B, Brown D, Osborne KS, Koziol C, Ayoub PG, Smith OB, O'Brien R, Tam C, Miyahira E, Ruiz M, Quintos JP, Senadheera S, Hollis RP, Kohn DB | Mol. Ther. | 2020 |
| Thalassemia: Common Clinical Queries in Management. | Lal A, Bansal D | Indian J Pediatr | 2020 |
| Innovations in Targeted Anti-Adhesion Treatment for Sickle Cell Disease. | Kanter J, Lanzkron S | Clin. Pharmacol. Ther. | 2020 |
| Management of cesarean delivery in a parturient with sickle cell disease. | Romano D, Craig H, Katz D | Int J Obstet Anesth | 2020 |
| Generation of an in vitro model of β-thalassemia using the CRISPR/Cas9 genome editing system. | Ajami M, Atashi A, Kaviani S, Kiani J, Soleimani M | J. Cell. Biochem. | 2020 |
| Improvement in processing speed following haploidentical bone marrow transplant with posttransplant cytoxan in children and adolescents with sickle cell disease. | Prussien KV, Patel DA, Wilkerson K, Armstrong B, Karnik L, de la Fuente J, Kassim AA | Pediatr Blood Cancer | 2020 |
| Opioid treatment for acute and chronic pain in patients with sickle cell disease. | Carroll CP | Neurosci. Lett. | 2020 |
| Methodological aspects of the oxygenscan in sickle cell disease: A need for standardization. | Rab MAE, Kanne CK, Bos J, Boisson C, van Oirschot BA, Nader E, Renoux C, Joly P, Fort R, van Beers EJ, Sheehan VA, van Wijk R, Connes P | Am. J. Hematol. | 2020 |
| Intima-media thickness of the common carotid arteries as a marker of retinopathy and nephropathy in sickle cell disease. | Ayoola OO, Bolarinwa RA, Onakpoya OH, Onigbinde SO, Asaleye CM, Odedeyi AA | Ultrasonography | 2020 |
| Hereditary xerocytosis - spectrum and clinical manifestations of variants in the PIEZO1 gene, including co-occurrence with a novel β-globin mutation. | Maciak K, Adamowicz-Salach A, Siwicka A, Poznanski J, Urasinski T, Plochocka D, Gora M, Burzynska B | Blood Cells Mol. Dis. | 2020 |
| Polymorphisms in genes that affect the variation of lipid levels in a Brazilian pediatric population with sickle cell disease: rs662799 APOA5 and rs964184 ZPR1. | Valente-Frossard TNS, Cruz NRC, Ferreira FO, Belisario AR, Pereira BM, Gomides AFF, Resende GAD, Carlos AM, Moraes-Souza H, Velloso-Rodrigues C | Blood Cells Mol. Dis. | 2020 |
| Prevalence and predictive factors of splenic sequestration crisis among 423 pediatric patients with sickle cell disease in Tunisia. | Ben Khaled M, Ouederni M, Mankai Y, Rekaya S, Ben Fraj I, Dhouib N, Kouki R, Mellouli F, Bejaoui M | Blood Cells Mol. Dis. | 2020 |
| Pattern of Renal Blood Flow and Renovascular Parameters in Adult Patients With Sickle Cell Disease. | Asbeutah AM, Adekile A, AlMajran AA, Asbeutah AAA, Naief AA, Al-Jafar H | J Ultrasound Med | 2020 |
| Management of age-associated medical complications in patients with β-thalassemia. | Motta I, Mancarella M, Marcon A, Vicenzi M, Cappellini MD | Expert Rev Hematol | 2020 |
| Prenatal diagnosis of α- and β-thalassemias in southern Thailand. | Nopparatana C, Nopparatana C, Saechan V, Karnchanaopas S, Srewaradachpisal K | Int. J. Hematol. | 2020 |
| Mouse models in hematopoietic stem cell gene therapy and genome editing. | Radtke S, Humbert O, Kiem HP | Biochem. Pharmacol. | 2020 |
| Regulators' Advice Can Make a Difference: European Medicines Agency Approval of Zynteglo for Beta Thalassemia. | Schuessler-Lenz M, Enzmann H, Vamvakas S | Clin. Pharmacol. Ther. | 2020 |
| Co-inheritance of alpha globin gene deletion lowering serum iron level in female beta thalassemia patients. | AbdulAzeez S, Almandil NB, Naserullah ZA, Al-Jarrash S, Al-Suliman AM, ElFakharay HI, Borgio JF | Mol. Biol. Rep. | 2020 |
| Effect of photodynamic therapy on gingival inflammation in patients with thalassemia. | Al Asmari D, Khan MK | Photodiagnosis Photodyn Ther | 2020 |
| Improving the justice-based argument for conducting human gene editing research to cure sickle cell disease. | Chan B | Bioethics | 2020 |
| Molecular basis of Hb H and AEBart's diseases in the Lao People's Democratic Republic. | Singha K, Srivorakun H, Fucharoen G, Fucharoen S | Int J Lab Hematol | 2020 |
| Intestinal pathophysiological and microbial changes in sickle cell disease: Potential targets for therapeutic intervention. | Dutta D, Aujla A, Knoll BM, Lim SH | Br. J. Haematol. | 2020 |
| Sickle cell disease subjects and mouse models have elevated nitrite and cGMP levels in blood compartments. | Almeida LEF, Kamimura S, de Souza Batista CM, Spornick N, Nettleton MY, Walek E, Smith ML, Finkel JC, Darbari DS, Wakim P, Quezado ZMN | Nitric Oxide | 2020 |
| Cold External Temperatures and Sickle Cell Morbidity in Children: A Retrospective Analysis. | Wachnian C, Tompkins N, Corriveau-Bourque C, Belletrutti M, Bruce AAK | J. Pediatr. Hematol. Oncol. | 2020 |
| New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level. | Chaouch L, Sellami H, Kalai M, Darragi I, Boudrigua I, Chaouachi D, Abbes S, Mnif S | J. Pediatr. Hematol. Oncol. | 2020 |
| The Adolescent and Caregiver Sickle Cell Disease Self-management Skills Checklist: Preliminary Reliability and Validity. | Loew M, Williams JL, Russell K, Rupff R, Hankins JS, Porter J | J. Pediatr. Hematol. Oncol. | 2020 |
| Inpatient Ordering of Home Hydroxyurea by Residents for Hospitalized Patients With Sickle Cell Disease. | Shaw R, Kappa S, Nickel RS | J. Pediatr. Hematol. Oncol. | 2020 |
| HbE-Beta Thalassemia with Moyamoya Syndrome: A Rare Association. | Agrawal A, Bhinder OS, Mishra D, Juneja M | Indian J Pediatr | 2020 |
| Craniofacial Deformities in Patients With Beta-Thalassemia: Orthodontic Versus Surgical Correction-A Systematic Review. | Einy S, Ben-Barak A, Kridin K, Aizenbud D | J. Pediatr. Hematol. Oncol. | 2020 |
| Evaluation of Ocular Complications by Using Optical Coherence Tomography in Children With Sickle Cell Disease Eye Findings in Children With Sickle Cell Disease. | Vatansever E, Vatansever M, Dinç E, Temel GÖ, Ünal S | J. Pediatr. Hematol. Oncol. | 2020 |
| Emerging drugs in randomized controlled trials for sickle cell disease: are we on the brink of a new era in research and treatment? | Matte A, Cappellini MD, Iolascon A, Enrica F, De Franceschi L | Expert Opin Investig Drugs | 2020 |
| 50 Years Ago in TheJournal ofPediatrics: A New Diagnostic Test for Hemoglobin S. | Ross LF | J. Pediatr. | 2020 |
| Electrophoresis features and genotypes of Hb bart's hydrops fetalis. | Li Y, Liang L, Tian M, Qing T, Wu X | Scand. J. Clin. Lab. Invest. | 2020 |
| A Sickle Cell Crisis in a Blood Culture Bottle. | Kamada K, Matsuda T, Konno S, Oka H | Intern. Med. | 2020 |
| Practice patterns for stroke prevention using transcranial Doppler in sickle cell anemia: DISPLACE Consortium. | Schlenz AM, Phillips S, Mueller M, Melvin C, Adams RJ, Kanter J, | Pediatr Blood Cancer | 2020 |
| Sex differences in the trajectory of glomerular filtration rate in pediatric and murine sickle cell anemia. | Kasztan M, Aban I, Hande SP, Pollock DM, Lebensburger JD | Blood Adv | 2020 |
| Consumption of a green tea extract-curcumin drink decreases blood urea nitrogen and redox iron in β-thalassemia patients. | Koonyosying P, Tantiworawit A, Hantrakool S, Utama-Ang N, Cresswell M, Fucharoen S, Porter JB, Srichairatanakool S | Food Funct | 2020 |
| [Research advances in transplantation for thalassemia major]. | Huang CW, Jiang H | Zhongguo Dang Dai Er Ke Za Zhi | 2020 |
| Blood rheology biomarkers in sickle cell disease. | Lu M, Rab MA, Shevkoplyas SS, Sheehan VA | Exp. Biol. Med. (Maywood) | 2020 |
| Proteomic Studies for the Investigation of γ-Globin Induction by Decitabine in Human Primary Erythroid Progenitor Cultures. | Theodorou A, Phylactides M, Katsantoni E, Vougas K, Garbis SD, Fanis P, Sitarou M, Thein SL, Kleanthous M | J Clin Med | 2020 |
| One-Fifth of Children with Sickle Cell Anemia Show Exercise-Induced Hemoglobin Desaturation: Rate of Perceived Exertion and Role of Blood Rheology. | Brousse V, Pondarre C, Arnaud C, Kamden A, de Montalembert M, Boutonnat-Faucher B, Bourdeau H, Charlot K, Grévent D, Verlhac S, da Costa L, Connes P | J Clin Med | 2020 |
| Correction: Determining Glomerular Filtration Rate in Homozygous Sickle Cell Disease: Utility of Serum Creatinine Based Estimating Equations. | | PLoS ONE | 2020 |
| Characterization and identification of Hb Bart's hydrops fetalis caused by a compound heterozygous mutation -- /-- , a novel α -thalassemia deletion. | Ruengdit C, Panyasai S, Kunyanone N, Phornsiricharoenphant W, Ngamphiw C, Tongsima S, Sripichai O, Pissard S, Pornprasert S | Int J Lab Hematol | 2020 |
| Effect of Hydroxyurea Treatment on the Inflammatory Markers Among Children With Sickle Cell Disease. | Zahran AM, Nafady A, Saad K, Hetta HF, Abdallah AM, Abdel-Aziz SM, Embaby MM, Abo Elgheet AM, Darwish SF, Abo-Elela MGM, Elhoufey A, Elsayh KI | Clin. Appl. Thromb. Hemost. | 2020 |
| Blood transfusions for treating acute chest syndrome in people with sickle cell disease. | Dolatkhah R, Dastgiri S | Cochrane Database Syst Rev | 2020 |
| The HLA-DRB1*11 group-specific allele is a predictor for alloantibody production in the transfusion-dependent thalassemia patients. | Ebrahimi M, Maleknia M, Parav N, Mohammadi MB, Mortazavi Y, Saki N, Rahim F | Transfus. Apher. Sci. | 2020 |
| Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population. | Noor FA, Sultana N, Bhuyan GS, Islam MT, Hossain M, Sarker SK, Islam K, Khan WA, Rahman M, Qadri SK, Shekhar HU, Qadri F, Qadri SS, Mannoor K | Orphanet J Rare Dis | 2020 |
| A Novel β-Thalassemia Mutation [IVS-I-6 (T>G), : c.92+6T>G] in a Chinese Family. | Luo H, Zou Y, Liu Y | Hemoglobin | 2020 |
| Luspatercept: First Approval. | Markham A | Drugs | 2020 |
| Alpha-Thalassemia Carrier due to -α3.7 Deletion: Not So Silent. | Gilad O, Steinberg-Shemer O, Dgany O, Krasnov T, Noy-Lotan S, Tamary H, Yacobovich J | Acta Haematol. | 2020 |
| The History of Deferiprone (L1) and the Paradigm of the Complete Treatment of Iron Overload in Thalassaemia. | Kontoghiorghes GJ, Kleanthous M, Kontoghiorghe CN | Mediterr J Hematol Infect Dis | 2020 |
| The Evolving Pharmacotherapeutic Landscape for the Treatment of Sickle Cell Disease. | Ballas SK | Mediterr J Hematol Infect Dis | 2020 |
| A Concise Review on the Frequency, Major Risk Factors and Surveillance of Hepatocellular Carcinoma (HCC) in β-Thalassemias: Past, Present and Future Perspectives and the ICET-A Experience. | De Sanctis V, Soliman AT, Daar S, Alansary N, Kattamis A, Skafida M, Galati MC, Christou S, Campisi S, Messina G, Yassin MA, Canatan D, Di Maio S, Al Jaouni S, Raiola G, Karimi M, Kaleva V, Kakkar S, Mariannis D, Kattamis C | Mediterr J Hematol Infect Dis | 2020 |
| Diagnosis and Prenatal Diagnosis in a Chinese Family Carrying the Rare α-Thalassemia Gene : c.1A>G Mutation. | Chen X, Luo S, Huang J, Yuan D, Yan T, Cai R, Tang N | Hemoglobin | 2020 |
| Variable Phenotypic Presentation of Two Siblings with Hemoglobin SD Disease. | Aggarwal P, Jain A, Mishra OP, Gupta V | Indian J Pediatr | 2020 |
| The relationship between frequency and severity of vaso-occlusive crises and health-related quality of life and work productivity in adults with sickle cell disease. | Rizio AA, Bhor M, Lin X, McCausland KL, White MK, Paulose J, Nandal S, Halloway RI, Bronté-Hall L | Qual Life Res | 2020 |
| Corrigendum to | Shmukler BE, Rivera A, Bhargava P, Nishimura K, Hsu A, Kim EH, Trudel M, Rust MB, Hubner CA, Brugnara C, Alper SL | Blood Cells Mol. Dis. | 2020 |
| Comparison Between Three Molecular Diagnostics for the Identification of Heterozygous Hemoglobin E. | Arif AA, An-Nizamiya AD, Putri C, Nashrurrokhman M, Husna N, Mulyati , Hadisusanto S, Handayani NSN | Pak. J. Biol. Sci. | 2020 |
| Compound heterozygosity of a silent beta-thalassemia mutation at the 3'-untranslated region (HBB: c.*132 C>T) and beta-zero thalassemia results in thalassemia intermedia. | Sripusanapan A, Phusua A, Fanhchaksai K, Charoenkwan P | Pediatr Blood Cancer | 2020 |
| Sickle Cell Disease: A Primer for Primary Care Providers. | Kimrey S, Saving KL | Pediatr Ann | 2020 |
| Body Composition in Egyptian Children With Transfusion-dependent Thalassemia: The Impact of Nutrition and Metabolic Profile. | Elalfy MS, Ebeid FSE, El Gendy YG, Zaki MM, Kalifa ASA | J. Pediatr. Hematol. Oncol. | 2020 |
| Hydroxyurea for ALL children with sickle cell anemia: What can we learn from Africa? | Aygun B | Pediatr Blood Cancer | 2020 |
| Treating sickle cell anemia: A new era dawns. | Steinberg MH | Am. J. Hematol. | 2020 |
| Rifaximin on intestinally-related pathologic changes in sickle cell disease. | Dutta D, Li K, Methe B, Lim SH | Am. J. Hematol. | 2020 |
| [Hematological and genotypic features of 100 patients with hemoglobin E disorders from Yunnan Province]. | Yang J, Wang H, Zhang Z, Qian Y, Zhang L, Lu L, Wang K | Zhonghua Yi Xue Yi Chuan Xue Za Zhi | 2020 |
| Haptoglobin genotype predicts severe acute vaso-occlusive pain episodes in children with sickle cell anemia. | Willen SM, McNeil JB, Rodeghier M, Kerchberger VE, Shaver CM, Bastarache JA, Steinberg MH, DeBaun MR, Ware LB | Am. J. Hematol. | 2020 |
| Innate immune cells, major protagonists of sickle cell disease pathophysiology. | Allali S, Maciel TT, Hermine O, de Montalembert M | Haematologica | 2020 |
| Mortality in children with sickle cell disease in mainland France from 2000 to 2015. | Desselas E, Thuret I, Kaguelidou F, Benkerrou M, de Montalembert M, Odièvre MH, Lesprit E, Rumpler E, Fontanet A, Pondarre C, Brousse V | Haematologica | 2020 |
| Headache in beta-thalassemia: An Italian multicenter clinical, conventional MRI and MR-angiography case-control study. | Tartaglione I, Caiazza M, Di Concilio R, Ciancio A, De Michele E, Maietta C, Valentino MS, Russo C, Roberti D, Casale M, Elefante A, Femina G, Esposito F, Ponticorvo S, Russo AG, Canna A, Ermani M, Cirillo M, Perrotta S, Manara R | Blood Cells Mol. Dis. | 2020 |
| Transfusion-transmitted hepatitis C: A cluster of cases in transfusion-dependent thalassaemia patients in Sri Lanka. | Perera S, Bonsall D, Niriella MA, Allen A, Peries AC, Nelumdeniya UB, Dissanayake R, Silva I, de Cesare M, Klenerman P, Weatherall DJ, Roberts DJ, Premawardhena AP | Transfus Med | 2020 |
| Performance of ICD-10-CM diagnosis codes for identifying children with Sickle Cell Anemia. | Reeves SL, Madden B, Wu M, Miller LS, Anders D, Caggana M, Cogan LW, Kleyn M, Hurden I, Freed GL, Dombkowski KJ | Health Serv Res | 2020 |
| The role of hydroxyurea in decreasing the occurrence of vasso-occulusive crisis in pediatric patients with sickle cell disease at King Saud Medical City in Riyadh, Saudi Arabia. | Azmet FR, Al-Kasim F, Alashram WM, Siddique K | Saudi Med J | 2020 |
| A Japanese Family with the Unstable Hb Sydney (: c.203T>C) Variant and Persistent Low Hemoglobin Oxygen Saturation. | Sakamoto A, Nakadate H, Tada K, Yamashiro Y, Ishiguro A | Hemoglobin | 2020 |
| Reactivation of γ-globin expression through Cas9 or base editor to treat β-hemoglobinopathies. | Wang L, Li L, Ma Y, Hu H, Li Q, Yang Y, Liu W, Yin S, Li W, Fu B, Kurita R, Nakamura Y, Liu M, Lai Y, Li D | Cell Res. | 2020 |
| New Option for Sickle Cell Disease. | Voelker R | JAMA | 2020 |
| Web-Based Technology to Improve Disease Knowledge Among Adolescents With Sickle Cell Disease: Pilot Study. | Saulsberry AC, Hodges JR, Cole A, Porter JS, Hankins J | JMIR Pediatr Parent | 2020 |
| Iron Overload Associated Endocrine Dysfunction Leading to Lower Bone Mineral Density in Thalassemia Major. | Yang WP, Chang HH, Li HY, Lai YC, Huang TY, Tsai KS, Lin KH, Lin DT, Jou ST, Lu MY, Yang YL, Chou SW, Shih SR | J. Clin. Endocrinol. Metab. | 2020 |
| Sickle cell disease celebration. | Mullard A | Nat Rev Drug Discov | 2020 |
| Sickle-Cell Disease Co-Management, Health Care Utilization, and Hydroxyurea Use. | Crego N, Douglas C, Bonnabeau E, Earls M, Eason K, Merwin E, Rains G, Tanabe P, Shah N | J Am Board Fam Med | 2020 |
| Alpha and beta-Thalassemia mutations in Hubei area of China. | Zhu Y, Shen N, Wang X, Xiao J, Lu Y | BMC Med. Genet. | 2020 |
| World Health Organization's Growth Reference Overestimates the Prevalence of Severe Malnutrition in Children with Sickle Cell Anemia in Africa. | Ghafuri DL, Abdullahi SU, Jibir BW, Gambo S, Bello-Manga H, Haliru L, Bulama K, Usman FM, Gambo A, Aliyu MH, Greene BC, Kassim AA, Slaughter C, Rodeghier M, DeBaun MR | J Clin Med | 2020 |
| Sickle cell disease in Germany: Early insights from a national registry. | Odame I | Pediatr Blood Cancer | 2020 |
| Genotype/Phenotype Correlation of β-Thalassemia in Syrian Patients: A Cross-Sectional Study. | Shoujaa A, Moasses F, Mukhalalaty Y, Murad H, Al-Quobaili F | Hemoglobin | 2020 |
| Optical coherence tomography angiography findings in young β-thalassemia patients. | Güler Kazancı E, Korkmaz MF, Can ME | Eur J Ophthalmol | 2020 |
| Decreased erythrocyte binding of Siglec-9 increases neutrophil activation in sickle cell disease. | Kiser ZM, Lizcano A, Nguyen J, Becker GL, Belcher JD, Varki AP, Vercellotti GM | Blood Cells Mol. Dis. | 2020 |
| Sharpening the Molecular Scissors: Advances in Gene-Editing Technology. | Broeders M, Herrero-Hernandez P, Ernst MPT, van der Ploeg AT, Pijnappel WWMP | iScience | 2020 |
| Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central Iran. | Sajadpour Z, Amini-Farsani Z, Motovali-Bashi M, Yadollahi M, Khosravi-Farsani N | Hemoglobin | 2020 |
| Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α-thalassemia by targeted next-generation sequencing. | Li Z, Shang X, Luo S, Zhu F, Wei X, Zhou W, Ye Y, Yan T, Cai R, Xu X | Mol. Genet. Genomics | 2020 |
| Immunization Adherence in Children With Sickle Cell Disease: A Single-Institution Experience. | Infanti LM, Elder JJ, Franco K, Simms S, Statler VA, Raj A | J Pediatr Pharmacol Ther | 2020 |
| Alpha-hemoglobin-stabilizing protein (AHSP): a modulatory factor in β-thalassemia. | Che Yaacob NS, Islam MA, Alsaleh H, Ibrahim IK, Hassan R | Int. J. Hematol. | 2020 |
| Assessment of health-related quality of life among adults hospitalized with sickle cell disease vaso-occlusive crisis. | Esham KS, Rodday AM, Smith HP, Noubary F, Weidner RA, Buchsbaum RJ, Parsons SK | Blood Adv | 2020 |
| Expression analysis data of BCL11A and γ-globin genes in KU812 and KG-1 cell lines after CRISPR/Cas9-mediated BCL11A enhancer deletion. | Khosravi MA, Abbasalipour M, Concordet JP, Berg JV, Zeinali S, Arashkia A, Buch T, Karimipoor M | Data Brief | 2020 |
| Cd60 (GTG > GAG)/Hb Cagliari mutation was found in scanning of β-thalassemia alleles from patients of East Kalimantan, Indonesia. | Susanto Z, Siswandari W, Rujito L | Mol Genet Metab Rep | 2020 |
| 5-(Hydroxymethyl)furfural restores low-oxygen rheology of sickle trait blood in vitro. | Hansen S, Wood DK, Higgins JM | Br. J. Haematol. | 2020 |
| Increased ferritin levels in non-transfusion-dependent β°-thalassaemia/HbE are associated with reduced CXCR2 expression and neutrophil migration. | Thiengtavor C, Siriworadetkun S, Paiboonsukwong K, Fucharoen S, Pattanapanyasat K, Vadolas J, Svasti S, Chaichompoo P | Br. J. Haematol. | 2020 |
| Derivation of human embryonic stem cell line MUSIe001-A from an embryo with homozygous α-thalassemia (SEA deletion). | Laowtammathron C, Chingsuwanrote P, Choavaratana R, Phornwilardsiri S, Sitthirit K, Kaewjunun C, Makemaharn O, Terbto P, Waeteekul S, Lorthongpanich C, U-Pratya Y, Srisook P, Kheolamai P, Issaragrisil S | Stem Cell Res | 2020 |
| Emerging point-of-care technologies for sickle cell disease diagnostics. | Ilyas S, Simonson AE, Asghar W | Clin. Chim. Acta | 2020 |
| Urinary cross-linked carboxyterminal telopeptide, a bone resorption marker, decreases after vaso-occlusive crises in adults with sickle cell disease. | Adesina OO, Jenkins IC, Wu QV, Fung EB, Narla RR, Lipkin EW, Mahajan K, Konkle BA, Kruse-Jarres R | Blood Cells Mol. Dis. | 2020 |
| Renal Functional Decline in Sickle Cell Disease and Trait. | Nath KA, Vercellotti GM | J. Am. Soc. Nephrol. | 2020 |
| Combined use of gap-PCR and next-generation sequencing improves thalassaemia carrier screening among premarital adults in China. | Zhao J, Li J, Lai Q, Yu Y | J. Clin. Pathol. | 2020 |
| Study of Iron Status in Sickle cell disorder. | Varshney P | J Assoc Physicians India | 2020 |
| Sickle cell disease (SCD) causing cirrhosis presenting as Acute on Chronic Liver Failure(ACLF) due to viral hepatitis. | Yellapu V, Mohanty AP, Mohanty L, Yellapu V | J Assoc Physicians India | 2020 |
| Insulin resistance in transfusion dependent adult beta thalassemia major subjects with metabolic syndrome. | Pasricha N, Aggarwal R, Jain SK, Prakash A, Jain A | J Assoc Physicians India | 2020 |
| Primary Hyperparathyroidism in Sickle Cell Disease: An Unknown Complication of the Disease in Adulthood. | Denoix E, Bomahou C, Clavier L, Ribeil JA, Lionnet F, Bartolucci P, Courbebaisse M, Pouchot J, Arlet JB | J Clin Med | 2020 |
| Thrombin activation of PAR-1 contributes to microvascular stasis in mouse models of sickle cell disease. | Sparkenbaugh EM, Chen C, Brzoska T, Nguyen J, Wang S, Vercellotti GM, Key NS, Sundd P, Belcher JD, Pawlinski R | Blood | 2020 |
| Incidental Findings of Sickle Cell Trait From an Everyday Diabetes Test: Should General Health Care Providers and Testing Centers Report, Retest, or Refer? | Cronin de Chavez A, Atkin KM, Babbington F, Berghs MJ, Dyson SM, Miller A, Whitelaw DC | Clin Diabetes | 2020 |
| Splenic function is not maintained long-term after partial splenectomy in children with sickle cell disease. | El-Gohary Y, Khan S, Hodgman E, Wynn L, Kimble A, Abdelhafeez A, Talbot L, Wang W, Davidoff AM, Murphy AJ | J. Pediatr. Surg. | 2020 |
| Cardiovascular changes in children with sickle cell crisis. | Onalo R, Cooper P, Cilliers A, Nnebe-Agumadu U | Cardiol Young | 2020 |
| An Unusual Compound Heterozygosity for Hb O-Arab (: c.364G>A) and Hb D-Los Angeles (: c.364G>C). | van Gammeren AJ, Pelkmans L, Endschot CCWV, Roelofsen-de Beer RJAC, Harteveld CL | Hemoglobin | 2020 |
| Screening Readthrough Compounds to Suppress Nonsense Mutations: Possible Application to β-Thalassemia. | Borgatti M, Altamura E, Salvatori F, D'Aversa E, Altamura N | J Clin Med | 2020 |
| Evaluation of the effectiveness of prophylactic oral vitamin D (cholecalciferol) in children with sickle cell disease. | Garrido C, Bardón-Cancho EJ, Fajardo-Sánchez VLÁ, Cascón-Pérez-Teijón ME, García-Morín M, Cela E, | Bone | 2020 |
| Comparison of liver MRI R2(FerriScan®) VS liver MRI T2* as a measure of body iron load in a cohort of beta thalassaemia major patients. | Padeniya P, Siriwardana S, Ediriweera D, Samarasinghe N, Silva S, Silva I, Ahamed N, Niriella M, Premawardhena A | Orphanet J Rare Dis | 2020 |
| Correlates of Cognitive Function in Sickle Cell Disease: A Meta-Analysis. | Prussien KV, Siciliano RE, Ciriegio AE, Anderson AS, Sathanayagam R, DeBaun MR, Jordan LC, Compas BE | J Pediatr Psychol | 2020 |
| P-selectin-deficient mice to study pathophysiology of sickle cell disease. | Bennewitz MF, Tutuncuoglu E, Gudapati S, Brzoska T, Watkins SC, Monga SP, Pradhan-Sundd T, Sundd P | Blood Adv | 2020 |
| Prevalence and Risk Factors for Microalbuminuria in Children with Sickle Cell Disease at King Abdulaziz University Hospital: A Retrospective Cross-sectional Study. | Alzahrani YA, Algarni MA, Alnashri MM, AlSayyad HM, Aljahdali KM, Alead JE, Alhjrsy YA, Alzahrani F, Safdar O | Cureus | 2020 |
| Pharmacy hydroxyurea education materials for patients with sickle cell disease: An environmental scan and assessment of accuracy. | Cervi A, Diamantouros A, Azzam M, Lane SJ, Sapru H, Verhovsek M | Pediatr Blood Cancer | 2020 |
| Hyperuricemia is associated with a lower glomerular filtration rate in pediatric sickle cell disease patients. | Kaspar CDW, Beach I, Newlin J, Sisler I, Feig D, Smith W | Pediatr. Nephrol. | 2020 |
| Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation. | Basak A, Munschauer M, Lareau CA, Montbleau KE, Ulirsch JC, Hartigan CR, Schenone M, Lian J, Wang Y, Huang Y, Wu X, Gehrke L, Rice CM, An X, Christou HA, Mohandas N, Carr SA, Chen JJ, Orkin SH, Lander ES, Sankaran VG | Nat. Genet. | 2020 |
| Asymptomatic intracranial aneurysms in beta-thalassemia: a three-year follow-up report. | Manara R, Caiazza M, Di Concilio R, Ciancio A, De Michele E, Maietta C, Capalbo D, Russo C, Roberti D, Casale M, Elefante A, Esposito F, Ponticorvo S, Russo AG, Canna A, Cirillo M, Perrotta S, Tartaglione I | Orphanet J Rare Dis | 2020 |
| Aura and mental stress are associated with reports of pain in sickle cell disease-a pilot study using a mobile application. | Espinoza J, Shah P, Veluswamy S, Zeltzer L, Khoo MCK, Coates TD, Baskin J | Am. J. Hematol. | 2020 |
| Now I Am The Voice: | Hadjidemetriou M | Am. J. Hematol. | 2020 |
| Malnutrition, Its Attributes, and Impact on Quality of Life: An Epidemiological Study among β-Thalassemia Major Children. | Biswas B, Naskar NN, Basu K, Dasgupta A, Basu R, Paul B | Korean J Fam Med | 2020 |
| Prevalence of endocrine complications in transfusion dependent thalassemia in Hospital Pulau Pinang: A pilot study. | Lee KT, Lim SL, Goh AS | Med. J. Malaysia | 2020 |
| Zinc supplementation improves glucose homeostasis in patients with β-thalassemia major complicated with diabetes mellitus: A randomized controlled trial. | Matter RM, Elbarbary NS, Ismail EAR, Darwish YW, Nada AS, Banoub VP | Nutrition | 2020 |
| Goal-Oriented Monitoring of Cyclosporine Is Effective for Graft-versus-Host Disease Prevention after Hematopoietic Stem Cell Transplantation in Sickle Cell Disease and Thalassemia Major. | Gauthier A, Bleyzac N, Garnier N, Kebaili K, Joly P, Goutagny MP, Mollet I, Goutelle S, Renard C, Bertrand Y | Biol. Blood Marrow Transplant. | 2020 |
| Usefulness of azacitidine therapy in a sickle cell disease patient with myelodysplastic syndrome. | De Luna G, Darnige L, Roueff S, Peyrard T, Pouchot J, Arlet JB | Ann. Hematol. | 2020 |
| Pulmonary dysfunction among adolescents and adults with sickle cell disease in Nigeria: Implications for monitoring. | Al-Mendalawi MD | Ann Thorac Med | 2020 |
| Whole genome sequence-based haplotypes reveal a single origin of the 1393 bp deletion. | Wang X, Xu JZ, Conrey A, Mendelsohn L, Shriner D, Pirooznia M, Thein SL | J. Med. Genet. | 2020 |
| Nondeletional α-Thalassemia: Two New Mutations on the α2 Gene. | Ropero P, Arbeteta J, Nieto JM, González FA, González B, Villegas A, Benavente C | Hemoglobin | 2020 |
| Reproductive health issues in female patients with beta-thalassaemia major: a narrative literature review. | Nourollahpour Shiadeh M, Cassinerio E, Modarres M, Zareiyan A, Hamzehgardeshi Z, Behboodi Moghadam Z | J Obstet Gynaecol | 2020 |
| Sickle cell disease: A distinction of two most frequent genotypes (HbSS and HbSC). | da Guarda CC, Yahouédéhou SCMA, Santiago RP, Neres JSDS, Fernandes CFL, Aleluia MM, Figueiredo CVB, Fiuza LM, Carvalho SP, Oliveira RM, Fonseca CA, Ndidi US, Nascimento VML, Rocha LC, Goncalves MS | PLoS ONE | 2020 |
| Perinatal Management of Bart's Hemoglobinopathy: Paradoxical Effects of Intrauterine, Transplacental, and Partial Exchange Transfusions. | Curran M, Mikhael M, Sun WD, Lim J, Leung A, Morchi G, Chmait RH | AJP Rep | 2020 |
| Patients With Sickle Cell Disease Between Ages 0 and 20 Years Presenting With Acute Chest Syndrome in the United States. | Ramphul K, Mejias SG, Joynauth J | J. Pediatr. Hematol. Oncol. | 2020 |
| Gene therapy in sickle cell disease: Possible utility and impact. | Curtis SA, Shah NC | Cleve Clin J Med | 2020 |
| Sickle cell disease: A primary care update. | Onimoe G, Rotz S | Cleve Clin J Med | 2020 |
| Complement activation in sickle cell disease: Dependence on cell density, hemolysis and modulation by hydroxyurea therapy. | Roumenina LT, Chadebech P, Bodivit G, Vieira-Martins P, Grunenwald A, Boudhabhay I, Poillerat V, Pakdaman S, Kiger L, Jouard A, Audureau E, Pirenne F, Galactéros F, Frémeaux-Bacchi V, Bartolucci P | Am. J. Hematol. | 2020 |
| Development of gene editing strategies for human β-globin (HBB) gene mutations. | Kalkan BM, Kala EY, Yuce M, Karadag Alpaslan M, Kocabas F | Gene | 2020 |
| American Society of Hematology 2020 guidelines for sickle cell disease: transfusion support | Chou ST, Alsawas M, Fasano RM, Field JJ, Hendrickson JE, Howard J, Kameka M, Kwiatkowski JL, Pirenne F, Shi PA, Stowell SR, Thein SL, Westhoff CM, Wong TE, Akl EA. | Blood Adv | 2020 |
| First Detection of Hb Cenxi [β46(CD5)Gly→Arg (GG>GG), : c.139G>C] by Capillary Electrophoresis. | Li YQ, Li YW, Liang L, Meng MH, Zhang XQ | Hemoglobin | 2020 |
| Hb F-Wentzville [γ24(B6)Gly→Glu; : c.74G>A, p.Gly25Glu]: An Unstable γ-Globin Variant Associated with Neonatal Hemolytic Anemia. | Semkiu KM, Oliveira JL, Nguyen PL, Porter TR, Wilson DB | Hemoglobin | 2020 |
| L-glutamine for sickle cell disease: Knight or pawn? | Sadaf A, Quinn CT | Exp. Biol. Med. (Maywood) | 2020 |
| Evaluation of regulatory T cells frequency and FoxP3/GDF-15 gene expression in β-thalassemia major patients with and without alloantibody; correlation with serum ferritin and folate levels. | Shokrgozar N, Amirian N, Ranjbaran R, Bazrafshan A, Sharifzadeh S | Ann. Hematol. | 2020 |
| False positive testing for sickle hemoglobin in a blood donor with mild erythrocytosis and hemoglobin Geldrop St. Anna. | Dunseth CD, Schlueter AJ, Knudson CM | Transfus. Apher. Sci. | 2020 |
| Distribution of sickle cell disease and assessment of risk factors based on transcranial Doppler values in the Gulf region. | Wali Y, Kini V, Yassin MA | Hematology | 2020 |
| Systemo-pulmonary shunting and acute chest syndrome in a patient with SC sickle-cell disease. | Schlemmer F, Gellen-Dautremer J, Carette MF, de Prost N, Spagnolo S, Deux JF, Fartoukh M, Naccache JM, Habibi A, Mahevas M, Bartolucci P, Mekontso Dessap A, Maitre B | Respir Med Res | 2020 |
| Discrimination of β-thalassemia and iron deficiency anemia through extreme learning machine and regularized extreme learning machine based decision support system. | Çil B, Ayyıldız H, Tuncer T | Med. Hypotheses | 2020 |
| Ghana takes on sickle-cell disease. | Adepoju P | Lancet | 2020 |
| Biallelic correction of sickle cell disease-derived induced pluripotent stem cells (iPSCs) confirmed at the protein level through serum-free iPS-sac/erythroid differentiation. | Haro-Mora JJ, Uchida N, Demirci S, Wang Q, Zou J, Tisdale JF | Stem Cells Transl Med | 2020 |
| Curative options for sickle cell disease: haploidentical stem cell transplantation or gene therapy? | Leonard A, Tisdale J, Abraham A | Br. J. Haematol. | 2020 |
| Epidemiology and Predictors of all-cause 30-Day readmission in patients with sickle cell crisis. | Kumar V, Chaudhary N, Achebe MM | Sci Rep | 2020 |
| haemoglobin sabine masquerading as double heterozygosity for HbQ-India and β-thalassemia trait: first report from South Asia. | Jamwal M, Kaur J, Chhabra S, Trehan A, Sharma P, Das R | J. Clin. Pathol. | 2020 |
| Relation Between Cardiac T2* Values and Electrocardiographic Parameters in Children With Transfusion-dependent Thalassemia. | Aggarwal P, Kumar I, Jain A, Verma A, Gupta V | J. Pediatr. Hematol. Oncol. | 2020 |
| Liver Stiffness Measurement by Vibration Controlled Transient Elastography Does Not Correlate to Hepatic Iron Overload in Children With Sickle Cell Disease. | Costa P, Rudolph B, Kogan-Liberman D, Manwani D, Silver EJ, Ovchinsky N | J. Pediatr. Hematol. Oncol. | 2020 |
| Coinheritance of Triplicated Alpha-Globin Gene and Beta-Thalassemia Mutations in Adulthood: Ten Years of Referrals in Northern Greece. | Theodoridou S, Balassopoulou A, Boutou E, Delaki EE, Yfanti E, Vyzantiadis TA, Vetsiou E, Voskaridou E, Vlachaki E | J. Pediatr. Hematol. Oncol. | 2020 |
| The effect of Islamic semanticism on self-reporting and lifestyles of mothers of adolescents with thalassemia. | Yolme ABS, Hojjati H, Akhoundzadeh G | Int J Adolesc Med Health | 2020 |
| Investigating the suitability of high-resolution mass spectrometry for newborn screening: identification of hemoglobinopathies and β-thalassemias in dried blood spots. | Wiesinger T, Mechtler T, Schwarz M, Xie X, Grosse R, Nieves Cobos P, Kasper D, Lukacs Z | Clin. Chem. Lab. Med. | 2020 |
| Correlates of hopelessness in clinically stable nigerian adults with sickle cell disease. | Aloba O, Eyiolawi D | Niger J Clin Pract | 2020 |
| [Coexistence of sickle cell disease and systemic lupus erythematosus]. | Christiaens C, Florkin B, Philippet P | Rev Med Liege | 2020 |
| Regulation of iron homeostasis through the erythroferrone-hepcidin axis in sickle cell disease. | Mangaonkar AA, Thawer F, Son J, Ajebo G, Xu H, Barrett NJ, Wells LG, Bowman L, Clair B, Patel N, Bora P, Jung G, Nemeth E, Kutlar A | Br. J. Haematol. | 2020 |
| Acute kidney injury in paediatric patients with sickle cell disease is associated with increased morbidity and resource utilization. | McCormick M, Richardson T, Warady BA, Novelli EM, Kalpatthi R | Br. J. Haematol. | 2020 |
| Knowledge, Experiences and Coping Mechanisms for Priapism among Persons with Sickle Cell Disease in Ibadan, Nigeria. | Raji OH, Shokunbi WA, Ajuwon AJ | West Afr J Med | 2020 |
| Hemolytic transfusion reactions in sickle cell disease: underappreciated and potentially fatal. | Thein SL, Pirenne F, Fasano RM, Habibi A, Bartolucci P, Chonat S, Hendrickson JE, Stowell SR | Haematologica | 2020 |
| Hemolytic anemia due to the unstable hemoglobin Wien: manifestations and long-term course in the largest pedigree identified to date. | Hilbert S, Voill-Glaninger A, Höller B, Minkov M | Haematologica | 2020 |
| Understanding sickle cell disease: impact of surveillance and gaps in knowledge. | Kaur M, Brown M, Love TW, Thompson A, Treadwell M, Smith-Whitley K | Blood Adv | 2020 |
| [Application Value of Capillary Electrophoresis in Screeningβ-Thalassemia of Children]. | Ren ZM, Li CG, Xu G, Huang J, Lin ZH, Luo MZ, Chen SY, Chen YS | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2020 |
| Can PROMIS domains of pain and physical functioning detect changes in health over time for children with sickle cell disease? | Singh A, Dasgupta M, Simpson PM, Brousseau DC, Panepinto JA | Pediatr Blood Cancer | 2020 |
| Two novel polymorphic forms of iron-chelating agent deferiprone. | Rajendrakumar S, Durga ASVS, Nanubolu JB, Balasubramanian S | Acta Crystallogr C Struct Chem | 2020 |
| Total hip arthroplasty: Concerns and precautions in sickle-cell trait. | Pisanu F, Pes M, Caggiari G, Ortu S, Satta ML, Amorese V, Doria C | J Orthop | 2020 |
| Level of agreement between adolescents' self-assessment and parent proxy report of health-related quality of life in adolescents with sickle cell disease. | Blake A, Guthrie-Dixon N, Grindley M, Barton-Gooden A, Knight-Madden J, Asnani M | Pediatr Blood Cancer | 2020 |
| Endocrinopathies complicating transfusion-dependent hemoglobinopathy. | Al-Agha AE, Bawahab NS, Nagadi SA, Alghamdi SA, Felemban DA, Milyani AA | Saudi Med J | 2020 |
| Comparison of efficacy of packed red blood cell transfusion based on its hemoglobin content versus the standard transfusion practice in thalassemia major patients (HEMOCON study). | Raja A, Jain A, Marwaha N, Trehan A | Transfus. Apher. Sci. | 2020 |
| α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region. | Al-Riyami AZ, Daar S, Kindi SA, Madhani AA, Wali Y, Rawahi MA, Zadjali SA | Hemoglobin | 2020 |
| Atypical Retro Internal Limiting Membrane Haemorrhage in Homozygous Sickle Cell Disease. | Voide N, Mantel I, Ambresin A | Klin Monbl Augenheilkd | 2020 |
| Cerebral Revascularization for Moyamoya Syndrome Associated with Sickle Cell Disease: A Systematic Review of the Literature on the Role of Extracranial-Intracranial Bypass in Treating Neurologic Manifestations of Pediatric Patients with Sickle Cell Disease. | Terrell D, Savardekar AR, Whipple SG, Dossani RH, Spetzler RF, Sun H | World Neurosurg | 2020 |
| Reticulocyte hemoglobin content. | Ogawa C, Tsuchiya K, Maeda K | Clin. Chim. Acta | 2020 |
| Prevalence of spp. Infection in Patients with Sickle Cell Disease. | Soares TCB, Isaias GAB, Almeida AR, Drummond MR, da Silva MN, Lania BG, Vieira-Damiani G, Saad STO, Ericson ME, Gupta K, Velho PENF | Vector Borne Zoonotic Dis. | 2020 |
| Ocular Manifestations of Sickle Cell Disease: Signs, Symptoms and Complications. | AlRyalat SA, Nawaiseh M, Aladwan B, Roto A, Alessa Z, Al-Omar A | Ophthalmic Epidemiol | 2020 |
| An Evaluation of Bone Health Parameters in Regularly Transfused Beta-Thalassemia Major Patients. | Kothimira VK, Kumar A, Richhele LR, Sood N, Gulati A | J. Pediatr. Hematol. Oncol. | 2020 |
| The Adverse Impact of Thalassemia Major on Adolescents' Oral Health-related Quality of Life. | Ebeid FSE, Khan NIH | J. Pediatr. Hematol. Oncol. | 2020 |
| Wrist Joint Skeletal Changes in Children With Transfusion-Dependent Thalassemia. | Dhawan P, Kanojia RK, Chandra J, Kumar A, Anand R, Gupta S | J Pediatr Orthop | 2020 |
| Hemolysis and Fetal Fraction in Cell-Free DNA Blood Collection Tubes for Noninvasive Prenatal Testing. | Stokowski R, White K, Hacker C, Doshi J, Schmid M | Mol Diagn Ther | 2020 |
| Safe and efficient peripheral blood stem cell collection in patients with sickle cell disease using plerixafor. | Uchida N, Leonard A, Stroncek D, Panch SR, West K, Molloy E, Hughes TE, Hauffe S, Taylor T, Fitzhugh C, Hankins JS, Wilson M, Sharma A, Tsai SQ, Weiss MJ, Hsieh M, Tisdale JF | Haematologica | 2020 |
| A New Indicator Derived From Reticulocyte Hemoglobin Content for Screening Iron Deficiency in an Area Prevalent for Thalassemia. | Jamnok J, Sanchaisuriya K, Chaitriphop C, Sanchaisuriya P, Fucharoen G, Fucharoen S | Lab Med | 2020 |
| Hemoglobins F, A , and E levels in Laotian children aged 6-23 months with Hb E disorders: Effect of age, sex, and thalassemia types. | Kingchaiyaphum B, Sanchaisuriya K, Fucharoen G, Chaibunruang A, Hess SY, Hinnouho GM, Barffour MA, Wessells KR, Kounnavong S, Fucharoen S | Int J Lab Hematol | 2020 |
| Laparoscopic cholecystectomy in children with sickle cell disease: A simple modified technique. | Al Hindi S, Al Aradi H, Mubarak M | Asian J Endosc Surg | 2020 |
| Peptide Nucleic Acids and Gene Editing: Perspectives on Structure and Repair. | Economos NG, Oyaghire S, Quijano E, Ricciardi AS, Saltzman WM, Glazer PM | Molecules | 2020 |
| Psychological morbidity among children with transfusion dependent β-thalassaemia and their parents in Sri Lanka. | Mettananda S, Peiris R, Pathiraja H, Chandradasa M, Bandara D, de Silva U, Mettananda C, Premawardhena A | PLoS ONE | 2020 |
| Dapagliflozin Suppresses Hepcidin And Increases Erythropoiesis. | Ghanim H, Abuaysheh S, Hejna J, Green K, Batra M, Makdissi A, Chaudhuri A, Dandona P | J. Clin. Endocrinol. Metab. | 2020 |
| The problems in evaluation of sleep disordered breathing in adults with sickle cell disease. | Roizenblatt S, Togeiro SMGP, Cabanas-Pedro AC, Figueredo MS | Sleep Med. | 2020 |
| Fever Management in Sickle Cell Disease in Low- and Middle-Income Countries: A Survey of SCD Management Programs. | Coria AL, Taylor CM, Tubman VN | Am. J. Trop. Med. Hyg. | 2020 |
| Hemopexin deficiency promotes acute kidney injury in sickle cell disease. | Ofori-Acquah SF, Hazra R, Orikogbo OO, Crosby D, Flage B, Ackah EB, Lenhart D, Tan RJ, Vitturi DA, Paintsil V, Owusu-Dabo E, Ghosh S, | Blood | 2020 |
| Prevalence of 3.7 and 4.2 deletions in Sudanese patients with red cells hypochromia and microcytosis. | Osman HA, Hamid MMA, Ahmad RB, Saleem M, Abdallah SA | BMC Res Notes | 2020 |
| Clinical Impact of Warmed Intravenous Saline in Sickle Cell Patients With Vasoocclusive Episodes. | Quarrie RP, Stoner MJ, Choueiki JM, Bonsu BK, Cohen DM | Pediatr Emerg Care | 2020 |
| Use of deferoxamine (DFO) in transfusion-dependent β-thalassemia during pregnancy: A retrospective study. | Piccioni MG, Capone C, Vena F, Del Negro V, Schiavi MC, D'Ambrosio V, Giancotti A, Smacchia MP, Brunelli R | Taiwan J Obstet Gynecol | 2020 |
| Impact of a paediatric-adult care transition programme on the health status of patients with sickle cell disease: study protocol for a randomised controlled trial (the DREPADO trial). | Hoegy D, Bleyzac N, Gauthier-Vasserot A, Cannas G, Denis A, Hot A, Bertrand Y, Occelli P, Touzet S, Dussart C, Janoly-Dumenil A, | Trials | 2020 |
| Addressing social determinants of health in sickle cell disease: The role of Medicaid policy. | Raphael JL | Pediatr Blood Cancer | 2020 |
| Pediatric Hematologists Report Infrequent Prognosis Discussions in the Routine Care of Children with Sickle Cell Disease. | Pecker LH, Silver EJ, Roth M, Manwani D | J Health Care Poor Underserved | 2020 |
| Engaging Individuals with Sickle Cell Disease in Patient-Centered Outcomes Research: A Community Health Ambassador Training Model. | Mayo-Gamble TL, Murry VM, Cunningham-Erves J, Cronin RM, Lari N, Gorden A, Scott L, DeBaun MR, Thompson T | J Health Care Poor Underserved | 2020 |
| The planimetric Grothoff's criteria by cardiac magnetic resonance can improve the specificity of left ventricular non-compaction diagnosis in thalassemia intermedia. | Macaione F, Meloni A, Positano V, Pistoia L, Barison A, Di Lisi D, Spasiano A, Campisi S, Spiga A, Righi R, Novo G, Novo S, Pepe A | Int J Cardiovasc Imaging | 2020 |
| Less 'reds' more 'blues': hemoglobin level and depression in non-transfusion-dependent thalassemia. | Mihailescu AM, Musallam KM, Cappellini MD, Taher AT | Ann. Hematol. | 2020 |
| Lack of knowledge and misperceptions about thalassaemia among college students in Bangladesh: a cross-sectional baseline study. | Hossain MS, Hasan MM, Raheem E, Islam MS, Al Mosabbir A, Petrou M, Telfer P, Siddiqee MH | Orphanet J Rare Dis | 2020 |
| A pilot study to screen for poor academic performance in children with sickle cell disease in the outpatient setting. | Karkoska K, Zaheer S, Chen V, Fishbein J, Appiah-Kubi A, Aygun B | Pediatr Blood Cancer | 2020 |
| Prevalence and risk factors for albuminuria and glomerular hyperfiltration in a large cohort of children with sickle cell anemia. | Belisário AR, de Almeida JA, Mendes FG, da Silva DMM, Planes W, Rezende PV, Silva CM, Brito AC, Sales RR, Viana MB, Simões E Silva AC | Am. J. Hematol. | 2020 |
| Two New Drugs for Sickle Cell Disease. | Aschenbrenner DS | Am J Nurs | 2020 |
| Molecular Heterogeneity of β-Thalassemia in the Kohat Region, Khyber Pakhtunkhwa Province, Pakistan. | Naz S, Rehman SU, Shakeel M, Rehman H, Hussain M, Haider A | Hemoglobin | 2020 |
| Increased Bone Marrow F-Choline Uptake in a Patient with Hepatocellular Carcinoma and Thalassemia Intermedia | Filippi L | Mol Imaging Radionucl Ther | 2020 |
| Corrigendum to | Valente-Frossard TNS, Cruz NRC, Ferreira FO, Belisario AR, Pereira BM, de Freitas Gomides AF, Resende GAD, Carlos AM, Moraes-Souza H, Velloso-Rodrigues C | Blood Cells Mol. Dis. | 2020 |
| Genetic polymorphisms of HbE/beta thalassemia related to clinical presentation: implications for clinical diversity. | Azman NF, Abdullah WZ, Hanafi S, Diana R, Bahar R, Johan MF, Zilfalil BA, Hassan R | Ann. Hematol. | 2020 |
| α-Thalassemia Mutations in Ilam Province, West Iran. | Moradi K, Aznab M, Azimi A, Biglari M, Shafieenia S, Alibakhshi R | Hemoglobin | 2020 |
| Microcytic anemia in children: parallel screening for iron deficiency and thalassemia provides a useful opportunity for thalassemia prevention in low- and middle-income countries. | Mettananda S, Paranamana S, Fernando R, Suranjan M, Rodrigo R, Perera L, Vipulaguna T, Fernando P, Fernando M, Dayanath BKTP, Costa Y, Premawardhena A | Pediatr Hematol Oncol | 2020 |
| Hemoglobin F mitigation of sickle cell complications decreases with aging. | Tolu SS, Reyes-Gil M, Ogu UO, Thomas M, Bouhassira EE, Minniti CP | Am. J. Hematol. | 2020 |
| The association of psychiatric comorbidities with emergency visits and hospitalisations in adult sickle-cell patients: a cohort study. | Fayand A, Dzierzynski N, Georgin-Lavialle S, Bachmeyer C, Mattioni S, Stankovic-Stojanovic K, Lionnet F, Steichen O | Br. J. Haematol. | 2020 |
| Students' knowledge on sickle cell disease in Kisangani, Democratic Republic of the Congo. | Kambale-Kombi P, Marini Djang'eing'a R, Alworong'a Opara JP, Tonen-Wolyec S, Kayembe Tshilumba C, Batina-Agasa S | Hematology | 2020 |
| Two Rare Pathogenic Variants in a Patient with β-Thalassemia Intermedia | Hançer VS, Fışgın T, Büyükdoğan M | Turk J Haematol | 2020 |
| Association of polymorphisms in the HBG1-HBD intergenic region with HbF levels. | Hu L, Huang L, Han Y, Jin T, Liu J, Jiang M, Liu X, Li Y, Han W, An B, Huang S | J. Clin. Lab. Anal. | 2020 |
| Effects of the dual sodium-glucose linked transporter inhibitor, licogliflozin vs placebo or empagliflozin in patients with type 2 diabetes and heart failure. | de Boer RA, Núñez J, Kozlovski P, Wang Y, Proot P, Keefe D | Br J Clin Pharmacol | 2020 |
| Recent insight on improving the iron chelation efficacy of deferasirox by adjuvant therapy in transfusion dependent beta thalassemia children with sluggish response. | Hamed EM, Meabed MH, Hussein RRS, Aly UF | Expert Opin Drug Metab Toxicol | 2020 |
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| Clinical Utility of Confirmatory Genetic Testing to Differentiate Sickle Cell Trait from Sickle-β-Thalassemia by Newborn Screening. | Shook LM, Haygood D, Quinn CT | Int J Neonatal Screen | 2020 |
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| Beta thalassemia major and Noonan syndrome - Two genetic disorders manifest in the blood film. | Tseu B, Siow W, Pushkaran B, Cheesebrough B, Bain BJ | Am. J. Hematol. | 2020 |
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| Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China. | Jiang F, Zuo L, Li D, Li J, Tang X, Chen G, Zhou J, Lu H, Liao C | BMC Med. Genet. | 2020 |
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| Association of hemoglobinosis D-Punjab and β-thalassemia in a Moroccan family. | Saoud MZ, Biaz A, Rachid A, El Amin G, Dami A, Ouzzif Z | Ann. Biol. Clin. (Paris) | 2020 |
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| High bias and low precision for estimated versus measured glomerular filtration rate in pediatric sickle cell anemia. | Lebensburger JD, Gossett J, Zahr R, Wang WC, Ataga KI, Estepp JH, Kang G, Hankins JS | Haematologica | 2020 |
| The Coup-TFII orphan nuclear receptor is an activator of the γ-globin gene. | Fugazza C, Barbarani G, Elangovan S, Marini MG, Giolitto S, Font-Monclus I, Marongiu MF, Manunza L, Strouboulis J, Cantù C, Gasparri F, Barabino SML, Nakamura Y, Ottolenghi S, Moi P, Ronchi AE | Haematologica | 2020 |
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| Association between hydroxycarbamide exposure and neurocognitive function in adolescents with sickle cell disease. | Partanen M, Kang G, Wang WC, Krull K, King AA, Schreiber JE, Porter JS, Hodges J, Hankins JS, Jacola LM | Br. J. Haematol. | 2020 |
| Attention difficulties are associated with lower engagement in adult care amongst youth with sickle cell disease. | Ali JS, Andrasik F, Berlin KS, Porter J, Hankins J, Anderson S, Schreiber JE | Br. J. Haematol. | 2020 |
| Changes in Mean Corpuscular Volume and RBC Distribution Width Predict Erythrocyte Engraftment Following ABO-Incompatible Hematopoietic Stem Cell Transplantation. | Sanford K, Case N, Blake B, Michaud T, McPherson RA, Roseff SD | Am. J. Clin. Pathol. | 2020 |
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| Improved health care utilization and costs in transplanted versus non-transplanted adults with sickle cell disease. | Saraf SL, Ghimire K, Patel P, Sweiss K, Gowhari M, Molokie RE, Gordeuk VR, Rondelli D | PLoS ONE | 2020 |
| A novel non-invasive prenatal sickle cell disease test for all at-risk pregnancies. | van Campen J, Silcock L, Yau S, Daniel Y, Ahn JW, Ogilvie C, Mann K, Oteng-Ntim E | Br. J. Haematol. | 2020 |
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| Editing a γ-globin repressor binding site restores fetal hemoglobin synthesis and corrects the sickle cell disease phenotype. | Weber L, Frati G, Felix T, Hardouin G, Casini A, Wollenschlaeger C, Meneghini V, Masson C, De Cian A, Chalumeau A, Mavilio F, Amendola M, Andre-Schmutz I, Cereseto A, El Nemer W, Concordet JP, Giovannangeli C, Cavazzana M, Miccio A | Sci Adv | 2020 |
| Profound Presentation of Retinopathy in a Patient with Sickle Cell Trait and Diabetes Mellitus. | Vangipuarm G, Saraf SS, Zhang Q, Wang R, Rezaei KA | J Ophthalmic Vis Res | 2020 |
| The Effect of Serum Ferritin Level on Gonadal, Prolactin, Thyroid Hormones, and Thyroid Stimulating Hormone in Adult Males with Sickle Cell Anemia. | Mostafa GG, Zahran FE, Omer SA, Ibrahim A, Elhakeem H | J Blood Med | 2020 |
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| Atypical presentation of acute post-infectious glomerulonephritis in patients with sickle cell disease: report of two cases. | de Menezes Neves PDM, Reichert BV, Bridi RA, Yu L, Dias CB, Pinheiro RBB, de Abreu Testagrossa L, Cavalcante LB, Malheiros DMAC, Jorge LB, Woronik V | BMC Nephrol | 2020 |
| ERFE regulation in sickle cell disease: complex but promising. | Girelli D, Busti F | Br. J. Haematol. | 2020 |
| Prevalence of Hemoglobinopathies (β-Thalassemia and Sickle Cell Trait) in the Adult Population of Al Majma'ah, Saudi Arabia. | Mir SA, Alshehri BM, Alaidarous M, Banawas SS, Dukhyil AAAB, Alturki MK | Hemoglobin | 2020 |
| Sickle Cell Disease is Associated with Increased Morbidity, Resource Utilization, and Readmissions after Common Abdominal Surgeries: A Multistate Analysis, 2007-2014. | Brumm J, White RS, Arroyo NS, Gaber-Baylis LK, Gupta S, Turnbull ZA, Mehta N | J Natl Med Assoc | 2020 |
| Correlation of lipid peroxidation and nitric oxide metabolites, trace elements, and antioxidant enzymes in patients with sickle cell disease. | Antwi-Boasiako C, Dankwah GB, Aryee R, Hayfron-Benjamin C, Aboagye G, Campbell AD | J. Clin. Lab. Anal. | 2020 |
| The association between vitamin D deficiency and hospitalization outcomes in pediatric patients with sickle cell disease. | Brown B, Long K, Agdere L, Kulpa J, Zarzoso-Fernandez S, Choudhary D, Sundarum R | Blood Cells Mol. Dis. | 2020 |
| When basic science reaches into rational therapeutic design: from historical to novel leads for the treatment of β-globinopathies. | Andrieu-Soler C, Soler E | Curr. Opin. Hematol. | 2020 |
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| Oxidative stress assessment in sickle cell anemia patients treated with hydroxyurea. | Renó CO, Barbosa AR, de Carvalho SS, Pinheiro MB, Rios DR, Cortes VF, Barbosa LA, Santos HL | Ann. Hematol. | 2020 |
| Treating sickle cell anemia. | Tisdale JF, Thein SL, Eaton WA | Science | 2020 |
| Genetic epidemiology of beta-thalassemia in the Maldives: 23 years of a beta-thalassemia screening program. | Mustafa I, Firdous N, Shebl FM, Shi Z, Saeed M, Zahir Z, Zayed H | Gene | 2020 |
| Phenylethanolamine -methyltransferase gene polymorphisms associate with crisis pain in sickle cell disease patients. | Sadhu N, Jhun EH, Posen A, Yao Y, He Y, Molokie RE, Wilkie DJ, Wang ZJ | Pharmacogenomics | 2020 |
| Indicators of male fertility potential in adult patients with beta-thalassemia major: a comparative study between patients undergone allogeneic stem cell transplantation and transfusion-dependent patients. | Rostami T, Mohammadifard MA, Ansari S, Kiumarsi A, Maleki N, Kasaeian A, Aghamahdi F, Rad S, Ghavamzadeh A | Fertil Res Pract | 2020 |
| Validation of the breathmobile case identification survey for asthma screening in children with sickle cell disease. | Patel AP, Krupani S, Stark JM, Mosquera RA, Waller DK, Gonzales T, Brown DL, Nguyen TT, Jon CK, Yadav A | J Asthma | 2020 |
| SPATIAL DISTRIBUTION OF NEWBORNS WITH SICKLE CELL TRAIT IN SERGIPE, BRAZIL. | Leite DCF, Cipolotti R, Gurgel RQ, Martins Filho PRS, Lopes GD | Rev Paul Pediatr | 2020 |
| Laboratory Biomarkers, Cerebral Blood Flow Velocity, and Intellectual Function in Children with Sickle Cell Disease. | Apollonsky N, Lerner NB, Zhang F, Raybagkar D, Eng J, Tarazi R | Adv Hematol | 2020 |
| Parental Knowledge on Thalassaemia and Factors Associated with Refusal to Screen Their Children. | Mat MAC, Yaacob LH, Zakaria R | Malays J Med Sci | 2020 |
| A Case of Hemoglobin Sickle-D Punjab. | Ali W, Jain M, Agarwal S, Kumar A | Indian J Hematol Blood Transfus | 2020 |
| Hemoglobin Henri Mondor [β26(B8) Glu → Val, GAG > GTG], A First Case Report in South-East Asia. | Panyasai S, Jaiping K, Khantarag P, Pornprasert S | Indian J Hematol Blood Transfus | 2020 |
| Key Determinants of Phenotypic Heterogeneity of Hb E/β Thalassemia: A Comparative Study from Eastern India. | Kalantri SA, Ray R, Choudhuri S, Roy S, Bhattacharyya M | Indian J Hematol Blood Transfus | 2020 |
| Phenotypic Diversity and Clinico-Hematological Profile of Hb E-Beta Thalassemic Children. | Baruah A, Baruah MK | Indian J Hematol Blood Transfus | 2020 |
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| The role of HLA matching in unrelated donor hematopoietic stem cell transplantation for sickle cell disease in Europe. | Gluckman E, Fuente J, Cappelli B, Scigliuolo GM, Volt F, Tozatto-Maio K, Rocha V, Tommaso M, O'Boyle F, Smiers F, Cunha-Riehm CBD, Calore E, Bonanomi S, Graphakos S, Paisiou A, Albert MH, Ruggeri A, Zecca M, Lankester AC, Corbacioglu S, | Bone Marrow Transplant. | 2020 |
| Cardiomyopathy in Thalassemia: Quick Review from Cellular Aspects to Diagnosis and Current Treatments. | Ghanavat M, Haybar H, Pezeshki SMS, Shahjahani M, Jodat H, Elyasi M, Saki N | Lab Med | 2020 |
| The mRNA-Binding Protein IGF2BP1 Restores Fetal Hemoglobin in Cultured Erythroid Cells from Patients with β-Hemoglobin Disorders. | Chambers CB, Gross J, Pratt K, Guo X, Byrnes C, Lee YT, Lavelle D, Dean A, Miller JL, Wilber A | Mol Ther Methods Clin Dev | 2020 |
| Life-Threatening Infectious Complications in Sickle Cell Disease: A Concise Narrative Review. | Ochocinski D, Dalal M, Black LV, Carr S, Lew J, Sullivan K, Kissoon N | Front Pediatr | 2020 |
| Fetal subdural hematoma, sickle cell disease and storage pool disease: A case report. | Iannaccone A, Darkwah Oppong M, Dammann P, Kimmig R, Köninger A | Case Rep Womens Health | 2020 |
| Eleven healthy live births: a result of simultaneous preimplantation genetic testing of α- and β-double thalassemia and aneuploidy screening. | Chen D, Shen X, Wu C, Xu Y, Ding C, Zhang G, Xu Y, Zhou C | J. Assist. Reprod. Genet. | 2020 |
| Novel High Oxygen Affinity Hemoglobin Variant in a Patient with Polycythemia: Hb Kennisis [β85(F1)Phe→Leu (TT>TT); : c.258T>G]. | Nabhani IA, Aneke JC, Verhovsek M, Eng B, Kuo KHM, Rudinskas LC, Waye JS | Hemoglobin | 2020 |
| Osteoarticular infections in paediatric sickle cell disease: in the era of multidrugresistant bacteria. | Gouveia C, Duarte M, Norte S, Alves P, Kjöllerström P, Brito M, Tavares D | Br. J. Haematol. | 2020 |
| Impact of Medicaid expansion on access and healthcare among individuals with sickle cell disease. | Kayle M, Valle J, Paulukonis S, Holl JL, Tanabe P, French DD, Garg R, Liem RI, Badawy SM, Treadwell MJ | Pediatr Blood Cancer | 2020 |
| MINOCA in a Patient with Sickle Cell Disease. | Lee S, Kaplin S, Tamis-Holland J, Talebi S | Am. J. Med. | 2020 |
| Vitamin D supplementation and pain-related emergency department visits in children with sickle cell disease. | Hood AM, Quinn CT, King CD, Shook LM, Peugh JL, Crosby LE | Complement Ther Med | 2020 |
| Review/overview of pain in sickle cell disease. | Ballas SK, Darbari DS | Complement Ther Med | 2020 |
| Incorporating integrative medicine and patient preferences into a pilot interdisciplinary sickle cell wellness clinic. | Junghans-Rutelonis AN, Moquist KL, Blaylark RM, Anderson N, Brown ML | Complement Ther Med | 2020 |
| Preliminary evaluation of the clinical implementation of cognitive-behavioral therapy for chronic pain management in pediatric sickle cell disease. | Sil S, Lai K, Lee JL, Gilleland Marchak J, Thompson B, Cohen L, Lane P, Dampier C | Complement Ther Med | 2020 |
| Autonomically-mediated decrease in microvascular blood flow due to mental stress and pain in sickle cell disease: A target for neuromodulatory interventions. | Martin SR, Shah P, Denton C, Zeltzer LK, Veluswamy S, Khoo MCK, Coates TD | Complement Ther Med | 2020 |
| A Comprehensive Review of the Treatment and Management of Pain in Sickle Cell Disease. | Fiocchi J, Urits I, Orhurhu V, Orhurhu MS, Giacomazzi S, Hoyt B, Kaye AD, Kaye RJ, Viswanath O | Curr Pain Headache Rep | 2020 |
| Matched Family versus Alternative Donor Hematopoietic Stem Cell Transplantation for Patients with Thalassemia Major: Experience from a Tertiary Referral Center in South India. | Swaminathan VV, Uppuluri R, Patel S, Ravichandran N, Ramanan KM, Vaidhyanathan L, Ramakrishnan B, Jayakumar I, Raj R | Biol. Blood Marrow Transplant. | 2020 |
| Motivations and Decision-Making of Adult Sickle Cell Patients in High-Risk Clinical Research. | Cho HL, Kim SYH, Fitzhugh C, Hsieh M, Tisdale J, Grady C | Biol. Blood Marrow Transplant. | 2020 |
| Hb Sun Prairie: A rare cause of chronic hemolysis in an Indian patient. | Jain A, Prasad P, Chaudhry S, Gupta DK, Saluja S | Hematol Oncol Stem Cell Ther | 2020 |
| Prognostic Value of Hyponatremia During Acute Painful Episodes in Sickle Cell Disease. | Rech JS, Yao K, Bachmeyer C, Bailleul S, Javier O, Grateau G, Lionnet F, Steichen O | Am. J. Med. | 2020 |
| Platelet and megakaryocyte CD40L expression in β-Thalassemic patients. | Morsilli O, Guerriero R, Lulli V, Maffei L, Pasquini L, Pulcinelli FM, Sorrentino F, Gabbianelli M | Thromb. Res. | 2020 |
| The changing epidemiology of the ageing thalassaemia populations: A position statement of the Thalassaemia International Federation. | Farmakis D, Giakoumis A, Angastiniotis M, Eleftheriou A | Eur. J. Haematol. | 2020 |
| White matter volume changes in adult beta-thalassemia: Negligible and unrelated to anemia and cognitive performances. | Manara R, Canna A, Caiazza M, Ponticorvo S, Russo AG, Di Concilio R, Ciancio A, De Michele E, Carafa PA, Ammendola F, Roberti D, Casale M, Elefante A, Cirillo M, Di Salle F, Esposito F, Perrotta S, Tartaglione I | Am. J. Hematol. | 2020 |
| Nitrous oxide and vitamin B12 in sickle cell disease: Not a laughing situation. | Desprairies C, Imbard A, Koehl B, Lorrot M, Gaschignard J, Sommet J, Pichard S, Holvoet L, Faye A, Benkerrou M, Benoist JF, Schiff M | Mol Genet Metab Rep | 2020 |
| Using novel magnetic resonance imaging methods to predict stroke risk in individuals with sickle cell anemia. | Jordan LC, Kassim AA, Wilkerson KL, Lee CA, Waddle SL, Donahue MJ | Hematol Oncol Stem Cell Ther | 2020 |
| Editorial commentary: Sickle cell disease: Diagnosing the heart of the matter. | Caughey MC, Novelli EM | Trends Cardiovasc. Med. | 2020 |
| Amino acids and fatty acids in patients with beta thalassemia major. | Koca T, Canatan D, Örmeci AR, Koca YS, Duman H, Baykal A, Akcam M | Acta Biomed | 2020 |
| Mechanisms underlying priapism in sickle cell disease: targeting and key innovations on the preclinical landscape. | Musicki B, Burnett AL | Expert Opin. Ther. Targets | 2020 |
| Impaired bile secretion promotes hepatobiliary injury in Sickle Cell Disease. | Vats R, Liu S, Zhu J, Mukhi D, Tutuncuoglu E, Cardenes N, Singh S, Brzoska T, Kosar K, Bamne M, Jonassaint J, Adebayo Michael A, Watkins SC, Hillery C, Ma X, Nejak-Bowen K, Rojas M, Gladwin MT, Kato GJ, Ramakrishnan S, Sundd P, Monga SP, Pradhan-Sundd T | Hepatology | 2020 |
| A Quality Initiative to Decrease Time to Antibiotics in Children with Sickle Cell Disease and Fever. | McKinney C, Caruso-Brown A, Montgomery K, Gillespie A, Coughlin R, Law D, Brouwer A, Tytler L, Hilden J, Nuss R | Pediatr Qual Saf | 2020 |
| Beta-Thalassemia Intermedia: A Single Thalassemia Center Experience from Northeastern Iraq. | Amin SS, Jalal SD, Ali KM, Mohammed AI, Rasool LK, Osman TJ | Biomed Res Int | 2020 |
| Identification of seven novel variants in the β-globin gene in transfusion-dependent and normal patients. | Aldakeel SA, Ghanem NZ, Al-Amodi AM, Osman AK, Al Asoom LI, Ahmed NR, Almandil NB, Akhtar MS, Azeez SA, Borgio JF | Arch Med Sci | 2020 |
| Sickle cell disease presenting in the third trimester of pregnancy: Delayed detection heralding a public health problem? | Sharma A, Gaur K, Tiwari VP, Shukla S | Indian J Public Health | 2020 |
| Iron overload and periodontal status in patients with sickle cell anaemia: A case series. | Costa SA, Moreira ARO, Costa CPS, Carvalho Souza SF | J. Clin. Periodontol. | 2020 |
| Hemoglobin: Structure, Function and Allostery. | Ahmed MH, Ghatge MS, Safo MK | Subcell. Biochem. | 2020 |
| Sickle Cell Hemoglobin. | Mandal AK, Mitra A, Das R | Subcell. Biochem. | 2020 |
| Embryonic and Fetal Human Hemoglobins: Structures, Oxygen Binding, and Physiological Roles. | Manning JM, Manning LR, Dumoulin A, Padovan JC, Chait B | Subcell. Biochem. | 2020 |
| Potential Contribution of Pulmonary Thromboembolic Disease in Pulmonary Hypertension in Sickle Cell Disease. | Nouraie M, Zhang X, Srisuwananukorn A, Machado RF, Gordeuk VR, Gladwin MT, Saraf S | Ann Am Thorac Soc | 2020 |
| Failure of response to combination therapy of adalimumab and infliximab in a recalcitrant patient of severe psoriasis and major thalassemia: A case report. | Goldust M, Rahmatpour Rokni G, Gupta M, Lotti T, Bathaei M | Clin Case Rep | 2020 |
| Outcome of short-term emergency department observation care of children with sickle cell disease and vaso-occlusive crises: initial experience from south-western Nigeria. | Adegoke SA, Oladimeji OI, Ologun BG, Aladekomo TA, Oyelami OA | Trans. R. Soc. Trop. Med. Hyg. | 2020 |
| Characteristics and Prognosis of Hepatocellular Carcinoma in Multi-Transfused Patients with β-Thalassemia. Experience of a Single Tertiary Center. | Papadopoulos N, Kountouras D, Malagari K, Tampaki M, Theochari M, Koskinas J | Mediterr J Hematol Infect Dis | 2020 |
| Lower white matter volume in beta-thalassemia associated with anemia and cognitive performance. | Choi S, Leahy RM, Wood JC | Am. J. Hematol. | 2020 |
| Re: Abnormally Low Hemoglobin A1c as Harbinger of Hemoglobinopathy. | Mungmungpuntipantip R, Wiwanitkit V, Bitencourt SE, Rodrigues de Aguiar D, Baggio A, Marcon CEM | J Am Board Fam Med | 2020 |
| Ambient air pollution and sickle cell disease-related emergency department visits in Atlanta, GA. | Blumberg AH, Ebelt ST, Liang D, Morris CR, Sarnat JA | Environ. Res. | 2020 |
| Salbutamol Worsens the Autonomic Nervous System Dysfunction of Children With Sickle Cell Disease. | Bokov P, El Jurdi H, Denjoy I, Peiffer C, Medjahdi N, Holvoet L, Benkerrou M, Delclaux C | Front Physiol | 2020 |
| Hb S/-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics. | Belisário AR, Carneiro-Proietti AB, Sabino EC, Araújo A, Loureiro P, Máximo C, Flor-Park MV, Rodrigues DDOW, Ozahata MC, McClure C, Mota RA, Gomes Moura IC, Custer B, Kelly S, | Hemoglobin | 2020 |
| Paediatric to adult transition care for patients with sickle cell disease: a global perspective. | Inusa BPD, Stewart CE, Mathurin-Charles S, Porter J, Hsu LL, Atoyebi W, De Montalembert M, Diaku-Akinwumi I, Akinola NO, Andemariam B, Abboud MR, Treadwell M | Lancet Haematol | 2020 |
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| Comparison of US Federal and Foundation Funding of Research for Sickle Cell Disease and Cystic Fibrosis and Factors Associated With Research Productivity. | Farooq F, Mogayzel PJ, Lanzkron S, Haywood C, Strouse JJ | JAMA Netw Open | 2020 |
| Heme A1M'ed at the kidney in sickle cell disease. | Saraf SL | Blood | 2020 |
| Iron homeostasis in a mouse model of thalassemia intermedia is altered between adolescence and adulthood. | Sanyear C, Butthep P, Eamsaard W, Fucharoen S, Svasti S, Masaratana P | PeerJ | 2020 |
| Renal medullary carcinoma and its association with sickle cell trait: a case report and literature review. | Holland P, Merrimen J, Pringle C, Wood LA | Curr Oncol | 2020 |
| Fibroblast Growth Factor 23 (FGF23) and Klotho Protein in Beta-Thalassemia. | Stefanopoulos D, Nasiri-Ansari N, Dontas I, Vryonidou A, Galanos A, Psaridi L, Fatouros IG, Mastorakos G, Papavassiliou AG, Kassi E, Tournis S | Horm. Metab. Res. | 2020 |
| Iron and Heart Failure: Diagnosis, Therapies, and Future Directions. | Ghafourian K, Shapiro JS, Goodman L, Ardehali H | JACC Basic Transl Sci | 2020 |
| A Phase 3 Trial of Luspatercept in Patients with Transfusion-Dependent β-Thalassemia. | Cappellini MD, Viprakasit V, Taher AT, Georgiev P, Kuo KHM, Coates T, Voskaridou E, Liew HK, Pazgal-Kobrowski I, Forni GL, Perrotta S, Khelif A, Lal A, Kattamis A, Vlachaki E, Origa R, Aydinok Y, Bejaoui M, Ho PJ, Chew LP, Bee PC, Lim SM, Lu MY, Tantiworawit A, Ganeva P, Gercheva L, Shah F, Neufeld EJ, Thompson A, Laadem A, Shetty JK, Zou J, Zhang J, Miteva D, Zinger T, Linde PG, Sherman ML, Hermine O, Porter J, Piga A, | N. Engl. J. Med. | 2020 |
| Quantifying Areas of Vascular Leakage in Sickle Cell Retinopathy Using Standard and Widefield Fluorescein Angiography. | Barbosa J, Malbin B, Le K, Lin X | Ophthalmic Surg Lasers Imaging Retina | 2020 |
| Phase 2 trial of montelukast for prevention of pain in sickle cell disease. | Field JJ, Kassim A, Brandow A, Embury SH, Matsui N, Wilkerson K, Bryant V, Zhang L, Simpson P, DeBaun MR | Blood Adv | 2020 |
| Leukocyte adhesion to P-selectin and the inhibitory role of Crizanlizumab in sickle cell disease: A standardized microfluidic assessment. | Man Y, Goreke U, Kucukal E, Hill A, An R, Liu S, Bode A, Solis-Fuentes A, Nayak LV, Little JA, Gurkan UA | Blood Cells Mol. Dis. | 2020 |
| Gene editing and CRISPR in the clinic: current and future perspectives. | Hirakawa MP, Krishnakumar R, Timlin JA, Carney JP, Butler KS | Biosci. Rep. | 2020 |
| Catheter associated thromboses in patients with sickle cell anaemia and dual lumen Vortex apheresis ports are common and can be clinically asymptomatic. | Brewin JN, Crowley MP, Kesse-Adu R, Stuart-Smith S, Awogbade M, Howard J | Br. J. Haematol. | 2020 |
| Longitudinal Description of Gonadal Function in Sickle-Cell Patients Treated With Hematopoietic Stem Cell Transplant Using Alkylator-based Conditioning Regimens. | Elchuri SV, Williamson Lewis R, Quarmyne MO, Haight AE, Cottrell HN, Meacham LR | J. Pediatr. Hematol. Oncol. | 2020 |
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| Current and future gene therapies for hemoglobinopathies. | Brendel C, Williams DA | Curr. Opin. Hematol. | 2020 |
| Haploidentical bone marrow transplant with posttransplant cyclophosphamide for sickle cell disease: An update. | Patel DA, Akinsete AM, de la Fuente J, Kassim AA | Hematol Oncol Stem Cell Ther | 2020 |
| Hematopoietic stem cell transplantation for patients with sickle cell disease in the Eastern Mediterranean. | Alahmari AD, Aljurf M, Alseraihy A, Hamidieh AA, Alkindi S, Rihani R, Satti T, Jastaniah W, Alsaedi H, Almohareb F, Al-Jefri A, Rasheed W | Hematol Oncol Stem Cell Ther | 2020 |
| Is sickle cell disease-related neurotoxicity a systemic endotheliopathy? | Palomo M, Diaz-Ricart M, Carreras E | Hematol Oncol Stem Cell Ther | 2020 |
| Alternative donor: αß/CD19 T-cell-depleted haploidentical hematopoietic stem cell transplantation for sickle cell disease. | Foell J, Kleinschmidt K, Jakob M, Troeger A, Corbacioglu S | Hematol Oncol Stem Cell Ther | 2020 |
| Standard management of sickle cell disease complications. | Abboud MR | Hematol Oncol Stem Cell Ther | 2020 |
| Status quo of allogeneic stem cell transplantation for patients with sickle cell disease using matched unrelated donors. | Oevermann L, Sodani P | Hematol Oncol Stem Cell Ther | 2020 |
| What is the place of hematopoietic stem cell transplantation in the management of cerebral vasculopathy in children with sickle cell anemia? | Bernaudin F | Hematol Oncol Stem Cell Ther | 2020 |
| Proceeding of the European Group for Blood and Marrow Transplantation (EBMT) congress on sickle cell disease, 16-17 may 2019, Regensburg, Germany: What is the impact of antithymocyte globulin pharmacokinetics on haploidentical hematopoietic stem cell transplantation? | Oostenbrink LVE, Jol-van der Zijde CM, Jansen-Hoogendijk AM, Pool ES, van Halteren AGS, Moes DJAR, Bredius RGM, Mohseny AB, Smiers FJW, van Tol MJD, Schilham MW, Lankester AC | Hematol Oncol Stem Cell Ther | 2020 |
| Alternative donor hematopoietic stem cell transplantation for sickle cell disease in Europe. | Gluckman E, Cappelli B, Scigliuolo GM, De la Fuente J, Corbacioglu S | Hematol Oncol Stem Cell Ther | 2020 |
| How to setup a successful transplant program for hemoglobinopathies in developing countries: The Cure2Children approach. | Faulkner L | Hematol Oncol Stem Cell Ther | 2020 |
| Curative options for sickle cell disease in Africa: Approach in Tanzania. | Makani J, | Hematol Oncol Stem Cell Ther | 2020 |
| The effect of transfusion on immune responses in thalassemia. | Politou M, Komninaka V, Valsami S, Kapsimali V, Pouliakis A, Koutsouri T, Panayiotakopoulos G, Kotsianidis I, Voskaridou E | Blood Cells Mol. Dis. | 2020 |
| Tandem P-selectin glycoprotein ligand immunoglobulin prevents lung vaso-occlusion in sickle cell disease mice. | Vats R, Tutuncuoglu E, Pradhan-Sundd T, Tejero J, Shaw GD, Sundd P | Exp. Hematol. | 2020 |
| COVID-19 pneumonia as a cause of acute chest syndrome in an adult sickle cell patient. | Beerkens F, John M, Puliafito B, Corbett V, Edwards C, Tremblay D | Am. J. Hematol. | 2020 |
| Tricuspid regurgitation velocity and other biomarkers of mortality in children, adolescents and young adults with sickle cell disease in the United States: The PUSH study. | Nouraie M, Darbari DS, Rana S, Minniti CP, Castro OL, Luchtman-Jones L, Sable C, Dham N, Kato GJ, Gladwin MT, Ensing G, Arteta M, Campbell A, Taylor JG, Nekhai S, Gordeuk VR | Am. J. Hematol. | 2020 |
| Clinicopathologic consequences following discontinuation of rifaximin in patients with sickle cell disease. | Lim SH, Dutta D | Am. J. Hematol. | 2020 |
| Rate of Food Insecurity Among Households with Children with Sickle Cell Disease is Above the National Average. | Ghafuri DL, Rodeghier M, DeBaun MR | South. Med. J. | 2020 |
| Pulmonary thromboendarterectomy in patients with chronic thromboembolic pulmonary hypertension and hemoglobinopathies. | Sousa ACC, Campos FTAF, Bernardes RC, Ivo MB, Corrêa RA | J Bras Pneumol | 2020 |
| The Sickle Cell Disease Multidisciplinary Clinic at the Lifespan Cancer Institute. | Sokolic R | R I Med J (2013) | 2020 |
| Outcome of pregnancies among women with sickle cell disease. | Nkwabong E, Ngoundjou Dongmo P, Tayou C, Nana Njamen T | J. Matern. Fetal. Neonatal. Med. | 2020 |
| Increased iron stores influence glucose metabolism in sickle cell anaemia. | Shah BN, Hassan TO, Zhang X, McClain DA, Gordeuk VR | Br. J. Haematol. | 2020 |
| Stress and the Home Environment in Caregivers of Children with Sickle Cell. | Varughese TE, Hoyt CR, L'Hotta AJ, Ikemenogo PA, Howdeshell SG, Housten AJ, Abel RA, King AA | J Pediatr Psychol | 2020 |
| Hardy-Weinberg Equilibrium in the Large Scale Genomic Sequencing Era. | Abramovs N, Brass A, Tassabehji M | Front Genet | 2020 |
| The Red Blood Cell-Inflammation Vicious Circle in Sickle Cell Disease. | Nader E, Romana M, Connes P | Front Immunol | 2020 |
| Generation of hematopoietic stem/progenitor cells with sickle cell mutation from induced pluripotent stem cell in serum-free system. | Paes BCMF, Stabeli LCJR, Costa PNM, Orellana MD, Kashima S, Covas DT, Picanço-Castro V | Hematol Transfus Cell Ther | 2020 |
| Association between HLA-DRB1*01 and HLA-DRB1*15 with alloimmunisation in transfusion-dependent patients with thalassaemia. | Ebrahimi M, Dayer D, Jalalifar MA, Keikhaei B, Tahan Nejad Asadi Z | Transfus Med | 2020 |
| Prolonged Weakness and Paresthesia After Revision Total Hip Arthroplasty in a Patient with Sickle Cell Anemia Receiving Spinal Anesthesia: A Case Report. | Yancey HB, Langfitt MK | JBJS Case Connect | 2020 |
| The Effect of Progressive Muscle Relaxation Exercises on Pain on Patients with Sickle Cell Disease: Randomized Controlled Study. | Kazak A, Ozkaraman A | Pain Manag Nurs | 2020 |
| Diagnosis support of sickle cell anemia by classifying red blood cell shape in peripheral blood images. | Delgado-Font W, Escobedo-Nicot M, González-Hidalgo M, Herold-Garcia S, Jaume-I-Capó A, Mir A | Med Biol Eng Comput | 2020 |
| New haematologic score to discriminate beta thalassemia trait from iron deficiency anaemia in a Spanish Mediterranean region. | Carla MG, Rafael SP, Isabel FG, Cristina GF, Teresa SM | Clin. Chim. Acta | 2020 |
| Patient and family experience with chronic transfusion therapy for sickle cell disease: A qualitative study. | Hawkins LM, Sinha CB, Ross D, Yee MEM, Quarmyne MO, Krishnamurti L, Bakshi N | BMC Pediatr | 2020 |
| The vaso-occlusive pain crisis in sickle cell disease: Definition, pathophysiology, and management. | Darbari DS, Sheehan VA, Ballas SK | Eur. J. Haematol. | 2020 |
| Preclinical Evaluation of a Novel Lentiviral Vector Driving Lineage-Specific BCL11A Knockdown for Sickle Cell Gene Therapy. | Brendel C, Negre O, Rothe M, Guda S, Parsons G, Harris C, McGuinness M, Abriss D, Tsytsykova A, Klatt D, Bentler M, Pellin D, Christiansen L, Schambach A, Manis J, Trebeden-Negre H, Bonner M, Esrick E, Veres G, Armant M, Williams DA | Mol Ther Methods Clin Dev | 2020 |
| The HRI-regulated transcription factor ATF4 activates BCL11A transcription to silence fetal hemoglobin expression. | Huang P, Peslak SA, Lan X, Khandros E, Yano JA, Sharma M, Keller CA, Giardine B, Qin K, Abdulmalik O, Hardison RC, Shi J, Blobel GA | Blood | 2020 |
| American Society of Hematology 2020 guidelines for sickle cell disease: prevention, diagnosis, and treatment of cerebrovascular disease in children and adults. | DeBaun MR, Jordan LC, King AA, Schatz J, Vichinsky E, Fox CK, McKinstry RC, Telfer P, Kraut MA, Daraz L, Kirkham FJ, Murad MH | Blood Adv | 2020 |
| Development of a genomic DNA reference material panel for thalassemia genetic testing. | Yin Z, Qu S, Huang C, Chen F, Li J, Chen S, Ye J, Yang Y, Zheng Y, Zhang X, Yang X, Xie L, Wei J, Wei F, Guo J, Huang J | Int J Lab Hematol | 2020 |
| Biallelic rare 17 bp deletion mutation (HBB:c.380_396 del TGCAGGCTGCCTATCAG) in a transfusion depended form of thalassemia. | Tripathi P, Agarwal S, Gupta A, Mandal K | Ann. Hematol. | 2020 |
| Total hip arthroplasty in sickle cell disease: a systematic review. | Kenanidis E, Kapriniotis K, Anagnostis P, Potoupnis M, Christofilopoulos P, Tsiridis E | EFORT Open Rev | 2020 |
| Prenatal diagnosis of rare genetic conditions at a tertiary care hospital in Karachi. | Karim K, Dileep D, Munim S | J Pak Med Assoc | 2020 |
| Sickle Cell Disease: Metabolomic Profiles of Vaso-Occlusive Crisis in Plasma and Erythrocytes. | Dembélé KC, Veyrat-Durebex C, Aldiouma G, Chupin S, Tessier L, Goïta Y, Baraïka MA, Diallo M, Touré BA, Homedan C, Mirebeau-Prunier D, Simard G, Diallo D, Cissé BM, Reynier P, Chao de la Barca JM | J Clin Med | 2020 |
| Progression of albuminuria in patients with sickle cell anemia: a multicenter, longitudinal study. | Niss O, Lane A, Asnani MR, Yee ME, Raj A, Creary S, Fitzhugh C, Bodas P, Saraf SL, Sarnaik S, Devarajan P, Malik P | Blood Adv | 2020 |
| Changes in Pain and Psychosocial Functioning and Transition to Chronic Pain in Pediatric Sickle Cell Disease: A Cohort Follow-up Study. | Sil S, Cohen LL, Bakshi N, Watt A, Hathaway M, Abudulai F, Dampier C | Clin J Pain | 2020 |
| Tilt-table Echocardiography Unmasks Early Diastolic Dysfunction in Patients With Hemoglobinopathies. | Mah K, Bruce A, Zahari N, Venner MA, Chow K, Thompson RB, Khoo NS, Tham EB | J. Pediatr. Hematol. Oncol. | 2020 |
| Parental Notification Via Text Messaging for Infant Sickle Screening Programs: Exploration of Feasibility and Acceptability in Uganda. | Fashakin V, Mathur S, Kwagala P, Mupere E, Kiguli S, Kitaka SB, Henry MB, Van Ells L, Tusuubira S, Mulumba L, Duong J, Stockwell MS, LaRussa P, Green NS | J. Pediatr. Hematol. Oncol. | 2020 |
| Leg Ulcers in Sickle-Cell Disease: Treatment Update. | Monfort JB, Senet P | Adv Wound Care (New Rochelle) | 2020 |
| Therapeutic base editing of human hematopoietic stem cells. | Zeng J, Wu Y, Ren C, Bonanno J, Shen AH, Shea D, Gehrke JM, Clement K, Luk K, Yao Q, Kim R, Wolfe SA, Manis JP, Pinello L, Joung JK, Bauer DE | Nat. Med. | 2020 |
| Directed evolution of adenine base editors with increased activity and therapeutic application. | Gaudelli NM, Lam DK, Rees HA, Solá-Esteves NM, Barrera LA, Born DA, Edwards A, Gehrke JM, Lee SJ, Liquori AJ, Murray R, Packer MS, Rinaldi C, Slaymaker IM, Yen J, Young LE, Ciaramella G | Nat. Biotechnol. | 2020 |
| Veno-Venous Extracorporeal Membrane Oxygenation in Adult Patients with Sickle Cell Disease and Acute Chest Syndrome: a Single-Center Experience. | Alashkar F, Herbstreit F, Carpinteiro A, Baum J, Tzalavras A, Aramayo-Singelmann C, Vance C, Lenz V, Gulbins E, Reinhardt D, Beelen DW, Dührsen U, Röth A, Koldehoff M, Liebregts T | Hemoglobin | 2020 |
| Rapid and severe Covid-19 pneumonia with severe acute chest syndrome in a sickle cell patient successfully treated with tocilizumab. | De Luna G, Habibi A, Deux JF, Colard M, Pham Hung d'Alexandry d'Orengiani AL, Schlemmer F, Joher N, Kassasseya C, Pawlotsky JM, Ourghanlian C, Michel M, Mekontso-Dessap A, Bartolucci P | Am. J. Hematol. | 2020 |
| A Chinese Male with Normal Hematological Indices and High Hb A Levels in β-Thalassemia Trait. | Chen YJ, Li YQ, Liu Q, Tang LY, Lv FT | Hemoglobin | 2020 |
| Distribution of Hemoglobinopathy in Nepalese Population. | Shrestha RM, Pandit R, Yadav UK, Das R, Yadav BK, Upreti HC | J Nepal Health Res Counc | 2020 |
| Mitigating the effect of the COVID-19 pandemic on sickle cell disease services in African countries. | Dexter D, Simons D, Kiyaga C, Kapata N, Ntoumi F, Kock R, Zumla A | Lancet Haematol | 2020 |
| Sickle cell disease and malaria: decreased exposure and asplenia can modulate the risk from Plasmodium falciparum. | Mwaiswelo RO, Mawala W, Iversen PO, de Montalembert M, Luzzatto L, Makani J | Malar. J. | 2020 |
| Impact of sickle cell disease on presentation and progression of paediatric HIV: a retrospective cohort study. | Ssenyondwa J, George PE, Carlos Bazo-Alvarez J, Mercedes R, Kanywa JB, Naturinda E, Wasswa PLM, Lubega J | Trop. Med. Int. Health | 2020 |
| Prevalence of priapism in individuals with sickle cell disease and implications on male sexual function. | Alvaia MA, Maia HAADS, Nelli AM, Guimarães COS, Carvalho ESS, Netto JMB, Miranda EP, Gomes CM, Bessa Júnior J | Einstein (Sao Paulo) | 2020 |
| [Gene Diagnosis and Phenotypic Analysis of β-Thalassemia Caused from a Rare Synonymous Mutation CD29 (C>T)]. | Qin DQ, DU L, Ding HK, Wang JC, Yuan TL, Yao CZ, Lan FF | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2020 |
| Multi-Locus Models to Address Hb F Variability in Portuguese β-Thalassemia Carriers. | Manco L, Bento C, Relvas L, Cunha E, Pereira J, Moreira V, Alvarez M, Maia T, Ribeiro ML | Hemoglobin | 2020 |
| Growth pattern in thalassemic children and their correlation with serum ferritin. | Rathaur VK, Imran A, Pathania M | J Family Med Prim Care | 2020 |
| Fertility Concerns and Access to Care for Stem Cell Transplantation Candidates with Sickle Cell Disease. | Mishkin AD, Mapara MY, Barhaghi M, Reshef R | Biol. Blood Marrow Transplant. | 2020 |
| COVID-19 infection in patients with sickle cell disease. | Hussain FA, Njoku FU, Saraf SL, Molokie RE, Gordeuk VR, Han J | Br. J. Haematol. | 2020 |
| Using arterial-venous oxygen difference to guide red blood cell transfusion strategy. | Fogagnolo A, Taccone FS, Vincent JL, Benetto G, Cavalcante E, Marangoni E, Ragazzi R, Creteur J, Volta CA, Spadaro S | Crit Care | 2020 |
| Biventricular Reference Values by Body Surface Area, Age, and Gender in a Large Cohort of Well-Treated Thalassemia Major Patients Without Heart Damage Using a Multiparametric CMR Approach. | Meloni A, Righi R, Missere M, Renne S, Schicchi N, Gamberini MR, Cuccia L, Lisi R, Spasiano A, Roberti MG, Zuccarelli A, Ait-Ali L, Festa P, Aquaro GD, Mangione M, Barra V, Positano V, Pepe A | J Magn Reson Imaging | 2020 |
| SARS-CoV-2 infection in beta thalassemia: Preliminary data from the Italian experience. | Motta I, Migone De Amicis M, Pinto VM, Balocco M, Longo F, Bonetti F, Gianesin B, Graziadei G, Cappellini MD, De Franceschi L, Piga A, Forni GL | Am. J. Hematol. | 2020 |
| L-Glutamine in sickle cell disease. | Cox SE, Hart E, Kirkham FJ, Stotesbury H | Drugs Today | 2020 |
| Establishment and Evaluation of a Novel Method Based on Loop-Mediated Isothermal Amplification for the Rapid Diagnosis of Thalassemia Genes. | Wang WH, Lin M, Li HL, Huang JY, Chen JT, Fang XS, Huang DM, Xi XX, Zhao QF, Song FL, Huang S, Zhong TY | Risk Manag Healthc Policy | 2020 |
| Depression and Anxiety as Moderators of the Pain-Social Functioning Relationship in Youth with Sickle Cell Disease. | Valrie C, Floyd A, Sisler I, Redding-Lallinger R, Fuh B | J Pain Res | 2020 |
| Effect of the Hydoxyurea in Yemeni Transfusion-Dependent β-Thalassemia Patients. | Al-Nood HA, Al-Nood RM, Ghanem NS, Al-Hadi AM | Hemoglobin | 2020 |
| Gut leakage enhances sepsis susceptibility in iron-overloaded β-thalassemia mice through macrophage hyperinflammatory responses. | Visitchanakun P, Saisorn W, Wongphoom J, Chatthanathon P, Somboonna N, Svasti S, Fucharoen S, Leelahavanichkul A | Am. J. Physiol. Gastrointest. Liver Physiol. | 2020 |
| Homocysteine is associated with severity of microvasculopathy in sickle cell disease patients. | Samarron SL, Miller JW, Cheung AT, Chen PC, Lin X, Zwerdling T, Wun T, Green R | Br. J. Haematol. | 2020 |
| High-level induction of fetal haemoglobin by pomalidomide in β-thalassaemia/HbE erythroid progenitor cells. | Khamphikham P, Nualkaew T, Pongpaksupasin P, Kaewsakulthong W, Songdej D, Paiboonsukwong K, Engel JD, Hongeng S, Fucharoen S, Sripichai O, Jearawiriyapaisarn N | Br. J. Haematol. | 2020 |
| Dramatic improvement after tocilizumab of severe COVID-19 in a child with sickle cell disease and acute chest syndrome. | Odièvre MH, de Marcellus C, Ducou Le Pointe H, Allali S, Romain AS, Youn J, Taytard J, Nathan N, Corvol H | Am. J. Hematol. | 2020 |
| A Novel Method to Identify Autoantibodies against Putative Target Proteins in Serum from beta-Thalassemia Major: A Pilot Study. | Sumera A, Anuar ND, Radhakrishnan AK, Ibrahim H, Rutt NH, Ismail NH, Tan TM, Baba AA | Biomedicines | 2020 |
| The Effects of Postprandial Resistance Exercise on Blood Glucose and Lipids in Prediabetic, Beta-Thalassemia Major Patients. | Georgakouli K, Stamperna A, Deli CK, Syrou N, Draganidis D, Fatouros IG, Jamurtas AZ | Sports (Basel) | 2020 |
| The Imperative of Dengue Vaccination for Children with Sickle Cell Disease. | Elenga N, Nacher M, Trehan I | J. Trop. Pediatr. | 2020 |
| Genetic testing costs and compliance with clinical best practices. | Montanez K, Berninger T, Willis M, Harding A, Lutgendorf MA | J Genet Couns | 2020 |
| Lessons learned from a prenatal diagnosis program for thalassemia in Thailand. | Wong P, Suannum P, Jermnim S, Charoenporn P, Chan-In M, Tapprom A, Deoisares R | Prenat. Diagn. | 2020 |
| Short-Term Outcome and MRI Changes in Three Adult Patients with Sickle Cell Disease and Aseptic Osteonecrosis after Treatment with Hyperbaric Oxygen Therapy: A Preliminary Report. | Shier A, Abdelrazek M, Soliman A, De Sanctis V, Elsayed A, Abdulla M, Mohamed S, Yassin K, Bilal I, Yassin M | Case Rep Oncol | 2020 |
| Advances in genome editing: the technology of choice for precise and efficient β-thalassemia treatment. | Ali G, Tariq MA, Shahid K, Ahmad FJ, Akram J | Gene Ther. | 2020 |
| Concomitant Existence of Paroxysmal Nocturnal Hemoglobinuria in a Patient with Hb E (: c.79G>A) Trait. | Halder R, Sundaram UKD, Veetil KK, Rath A, Seth T, Tyagi S, Pati HP | Hemoglobin | 2020 |
| Nasal Colonization among Children with Sickle Cell Disease at the Children's Hospital, Accra: Prevalence, Risk Factors, and Antibiotic Resistance. | Appiah VA, Pesewu GA, Kotey FCN, Boakye AN, Duodu S, Tette EMA, Nyarko MY, Donkor ES | Pathogens | 2020 |
| Gene expression of HIF-1α and VEGF in response to hypoxia in sickle cell anaemia: Influence of hydroxycarbamide. | Pedrosa AM, Lemes RPG | Br. J. Haematol. | 2020 |
| Microvasculopathy and biomarkers in sickle cell disease: the promise of non-invasive real-time in vivo tools. | Colombatti R, Andemariam B | Br. J. Haematol. | 2020 |
| Gene Mutation Spectrum of Thalassemia Among Children in Yunnan Province. | Huang TL, Zhang TY, Song CY, Lin YB, Sang BH, Lei QL, Lv Y, Yang CH, Li N, Tian X, Yang YH, Zhang XW | Front Pediatr | 2020 |
| Two Consecutive Episodes of Severe Delayed Hemolytic Transfusion Reaction in a Sickle Cell Disease Patient. | Mpinganzima C, Haaland A, Holm AGV, Thein SL, Tjønnfjord GE, Iversen PO | Case Rep Hematol | 2020 |
| Deletional Alpha-Thalassemia Alleles in Amazon Blood Donors. | Anselmo FC, Ferreira NS, da Mota AJ, Gonçalves MS, Albuquerque SRL, Fraiji NA, Ferreira ACD, de Moura Neto JP | Adv Hematol | 2020 |
| Rare Case of Diffuse Splenic Uptake on Methylene Diphosphonate Bone Scan in a Patient with Sickle Cell Disease. | Parida GK, Mitra S, Muthu GS, Suman A | Indian J Nucl Med | 2020 |
| Smad2/3-pathway ligand trap luspatercept enhances erythroid differentiation in murine β-thalassaemia by increasing GATA-1 availability. | Martinez PA, Li R, Ramanathan HN, Bhasin M, Pearsall RS, Kumar R, Suragani RNVS | J. Cell. Mol. Med. | 2020 |
| Systematic Review of Crizanlizumab: A New Parenteral Option to Reduce Vaso-occlusive Pain Crises in Patients with Sickle Cell Disease. | Han J, Saraf SL, Gordeuk VR | Pharmacotherapy | 2020 |
| The prevalence of hepatitis C virus infection in β-thalassemia patients in Pakistan: a systematic review and meta-analysis. | Akhtar S, Nasir JA, Hinde A | BMC Public Health | 2020 |
| Inhibition of Band 3 tyrosine phosphorylation: a new mechanism for treatment of sickle cell disease. | Noomuna P, Risinger M, Zhou S, Seu K, Man Y, An R, Sheik DA, Wan J, Little JA, Gurkan UA, Turrini FM, Kalfa T, Low PS | Br. J. Haematol. | 2020 |
| Comparison of global strain values of myocardium in beta-thalassemia major patients with iron load using specific feature tracking in cardiac magnetic resonance imaging. | Rezaeian N, Mohtasham MA, Khaleel AJ, Parnianfard N, Kasani K, Golshan R | Int J Cardiovasc Imaging | 2020 |
| New mutations of locus control region in Saudi sickle patients. | Alenzi FQ | Saudi J Biol Sci | 2020 |
| Pulmonary complications for women with sickle cell disease in pregnancy: systematic review and meta-analysis. | Inparaj S, Buckingham M, Oakley L, Seed PT, Lucas S, Oteng-Ntim E | Thorax | 2020 |
| Oxidation Impacts the Intracellular Signaling Machinery in Hematological Disorders. | Tibaldi E, Federti E, Matte A, Iatcenko I, Wilson AB, Riccardi V, Pagano MA, De Franceschi L | Antioxidants (Basel) | 2020 |
| Hematopoietic stem cell function in β-thalassemia is impaired and is rescued by targeting the bone marrow niche. | Aprile A, Gulino A, Storto M, Villa I, Beretta S, Merelli I, Rubinacci A, Ponzoni M, Marktel S, Tripodo C, Lidonnici MR, Ferrari G | Blood | 2020 |
| Systematic Review of Voxelotor: A First-in-Class Sickle Hemoglobin Polymerization Inhibitor for Management of Sickle Cell Disease. | Han J, Saraf SL, Gordeuk VR | Pharmacotherapy | 2020 |
| Sexual dysfunction in female subjects with beta-thalassemia minor. | Keşkek ŞÖ, Demirtaş D, Uysal G, Başaran E | Int. J. Impot. Res. | 2020 |
| Caring for Africa's sickle cell children: will we rise to the challenge? | Oron AP, Chao DL, Ezeanolue EE, Ezenwa LN, Piel FB, Ojogun OT, Uyoga S, Williams TN, Nnodu OE | BMC Med | 2020 |
| Celocentesis for early prenatal diagnosis of hemoglobinopathies. | Makrydimas G, Damiani G, Jakil C, Cigna V, Orlandi M, Picciotto F, Schillaci G, Cassarà F, Vinciguerra M, Leto F, Giambona A, Maggio A, Nicolaides KH | Ultrasound Obstet Gynecol | 2020 |
| Hematological Characteristics of Hb Constant Spring (: c.427T>C) Carriers in Mainland China. | Jiang F, Xu LL, Chen GL, Zhou JY, Li J, Tang XW, Zuo LD, Li DZ | Hemoglobin | 2020 |
| The Relation between Different Aspects of Quality of Life with Coping Style in Adolescents with Thalassemia in Comparison to a Healthy Group. | Abbasi S, Shahriari M, Ghanavat M, Talakoub S, Mosavi Asl FS, Hemati Z | Int J Hematol Oncol Stem Cell Res | 2020 |
| The association of HBG2, BCL11A, and HBS1L-MYB polymorphisms to thalidomide response in Chinese β-thalassemia patients. | Yang K, Wu Y, Ma Y, Xiao J, Zhou Y, Yin X | Blood Cells Mol. Dis. | 2020 |
| Biochemical and imaging markers in patients with thalassaemia. | Vlachou M, Kamperidis V, Giannakoulas G, Karamitsos T, Vlachaki E, Karvounis H | Hellenic J Cardiol | 2020 |
| Voxelotor for the Treatment of Sickle Cell Disease. | Fantasia HC, Morse BL | Nurs Womens Health | 2020 |
| Experience with Parent Follow-Up for Communication Outcomes after Newborn Screening Identifies Carrier Status. | Farrell MH, La Pean Kirschner A, Tluczek A, Farrell PM | J. Pediatr. | 2020 |
| Measuring hydroxyurea adherence by pharmacy and laboratory data compared with video observation in children with sickle cell disease. | Creary S, Chisolm D, Stanek J, Neville K, Garg U, Hankins JS, O'Brien SH | Pediatr Blood Cancer | 2020 |
| Nephrectomy Does not Exacerbate Cancellous Bone loss in Thalassemic Mice. | Lotinun S, Atjanasuppat K, Limsuvech J, Leelahavanichkul A, Svasti S, Krishnamra N | Sci Rep | 2020 |
| Clinical, laboratory, and genetic risk factors for thrombosis in sickle cell disease. | Srisuwananukorn A, Raslan R, Zhang X, Shah BN, Han J, Gowhari M, Molokie RE, Gordeuk VR, Saraf SL | Blood Adv | 2020 |
| Impact of Arginine Therapy on Mitochondrial Function in Children with Sickle Cell Disease during Vaso-occlusive Pain. | Morris CR, Brown LA, Reynolds M, Dampier CD, Lane P, Watt A, Kumari P, Harris F, Manoranjithan S, Mendis RD, Figueroa J, Shiva S | Blood | 2020 |
| Development of the InCharge Health Mobile App to Improve Adherence to Hydroxyurea in Patients With Sickle Cell Disease: User-Centered Design Approach. | Alberts NM, Badawy SM, Hodges J, Estepp JH, Nwosu C, Khan H, Smeltzer MP, Homayouni R, Norell S, Klesges L, Porter JS, Hankins JS | JMIR Mhealth Uhealth | 2020 |
| Detecting HbE Gene Using DNA Extracted from Urine Sediments by Chelex-plus-Heating Technique. | Pankham A, Tatu T | J Biomol Tech | 2020 |
| Microsurgery in the sickle cell trait population: is it actually safe? | Abraham PF, Allam O, Park KE, Alperovich M | BMJ Case Rep | 2020 |
| Hematologist and transplant physicians: How and where to meet for the best of sickle cell disease patients? | Dalle JH | Hematol Oncol Stem Cell Ther | 2020 |
| S100B single nucleotide polymorphisms exhibit sex-specific associations with chronic pain in sickle cell disease in a largely African-American cohort. | Jhun EH, Sadhu N, He Y, Yao Y, Wilkie DJ, Molokie RE, Wang ZJ | PLoS ONE | 2020 |
| A study of the geographic distribution and associated risk factors of leg ulcers within an international cohort of sickle cell disease patients: the CASiRe group analysis. | Antwi-Boasiako C, Andemariam B, Colombatti R, Asare EV, Strunk C, Piccone CM, Manwani D, Boruchov D, Farooq F, Urbonya R, Wilson S, Boatemaa GD, Perrotta S, Sainati L, Rivers A, Rao S, Zempsky W, Ekem I, Sey F, Segbefia C, Inusa B, Tartaglione I, Campbell AD | Ann. Hematol. | 2020 |
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| Genetic counselling in sickle cell disease: views of single young adults in Ghana. | Appiah S, Korsah KA, AmpongAdjei C, Appiah OE | J Community Genet | 2020 |
| In Vitro Lymphocyte Functions in Undernourished Children With Sickle Cell Anemia. | Kuvibidila SR, Gardner R, Velez MC, Yu L, Warrier RP | Ochsner J | 2020 |
| Replacing the suppressed hormone: toward a better treatment for iron overload in β-thalassemia major? | Girelli D, Busti F | Haematologica | 2020 |
| Necrobiosis Lipoidica in a Patient with β-Thalassemia Major: A Case Report and Review of the Literature. | Vetsiou E, Mpouras V, Nikolaidou C, Klonizakis P, Mandala E, Vamvakis K, Psarras K, Vlachaki E | Hemoglobin | 2020 |
| Utilising red cell antigen genotyping and serological phenotyping in sickle cell disease patients to risk-stratify patients for alloimmunisation risk. | Shih AW, Yan MTS, Elahie AL, Barty RL, Liu Y, Berardi P, Azzam M, Siddiqui R, Parvizian MK, Mcdougall T, Heddle NM, Al-Habsi KS, Goldman M, Cote J, Athale U, Verhovsek MM | Transfus Med | 2020 |
| A Woman with Missing Hb A Due to a Novel (εγ)δβ-Thalassemia and a Novel δ-Globin Variant Hb A-Gebenstorf (: c.209G>A). | Saller E, Knijnenburg J, Harteveld CL, Dutly F | Hemoglobin | 2020 |
| Umbilical Cord Blood Screening for the Detection of Common Deletional Mutations of α-Thalassemia in Bangladesh. | Anwar S, Taslem Mourosi J, Hasan MK, Hosen MJ, Miah MF | Hemoglobin | 2020 |
| Iconic Visualization of Sickle Cell Patients Current and Past Health Status. | Diallo AH, Camara G, Lo M, Diagne I, Lamy JB | Stud Health Technol Inform | 2020 |
| Potential Risk Factors Associated With Graft Failure of Haploidentical Hematopoietic Stem Cell Transplantation (HSCT) in Children With Sickle Cell Disease (SCD). | Yu J, Black V, Lamba J, Horn B | J Pediatr Hematol Oncol | 2020 |
| Observational study on the current status of thalassaemia in Malaysia: a report from the Malaysian Thalassaemia Registry. | Mohd Ibrahim H, Muda Z, Othman IS, Mohamed Unni MN, Teh KH, Thevarajah A, Gunasagaran K, Ong GB, Yeoh SL, Muhammad Rivai A, Che Mohd Razali CH, Din ND, Abdul Latiff Z, Jamal R, Mohamad N, Mohd Ariffin H, Alias H | BMJ Open | 2020 |
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| Folic acid supplementation in children with sickle cell disease: study protocol for a double-blind randomized cross-over trial. | Williams BA, McCartney H, Adams E, Devlin AM, Singer J, Vercauteren S, Wu JK, Karakochuk CD | Trials | 2020 |
| Silent Cerebral Infarct in Sickle Cell Anemia Patients of South Turkey. | Nafİle Sayman E, Leblebİsatan G, Leblebİsatan Ş, BiÇakci YK, KilinÇ Y, BarutÇu A | Turk J Med Sci | 2020 |
| Validation of the fine motor subtest of the Bayley-III with children with sickle cell disease using Rasch analysis. | L'Hotta AJ, Hoyt CR, Lindsey T, Abel RA, Chang CH, King AA | Child Care Health Dev | 2020 |
| The Economic Burden of End-Organ Damage Among Medicaid Patients with Sickle Cell Disease in the United States: A Population-Based Longitudinal Claims Study. | Campbell A, Cong Z, Agodoa I, Song X, Martinez DJ, Black D, Lew CR, Varker H, Chan C, Lanzkron S | J Manag Care Spec Pharm | 2020 |
| A Wide Spectrum Study of α-Globin Chain Variants: Cases from the UK. | Khalil MSM, Timbs AT, Henderson SJ, Schuh A, El-Khawanky MM, Old JM | Hemoglobin | 2020 |
| Management of haemoglobin Barts hydrops fetalis syndrome with exchange transfusions. | Ong J, Bowden D, Kaplan Z | Intern Med J | 2020 |
| Identification of a new hemoglobin variant Hb Liuzhou [:C.182A→G] by MALDI-TOF mass spectrometry during HbA measurement. | Xu A, Chen W, Xie W, Ji L | Scand J Clin Lab Invest | 2020 |
| Red Blood Cell-Mediated S-Nitrosohemoglobin-Dependent Vasodilation: Lessons Learned from a β-Globin Cys93 Knock-in Mouse. | Premont RT, Reynolds JD, Zhang R, Stamler JS | Antioxid Redox Signal | 2020 |
| Epigenetic Reexpression of Hemoglobin F Using Reversible LSD1 Inhibitors: Potential Therapies for Sickle Cell Disease. | Holshouser S, Cafiero R, Robinson M, Kirkpatrick J, Casero RA, Hyacinth HI, Woster PM | ACS Omega | 2020 |
| Hemoglobin S/O: Retinal Manifestations of a Rare Hemoglobinopathy. | Sanders R, Ly V, Ahmad K, Swift J, Sallam A, Uwaydat S | Case Rep Ophthalmol | 2020 |
| Differences among hemoglobin thresholds for red blood cell transfusions in patients with hematological diseases in teaching hospitals: a real world data in Japan. | Yokohama A, Okuyama Y, Ueda Y, Itoh M, Fujiwara SI, Hasegawa Y, Nagai K, Arakawa K, Miyazaki K, Makita M, Watanabe M, Ikeda K, Tanaka A, Fujino K, Matsumoto M, Makino S, Kino S, Takeshita A, Muroi K | Int J Hematol | 2020 |
| Combating iron overload: a case for deferoxamine-based nanochelators. | Jones G, Goswami SK, Kang H, Choi HS, Kim J | Nanomedicine (Lond) | 2020 |
| FcγR2B B2.4 haplotype predicts increased risk of red blood cell alloimmunization in sickle cell disease patients. | Costa Neto A, Santos F, Ribeiro I, Oliveira V, Dezan M, Kashima S, Covas D, Pereira A, Fonseca G, Moreira F, Krieger J, Gualandro S, Rocha V, Mendrone A, Dinardo CL | Transfusion | 2020 |
| Individual red blood cell fetal hemoglobin quantification allows to determine protective thresholds in sickle cell disease. | Hebert N, Rakotoson MG, Bodivit G, Audureau E, Bencheikh L, Kiger L, Oubaya N, Pakdaman S, Sakka M, Di Liberto G, Chadebech P, Vingert B, Pirenne F, Galactéros F, Cambot M, Bartolucci P | Am J Hematol | 2020 |
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| Label-free detection of thalassemia and other ROS impairing diseases. | Chakraborty A, Chatterjee SK, Dasgupta AK | Med Biol Eng Comput | 2020 |
| Effectiveness of a home-based therapeutic exercise program on lower back pain and functionality in Sickle Cell Disease (SCD) patients. | Zanoni CT, Galvão F, Maria RM, Zulli R, Ricciardi JB, Cliquet A, Saad STO | Hematol Transfus Cell Ther | 2020 |
| Effect of Inhaled Cannabis for Pain in Adults With Sickle Cell Disease: A Randomized Clinical Trial. | Abrams DI, Couey P, Dixit N, Sagi V, Hagar W, Vichinsky E, Kelly ME, Connett JE, Gupta K | JAMA Netw Open | 2020 |
| Young Adults With Sickle Cell Disease: Challenges With Transition to Adult Health Care. | Varty M, Popejoy LL | Clin J Oncol Nurs | 2020 |
| Analysis of the foveal microvasculature in sickle cell disease using swept-source optical coherence tomography angiography. | Mokrane A, Gazeau G, Lévy V, Fajnkuchen F, Giocanti-Aurégan A | Sci Rep | 2020 |
| The safety and effectiveness of genetically corrected iPSCs derived from β-thalassaemia patients in nonmyeloablative β-thalassaemic mice. | Xian Y, Xie Y, Song B, Ou Z, Ouyang S, Xie Y, Yang Y, Xiong Z, Li H, Sun X | Stem Cell Res Ther | 2020 |
| A high frequency of Gilbert syndrome (UGT1A1*28/*28) and associated hyperbilirubinemia but not cholelithiasis in adolescent and adult north Indian patients with transfusion-dependent β-thalassemia. | Shrestha O, Khadwal AR, Singhal M, Trehan A, Bansal D, Jain R, Pal A, Hira JK, Chhabra S, Malhotra P, Das R, Sharma P | Ann Hematol | 2020 |
| CTLA4Ig in an Extended Schedule along with Sirolimus Improves Outcome with a Distinct Pattern of Immune Reconstitution Following Post-Transplantation Cyclophosphamide-Based Haploidentical Transplantation for Hemoglobinopathies. | Jaiswal SR, Bhakuni P, Aiyer HM, Soni M, Bansal S, Chakrabarti S | Biol. Blood Marrow Transplant. | 2020 |
| Hemoglobin SS Nigerian Woman First Diagnosed at the Age of 52 years with Manifestation Mimicking Tuberculosis of the Spine. | Ugwu NI, Nna EO, Egwu AN, Okoye EA | Niger Med J | 2020 |
| The Effect of Five Single Nucleotide Polymorphisms on Hb F Variation of β-Thalassemia Traits and Hematologically Normal Individuals in Southeast Turkey. | Genc A, Tastemir Korkmaz D, Bayram S, Rencuzogullari E | Hemoglobin | 2020 |
| Hematological Characteristics of β-Globin Gene Mutation -50 (G>A) (: c.-100G>A) Carriers in Mainland China. | Zhao Y, Jiang F, Li DZ | Hemoglobin | 2020 |
| Voxelotor: A Novel Treatment for Sickle Cell Disease. | Herity LB, Vaughan DM, Rodriguez LR, Lowe DK | Ann Pharmacother | 2020 |
| Antioxidant nutrients and hemolysis in sickle cell disease. | Delesderrier E, Curioni C, Omena J, Macedo CR, Cople-Rodrigues C, Citelli M | Clin Chim Acta | 2020 |
| Computer Algorithm-Based Hydroxyurea Dosing Facilitates Titration to Maximum Tolerated Dose in Sickle Cell Anemia. | Oldham M, Conrey A, Pittman C, Fisher C, Hargrett S, West K, Jackson M, Martin S, Hsieh MM, Jeffries N, Kaplarevic M, Johnson D, Olkhanud P, Fitzhugh CD | J Clin Pharmacol | 2020 |
| Stable renal function in children and adolescents with sickle cell disease after nonmyeloablative hematopoietic stem cell transplantation. | Pedersen SJV, Monagel DA, Mammen C, Lewis VA, Guilcher GMT, Bruce AA | Pediatr Blood Cancer | 2020 |
| Longitudinal follow-up of patients with thalassaemia intermedia who started transfusion therapy in adulthood: a cohort study. | Ricchi P, Meloni A, Pistoia L, Spasiano A, Rita Gamberini M, Maggio A, Gerardi C, Messina G, Campisi S, Allò M, Renne S, Righi R, Midiri M, Positano V, Filosa A, Pepe A | Br. J. Haematol. | 2020 |
| Cost of health care for paediatric patients with sickle cell disease: An analysis of resource use and costs in a European country. | Thielen FW, Houwing ME, Cnossen MH, Al Hadithy-Irgiztseva IA, Hazelzet JA, Groot CAU, de Pagter APJ, Blommestein HM | Pediatr Blood Cancer | 2020 |
| Osteomyelitis in sickle cell disease: You know it when you see it? | Rothman JA | Pediatr Blood Cancer | 2020 |
| Two Novel and Five Rare Mutations in the Non Coding Regions of the β-Globin Gene in the Iranian Population. | Hamid M, Zargan Nezhad E, Keikhaei B, Galehdari H, Saberi A, Sedaghat A, Mohammadi-Anaei M, Shariati G | Hemoglobin | 2020 |
| Update in Laboratory Diagnosis of Thalassemia. | Munkongdee T, Chen P, Winichagoon P, Fucharoen S, Paiboonsukwong K | Front Mol Biosci | 2020 |
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| Impact of SARS CoV-2 in Hemoglobinopathies with Immune Disfunction and Epidemiology. A Protective Mechanism from Beta Chain Hemoglobin Defects? | Torti L, Maffei L, Sorrentino F, De Fabritiis P, Miceli R, Abruzzese E | Mediterr J Hematol Infect Dis | 2020 |
| Preliminary Data on COVID-19 in Patients with Hemoglobinopathies: A Multicentre ICET-A Study. | de Sanctis V, Canatan D, Corrons JLV, Karimi M, Daar S, Kattamis C, Soliman AT, Wali Y, Alkindi S, Huseynov V, Nasibova A, Tiryaki TO, Evim MS, Gunes AM, Karakas Z, Christou S, Campisi S, Zarei T, Khater D, Oymak Y, Kaleva V, Stoyanova D, Banchev A, Galati MC, Yassin MA, Kakar S, Skafida M, Kilinc Y, Alyaarubi S, Verdiyevas N, Stoeva I, Raiola G, Mariannis D, Ruggiero L, Di Maio S | Mediterr J Hematol Infect Dis | 2020 |
| Creating New β-Globin-Expressing Lentiviral Vectors by High-Resolution Mapping of Locus Control Region Enhancer Sequences. | Morgan RA, Ma F, Unti MJ, Brown D, Ayoub PG, Tam C, Lathrop L, Aleshe B, Kurita R, Nakamura Y, Senadheera S, Wong RL, Hollis RP, Pellegrini M, Kohn DB | Mol Ther Methods Clin Dev | 2020 |
| Seroprevalence of HBV, HCV and HIV-1 and Correlation with Molecular Markers among Multi-Transfused Thalassemia Patients in Western India. | Mishra K, Shah A, Patel K, Ghosh K, Bharadva S | Mediterr J Hematol Infect Dis | 2020 |
| Association of rs4701 Variant, but not -α Over-Expression with Bone Mineral Density in Pediatric Well-Chelated β-Thalassemia Patients. | Sahmoud S, Ibrahim MS, Toraih EA, Kamel N, Fawzy MS, Elfiky S | Mediterr J Hematol Infect Dis | 2020 |
| Prevalence and predictors of chronic pain intensity and disability among adults with sickle cell disease. | Matthie N, Jenerette C, Gibson A, Paul S, Higgins M, Krishnamurti L | Health Psychol Open | 2020 |
| Health-Related Quality of Life in Thai Children with Thalassemia as Evaluated by PedsQL and EQ-5D-Y: A Single-Center Experience. | Sinlapamongkolkul P, Surapolchai P | Mediterr J Hematol Infect Dis | 2020 |
| Re: Renal medullary carcinoma and its association with sickle cell trait: a case report and literature review. | Riminucci M, Corsi A | Curr Oncol | 2020 |
| Effects of α-tocopherol on hemolysis and oxidative stress markers on red blood cells in β-thalassemia major. | Sovira N, Lubis M, Wahidiyat PA, Suyatna FD, Gatot D, Bardosono S, Sadikin M | Clin Exp Pediatr | 2020 |
| Reduction of Liver Iron Load in Adult Patients with β-Thalassemia Major Treated with Modern Chelation Modalities. | Georgiev PG, Sapunarova KG, Goranova-Marinova VS, Goranov SE | Folia Med (Plovdiv) | 2020 |
| Inadequate Pre-conception Counseling is a Major Challenge for Antenatal Management of β-Thalassemia: Experience from a Referral Centre in India. | Shetty M, Balakrishna S, Hegde S | Indian J Hematol Blood Transfus | 2020 |
| Thalidomide in Patients with Transfusion-Dependent E-Beta Thalassemia Refractory to Hydroxyurea: A Single-Center Experience. | Nag A, Radhakrishnan VS, Kumar J, Bhave S, Mishra DK, Nair R, Chandy M | Indian J Hematol Blood Transfus | 2020 |
| Association of HMIP1 C-893A polymorphism and disease severity in patients with sickle cell anemia. | Pereira-Martins DA, Domingos IF, Belini-Junior E, Coelho-Silva JL, Weinhäuser I, Araújo AS, Lobo CL, Bonini-Domingos CR, Bezerra MA, Lucena-Araujo AR | Hematol Transfus Cell Ther | 2020 |
| β-Globin Gene Mutations in Pediatric Patients with β-Thalassemia in the Region of Çukurova, Turkey. | Guzelgul F, Seydel GS, Aksoy K | Hemoglobin | 2020 |
| Cost-utility of new film-coated tablet formulation of deferasirox vs deferoxamine among major beta-thalassemia patients in Iran. | Saiyarsarai P, Khorasani E, Photogeraphy H, Ghaffari Darab M, Seyedifar M | Medicine (Baltimore) | 2020 |
| Promising Response to Thalidomide in Symptomatic β-Thalassemia. | Yassin AK | Indian J Hematol Blood Transfus | 2020 |
| Alternative Strategies in Thalassemia: Focus on Thalidomide. | Naithani R, Jeyaraman P, Mahapatra M | Indian J Hematol Blood Transfus | 2020 |
| A New α Chain Variant, Hb Heilongjiang (: c.49A>C), Found During Hb A Measurement. | Xu A, Chen W, Xie W, Ji L, Wang Y, Xu M | Hemoglobin | 2020 |
| Marijuana use and health behaviors in a US clinic sample of patients with sickle cell disease. | Wilson JD, Pecker LH, Lanzkron S, Bediako SM, Han D, Beach MC | PLoS One | 2020 |
| Serum folate and cytokines in heterozygous β-thalassemia. | Paniz C, Lucena MR, Bertinato JF, Dos Santos MNN, Gomes GW, Figueiredo MS, Sonati MF, Blaia-D Avila VLN, Green R, Guerra-Shinohara EM | Int J Lab Hematol | 2020 |
| Self-management recommendations for sickle cell disease: A content analysis of websites. | Druye AA, Nelson K, Robinson B | Nurs Health Sci | 2020 |
| Efficacy and Safety of Combined Oral Chelation with Deferiprone and Deferasirox on Iron Overload in Transfusion Dependent Children with Thalassemia - A Prospective Observational Study. | DivakarJose RR, Delhikumar CG, Ram Kumar G | Indian J Pediatr | 2020 |
| Haptoglobin: From hemoglobin scavenging to human health. | di Masi A, De Simone G, Ciaccio C, D'Orso S, Coletta M, Ascenzi P | Mol Aspects Med | 2020 |
| Extensive Extramedullary Hematopoiesis in Thalassemia: Soft Tissue Uptake on 99mTc-MDP SPECT/CT. | Usmani S, Ahmed N, Muzaffar S, Al Kandari F | Clin Nucl Med | 2020 |
| Hemoglobin S/Hemoglobin Quebec-Chori Presenting as Sickle Cell Disease: A Case Report. | Goode E, Boruchov D, Oliveira JL, Lau CC | J Pediatr Hematol Oncol | 2020 |
| Vulnerability of sickle cell disease persons to the COVID-19 in sub-Saharan Africa. | Tonen-Wolyec S, Marini Djang'eing'a R, Kambale-Kombi P, Tshilumba CK, Bélec L, Batina-Agasa S | Hematology | 2020 |
| Whole blood viscosity and red blood cell adhesion: Potential biomarkers for targeted and curative therapies in sickle cell disease. | Kucukal E, Man Y, Hill A, Liu S, Bode A, An R, Kadambi J, Little JA, Gurkan UA | Am J Hematol | 2020 |
| The effect of dietary nitrate supplementation on the speed-duration relationship in mice with sickle cell disease. | Ferguson SK, Redinius KM, Harral JW, Pak DI, Swindle DC, Hirai DM, Blackwell JR, Jones AM, Stenmark KR, Buehler PW, Irwin DC | J Appl Physiol (1985) | 2020 |
| Men with sickle cell disease experience greater sexual dysfunction when compared with men without sickle cell disease. | Idris IM, Abba A, Galadanci JA, Mashi SA, Hussaini N, Gumel SA, Burnett AL, DeBaun MR | Blood Adv | 2020 |
| Cohort profile: targeted antenatal screening for haemoglobinopathies in Basel. | Amstad Bencaiova G, Geissler F, Hoesli I | BMJ Open | 2020 |
| Improving self-management in adolescents with sickle cell disease. | Crosby LE, Hood A, Kidwell K, Nwankwo C, Peugh J, Strong H, Quinn C, Britto MT | Pediatr Blood Cancer | 2020 |
| A Case of COVID-19 in a Patient with Asymptomatic Hemoglobin D Thalassemia and Glucose-6-Phosphate Dehydrogenase Deficiency. | Sasi S, Yassin MA, Nair AP, Al Maslamani MS | Am J Case Rep | 2020 |
| The CYB5R3 and G6PD A alleles modify severity of anemia in malaria and sickle cell disease. | Gordeuk VR, Shah BN, Zhang X, Thuma PE, Zulu S, Moono R, Reading NS, Song J, Zhang Y, Nouraie M, Campbell A, Minniti CP, Rana SR, Darbari DS, Kato GJ, Niu M, Castro OL, Machado R, Gladwin MT, Prchal JT | Am J Hematol | 2020 |
| Socio-religious Prognosticators of Psychosocial Burden of Beta Thalassemia Major. | Ul Hassan Rashid MA, Abbasi SS, Manzoor MM | J Relig Health | 2020 |
| Mild Thalassemia Intermedia Due to Interaction of δβ-Thalassemia with Triplicated α-Globin Genes. | Payán-Pernía S, Bernal Noguera S, Rojas Rodríguez E, Serra Ferrer M, Remacha Sevilla ÁF | Hemoglobin | 2020 |
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| Analysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia. | Horri-Naceur A, Timson DJ | Hemoglobin | 2020 |
| Chronic opioid use can be reduced or discontinued after haematopoietic stem cell transplantation for sickle cell disease. | Han J, Holden CC, Ahluwalia AY, Molokie RE, Gowhari M, Sweiss K, Patel PR, Gordeuk VR, Rondelli D, Saraf SL | Br J Haematol | 2020 |
| Molecular Understanding of Severe Cases of β-Thalassemia in the Nablus Region, West Bank, Palestine. | Samha L, Sirdah MM, Reading NS, Karmi B, Agarwal AM | Hemoglobin | 2020 |
| Long-Molecule Sequencing: A New Approach for Identification of Clinically Significant DNA Variants in α-Thalassemia and β-Thalassemia Carriers. | Xu L, Mao A, Liu H, Gui B, Choy KW, Huang H, Yu Q, Zhang X, Chen M, Lin N, Chen L, Han J, Wang Y, Zhang M, Li X, He D, Lin Y, Zhang J, Cram DS, Cao H | J Mol Diagn | 2020 |
| Persons With Thalassemia Major May Have Increased Risk of Gingival Inflammation. | Ayilavarapu S | J Evid Based Dent Pract | 2020 |
| Novel dose escalation to predict treatment with hydroxyurea (NDEPTH): A randomized controlled trial of a dose-prediction equation to determine maximum tolerated dose of hydroxyurea in pediatric sickle cell disease. | George A, Dinu B, Estrada N, Minard CG, Hurwitz R, Mahoney DH, Yates AM, Vaughan M, Carmouche A, Airewele G, Kirk SE, Fasipe T, Uwaezuoke P, Ware RE | Am. J. Hematol. | 2020 |
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| Racism and Health-Related Quality of Life in Pediatric Sickle Cell Disease: Roles of Depression and Support. | Mougianis I, Cohen LL, Martin S, Shneider C, Bishop M | J Pediatr Psychol | 2020 |
| Non-myeloablative matched sibling stem cell transplantation with the optional reinforced stem cell infusion for patients with hemoglobinopathies. | Shin SH, Park SS, Park S, Jeon YW, Yoon JH, Yahng SA, Cho BS, Kim YJ, Lee S, Kim HJ, Min CK, Cho SG, Kim DW, Lee JW, Eom KS | Eur. J. Haematol. | 2020 |
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| Assessment of Patient and Caregiver Attitudes and Approaches to Decision-Making Regarding Bone Marrow Transplant for Sickle Cell Disease: A Qualitative Study. | Bakshi N, Katoch D, Sinha CB, Ross D, Quarmyne MO, Loewenstein G, Krishnamurti L | JAMA Netw Open | 2020 |
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| Improving the Quality of Care for Adolescents and Adults With Sickle Cell Disease-It's a Long Road. | Oyedeji C, Strouse JJ | JAMA Netw Open | 2020 |
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| Graft Versus Host Disease Prophylaxis With Abatacept Reduces Severe Acute Graft Versus Host Disease in Allogeneic Hematopoietic Stem Cell Transplant for Beta Thalassemia Major with Busulfan, Fludarabine, and Thiotepa. | Khandelwal P, Yeh RF, Yu L, Lane A, Dandoy CE, El-Bietar J, Davies SM, Grimley MS | Transplantation | 2020 |
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| Long--Term Free Survival of Two Class III β-Thalassemic Patients after Non-Myeloablative Stem Cell Transplantation. | Adib Sereshki MM, Bahar B, Ghavamzadeh A, Mousavi SA, Alimoghaddam K | Int J Hematol Oncol Stem Cell Res | 2020 |
| Genetic Variation in SOD1 Gene Promoter Ins/Del and Its Influence on Oxidative Stress in Beta Thalassemia Major Patients. | Tripathi P, Agarwal S, Sarangi AN, Tewari S, Mandal K | Int J Hematol Oncol Stem Cell Res | 2020 |
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| A cost-of-illness analysis of β-Thalassaemia major in children in Sri Lanka - experience from a tertiary level teaching hospital. | Reed-Embleton H, Arambepola S, Dixon S, Maldonado BN, Premawardhena A, Arambepola M, Khan JAM, Allen S | BMC Pediatr | 2020 |
| BETA THALASSEMIA MINOR PATIENTS: NOT TIRED, BUT DEPRESSED AND ANXIOUS. | Eren R, Karışmaz A, Aslan C, Doğu MH, Altındal Ş, Yokuş O, Suyani E | Med Princ Pract | 2020 |
| Outcomes of a preoperative risk-based transfusion assignment protocol in sickle cell disease patients: a single-center retrospective study from Saudi Arabia. | Albolowi N, Mustafa O, Almohammadi M, Al-Hindi MY, Jastaniah W | Pediatr Hematol Oncol | 2020 |
| Sleep disturbance in adults with sickle cell disease: relationships with executive and psychological functioning. | Rhodes A, Martin S, Wolters P, Rodriguez Y, Toledo-Tamula MA, Struemph K, Fitzhugh C, Hsieh M, Tisdale J | Ann. Hematol. | 2020 |
| The Case of an Adolescent Male With Sickle Cell Disease and Atypical Leg Pain. | Millan J, Karrs J, Helou M, Dunbar EE | Clin Pediatr (Phila) | 2020 |
| Placental histopathology in sickle cell disease: A descriptive and hypothesis-generating study. | Malinowski AK, Dziegielewski C, Keating S, Parks T, Kingdom J, Shehata N, Rizov E, D'Souza R | Placenta | 2020 |
| Fifteen years of newborn sickle cell disease screening in Madrid, Spain: an emerging disease in a European country. | García-Morín M, Bardón-Cancho EJ, Beléndez C, Zamarro R, Béliz-Mendiola C, González-Rivera M, Vecilla C, Llorente-Otones L, Pérez-Alonso V, Román SS, Sebastián E, Dulín E, Cela E | Ann. Hematol. | 2020 |
| A biomathematical model of human erythropoiesis and iron metabolism. | Schirm S, Scholz M | Sci Rep | 2020 |
| Synthesis and evaluation of resveratrol derivatives as fetal hemoglobin inducers. | Bosquesi PL, Melchior ACB, Pavan AR, Lanaro C, de Souza CM, Rusinova R, Chelucci RC, Barbieri KP, Fernandes GFDS, Carlos IZ, Andersen OS, Costa FF, Dos Santos JL | Bioorg. Chem. | 2020 |
| Patient-reported outcomes in sickle cell disease and association with clinical and psychosocial factors: Report from the sickle cell disease implementation consortium. | Knisely MR, Pugh N, Kroner B, Masese R, Gordeuk V, King AA, Smith SM, Gurney JG, Adams R, Wun T, Snyder A, Glassberg J, Shah N, Treadwell M, | Am. J. Hematol. | 2020 |
| Potential Markers of Dietary Glycemic Exposures for Sustained Dietary Interventions in Populations without Diabetes. | Feskens E, Brennan L, Dussort P, Flourakis M, Lindner LME, Mela D, Rabbani N, Rathmann W, Respondek F, Stehouwer C, Theis S, Thornalley P, Vinoy S | Adv Nutr | 2020 |
| Sickle cell disease clinical phenotypes in Nigeria: A preliminary analysis of the Sickle Pan Africa Research Consortium Nigeria database. | Isa H, Adegoke S, Madu A, Hassan AA, Ohiaeri C, Chianumba R, Brown B, Okocha E, Ugwu N, Diaku-Akinwumi I, Adeyemo T, Kuliya-Gwarzo A, Dogara L, Lawal H, Tanko Y, Ladu A, Kangiwa U, Ekwem L, Oniyangi S, Wakama T, Umoru D, Olanrewaju O, Akinola N, Nnebe-Agumadu U, Asala S, Adekile A, Olaniyi J, Sangeda R, Sickle Africa Data Coordinating Center SADaCC , Nnodu O | Blood Cells Mol. Dis. | 2020 |
| Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania. | Nkya S, Mwita L, Mgaya J, Kumburu H, van Zwetselaar M, Menzel S, Mazandu GK, Sangeda R, Chimusa E, Makani J | BMC Med. Genet. | 2020 |
| Wrist Joint Skeletal Changes in Children With Transfusion-dependent Thalassemia. | Dhawan P, Kanojia RK, Chandra J, Kumar A, Anand R, Gupta S | J Pediatr Orthop | 2020 |
| The curious case of hemoglobin DC disease masquerading as sickle cell anemia. | Hirani S, Gupta S, Veillon D, Patan S, Master S, Mansour R | Hematol Rep | 2020 |
| Portal Vein Thrombosis with Splenic Infarct in β-Thalassemia Minor at High Altitude. | Yanamandra U, Bahl R, Mishra K, Kumar S | High Alt. Med. Biol. | 2020 |
| Severe α-Thalassemia Due to Compound Heterozygosity for Hb Adana (α59 Gly>Asp) (: c.179G > A) and Codon 127 (A > T) (: c.382A > T) in an Iranian Family. | Azimi A, Tahmasebi S, Moradi K, Nejati P, Alibakhshi R | Hemoglobin | 2020 |
| Probing the structure-function relationship of hemoglobin in living human red blood cells. | Dybas J, Bokamper MJ, Marzec KM, Mak PJ | Spectrochim Acta A Mol Biomol Spectrosc | 2020 |
| Comparative analysis of lentiviral gene transfer approaches designed to promote fetal hemoglobin production for the treatment of β-hemoglobinopathies. | Daniel-Moreno A, Lamsfus-Calle A, Wilber A, Chambers CB, Johnston I, Antony JS, Epting T, Handgretinger R, Mezger M | Blood Cells Mol. Dis. | 2020 |
| Characteristics and potential biomarkers of adult sickle cell patients with chronic pain. | Albo C, Kumar S, Pope M, Kidwell KM, Xu H, Bowman L, Wells L, Barrett N, Fields S, Bora P, Patel N, Kutlar A | Eur. J. Haematol. | 2020 |
| Sexual health of French adolescents with sickle cell disease. | Gros M, Jung C, Fourmaux C, Kamdem A, Arnaud C, Hau I, Pondarre C, Carlier-Gonod A | Eur J Contracept Reprod Health Care | 2020 |
| Fusobacterium nucleatum Multiple Liver Abscesses in an Adolescent With Hemoglobin SC Disease. | Pincez T, Ovetchkine P, Pastore Y | J. Pediatr. Hematol. Oncol. | 2020 |
| The effect of mother's β-thalassemia minor on placental histology and neonatal outcomes. | Vafaei H, Karimi S, Akbarzadeh Jahromi M, Asadi N, Kasraeian M | J. Matern. Fetal. Neonatal. Med. | 2020 |
| Effects of Alpha-Lipoic Acid Supplementation on Cardiovascular Disease Risk Factors in β-Thalassemia Major Patients: A Clinical Trial Crossover Study. | Jamshidi K, Abdollahzad H, Nachvak M, Rezaei M, Golpayegani MR, Sharifi Zahabi E | J Blood Med | 2020 |
| Brodie's Abscess Masquerading as Vaso-occlusive Crisis in a Sickle-cell Disease Patient. | Sheikh T, Fatima R, Aziz M, Balla M, Georgescu C | Cureus | 2020 |
| Zinc supplementation improves markers of glucose homeostasis in thalassaemia. | Fung EB, Ahmad T, Killilea DW, Hussain R, Lal A | Br. J. Haematol. | 2020 |
| Fetal haemoglobin H-Constant Spring disease: a role for intrauterine management. | Luewan S, Charoenkwan P, Sirichotiyakul S, Tongsong T | Br. J. Haematol. | 2020 |
| Alloimmunization and autoimmunization in adult transfusion-dependent thalassemia patients: a report from a comprehensive center in Israel. | Pazgal I, Yahalom V, Shalev B, Raanani P, Stark P | Ann. Hematol. | 2020 |
| Baseline and Disease-Induced Transcriptional Profiles in Children with Sickle Cell Disease. | Creary S, Shrestha CL, Kotha K, Minta A, Fitch J, Jaramillo L, Zhang S, Pinto S, Thompson R, Ramilo O, White P, Mejias A, Kopp BT | Sci Rep | 2020 |
| Leukocyte telomere length in patients with transfusion-dependent thalassemia. | Nanthatanti N, Tantiworawit A, Piriyakhuntorn P, Rattanathammethee T, Hantrakool S, Chai-Adisaksopha C, Rattarittamrong E, Norasetthada L, Tuntiwechapikul W, Fanhchaksai K, Charoenkwan P, Kumfu S, Chattipakorn N | BMC Med Genomics | 2020 |
| Pulmonary disease burden in Hispanic and non-Hispanic children with sickle cell disease. | Chen L, Gong J, Matta E, Morrone K, Manwani D, Rastogi D, De A | Pediatr. Pulmonol. | 2020 |
| A Nested Asymmetric PCR Melting Curve Assay for One-Step Genotyping of Nondeletional α-Thalassemia Mutations. | Qin J, Xu M, Zhang Q, Wen X, He S, Zhou Y, Liu H, Zhou W | J Mol Diagn | 2020 |
| Association of Hb A Variants with Several Forms of α- and β-Thalassemia in Thailand. | Panyasai S, Pornprasert S | Hemoglobin | 2020 |
| Mn porphyrins as a novel treatment targeting sickle cell NOXs to reverse and prevent acute vaso-occlusion in vivo. | Thamilarasan M, Estupinan R, Batinic-Haberle I, Zennadi R | Blood Adv | 2020 |
| Can CSF spectrophotometry for | Siu WY, Thomas W, Trivedi R, Hogan A, Siddiqi U, Sarker A, Besser MW | Clin Case Rep | 2020 |
| Renal failure in thalassemia: Thinking outside the box. | Kasinathan G | Clin Case Rep | 2020 |
| Locomotor mal-performance and gait adaptability deficits in sickle cell mice are associated with vascular and white matter abnormalities and oxidative stress in cerebellum. | Almeida LEF, Wang L, Kamimura S, Zerfas PM, Smith ML, Neto OLA, Vale T, Quezado MM, Horkayne-Szakaly I, Wakim P, Quezado ZMN | Brain Res. | 2020 |
| Development of the Thalassaemia Adult Life Index (ThALI). | Kantaris X, Shevlin M, Porter J, Myers L | Health Qual Life Outcomes | 2020 |
| JPP Student Journal Club Commentary: Review of Psychological Interventions Targeting Adherence Among Pediatric Sickle Cell Disease. | Durkin LK, Neff Greenley R | J Pediatr Psychol | 2020 |
| Delta-Globin Gene Expression Is Enhanced by Interferon Type I. | Manchinu MF, Simbula M, Caria CA, Musu E, Perseu L, Porcu S, Steri M, Poddie D, Frau J, Cocco E, Manunza L, Barella S, Ristaldi MS | Front Med (Lausanne) | 2020 |
| Trends in the Development of Diagnostic Tools for Red Blood Cell-Related Diseases and Anemias. | Kaestner L, Bianchi P | Front Physiol | 2020 |
| Allosteric control of hemoglobin S fiber formation by oxygen and its relation to the pathophysiology of sickle cell disease. | Henry ER, Cellmer T, Dunkelberger EB, Metaferia B, Hofrichter J, Li Q, Ostrowski D, Ghirlando R, Louis JM, Moutereau S, Galactéros F, Thein SL, Bartolucci P, Eaton WA | Proc. Natl. Acad. Sci. U.S.A. | 2020 |
| Comment on | Olatunya OS | Br. J. Haematol. | 2020 |
| Nights with sickle cell. | Mattingly DT | Fam Syst Health | 2020 |
| Genotypic-phenotypic heterogeneity of δβ-thalassemia and hereditary persistence of fetal hemoglobin (HPFH) in India. | Hariharan P, Kishnani P, Sawant P, Gorivale M, Mehta P, Kargutkar N, Colah R, Nadkarni A | Ann. Hematol. | 2020 |
| Neglected Pulmonary Arterial Hypertension in Sickle Cell Anaemia during Prenatal Care. | Karimi MB | Eur J Case Rep Intern Med | 2020 |
| Interocular asymmetry of foveal avascular zone morphology and parafoveal capillary density in sickle cell retinopathy. | Zhou DB, Scott AW, Linz MO, Han IC, Castanos MV, Lynch G, Andrade Romo JS, Linderman RE, Carroll J, Rosen RB, Chui TY | PLoS ONE | 2020 |
| Fetal Cardiac Cellular Damage Caused by Anemia in Utero in Hb Bart's Disease. | Jatavan P, Kumfu S, Tongsong T, Chattipakorn N | Curr. Mol. Med. | 2020 |
| Advances in Sickle Cell Disease Treatments. | Pavan AR, Dos Santos JL | Curr. Med. Chem. | 2020 |
| Optical coherence tomography (OCT) and OCT angiography allow early identification of sickle cell maculopathy in children and correlate it with systemic risk factors. | Grego L, Pignatto S, Alfier F, Arigliani M, Rizzetto F, Rassu N, Samassa F, Prosperi R, Barbieri F, Dall'Amico R, Cogo P, Lanzetta P | Graefes Arch. Clin. Exp. Ophthalmol. | 2020 |
| Risk score to predict event-free survival after hematopoietic cell transplant for sickle cell disease. | Brazauskas R, Scigliuolo GM, Wang HL, Cappelli B, Ruggeri A, Fitzhugh CD, Hankins JS, Kanter J, Meerpohl JJ, Panepinto JA, Rondelli D, Shenoy S, Walters MC, Wagner JE, Tisdale JF, Gluckman E, Eapen M | Blood | 2020 |
| Progressive vasoconstriction with sequential thermal stimulation indicates vascular dysautonomia in sickle cell disease. | Veluswamy S, Shah P, Khaleel M, Thuptimdang W, Chalacheva P, Sunwoo J, Denton CC, Kato R, Detterich J, Wood JC, Sposto R, Khoo MCK, Zeltzer L, Coates TD | Blood | 2020 |
| SEN virus genotype H distribution in β-thalassemic patients and in healthy donors in Iraq: Molecular and physiological study. | Al-Ouqaili MTS, Majeed YH, Al-Ani SK | PLoS Negl Trop Dis | 2020 |
| Moderate fixed-dose hydroxyurea for primary prevention of strokes in Nigerian children with sickle cell disease: Final results of the SPIN trial. | Galadanci NA, Abdullahi SU, Ali Abubakar S, Wudil Jibir B, Aminu H, Tijjani A, Abba MS, Tabari MA, Galadanci A, Borodo AM, Belonwu R, Salihu AS, Rodeghier M, Ghafuri DL, Covert C Greene BV, Neville K, Kassim AA, Kirkham FJ, Jordan LC, Aliyu MH, DeBaun MR | Am. J. Hematol. | 2020 |
| Recent Advances in the Treatment of Sickle Cell Disease. | Salinas Cisneros G, Thein SL | Front Physiol | 2020 |
| I Polymorphism in Sickle Cell Disease in North Morocco. | Alaoui-Ismaili FZ, Laghmich A, Ghailani-Nourouti N, Barakat A, Bennani-Mechita M | Hemoglobin | 2020 |
| Sickle cell disease perceptions of caregivers, adolescent, and adult patients: Barriers and facilitators to medical care adherence. | Hoegy D, Guilloux R, Bleyzac N, Gauthier-Vasserot A, Cannas G, Bertrand Y, Hot A, Dussart C, Janoly-Dumenil A | J Adv Nurs | 2020 |
| Development of the Next Generation Sequencing-Based Diagnostic Test for β-Thalassemia and its Validation in a Pashtun Family. | Sabiha B, Haider SA, Jan H, Yousafzai YM, Afridi OK, Khan AA, Ali J | Hemoglobin | 2020 |
| Rheumatoid arthritis and sickle cell disease: A potential association. | Roizenblatt S, Cabañas-Pedro AC, Figueiredo MS | Br J Haematol | 2020 |
| Manual erythroexchange in sickle cell disease: multicenter validation of a protocol predictive of volume to exchange and hemoglobin values. | Gianesin B, Pinto VM, Casale M, Corti P, Fidone C, Quintino S, Voi V, Forni GL | Ann Hematol | 2020 |
| Determination of von Willebrand factor level in patient with sickle cell diseasein vaso-occlusive crisis. | Akaba K, Nwogoh B, Oshatuyi O | Res Pract Thromb Haemost | 2020 |
| Association between Vaso-occlusive Crises and Opioid Prescriptions among Patients with Sickle Cell Disease: A Retrospective Claims-based Study. | Kang HA, Barner JC, Richards KM, Bhor M, Paulose J, Kutlar A | J Health Econ Outcomes Res | 2020 |
| Medical Resource Use and Costs of Treating Sickle Cell-related Vaso-occlusive Crisis Episodes: A Retrospective Claims Study. | Shah N, Bhor M, Xie L, Paulose J, Yuce H | J Health Econ Outcomes Res | 2020 |
| The First Asian, Single-Center Experience of Blastocyst Preimplantation Genetic Diagnosis with HLA Matching in Thailand for the Prevention of Thalassemia and Subsequent Curative Hematopoietic Stem Cell Transplantation of Twelve Affected Siblings. | Tiewsiri K, Manipalviratn S, Sutheesophon W, Vanichsetakul P, Thaijaroen P, Ketcharoon P, Bradley CK, McArthur SJ, Krutsawad W, Marshall JTA, Papadopoulos KI | Biomed Res Int | 2020 |
| Corrigendum to | Amin SS, Jalal SD, Ali KM, Mohammed AI, Rasool LK, Osman TJ | Biomed Res Int | 2020 |
| Frequency of thyroid nodules in patients with β-thalassemias in Southern Iran. | Haghpanah S, Pishdad P, Zarei T, Shahsavani A, Amirmoezi F, Ilkhanipoor H, Ilkhanipoor H, Safaei S, Setoodegan F, De Sanctis V, Karimi M | Acta Endocrinol (Buchar) | 2020 |
| The Predictor Role of Perceived Social Support and Spiritual Intelligence in Hope Among Thalassemia Patients. | Pasyar N, Rambod M, Behrouzi Z | Malays J Med Sci | 2020 |
| The Use of Extracorporeal Membrane Oxygenation During Acute Chest Crisis in an Adult Sickle Cell Disease Patient: Identification of Pearls and Pitfalls. | Tanenbaum MT, Shvygina A, Sridhar V, Vaughn JE, Joseph M | Am Surg | 2020 |
| Process mapping of the urgent red cell exchange procedure for patients with severe complications of sickle cell disease at a centralized hemapheresis service. | Smith JA, Seheult JN, Sevcik J, Kiss JE, Kaplan A | J Clin Apher | 2020 |
| Drug Therapies for the Management of Sickle Cell Disease. | Rai P, Ataga KI | F1000Res | 2020 |
| Evaluation of a clinical protocol using intranasal fentanyl for treatment of vaso-occlusive crisis in sickle cell patients in the emergency department. | Paquin H, Trottier ED, Pastore Y, Robitaille N, Dore Bergeron MJ, Bailey B | Paediatr Child Health | 2020 |
| Author Correction: Baseline and Disease-Induced Transcriptional Profiles in Children with Sickle Cell Disease. | Creary S, Shrestha CL, Kotha K, Minta A, Fitch J, Jaramillo L, Zhang S, Pinto S, Thompson R, Ramilo O, White P, Mejias A, Kopp BT | Sci Rep | 2020 |
| Nitric oxide donors offer protection to RBC from storage lesion. | Sengupta P, Mahalakshmi V, Stebin JJ, Ganesh S, Suganya N, Chatterjee S | Transfus Clin Biol | 2020 |
| Menstrual Type, Pain and Psychological Distress in Adult Women with Sickle Cell Disease (SCD). | Sollers JJ, Leach-Beale B, Barker CS, Wood M, Burford T, Bell K, Muhammad M, Lands JR, Smith N, Miller J, Jones B, Murrill AN, Killough A, Robinson E, Whitfield KE, Byrd GS, Edwards CL | J Natl Med Assoc | 2020 |
| Psychosocial and Clinical Risk Factors Associated with Substance Use in Observational Cohort of Patients with Sickle Cell Disease. | Wilson JD, Lanzkron S, Pecker LH, Bediako SM, Han D, Beach MC | Subst Use Misuse | 2020 |
| Assessment of cardiac and liver iron overload by magnetic resonance imaging in patients with thalassemia major: short-term follow-up. | Bayav M, Isiksalan Ozbulbul N, Bor O | J Int Med Res | 2020 |
| Unmasking hypertension in children and adolescents with sickle/beta-thalassemia. | Stabouli S, Antza C, Papadopoulou E, Teli A, Kotsis V, Economou M | J Clin Hypertens (Greenwich) | 2020 |
| Blood management during the COVID-19 pandemic. | Tolich D, Auron M, McCoy K, Dargis M, Quraishy N | Cleve Clin J Med | 2020 |
| Viral metagenomics in Brazilian multiply transfused patients with sickle cell disease as an indicator for blood transfusion safety. | Nunes Valença I, Silva-Pinto AC, Araújo da Silva Júnior W, Tadeu Covas D, Kashima S, Nanev Slavov S | Transfus Clin Biol | 2020 |
| Assessment of ventricular dysfunction in Egyptian children with Beta-thalassemia major. | Deraz SE, Abd El Naby SA, Mahmoud AA | Hematol Oncol Stem Cell Ther | 2020 |
| Ocular Manifestations of Sickle Cell Disease in Different Genotypes. | AlRyalat SA, Jaber BAM, Alzarea AA, Alzarea AA, Alosaimi WA, Al Saad M | Ophthalmic Epidemiol | 2020 |
| Existential analysis of mothers in the care of their children with Sickle Cell Disease. | Ramos CM, Pacheco ZML, Vargas IMÁ, Araújo PA | Rev Bras Enferm | 2020 |
| ATF4 Regulates MYB to Increase γ-Globin in Response to Loss of β-Globin. | Boontanrart MY, Schröder MS, Stehli GM, Banović M, Wyman SK, Lew RJ, Bordi M, Gowen BG, DeWitt MA, Corn JE | Cell Rep | 2020 |
| Elevated levels of circulating monocytic myeloid derived suppressor cells in splenectomised β-thalassaemia/HbE patients. | Siriworadetkun S, Thubthed R, Thiengtavor C, Paiboonsukwong K, Khuhapinant A, Fucharoen S, Pattanapanyasat K, Vadolas J, Svasti S, Chaichompoo P | Br J Haematol | 2020 |
| Has the time come to implement gene therapy for sickle cell disease? | Ginsberg N, Shulman LP | Arch Gynecol Obstet | 2020 |
| Patient-Reported Outcomes and Economic Burden of Adults with Sickle Cell Disease in the United States: A Systematic Review. | Lee S, Vania DK, Bhor M, Revicki D, Abogunrin S, Sarri G | Int J Gen Med | 2020 |
| Effect of Mutations on mRNA and Globin Stability: The Cases of Hb Bernalda/Groene Hart and Hb Southern Italy. | Cardiero G, Musollino G, Friscia MG, Testa R, Virruso L, Di Girgenti C, Caldora M, Colella Bisogno R, Gaudiano C, Manco G, Lacerra G | Genes (Basel) | 2020 |
| Automated Semantic Segmentation of Red Blood Cells for Sickle Cell Disease. | Zhang M, Li X, Xu M, Li Q | IEEE J Biomed Health Inform | 2020 |
| Cardiorenal syndrome in thalassemia patients. | Makmettakul S, Tantiworawit A, Phrommintikul A, Piriyakhuntorn P, Rattanathammethee T, Hantrakool S, Chai-Adisaksopha C, Rattarittamrong E, Norasetthada L, Fanhchaksai K, Charoenkwan P, Lekawanvijit S | BMC Nephrol | 2020 |
| Hepatocellular carcinoma in adult thalassemia patients: an expert opinion based on current evidence. | Mangia A, Bellini D, Cillo U, Laghi A, Pelle G, Valori VM, Caturelli E | BMC Gastroenterol | 2020 |
| Heparanase Level and Procoagulant Activity Are Increased in Thalassemia and Attenuated by Janus Kinase 2 Inhibition. | Ghoti H, Ackerman S, Rivella S, Casu C, Nadir Y | Am J Pathol | 2020 |
| Communicating and understanding pain: Limitations of pain scales for patients with sickle cell disorder and other painful conditions. | Collins PJ, Renedo A, Marston CA | J Health Psychol | 2020 |
| Accidental hydroxyurea overdosage in a child with sickle cell anemia: An African experience. | Nnebe-Agumadu U, Adebayo IA, Nnodu O, Adekile A | Pediatr Blood Cancer | 2020 |
| The effects of selective beta-adrenergic blockade on bone marrow dysfunction following severe trauma and chronic stress. | Miller ES, Apple CG, Kannan KB, Funk ZM, Efron PA, Mohr AM | Am J Surg | 2020 |
| Characterization of Sensorineural Hearing Loss in Adult Patients With Sickle Cell Disease: A Systematic Review and Meta-analysis. | Kapoor E, Strum D, Shim T, Kim S, Sabetrasekh P, Monfared A | Otol Neurotol | 2020 |
| The Liver in Sickle Cell Disease. | Lacaille F, Allali S, de Montalembert M | J Pediatr Gastroenterol Nutr | 2020 |
| COVID-19 Infection in a Child With Thalassemia Major After Hematopoietic Stem Cell Transplant. | Sarbay H, Atay A, Malbora B | J Pediatr Hematol Oncol | 2020 |
| Corrigendum to | Isa H, Adegoke S, Madu A, Hassan AA, Ohiaeri C, Chianumba R, Brown B, Okocha E, Ugwu N, Diaku-Akinwumi I, Adeyemo T, Kuliya-Gwarzo A, Dogara L, Lawal H, Tanko Y, Ladu A, Kangiwa U, Ekwem L, Oniyangi S, Wakama T, Umoru D, Olanrewaju O, Akinola N, Nnebe-Agumadu U, Asala S, Adekile A, Olaniyi J, Sangeda R, , Nnodu O | Blood Cells Mol Dis | 2020 |
| Combined chelation with high-dose deferiprone and deferoxamine to improve survival and restore cardiac function effectively in patients with transfusion-dependent thalassemia presenting severe cardiac complications. | Chuang TY, Li JP, Weng TF, Wu KH, Chao YH | Ann Hematol | 2020 |
| Vaso-occlusive crisis in a sickle cell patient after transfusion-transmitted dengue infection. | Santos FLS, Slavov SN, Bezerra RS, Santos EV, Silva-Pinto AC, Morais ALL, Sá MB, Ubiali EMA, De Santis GC, Covas DT, Kashima S | Transfusion | 2020 |
| Imaging review of sickle cell disease for the emergency radiologist. | Gilyard SN, Hamlin SL, Johnson JO, Herr KD | Emerg Radiol | 2020 |
| Effect of HBB genotype on survival in a cohort of transfusion-dependent thalassemia patients in Cyprus. | Kountouris P, Michailidou K, Christou S, Hadjigavriel M, Sitarou M, Kolnagou A, Kleanthous M, Telfer P | Haematologica | 2020 |
| Eculizumab for complement mediated thrombotic microangiopathy in sickle cell disease. | Chonat S, Graciaa S, Shin HS, Newton JG, Quarmyne MO, Boudreaux J, Tang A, Zerra PE, Rollins MR, Josephson CD, Brown C, Joiner CH, Fasano RM, Stowell SR | Haematologica | 2020 |
| Targeting the bone marrow niche in hemoglobinopathies. | Carlesso N | Blood | 2020 |
| Characterization of kidney complications in patients with sickle cell anemia. | Isaza-López MC, Rojas-Rosas LF, Echavarría-Ospina L, Serna-Higuita LM | Rev Chil Pediatr | 2020 |
| Smartphone-based sickle cell disease detection and monitoring for point-of-care settings. | Ilyas S, Sher M, Du E, Asghar W | Biosens Bioelectron | 2020 |
| Iron overload as a risk factor for poor graft function following allogeneic hematopoietic stem cell transplantation. | Wu XQ, Lin KN, Chen MM, Jiang PF, Zhang YX, Chen YQ, Chen QR, Xiao M, Zhu HJ, Issa HA, Chen SZ, Luo XF, Ren JH, Li Q, Zeng YL, Xu JJ, Lin YF, Zheng R, Zheng ZH, Chen ZZ, Hu JD, Yang T | Kaohsiung J Med Sci | 2020 |
| Early detection of ventricular dysfunction by tissue Doppler echocardiography related to cardiac iron overload in patients with thalassemia. | Silvilairat S, Charoenkwan P, Saekho S, Tantiworawit A, Srichairatanakool S | Int J Cardiovasc Imaging | 2020 |
| Analysis of Hb levels and degree of anemia in relation to genotype in 615 patients with hemoglobin H disease. | Luo S, Chen X, Chen L, Zhong Q, Wang Q, Xu Z, Huang J, Yan T, Tang N | Expert Rev Hematol | 2020 |
| α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser ( or c.96G>T or C)] with the α-Thalassemia-1 [- - (Southeast Asian)] Deletion in Thailand. | Panyasai S, Phasit A | Hemoglobin | 2020 |
| A Report on the Education, Employment and Marital Status of Thalassemia Patients from a Tertiary Care Center in the Middle East. | Bou-Fakhredin R, Ghanem NN, Kreidieh F, Tabbikha R, Daadaa H, Ajouz J, Koussa S, Taher AT | Hemoglobin | 2020 |
| Cellular and Molecular Aspects of Blood Cell-Endothelium Interactions in Vascular Disorders. | Wautier JL, Wautier MP | Int J Mol Sci | 2020 |
| Complications and Challenges in the Management of Iraqi Patients with β-Thalassemia Major: A Single-center Experience. | Sadullah RK, Atroshi SD, Al-Allawi NA | Oman Med J | 2020 |
| Time to apply a social determinants of health lens to addressing sickle cell disorders in sub-Saharan Africa. | Berghs M, Ola B, Cronin De Chavez A, Ebenso B | BMJ Glob Health | 2020 |
| Molecular spectrum of Hb H disease and characterization of rare deletional α-thalassemia found in Thailand. | Jomoui W, Tepakhan W, Satthakarn S, Panyasai S | Scand J Clin Lab Invest | 2020 |
| Novel α-Thalassemia Deletion Identified in an Indian Infant with Hb H Disease. | Moore JA, Pullon BM, Drake KM, Brennan SO | Hemoglobin | 2020 |
| Impact of COVID-19 Infection on 24 Patients with Sickle Cell Disease. One Center Urban Experience, Detroit, MI, USA. | Balanchivadze N, Kudirka AA, Askar S, Almadhoun K, Kuriakose P, Fadel R, Dabak V | Hemoglobin | 2020 |
| Sickle Cell Disease: A Paradigm for Venous Thrombosis Pathophysiology. | Lizarralde-Iragorri MA, Shet AS | Int J Mol Sci | 2020 |
| Analysis of rare thalassemia caused by HS-40 regulatory site deletion. | Luo S, Chen X, Zhong Q, Wang Q, Xu Z, Qin L, Wang J, Yuan D, Yan T, Tang N | Hematology | 2020 |
| Hydroxycarbamide decreases the free alpha-hemoglobin pool in red blood cells of adult patients with sickle cell anemia. | Domingues-Hamdi E, Vasseur C, Pakdaman S, Moutereau S, Habibi A, Bartolucci P, Galactéros F, Baudin-Creuza V | Am J Hematol | 2020 |
| Sickle cell disease: Progress made & challenges ahead. | Odame I, Jain D | Indian J Med Res | 2020 |
| Mutation spectrum and erythrocyte indices characterisation of α-thalassaemia and β-thalassaemia in Sichuan women in China: a thalassaemia screening survey of 42 155 women. | Li B, Han X, Ma J, Yang D | J Clin Pathol | 2020 |
| Evaluation of Erythroferrone, Hepcidin, and Iron Overload Status in Iraqi Transfusion-Dependent β-Thalassemia Major Patients. | Smesam HNK, Albuthabhak HAQ, Arjmand S, Al-Hakeim HK, R Siadat SO | Hemoglobin | 2020 |
| Design, synthesis, and optimization of a series of 2-azaspiro[3.3]heptane derivatives as orally bioavailable fetal hemoglobin inducers. | Katayama K, Tsunemi T, Miyazaki K, Uoto K, Yoshioka R, Terashima H, Terakawa M, Yamashiro K, Haruyama M, Maeda H, Makino T | Bioorg Med Chem Lett | 2020 |
| Blood transfusion for preventing primary and secondary stroke in people with sickle cell disease. | Estcourt LJ, Kohli R, Hopewell S, Trivella M, Wang WC | Cochrane Database Syst Rev | 2020 |
| Household material hardships impact emergency department reliance in pediatric patients with sickle cell disease. | Power-Hays A, Patterson A, Sobota A | Pediatr Blood Cancer | 2020 |
| NRF2 mediates γ-globin gene regulation through epigenetic modifications in a β-YAC transgenic mouse model. | Zhu X, Xi C, Ward A, Takezaki M, Shi H, Peterson KR, Pace BS | Exp Biol Med (Maywood) | 2020 |
| Hydroxycarbamide exposure and ovarian reserve in women with sickle cell disease in the Multicenter Study of Hydroxycarbamide. | Pecker LH, Hussain S, Christianson MS, Lanzkron S | Br J Haematol | 2020 |
| Molecular spectrum of α-thalassemia mutations in Erbil province of Iraqi Kurdistan. | Shamoon RP | Mol Biol Rep | 2020 |
| Biochemical and therapeutic effects of Omega-3 fatty acids in sickle cell disease. | Daak AA, Lopez-Toledano MA, Heeney MM | Complement Ther Med | 2020 |
| Randomized phase 2 trial of Intravenous Gamma Globulin (IVIG) for the treatment of acute vaso-occlusive crisis in patients with sickle cell disease: Lessons learned from the midpoint analysis. | Manwani D, Xu C, Lee SK, Amatuni G, Cohen HW, Carullo V, Morrone K, Davila J, Shi PA, Ireland K, Keenan J, Frenette PS | Complement Ther Med | 2020 |
| Moyamoya Syndrome in a 32-Year-Old Male With Sickle Cell Anemia. | Yamani M, Obaid EF, Hemida AH | Cureus | 2020 |
| Neurologic recovery in systemic nontraumatic fat embolism syndrome in an elderly patient with hemoglobin SC disease: A case report. | Ositelu A, Urrutia-Argueta S, Kapoor R | Clin Case Rep | 2020 |
| TLR4 Signaling by Heme and the Role of Heme-Binding Blood Proteins. | Janciauskiene S, Vijayan V, Immenschuh S | Front Immunol | 2020 |
| Nucleic Acid Therapy for β-Thalassemia. | d'Arqom A | Biologics | 2020 |
| 3 cases of variant hemoglobin Hb A2-Niigata detected by falsely high HbA1c values. | Ito M, Sano K, Koga M | Clin Chim Acta | 2020 |
| Cognitive functioning, patient health communication, and worry mediate pain predictive effects on health-related quality of life in youth with sickle cell disease. | Varni JW, Panepinto JA | Pediatr Blood Cancer | 2020 |
| Haemoglobin Constant Spring (HbA2: c.427T>C) and Haemoglobin Adana (HbA2: c.179G>A) in jaundiced Malaysian term neonates with clinically significant hyperbilirubinemia. | Shwe S, Boo NY, Ong HK, Chee SC, Maslina M, Ling MMM, Ahluwalia AK | Malays J Pathol | 2020 |
| Microcytic to hypochromic ratio as a discriminant index of thalassaemia trait in subjects with hypochromic anaemia. | Wee SY, Muhamed Said SS, Raja Sabudin RZA, Alauddin H, Ithnin A | Malays J Pathol | 2020 |
| Assessment of the Martín-Sánchez indices for distinguishing beta thalassemia trait from iron deficiency anemia. | Hoffmann JJML, Urrechaga E | Clin Chim Acta | 2020 |
| Prevalence of Sickle Cell Trait and Rare Hemoglobin Variants in the Metropolitan Washington DC Area. | Niu X, Parry CS, Mason A, Harrison B, Nouraie SM, Ammosova T, Salomon-Andonie J, Oneal PA, Gordeuk VR, Taylor JG, Nekhai S | J Hematol | 2020 |
| How to implement endurance exercise training in sickle cell disease. | Messonnier LA, Riccetti M, Chatel B, Galactéros F, Gellen B, Rupp T, Féasson L, Bartolucci P | Haematologica | 2020 |
| Fetal hemoglobin rescues ineffective erythropoiesis in sickle cell disease. | El Hoss S, Cochet S, Godard A, Yan H, Dussiot M, Frati G, Boutonnat-Faucher B, Laurance S, Renaud O, Joseph L, Miccio A, Brousse V, Mohandas N, El Nemer W | Haematologica | 2020 |
| Oxidative stress activates red cell adhesion to laminin in sickle cell disease. | Lizarralde-Iragorri MA, Lefevre SD, Cochet S, El Hoss S, Brousse V, Filipe A, Dussiot M, Azouzi S, Le Van Kim C, Rodrigues-Lima F, Français O, Le Pioufle B, Klei T, van Bruggen R, El Nemer W | Haematologica | 2020 |
| Evidence-based dental management in the new era of sickle cell disease: A scoping review. | Hsu LL, Fan-Hsu J | J Am Dent Assoc | 2020 |
| Association of HIV infection with clinical and laboratory characteristics of sickle cell disease. | Belisário AR, Blatyta PF, Vivanco D, Oliveira CDL, Carneiro-Proietti AB, Sabino EC, de Almeida-Neto C, Loureiro P, Máximo C, de Oliveira Garcia Mateos S, Flor-Park MV, de Oliveira Werneck Rodrigues D, Afonso Mota R, Gonçalez TT, Hoffmann TJ, Kelly S, Custer B, | BMC Infect Dis | 2020 |
| Sickle Cell-Related Complications in Patients Undergoing Cardiopulmonary Bypass. | Chacon-Portillo MA, Mossad EB, Zea-Vera R, Beckerman Z, Binsalamah ZM, Adachi I, Mery CM, Imamura M, Heinle JS, Fraser CD | World J Pediatr Congenit Heart Surg | 2020 |
| Peripartum hyperhemolysis prophylaxis and management in sickle cell disease: A case report and narrative review. | Vasanthamohan L, Choo S, Marshall T, Symons YT, Matsui D, Eastabrook G, Solh Z | Transfusion | 2020 |
| Epidemiology and treatment of beta thalassemia major in China. | Xu X, Wu X | Pediatr Investig | 2020 |
| An Innovative Multilevel Test for Hemoglobinopathies: TGA/Chemometrics Simultaneously Identifies and Classifies Sickle Cell Disease From Thalassemia. | Risoluti R, Caprari P, Gullifa G, Massimi S, Maffei L, Sorrentino F, Carcassi E, Materazzi S | Front Mol Biosci | 2020 |
| Chronic Thromboembolic Pulmonary Hypertension in a Child With Sickle Cell Disease. | Spencer R, Valencia Villeda G, Takeda K, Rosenzweig EB | Front Pediatr | 2020 |
| Post-translational modification as a response to cellular stress induced by hemoglobin oxidation in sickle cell disease. | Strader MB, Jana S, Meng F, Heaven MR, Shet AS, Thein SL, Alayash AI | Sci Rep | 2020 |
| Critical illness-associated cerebral microbleed in a patient with sickle cell disease: A case report and review of the literature. | Shafaat O, Sotoudeh H, Zandifar A, Chapman PR, Roberson GH, Sotoudeh E, Singhal A | Clin Imaging | 2020 |
| Acute lymphoblastic leukemia in a β-thalassemia intermedia child: A case report. | Sherief LM, Goneim E, Kamal NM, Ibraheim A, Alsofiani F, Alawur A | World J Clin Pediatr | 2020 |
| Diagnosis of Kikuchi-Fujimoto disease in an 11-year-old girl with fever and sickle cell disease. | Cannon L, Wang E, Becker M | BMJ Case Rep | 2020 |
| Multiple sclerosis in a young woman with sickle cell disease. | Kerpen K, Baptiste A, Yeshokumar AK | Mult Scler Relat Disord | 2020 |
| Age-dependent characterization of carotid and cerebral artery geometries in a transgenic mouse model of sickle cell anemia using ultrasound and microcomputed tomography. | Rivera CP, Li L, Cai S, Pei N, McAlear GE, Bollavaram K, Ariyo OV, Omojola VO, Song H, Alfonso AL, Tan W, Huo Y, Platt MO | Blood Cells Mol Dis | 2020 |
| Efficacy and safety of recently approved drugs for sickle cell disease: a review of clinical trials. | Ali MA, Ahmad A, Chaudry H, Aiman W, Aamir S, Anwar MY, Khan A | Exp Hematol | 2020 |
| Sickle cell disease and COVID-19: Atypical presentations and favorable outcomes. | Azerad MA, Bayoudh F, Weber T, Minon JM, Ketelslegers O, Hoyoux M, Ren X, Kaye O, De Marneffe N, Fraipont V, Masset C, Bouillon AS, Jaspers A, Tebache M, D'Hoen G, Habibi A, Efira A, Thachil J, Deckmyn H, Beguin Y | EJHaem | 2020 |
| Clinical management of a Nigerian patient affected by sickle cell disease with rare blood group and persistent SARS-CoV-2 positivity. | Quaresima M, Quaresima V, Naldini MM, Cirillo DM, Ferrari A, Mazzi A, Tesini EMC, Leone MC, Merli F | EJHaem | 2020 |
| Early Detection of Renal Injury in Children with Sickle Cell Anaemia using Microalbuminuria in a Tertiary Health Institution in Southern Nigeria. | Ekpenyong EE, Ikpeme EE, Bassey EG, Dixon-Umo OT | West Afr J Med | 2020 |
| Detection of Early Renal Disease In Children With Sickle Cell Anaemia Using Microalbuminuria As A Surrogate Marker. | Arogundade FA | West Afr J Med | 2020 |
| The Burden of Obstructive Sleep Apnea in Pediatric Sickle Cell Disease: a Kids' Inpatient Database Study. | Tsou PY, Cielo CM, Xanthopoulos MS, Wang YH, Kuo PL, Tapia IE | Sleep | 2020 |
| Alpha thalassemia genotypes in Kuwait. | Adekile A, Sukumaran J, Thomas D, D'Souza T, Haider M | BMC Med Genet | 2020 |
| Editorial for | Pattira B | J Magn Reson Imaging | 2020 |
| An Interrupted Time Series Analysis of the Dissemination of a Sickle Cell Vaso-Occlusive Episode Treatment Algorithm and a Case Management Referral Form for Individuals With Sickle Cell Disease in the Emergency Department. | Bulgin D, Bonnabeau E, Alexander A, Frederick E, Rains G, Shah N, Young M, Tanabe P | J Emerg Nurs | 2020 |
| Vulnerable Child Syndrome and Newborn Screening Carrier Results for Cystic Fibrosis or Sickle Cell. | Farrell MH, Sims AM, La Pean Kirschner A, Farrell PM, Tarini BA | J Pediatr | 2020 |
| Splenic Infarct Secondary to High Altitude Exposure in Sickle Cell Trait Patients: A Case Series. | Gonzalez L, Shapiro AF, Tafur A, Plaza-Meneses C, Sabando B | Cureus | 2020 |
| Mixed Bullous-Eczematous Contact Dermatitis From a Black Henna Tattoo in an African American Female With Sickle Cell Disease With Post-Dermatitis Pain. | Persaud-Sharma D, Govea M, Hernandez R | Cureus | 2020 |
| The Prevalence of Uterine Fibroids in African American Women with Hemoglobin SS Sickle Cell Disease as Determined by Pelvic Magnetic Resonance Imaging. | Jones DC, Ronald J, Pabon-Ramos W, Prescott J, Martin JG | Acad Radiol | 2020 |
| Screening for Obstructive Sleep Apnea in Children With Sickle Cell Disease: A Pilot Study. | Maroda AJ, Spence MN, Larson SR, Estepp JH, Gillespie MB, Harris AJ, Mamidala MP, Sheyn AM | Laryngoscope | 2020 |
| Long-term results of the NF-08-TM protocol in stem cell transplant for patients with thalassemia major: A multi-center large-sample study. | He Y, Jiang H, Li C, Zhu Y, Wu X, Liu S, Qu Y, Liao J, Feng X, Liu H, Peng Z, He L, Pu C, Gautam M, Leung W, Li C | Am J Hematol | 2020 |
| Severe delayed hemolytic transfusion reaction due to anti-Fy3 in a patient with sickle cell disease undergoing red cell exchange prior to hematopoietic progenitor cell collection for gene therapy. | Stone EF, Avecilla ST, Wuest DL, Lomas-Francis C, Westhoff CM, Diuguid DL, Sadelain M, Boulad F, Shi PA | Haematologica | 2020 |
| The molecular basis for the prothrombotic state in sickle cell disease. | Shet AS, Lizarralde-Iragorri MA, Naik RP | Haematologica | 2020 |
| Interleukin-1 receptor inhibition reduces stroke size in a murine model of sickle cell disease. | Venugopal J, Wang J, Mawri J, Guo C, Eitzman D | Haematologica | 2020 |
| De novo heterozygous Hb G-Waimanalo (α64(E13)Asp>Asn, CTG>CCG; HBA1:c.193G>A) variant in a sickle cell disease patient of an Indian tribe. | Kumar R, Mishra S, Uikey RS, Gwal A, Mun A, Bharti PK, Shanmugam R | J Clin Pathol | 2020 |
| Management of chronic respiratory complications in children and adolescents with sickle cell disease. | Arigliani M, Gupta A | Eur Respir Rev | 2020 |
| Retinal ultra-wide-field colour imaging versus dilated fundus examination to screen for sickle cell retinopathy. | Alabduljalil T, Cheung CS, VandenHoven C, Mackeen LD, Kirby-Allen M, Kertes PJ, Lam WC | Br J Ophthalmol | 2020 |
| Southeast Asian Ovalocytosis and Hemoglobinopathies in Newborns: Prevalence, Molecular, and Hematological Analyses. | Yamsri S, Kawon W, Duereh A, Fucharoen G, Fucharoen S | J Pediatr Hematol Oncol | 2020 |
| Assessment of Bone Metabolism Alterations in Transfusion-dependent Beta-thalassemia Major: An Observational Study. | Murtas A, Zanza C, Vacca N, Saderi L, Sotgiu G, Fozza C, Antonucci R | J Pediatr Hematol Oncol | 2020 |
| Physical Therapy in Pediatric and Young Adult Patients With Sickle Cell Disease: Assessing Potential Benefits and Barriers. | Callaway D, Chawla A, Sprinz P | J Pediatr Hematol Oncol | 2020 |
| Vaso-occlusive crises and costs of sickle cell disease in patients with commercial, Medicaid, and Medicare insurance - the perspective of private and public payers. | Shah NR, Bhor M, Latremouille-Viau D, Kumar Sharma V, Puckrein GA, Gagnon-Sanschagrin P, Khare A, Kumar Singh M, Serra E, Davidson M, Xu L, Guerin A | J Med Econ | 2020 |
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| Ultrasound Features of Fetal Anemia Lessons From Hemoglobin Bart Disease. | Thammavong K, Luewan S, Wanapirak C, Tongsong T | J Ultrasound Med | 2020 |
| Sickle cell anemia and COVID-19: Use of voxelotor to avoid transfusion. | Ershler WB, Holbrook ME | Transfusion | 2020 |
| Adherence to a selective antenatal haemoglobinopathy screening policy within a tertiary level obstetric unit in Australia. | Borbolla Foster A, Smith E, Ross B | Aust N Z J Obstet Gynaecol | 2020 |
| Curative in vivo hematopoietic stem cell gene therapy of murine thalassemia using large regulatory elements. | Wang H, Georgakopoulou A, Li C, Liu Z, Gil S, Bashyam A, Yannaki E, Anagnostopoulos A, Pande A, Izsvák Z, Papayannopoulou T, Lieber A | JCI Insight | 2020 |
| Characterising demographics, knowledge, practices and clinical care among patients attending sickle cell disease clinics in Eastern Uganda. | Olupot-Olupot P, Wabwire H, Ndila C, Adong R, Ochen L, Amorut D, Abongo G, Okalebo CB, Akello SR, Oketcho JB, Okiror W, Asio S, Odiit A, Alaroker F, Nyutu G, Maitland K, Williams TN | Wellcome Open Res | 2020 |
| Abatacept is effective as GVHD prophylaxis in unrelated donor stem cell transplantation for children with severe sickle cell disease. | Ngwube A, Shah N, Godder K, Jacobsohn D, Hulbert ML, Shenoy S | Blood Adv | 2020 |
| Appropriate thresholds for accurate screening for β-thalassemias in the newborn period: results from a French center for newborn screening. | Allaf B, Pondarre C, Allali S, De Montalembert M, Arnaud C, Barrey C, Benkerrou M, Benhaim P, Bensaid P, Brousse V, Dollfus C, Eyssette-Guerreau S, Galacteros F, Gajdos V, Garrec N, Guillaumat C, Guitton C, Monfort-Gouraud M, Gouraud F, Holvoet L, Ithier G, Kamdem A, Koehl B, Malric A, Missud F, Monier B, Odièvre MH, Joly P, Renoux C, Patin F, Pissard S, Couque N | Clin Chem Lab Med | 2020 |
| Pica behaviors in pediatric patients with sickle cell disease: a scoping review protocol. | Clark OM, Williams R | JBI Evid Synth | 2020 |
| Automated exchange compared to manual and simple blood transfusion attenuates rise in ferritin level after 1 year of regular blood transfusion therapy in chronically transfused children with sickle cell disease. | Kelly S, Rodeghier M, DeBaun MR | Transfusion | 2020 |
| Pedigree Analysis of Nonhomologous Sequence Recombination of and Genes. | Luo SQ, Chen XY, Tang N, Huang J, Zhong QY, Cai R, Yan TZ | Hemoglobin | 2020 |
| Consanguinity, the driving force behind inheritance of HbS-β thalassemia in Southern Districts of KP. | Khan J, Muhammad D, Ismail M, Khan I, , Niaz S | J Pak Med Assoc | 2020 |
| Fetal Hemoglobin in Sickle Cell Anemia. | Steinberg MH | Blood | 2020 |
| Germline Gene Editing for Sickle Cell Disease. | Sharma A, Bhakta N, Johnson LM | Am J Bioeth | 2020 |
| Extremely high birth prevalence of sickle cell disease in rural Tanzania. | Eastburg L, Peckham A, Kawira E, Chirangi B, Adler D, Akungo BD, Smart LR, Ambrose EE | Pediatr Blood Cancer | 2020 |
| Phenotypical and functional abnormalities of circulating neutrophils in patients with β-thalassemia. | Buttari B, Profumo E, Caprari P, Massimi S, Sorrentino F, Maffei L, Gabbianelli M, Riganò R | Ann Hematol | 2020 |
| Prediction, management, and prognosis of mixed chimerism after hematopoietic stem cell transplantation in transfusion-dependent pediatric thalassemia patients. | Chen H, Li XY, Zhan LP, Fang JP, Huang K, Li Y, Weng WJ, Xu LH, Xu HG, Zhou DH | Pediatr Transplant | 2020 |
| Allogeneic hematopoietic stem cell transplantation from sibling and unrelated donors in pediatric patients with sickle cell disease-A single center experience. | Kogel F, Hakimeh D, Sodani P, Lang P, Kühl JS, Hundsdoerfer P, Künkele A, Eggert A, Oevermann L, Schulte JH | Pediatr Transplant | 2020 |
| Supramolecular nanosubstrate-mediated delivery system enables CRISPR-Cas9 knockin of hemoglobin beta gene for hemoglobinopathies. | Yang P, Chou SJ, Li J, Hui W, Liu W, Sun N, Zhang RY, Zhu Y, Tsai ML, Lai HI, Smalley M, Zhang X, Chen J, Romero Z, Liu D, Ke Z, Zou C, Lee CF, Jonas SJ, Ban Q, Weiss PS, Kohn DB, Chen K, Chiou SH, Tseng HR | Sci Adv | 2020 |
| Characterization of HIV risks in a Brazilian sickle cell disease population. | Blatyta PF, Kelly S, Goncalez TT, Carneiro-Proietti AB, Salomon T, Miranda C, Sabino E, Preiss L, Maximo C, Loureiro P, Custer B, de Almeida-Neto C, | BMC Public Health | 2020 |
| Liver complications of haemoglobin H disease in adults. | Chan LKL, Mak VWM, Chan SCH, Yu ELM, Chan NCN, Leung KFS, Ng CKM, Ng MHL, Chan JCW, Lee HKK | Br J Haematol | 2020 |
| Oxygen gradient ektacytometry-derived biomarkers are associated with vaso-occlusive crises and correlate with treatment response in sickle cell disease. | Rab MAE, Kanne CK, Bos J, van Oirschot BA, Boisson C, Houwing ME, Gerritsma J, Teske E, Renoux C, Riedl J, Schutgens REG, Bartels M, Nur E, Joly P, Fort R, Cnossen MH, van Wijk R, Connes P, van Beers EJ, Sheehan VA | Am J Hematol | 2020 |
| Diaphragm ultrasonography in adults with sickle cell anemia: evaluation of morphological and functional aspects. | Zeitoune R, Mogami R, Koifman ACB, Lopes AJ, Soares AR, Martins RAG, Maioli MCP | Hematology | 2020 |
| Co-morbidities and mortality associated with transfusion-dependent beta-thalassaemia in patients in England: a 10-year retrospective cohort analysis. | Jobanputra M, Paramore C, Laird SG, McGahan M, Telfer P | Br J Haematol | 2020 |
| Investigating the missing heritability of foetal haemoglobin level in Africa. | Wonkam A | Br J Haematol | 2020 |
| The evolution of clinical research in thalassaemia: where has all the funding gone? | Rund D | Br J Haematol | 2020 |
| Complications of Central Venous Access Devices in Patients With Sickle Cell Disease and Thalassemia Major. | Ordóñez J, Del Cañizo A, Beléndez C, García-Morín M, Pérez-Egido L, Fanjul M, García-Casillas MA, Cerdá J, Peláez D, Bardón E, de Agustín JC, Cela E | J Pediatr Hematol Oncol | 2020 |
| Pain in Youth with Sickle Cell Disease: A Report from the Sickle Cell Clinical Research and Intervention Program. | Alberts NM, Kang G, Li C, Richardson PA, Hodges J, Hankins JS, Klosky JL | Clin J Pain | 2020 |
| Surgical and Medical Perioperative Management of Sickle Cell Retinopathy: A Literature Review. | Nithianandan H, Sridhar J | Int Ophthalmol Clin | 2020 |
| Unannotated single nucleotide polymorphisms in the TATA box of erythropoiesis genes show in vitro positive involvements in cognitive and mental disorders. | Ponomarenko M, Sharypova E, Drachkova I, Chadaeva I, Arkova O, Podkolodnaya O, Ponomarenko P, Kolchanov N, Savinkova L | BMC Med Genet | 2020 |
| Conformational changes of β-thalassemia major hemoglobin and oxidative status of plasma after in vitro exposure to extremely low-frequency electromagnetic fields: An artificial neural network analysis. | Rahmani S, Ansarihadipour H, Bayatiani MR, Khosrowbeygi A, Babaei S, Rasmi Y | Electromagn Biol Med | 2020 |
| Prenatal Diagnosis and Screening of Thalassemia Mutations in Bangladesh: Presence of Rare Mutations. | Aziz MA, Khan WA, Banu B, Das SA, Sadiya S, Begum S | Hemoglobin | 2020 |
| The impact of COVID-19 on transfusion-dependent thalassemia patients of Karachi, Pakistan: A single-center experience. | Arshad Ali S, Azim D, Hassan HM, Iqbal A, Ahmed N, Kumar S, Nasim S | Transfus Clin Biol | 2020 |
| Sophie Uyoga-reducing sickle cell stigma in Africa. | Kirby T | Lancet Haematol | 2020 |
| Prevalence of Sensorineural Hearing Loss in Pediatric Patients with Sickle Cell Disease: A Meta-analysis. | Strum D, Kapoor E, Shim T, Kim S, Sabetrasekh P, Monfared A | Laryngoscope | 2020 |
| Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study. | Barbanera Y, Arcioni F, Lancioni H, La Starza R, Cardinali I, Matteucci C, Nofrini V, Roetto A, Piga A, Grammatico P, Caniglia M, Mecucci C, Gorello P | PLoS One | 2020 |
| Spontaneous splenic rupture, mesenteric ischemia and spinal infarction after aortic repair for acute type A dissection in a patient with sickle cell trait. | Toyoda M, Kitamura T, Nakashima K, Matsunaga Y, Nie M, Miyaji K | Gen Thorac Cardiovasc Surg | 2020 |
| Distinguishing iron deficiency from beta-thalassemia trait by new generation ektacytometry. | Krishnevskaya E, Payán-Pernía S, Hernández-Rodríguez I, Remacha Sevilla ÁF, Ancochea Serra Á, Morales-Indiano C, Serra Ferrer M, Vives-Corrons JL | Int J Lab Hematol | 2020 |
| The Sickle Cell Pro-Inflammatory Response to Interval Testing Study (SPRINTS) in children and young adults with sickle cell anemia - Study design and methodological strategies. | Liem RI, Baynard T, Hsu LL, Garofano R, Green NS, Hankins JS, Ness KK, Rodeghier M, Radom-Aizik S | Contemp Clin Trials Commun | 2020 |
| Effects of Aquatic Exercise on Dimensions of Quality of Life and Blood Indicators in Patients with Beta-Thalassemia Major. | Hasanpour Dehkordi A, Hasani T, Fekri K, Deris F, Etemadifar S | Int J Prev Med | 2020 |
| Complete RH and Kell matching related to low alloimmunisation risk in sickle cell disease: prevalence and risk factors of alloimmunisation in a Spanish Tertiary Care National Reference Centre. | Regalado-Artamendi I, Pérez-Corral AM, García-Morín M, Cela E, Beléndez C, Bardón-Cancho EJ, Pérez-Rus G, Pérez-Sánchez I, Pascual C, Monsalvo S, Falero C, Díez-Martín JL, Anguita J | Blood Transfus | 2020 |
| Mechanisms of enhanced vascular smooth muscle contraction induced by sickle erythrocyte constituents. | Azubuike-Osu S, Uche OK, Ajayi IO, Ebeigbe AB | Niger J Physiol Sci | 2020 |
| Acute Soft Head Syndrome (Subgaleal Haematoma) with Periorbital Oedema as a Rare Presentation in Sickle Cell Disease. | Al-Ansari RY, Al Harbi M, Al-Jubair N, Abdalla L | Eur J Case Rep Intern Med | 2020 |
| Significance of variant annotation for molecular diagnosis of thalassaemia. | Poon KS, Koay ES, Tan KM | J Clin Pathol | 2020 |
| High prevalence of thalassemia with a novel α-thalassemia mutationin in Baoan populations in Guangdong province, China. | Yu Y, Yang Z, Yu H, Sun R, Zhu Y, Guo F | Eur J Obstet Gynecol Reprod Biol | 2020 |
| Using cyproterone acetate to treat recurrent ischemic priapism in a patient with sickle cell anemia as a comorbidity: a case report. | Alshahrani A | J Med Case Rep | 2020 |
| Femur Fracture in a Premature Infant: An Unusual Association of Sickle Cell Disease with Osteogenesis Imperfecta. | Gozum G, Bogdan M, Sundaram R, Kulpa J, Narula P, Agdere L | Am J Case Rep | 2020 |
| Manipulation of developmental gamma-globin gene expression: an approach for healing hemoglobinopathies. | Venkatesan V, Srinivasan S, Babu P, Thangavel S | Mol Cell Biol | 2020 |
| Codanin-1 mutations engineered in human erythroid cells demonstrate role of CDAN1 in terminal erythroid maturation. | Murphy ZC, Getman MR, Myers JA, Burgos Villar KN, Leshen E, Kurita R, Nakamura Y, Steiner LA | Exp Hematol | 2020 |
| Randomized Control Trial of Oral Arginine Therapy for Children with Sickle Cell Anemia Hospitalized for Pain in Nigeria. | Onalo R, Cooper P, Cilliers A, Vorster BC, Uche NA, Oluseyi OO, Onalo VD, Zubairu Y, Ayodele-Kehinde AU, Damilare OM, Figueroa J, Morris CR | Am J Hematol | 2020 |
| F cell numbers are associated with an X-linked genetic polymorphism and correlate with haematological parameters in patients with sickle cell disease. | Urio F, Nkya S, Rooks H, Mgaya JA, Masamu U, Zozimus Sangeda R, Mmbando BP, Brumat M, Mselle T, Menzel S, Luzzatto L, Makani J | Br J Haematol | 2020 |
| Generation of nine iPSC lines (HNMUi002-A, HNMUi003-A, HNMUi004-A, HNMUi005-A, HNMUi006-A, HNMUi007-A, HNMUi008-A, HNMUi009-A, HNMUi010-A) from three Chinese families with thalassemia. | Long P, Wang Z, Yang H, Liu Z, Wu B, Zhong G, Chen J, Sun C, Wang F, Zhou Y, Sun F, Li Q, Ma Y | Stem Cell Res | 2020 |
| Nanoscale adhesion profiling and membrane characterisation in sickle cell disease using hybrid atomic force microscopy-IR spectroscopy. | Fellows AP, Casford MTL, Davies PB, Gibson JS, Brewin JN, Rees DC | Colloids Surf B Biointerfaces | 2020 |
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| Effective Recruitment Strategies for a Sickle Cell Patient Registry Across Sites from the Sickle Cell Disease Implementation Consortium (SCDIC). | Masese RV, DeMartino T, Bonnabeau E, Burns EN, Preiss L, Varughese T, Nocek JM, Lasley P, Chen Y, Davila C, Nwosu C, Scott S, Bowman L, Gordon L, Clesca C, Peters-Lawrence M, Melvin C, Shah N, Tanabe P, | J Immigr Minor Health | 2020 |
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| Association of Hb Shenyang [α26(B7)Ala→Glu, GG>GG, : c.80C>A (or )] with Several Types of α-Thalassemia in Thailand. | Panyasai S, Kongthai K, Phasit A | Hemoglobin | 2020 |
| Computational and drug target analysis of functional single nucleotide polymorphisms associated with Haemoglobin Subunit Beta (HBB) gene. | Soremekun OS, Ezenwa C, Isewon I, Soliman M, Idowu O, Nashiru O, Fatumo S | Comput Biol Med | 2020 |
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| Non-hematopoietic deficiency of proprotein convertase subtilisin/kexin type 9 deficiency leads to more severe anemia in a murine model of sickle cell disease. | Venugopal J, Wang J, Guo C, Lu H, Chen YE, Eitzman DT | Sci Rep | 2020 |
| Successful Hematopoietic Stem Cell Transplantation from a Matched Related Donor with Beta-Thalassemia Minor for Severe Aplastic Anemia. | Jung MY, Lim YT, Lim H, Hah JO, Lee JM | Children (Basel) | 2020 |
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| Pregnancy Outcomes among Patients with Sickle Cell Disease in Brazzaville. | Galiba Atipo Tsiba FO, Itoua C, Ehourossika C, Ngakegni NY, Buambo G, Potokoue Mpia NSB, Elira Dokekias A | Anemia | 2020 |
| Polymorphisms in Inflammatory Genes Modulate Clinical Complications in Patients With Sickle Cell Disease. | Tozatto-Maio K, Girot R, Ly ID, Silva Pinto AC, Rocha V, Fernandes F, Diagne I, Benzerara Y, Dinardo CL, Soler JP, Kashima S, Araujo IL, Kenzey C, Fonseca GHH, Rodrigues ES, Volt F, Jarduli L, Ruggeri A, Mariaselvam C, Gualandro SFM, Rafii H, Cappelli B, Nogueira FM, Scigliuolo GM, Guerino-Cunha RL, Malmegrim KCR, Simões BP, Gluckman E, Tamouza R | Front Immunol | 2020 |
| Circulating Extracellular Vesicles and Endothelial Damage in Sickle Cell Disease. | Lapping-Carr G, Gemel J, Mao Y, Beyer EC | Front Physiol | 2020 |
| Sickle Cell Anemia: Variants in the , , and Genes Are Associated With Improved Hydroxyurea Response. | Yahouédéhou SCMA, Neres JSDS, da Guarda CC, Carvalho SP, Santiago RP, Figueiredo CVB, Fiuza LM, Ndidi US, de Oliveira RM, Fonseca CA, Nascimento VML, Rocha LC, Adanho CSA, da Rocha TSC, Adorno EV, Goncalves MS | Front Pharmacol | 2020 |
| CXCR4 effector neutrophils in sickle cell anemia: potential role for elevated circulating serotonin (5-HT) in CXCR4 neutrophil polarization. | Garcia F, Mendonça R, Miguel LI, Dominical VM, Saad STO, Costa FF, Conran N | Sci Rep | 2020 |
| Daily Cannabis Users with Sickle Cell Disease Show Fewer Admissions than Others with Similar Pain Complaints. | Curtis SA, Brandow AM, DeVeaux M, Zeltermam D, Devine L, Roberts JD | Cannabis Cannabinoid Res | 2020 |
| Management of Acute Pulmonary Embolism in a Patient with Sickle Cell Anemia Using Catheter-Directed Thrombolysis. | Bowers E, Mohapatra AA, Ali AA, Singh MJ | Ann Vasc Surg | 2020 |
| In Vivo HSC Gene Therapy Using a Bi-modular HDAd5/35++ Vector Cures Sickle Cell Disease in a Mouse Model. | Li C, Wang H, Georgakopoulou A, Gil S, Yannaki E, Lieber A | Mol Ther | 2020 |
| Crizanlizumab and comparators for adults with sickle cell disease: a systematic review and network meta-analysis. | Thom H, Jansen J, Shafrin J, Zhao L, Joseph G, Cheng HY, Gupta S, Shah N | BMJ Open | 2020 |
| Accelerated erythrocyte destruction mimicking post-transfusion hyperhaemolysis in the course of uncomplicated vaso-occlusive crisis associated with sickle cell disease. | Conrado MCAV, Fonseca GSVC, Dezan MR, Mendes FR, Hamasaki DT, Chinoca KZ, Fonseca GH, Gualandro SFM, Rocha V, Mendrone-Júnior A, Dinardo CL | Transfus Med | 2020 |
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| Severe infusion-related reaction to crizanlizumab in an adolescent with sickle cell disease. | Karkoska K, Quinn CT, Clapp K, McGann PT | Am J Hematol | 2020 |
| Tricuspid regurgitant jet velocity and myocardial tissue Doppler parameters predict mortality in a cohort of patients with sickle cell disease spanning from pediatric to adult age groups - revisiting this controversial concept after 16 years of additional evidence. | Shah P, Suriany S, Kato R, Bush AM, Chalacheva P, Veluswamy S, Denton CC, Russell K, Khaleel M, Forman HJ, Khoo MCK, Sposto R, Coates TD, Wood JC, Detterich J | Am J Hematol | 2020 |
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| Managing patients with sickle cell disease in primary care. | Hehre RJ | JAAPA | 2020 |
| Administrative data identify sickle cell disease: A critical review of approaches in U.S. health services research. | Grosse SD, Green NS, Reeves SL | Pediatr Blood Cancer | 2020 |
| Relative and Absolute Quantification of Aberrant and Normal Splice Variants in β-Thalassemia. | Patsali P, Papasavva P, Christou S, Sitarou M, Antoniou MN, Lederer CW, Kleanthous M | Int J Mol Sci | 2020 |
| Genetic research and clinical analysis of deletional Chinese γ(γδβ) -thalassemia and Southeast Asian HPFH in South China. | Wu Y, Yao Q, Zhong M, Wu J, Xie L, Su L, Yu F | Ann Hematol | 2020 |
| A stable version of capillary electrophoresis for determining human hemoglobin chains aiming at the screening and diagnosis of thalassemia. | Guo C, Zhang Q, Bao L, Li H, Zheng Q, Guo Z, Chen Y | Anal Methods | 2020 |
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| EDSC: Working to Improve Emergency Department Care of Individuals With Sickle Cell Disease. | Kavanagh PL, Hirshon JM | Ann Emerg Med | 2020 |
| A Caregiver's Perspective: Internist, Active Duty Service Member, and Mother of a Child Living With Sickle Cell Disease. | McGann S | Ann Emerg Med | 2020 |
| A Survey-Based Needs Assessment of Barriers to Optimal Sickle Cell Disease Care in the Emergency Department. | Linton EA, Goodin DA, Hankins JS, Kanter J, Preiss L, Simon J, Souffront K, Tanabe P, Gibson R, Hsu LL, King A, Richardsona LD, Glassberg JA, | Ann Emerg Med | 2020 |
| A Multiyear Cross-sectional Study of Guideline Adherence for the Timeliness of Opioid Administration in Children With Sickle Cell Pain Crisis. | Brousseau DC, Alpern ER, Chamberlain JM, Ellison AM, Bajaj L, Cohen DM, Hariharan S, Cook LJ, Harding M, Panepinto J, | Ann Emerg Med | 2020 |
| Emergency Department Utilization for Patients Living With Sickle Cell Disease: Psychosocial Predictors of Health Care Behaviors. | Abdallah K, Buscetta A, Cooper K, Byeon J, Crouch A, Pink S, Minniti C, Bonham VL | Ann Emerg Med | 2020 |
| Utility of Point-of-Care Lung Ultrasonography for Evaluating Acute Chest Syndrome in Young Patients With Sickle Cell Disease. | Cohen SG, Malik ZM, Friedman S, Russell S, Hagbom R, Alazraki A, McCracken CE, Figueroa J, Adisa OA, Mendis RD, Manoranjithan S, Simon HK, Morris CR | Ann Emerg Med | 2020 |
| Inconsistent Emergency Department Care: The Hidden Cost for Patients With Sickle Cell Disease. | Williams AF | Ann Emerg Med | 2020 |
| Association of Antibiotic Choice With Hospital Length of Stay and Risk Factors for Readmission in Patients With Sickle Cell Disease and Acute Chest Syndrome: An Observational Cohort Study. | Badaki-Makun O, Casella JF, Tackett S, Tao X, Chamberlain JM | Ann Emerg Med | 2020 |
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| The Effect of Use of Individualized Pain Plans in Sickle Cell Patients Presenting to the Emergency Department. | Della-Moretta S, Delatore L, Purcell M, Huang Y, Heinlein M, Adkins E, Desai P | Ann Emerg Med | 2020 |
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| The State of Sickle Cell Disease Care in the United States: How Can Emergency Medicine Contribute? | Giroir BP, Collins F | Ann Emerg Med | 2020 |
| Rapid Molecular Detection for Differentiation of Homozygous HbE and ß0-Thalassemia/HbE in Samples Related With HbE >80% and Variable HbF Levels. | Tepakhan W, Jomoui W | Lab Med | 2020 |
| Coinherited Hemoglobin H/Constant Spring Disease and Heterozygous Hemoglobin Tak Causing Severe Hemolytic Anemia in a Thai Boy. | Choed-Amphai C, Phusua A, Ittiwut C, Charoenkwan P, Suphapeetiporn K, Shotelersuk V | J Pediatr Hematol Oncol | 2020 |
| Association of HFE Gene Mutations With Serum Ferritin Level and Heart and Liver Iron Overload in Patients With Transfusion-dependent Beta-Thalassemia. | Zekavat OR, Zareian Jahromi M, Haghpanah S, Kargar Jahromi Z, Cohan N | J Pediatr Hematol Oncol | 2020 |
| Pain in Children and Adolescents With Sickle Cell Disease: Multidimensional Assessment. | Abadesso C, Pacheco S, Machado MC, Finley GA | J Pediatr Hematol Oncol | 2020 |
| Fifteen Cases of Hb J-Meerut: The Rare Association with Hb E and/or : c.-24C>G (or ) Variants. | Khalil MSM, Timbs AT, Henderson SJ, Schuh A, Old JM | Hemoglobin | 2020 |
| Genetic Analysis of Patients With Sickle Cell Anemia and Stroke Before 4 Years of Age Suggest an Important Role for Apoliprotein E. | Brewin JN, Smith AE, Cook R, Tewari S, Brent J, Wilkinson S, Brousse V, Inusa B, Menzel S, Rees DC | Circ Genom Precis Med | 2020 |
| Initial Dosage Optimization of Tacrolimus in Pediatric Patients With Thalassemia Major Undergoing Hematopoietic Stem Cell Transplantation Based on Population Pharmacokinetics. | Zhou S, Zhang R, Lv C, Lu J, Wei Y, Li C, Chen M, Li Q, Liu T | Ann Pharmacother | 2020 |
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| Challenging the Erythropoiesis Paradigm in β-Thalassemia. | Vinchi F, Vance SZ | Hemasphere | 2020 |
| Cognitive Correlates of Math Performance in School-Aged Children with Sickle Cell Disease and Silent Cerebral Infarcts. | Peterson RK, Williams S, Janzen L | Arch Clin Neuropsychol | 2020 |
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| "Pain is Subjective": A Mixed-Method Study of Provider Attitudes and Practices Regarding Pain Management in Sickle Cell Disease across Three Countries | Stewart KA, Parshad-Asnani M, Wonkam A, Bollinger J, Ngo Bitoungui V, Wonkam-Tingang E, Powell J, Desronvil K, Benson K, Clark A, Katz M, Martin B, Peterseim C, Williams C, Young N, Shah N, Babyak M, Tanabe P, Royal CD | J Pain Symptom Manage | 2020 |
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| Feasibility and preliminary outcomes of an integrated pediatric sickle cell disease and pulmonary care clinic for children with sickle cell disease. | Black LV, Ezmigna D, Wallace-Farquharson T, Wilkie DJ, Duckworth L | Pediatr Blood Cancer | 2020 |
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| Prenatal diagnosis of a rare β-thalassemia gene －90 (C>T) (HBB: c.-140 C>T) mutation associated with deletional Hb H disease (-- /-α ). | Qian H, Huang J, Xu J, Zhao W, Ye X, Liu W | Mol Genet Genomic Med | 2020 |
| MEMSID: Results From a Phase 2 Pilot Study on Memantine Treatment for Sickle Cell Disease. | Hegemann I, Sasselli C, Valeri F, Makhro A, Müller R, Bogdanova A, Manz MG, Gassmann M, Goede JS | Hemasphere | 2020 |
| Recommendations for Pregnancy in Rare Inherited Anemias. | Taher AT, Iolascon A, Matar CF, Bou-Fakhredin R, de Franceschi L, Cappellini MD, Barcellini W, Russo R, Andolfo I, Tyan P, Gulbis B, Aydinok Y, Anagnou NP, Bencaiova GA, Tamary H, Martinez PA, Forni G, Vindigni R | Hemasphere | 2020 |
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| Soluble transferrin receptor level, inflammation markers, malaria, alpha-thalassemia and selenium status are the major predictors of hemoglobin in children 6-23 months in Malawi. | Gebremedhin S | Food Sci Nutr | 2020 |
| Investigation of Lipid Profile and Clinical Manifestations in SCA Children. | da Guarda CC, Yahouédéhou SCMA, Santiago RP, Fernandes CFL, Neres JSDS, Oliveira AMJ, Aleluia MM, Figueiredo CVB, Fonseca CA, Fiuza LM, Carvalho SP, de Oliveira RM, Nascimento VML, Rocha LC, Gonçalves MS | Dis Markers | 2020 |
| Pure Erythroid Leukemia in a Sickle Cell Patient Treated with Hydroxyurea. | Yadav DK, Paul T, Alhamar M, Inamdar K, Guo Y | Case Rep Oncol | 2020 |
| The Use of Music by Adolescents and Young Adults With Sickle Cell Disease. | Solodiuk JC, Jantz B, Fuller M, Osterling D, Foxman H, Grafft N, Hanser S | Creat Nurs | 2020 |
| Evaluation of electrocardiographic markers of cardiac arrhythmic events and their correlation with cardiac iron overload in patients with β-thalassemia major. | Demircan T, Onder Sivis Z, Tatlı Güneş B, Karadeniz C | Cardiol Young | 2020 |
| Integrin VLA-4 as a PET imaging biomarker of hyper-adhesion in transgenic sickle mice. | Perkins LA, Nyiranshuti L, Little-Ihrig L, Latoche JD, Day KE, Zhu Q, Tavakoli S, Sundd P, Novelli EM, Anderson CJ | Blood Adv | 2020 |
| Influence of beta-cluster haplotypes, alpha-gene status and UGTA1 polymorphism on clinical and hematological data in sickle-cell disease children from French Guiana. | Elenga N, Cuadro-Alvarez E, Martin E, Njuieyon F, Defo A, Maniassom C | PLoS One | 2020 |
| Weight Loss as an Effective Strategy to Decrease Opioid Use and Frequency of Vaso-Occlusive Crises in Patients with Sickle Cell Disease. | Babroudi S, Vesel T | J Palliat Med | 2020 |
| [Prevalence of Chronic Complications of Sickle Cell Disease at the Bobo-Dioulasso Teaching Hospital, Burkina Faso]. | Traoré C, Kyelem CG, Semdé A, Koulidiati J, Sanou AF, Bokoum S, Kafando E | Bull Soc Pathol Exot | 2020 |
| Presumed Sickle Cell Retinopathy in an Elderly Woman. | Starr MR, Patel LG, Ho AC | JAMA Ophthalmol | 2020 |
| Association Between Genetic Polymorphisms and Hb F Levels in Heterozygous β-Thalassemia 3.5 kb Deletions. | Tepakhan W, Kanjanaopas S, Srewaradachpisal K | Hemoglobin | 2020 |
| Prevalence of Transfusion Transmissible Infections in Beta-Thalassemia Major Patients in Pakistan: A Systematic Review. | Ehsan H, Wahab A, Anwer F, Iftikhar R, Yousaf MN | Cureus | 2020 |
| Effectiveness of Deferasirox in Pediatric Thalassemia Patients: Experience from a Tertiary Care Hospital of Odisha. | Panigrahi M, Swain TR, Jena RK, Panigrahi A, Debta N | Indian J Pharmacol | 2020 |
| Precise and error-prone CRISPR-directed gene editing activity in human CD34+ cells varies widely among patient samples. | Modarai SR, Kanda S, Bloh K, Opdenaker LM, Kmiec EB | Gene Ther | 2020 |
| Receptor Activator of Nuclear Factor κ-Β Ligand/Osteoprotegerin Axis in Adults with Hb S/β-Thalassemia and β-Thalassemia Trait. | Tombak A, Boztepe B, Akbayir S, Dogru G, Sungur MA | Hemoglobin | 2020 |
| Challenges in the Management of Sickle Cell Disease During SARS-CoV-2 Pandemic. | Alsayegh F, Mousa SA | Clin Appl Thromb Hemost | 2020 |
| Preserved efficiency of sickle cell disease placentas despite altered morphology and function. | Cordier AG, Bouvier AS, Vibert F, Martinovic J, Couturier-Tarrade A, Lai-Kuen R, Curis E, Fournier T, Benachi A, Peoc'H K, Gil S | Placenta | 2020 |
| When Actions Speak Louder Than Words - Racism and Sickle Cell Disease. | Power-Hays A, McGann PT | N Engl J Med | 2020 |
| The opposing roles of the mTOR signaling pathway in different phases of human umbilical cord blood-derived CD34 cell erythropoiesis. | Liu Q, Luo L, Ren C, Zou M, Yang S, Cai B, Wu L, Wang Y, Fu S, Hua X, Tang N, Huang S, Huang X, Xin W, Chen F, Zhang X | Stem Cells | 2020 |
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| An assessment of the continuing medical education needs of US physicians in the management of patients with beta thalassemia. | Stacy S, Sheth S, Coleman B, Cerenzia W | Ann Hematol | 2020 |
| Distribution of Gene Mutations in the Kurdish Population of Ilam Province, West Iran. | Moradi K, Aznab M, Tahmasebi S, Omidniakan L, Bijari N, Alibakhshi R | Hemoglobin | 2020 |
| Functional Connectivity Decreases with Metabolic Stress in Sickle Cell Disease. | Fields ME, Mirro AE, Guilliams KP, Binkley MM, Gil Diaz L, Tan J, Fellah S, Eldeniz C, Chen Y, Ford AL, Shimony JS, King AA, An H, Smyser CD, Lee JM | Ann Neurol | 2020 |
| Changing the Clinical Paradigm of Hydroxyurea Treatment for Sickle Cell Anemia Through Precision Medicine. | Dong M, McGann PT | Clin Pharmacol Ther | 2020 |
| Clinical outcomes and healthcare utilization in patients with sickle cell disease: a nationwide cohort study of Medicaid beneficiaries. | Desai RJ, Mahesri M, Globe D, Mutebi A, Bohn R, Achebe M, Levin R, Schneeweiss S | Ann Hematol | 2020 |
| The Relationship Between Sickle Cell Disease and Sudden Onset Sensorineural Deafness. | Abdelmahmuod E, Yassin MA, Ahmed M, Ali E | Cureus | 2020 |
| Gender-specific transcriptional profiles identified in β-thalassemia patients. | Nanou A, Toumpeki C, Fanis P, Bianchi N, Cosenza LC, Zuccato C, Sentis G, Giagkas G, Stephanou C, Phylactides M, Christou S, Hadjigavriel M, Sitarou M, Lederer CW, Gambari R, Kleanthous M, Katsantoni E | Haematologica | 2020 |
| Visual cortex changes in children with sickle cell disease and normal visual acuity: a multimodal magnetic resonance imaging study. | Manara R, Dalla Torre A, Lucchetta M, Ermani M, Favaro A, Baracchini C, Favaretto S, Viaro F, Munaretto V, Sartori S, Ponticorvo S, Russo AG, Biffi A, Sainati L, Colombatti R | Br J Haematol | 2020 |
| Medical marijuana certification for patients with sickle cell disease: a report of a single center experience. | Curtis SA, Lew D, Spodick J, Hendrickson JE, Minniti CP, Roberts JD | Blood Adv | 2020 |
| Outcomes following kidney transplantation in patients with sickle cell disease: The impact of automated exchange blood transfusion. | Willis JC, Awogbade M, Howard J, Breen C, Abbas A, Harber M, Shendi AM, Andrews PA, Galliford J, Thuraisingham R, Gage A, Shah S, Sharpe CC | PLoS One | 2020 |
| Fetal Heart Diameter as a Predictor of Hemoglobin Bart Disease at Midpregnancy. | Nattawongsiri C, Tongprasert F, Tongsong T | J Ultrasound Med | 2020 |
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| Influence of gender norms in relation to child's quality of care: follow-up of families of children with SCD identified through NBS in Tanzania. | Bukini D, Mbekenga C, Nkya S, Malasa L, McCurdy S, Manji K, Makani J, Parker M | J Community Genet | 2020 |
| Cell-Derived Microparticles in Blood Products from Thalassemic Blood Donors. | Noulsri E, Lerdwana S, Palasuwan D, Palasuwan A | Lab Med | 2020 |
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| Incidence of sickle cell disease patients with pulmonary embolism admitted to the intensive care unit in Bahrain. | Mandeel FH, Saeed HM, Alsadah AH, Ahmed SA, Alhammam RA | Saudi Med J | 2020 |
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| Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects. | Kanter J, Smith WR, Desai PC, Treadwell M, Andemariam B, Little J, Nugent D, Claster S, Manwani DG, Baker J, Strouse JJ, Osunkwo I, Stewart RW, King A, Shook LM, Roberts JD, Lanzkron S | Blood Adv | 2020 |
| The participation of cohabitants with sickle cell disease in health care: a bibliographic study. | Lopes WSL, Gomes R | Cien Saude Colet | 2020 |
| Association between sickle cell disease and dental caries: a systematic review and meta-analysis. | Yue H, Xu X, Liu Q, Li X, Jiang W, Hu B | Hematology | 2020 |
| Using surveillance to determine the number of individuals with sickle cell disease in California and Georgia, 2005-2016. | Aluc A, Zhou M, Paulukonis ST, Snyder AB, Wong D, Hulihan MM | Pediatr Hematol Oncol | 2020 |
| Hb broomhill [α1 or α2 114(GH2) pro > ala; or :c.343C > G]: a rare Hb variant found in a diabetic chinese individual. | Yuan Y, Zhou X, Ren Q, Ji L | Scand J Clin Lab Invest | 2020 |
| Transient Second-Degree Atrioventricular Block: A Rare Finding in Sickle Cell Crisis. | Riaz S, Sampat PJ, Dhungana R, Bhatta L | Cureus | 2020 |
| Sickle Cell Trait and Risk of Ischemic Stroke in Young Adults. | Zhang RV, Ryan KA, Lopez H, Wozniak MA, Phipps MS, Cronin CA, Cole JW, Dutta TM, Mehndiratta P, Motta M, Merino JG, Kittner SJ | Stroke | 2020 |
| Using LIBS as a diagnostic tool in pediatrics beta-thalassemia. | Alsharnoubi J, Nassef Y, Fahmy RF, Gamal M | Lasers Med Sci | 2020 |
| Acute compartment syndrome in a patient with sickle cell disease. | Cochrane E, Young S, Shariff Z | Ann R Coll Surg Engl | 2020 |
| Pain Experience, Physical Function, Pain Coping, and Catastrophizing in Children With Sickle Cell Disease Who Had Normal and Abnormal Sensory Patterns. | Hyacinth O, Machado Silva-Rodrigues F, Darezzo Rodrigues Nunes M, Carlos Lopes L, Fernandes A, Castanheira Nascimento L, Jacob E | J Pain Symptom Manage | 2020 |
| Reduction in transcranial doppler ultrasound (TCD) velocity after regular blood transfusion therapy is associated with a change in hemoglobin S fraction in sickle cell anemia. | Jordan LC, Rodeghier M, Donahue MJ, DeBaun MR | Am J Hematol | 2020 |
| Red blood cell adhesion to ICAM-1 is mediated by fibrinogen and is associated with right-to-left shunts in sickle cell disease. | Kucukal E, Man Y, Quinn E, Tewari N, An R, Ilich A, Key NS, Little JA, Gurkan UA | Blood Adv | 2020 |
| Serum albumin is independently associated with higher mortality in adult sickle cell patients: Results of three independent cohorts. | Nouraie M, Ashley-Koch AE, Garrett ME, Sritharan N, Zhang Y, Little J, Gordeuk VR, Gladwin MT, Telen MJ, Kato GJ | PLoS One | 2020 |
| SARS-CoV-2 infection in pediatric patient with hemoglobin SC disease. | Dagalakis U, Hammershaimb E, McArthur MA, Macatangay RA | Pediatr Blood Cancer | 2020 |
| A pediatric patient with sickle cell disease presenting with severe anemia and splenic sequestration in the setting of COVID-19. | Jacob S, Dworkin A, Romanos-Sirakis E | Pediatr Blood Cancer | 2020 |
| The Trabecular Bone Score as a Predictor for Thalassemia-Induced Vertebral Fractures in Northeastern Thailand. | Teawtrakul N, Chukanhom S, Charoensri S, Somboonporn C, Pongchaiyakul C | Anemia | 2020 |
| Implications of COVID-19 infections in sickle cell disease. | John NA, John JE | Pan Afr Med J | 2020 |
| Prevalence of β thalassaemia trait and Haemoglobin E disorders among students aged between 14-17yrs in Kurunegala district, Sri Lanka. | Warushahennadi R, Wanasundara DH, Priyadarshani W, Abeysekara AM, Jiffry MN | Ceylon Med J | 2020 |
| Association between BCL11A, HSB1L-MYB, and XmnI γG-158 (C/T) gene polymorphism and hemoglobin F level in Egyptian sickle cell disease patients. | El-Ghamrawy M, Yassa ME, Tousson AMS, El-Hady MA, Mikhaeil E, Mohamed NB, Khorshied MM | Ann Hematol | 2020 |
| The risk of acute events among patients with sickle cell disease in relation to early or late initiation of care at a specialist center: evidence from a retrospective cohort study. | Rankine-Mullings AE, Logan TM, King LG, Cunningham-Myrie CA, Scott CR, Knight-Madden JM | BMC Pediatr | 2020 |
| [Effects of a standardized musical intervention on the management of pain and anxiety-state of sickle-cell adolescents]. | Martin J, Le Faucheur L, Pondarré C, Carlier-Gonod A, Baeza-Velasco C | Soins Pediatr Pueric | 2020 |
| Detection of a Hb A -Melbourne (HBD: c.130G>A) combined with β-thalassemia in a Chinese individual. | Li Y, Huang T, Mao T, Zhang X, Liang L, Meng M | J Clin Lab Anal | 2020 |
| Screening for Iron Deficiency Anemia in Infants in a Thalassemia-endemic Region. | Nanta N, Natesirinilkul R, Kittisakmontri K, Chimnuan K, Manowong S, Suanta S, Charoenkwan P | J Pediatr Hematol Oncol | 2020 |
| A microfluidic computational fluid dynamics model for cellular interaction studies of sickle cell disease vaso-occlusions. | Blakely IP, Horton RE | Microvasc Res | 2020 |
| Assessment of mandibular characteristics in patients affected with β-thalassaemia major: A retrospective case-control study. | Movahhedian N, Akbarizadeh F, Khojastepour L, Sardarian AR, Pakshir HR, Ahrari F | Int Orthod | 2020 |
| [Sickle cell trait complications: A case series of 6 patients]. | Marcombes C, Lafont E, Jullien V, Flamarion E, Dion J, Costedoat-Chalumeau N, Pouchot J, Arlet JB | Rev Med Interne | 2020 |
| Impact of relative systemic hypertension on the heart in sickle cell anaemia. | Oni OO, Adebiyi AA, Aje A, Akingbola TS | Indian Heart J | 2020 |
| Intracranial and Extracranial Vascular Stenosis as Risk Factors for Stroke in Sickle Cell Disease. | Schlotman AA, Donahue MJ, Kassim AA, Lee CA, Waddle SL, Pruthi S, Davis LT, Rodeghier M, DeBaun MR, Jordan LC | Pediatr Neurol | 2020 |
| Red blood cell exchange in an emergency in sickle cell disease. | Hequet O, Fort R, Driss F | Transfus Apher Sci | 2020 |
| Bone infarct transformation into undifferentiated pleomorphic sarcoma in sickle cell disease: A case report. | Alhamdan HA, Alrifai OI, Shaheen MF, Pant R, Altayeb MA | Int J Surg Case Rep | 2020 |
| Autoimmune Liver Disease in Patients With Sickle Cell Disease. | Waisbourd-Zinman O, Frenklak R, Hakakian O, Hilmara D, Lin H | J Pediatr Hematol Oncol | 2020 |
| The carriage rates of ααα, ααα, and HKαα in the population of Guangxi, China measured using a rapid detection qPCR system to determine CNV in the α-globin gene cluster. | Long J, Liu E | Gene | 2020 |
| A roadmap for the standardization of hemoglobin A. | Mosca A, Paleari R, Harteveld CL, | Clin Chim Acta | 2020 |
| Assessment of Complement Regulatory Proteins CD55 and CD59 on Erythrocytes in Beta-Thalassemia Major Patients. | Zahran AM, Shaltout AS, Hamada IH, Mohammed AM, Abo Elgheet AM, Elsayh KI | Egypt J Immunol | 2020 |
| Global loss of Tfr2 with concomitant induced iron deficiency greatly ameliorates the phenotype of a murine thalassemia intermedia model. | Schmidt PJ, Fitzgerald K, Butler JS, Fleming MD | Am J Hematol | 2020 |
| Rapid decline in estimated glomerular filtration rate in sickle cell anemia: results of a multicenter pooled analysis. | Ataga KI, Zhou Q, Derebail VK, Saraf SL, Hankins JS, Loehr LR, Garrett ME, Ashley-Koch AE, Cai J, Telen MJ | Haematologica | 2020 |
| Co-transplantation of bone marrow-derived mesenchymal stem cells with hematopoietic stem cells does not improve transplantation outcome in class III beta-thalassemia major: A prospective cohort study with long-term follow-up. | Rostami T, Maleki N, Kasaeian A, Nikbakht M, Kiumarsi A, Asadollah Mousavi S, Ghavamzadeh A | Pediatr Transplant | 2020 |
| Evaluation of Adipokines Concentration in Iraqi Patients with Major and Minor Beta Thalassemia. | Harbi NS, Jawad AH, Alsalman FK | Rep Biochem Mol Biol | 2020 |
| Epidemiology of Thalassemia in Gulf Cooperation Council Countries: A Systematic Review. | Abu-Shaheen A, Heena H, Nofal A, Abdelmoety DA, Almatary A, Alsheef M, AlFayyad I | Biomed Res Int | 2020 |
| EF Bart's Disease with Coinheritance of G-XmnI and A-Globin Polymorphisms: A Case of Nontransfusion-Dependant Thalassemia. | Laks KM, Hirner C, Gruner B, Coberly J, Laziuk K, Sathi BK | Case Rep Hematol | 2020 |
| Spatiotemporal Alterations in Gait in Humanized Transgenic Sickle Mice. | Kiven S, Wang Y, Aich A, Argueta DA, Lei J, Sagi V, Tennakoon M, Bedros SJ, Lambrecht N, Gupta K | Front Immunol | 2020 |
| Plasma Folate Levels in Acutely Ill and Steady State Pediatric Sickle Cell Disease Patients in Ghana. | Adjei GO, Sulley AM, Goka BQ, Enweronu-Laryea C, Amponsah SK, Alifrangis M, Kurtzhals JAL | J Blood Med | 2020 |
| Clinical management of sickle cell liver disease in children and young adults. | Kyrana E, Rees D, Lacaille F, Fitzpatrick E, Davenport M, Heaton N, Height S, Samyn M, Mavilio F, Brousse V, Suddle A, Chakravorty S, Verma A, Gupte G, Velangi M, Inusa B, Drasar E, Hadzic N, Grammatikopoulos T, Hind J, Deheragoda M, Sellars M, Dhawan A | Arch Dis Child | 2020 |
| Hyperhaemolytic Syndrome in Sickle cell disease: clearing the cobwebs. | Madu AJ, Ugwu AO, Efobi C | Med Princ Pract | 2020 |
| Abnormal Ambulatory Blood Pressure and Early Renal Dysfunction in Sickle Cell Disease. | Dubey SRK, Shrivastava N, Sharma T, Bhatt GC, Dhingra B, Pakhare AP, Goel SK, Joshi D | Indian J Pediatr | 2020 |
| GBT440 Increases Hematocrit and Improves Biventricular Function in Berkeley Sickle Cell Disease Mice. | Gassner R, Schreier DA, Hacker T, Tabima DM, Chesler N | J Biomech Eng | 2020 |
| Parental stress in the relationship with children affected by chronic hematological disease. | Ribilotta A, Sergio M, Scarponi D | Minerva Pediatr | 2020 |
| COVID-19 pneumonia and pulmonary microembolism in a patient with B-thalassemia major. | Marziali M, Ribersani M, Losardo AA, Taglietti F, Pugliese P, Micozzi A, Gentile G, Angeloni A | Clin Case Rep | 2020 |
| Fat Embolism Syndrome in Sickle Cell Disease. | Tsitsikas DA, Vize J, Abukar J | J Clin Med | 2020 |
| Comparison of two vitamin D supplementation strategies in children with sickle cell disease: a randomized controlled trial. | Grégoire-Pelchat P, Pastore Y, Robitaille N, LeMay S, Khamessan A, Kleiber N, Nyalendo C, Gagné N, Alos N, Mailhot G | Br J Haematol | 2020 |
| Machine-learning algorithms for predicting hospital re-admissions in sickle cell disease. | Patel A, Gan K, Li AA, Weiss J, Nouraie M, Tayur S, Novelli EM | Br J Haematol | 2020 |
| Multimodality Treatment for Nonhealing Wound With Osteomyelitis in Sickle Cell Disease. | Kakar J | Int J Low Extrem Wounds | 2020 |
| Implementation of the therapeutic use of hydroxyurea for sickle cell disease management in resource-constrained settings: a systematic review of adoption, cost and acceptability. | Ryan N, Dike L, Ojo T, Vieira D, Nnodu O, Gyamfi J, Peprah E | BMJ Open | 2020 |
| Multiple Enlarging Masses and Failure to Thrive in Infant With Sickle Cell Trait. | Jabbour AJ, Warrier R, Kretschmar P | Clin Pediatr (Phila) | 2020 |
| GDF-15 negatively regulates excess erythropoiesis and its overexpression is involved in erythroid hyperplasia. | Ranjbaran R, Abbasi M, Rahimian E, Dehbidi GR, Seyyedi N, Zare F, Behzad-Behbahani A | Exp Cell Res | 2020 |
| Association of Exon 14 of the Gene Sequence Variations with Response to Hydroxyurea Therapy in Patients Carrying Non Transfusion-Dependent Thalassemia. | Mohammadi Z, Mohammadi R, Haghpanah S, Moghadam M, Pazhoomand R, Karimi M | Hemoglobin | 2020 |
| Transcranial Doppler Velocities among Sickle Cell Disease Patients in Steady State. | Salama K, Rady R, Hashem RH, El-Ghamrawy M | Hemoglobin | 2020 |
| Inner Ear Complications in Children and Adolescents with Sickle Cell Disease. | Tantawy AAG, Ibrahim SW, Abdel-Aziz TT, Rabie AN, Makkeyah SM, Ragab IA | Hemoglobin | 2020 |
| Cytomegalovirus and Epstein-Barr Infections: Prevalence and Impact on Patients with Hematological Diseases. | de Melo Silva J, Pinheiro-Silva R, Dhyani A, Pontes GS | Biomed Res Int | 2020 |
| Fetal heterozygosity for both Hb G-Hsi-Tsou and beta thalassemia: A case report. | Alhazidou E, Androulaki M, Panagiotopoulos M, Boudouvas D, Lampropoulou D, Yfanti E, Delaki EE, Repa K, Petrakos G | Case Rep Womens Health | 2020 |
| Red blood cell exchange in sickle cell disease patient with multiple alloantibodies. | Aggarwal G, Tiwari AK, Dhiman P, Arora D, Pabbi SM, Setya D | Asian J Transfus Sci | 2020 |
| Generation of a human iPSC line CIBi008-A from amniotic fluid-derived cells of a fetus with β-thalassemia carrying variants of -28A > G and IVS-II-654C > T in HBB. | Wu S, Wei H, Chu M, Weng Z | Stem Cell Res | 2020 |
| Editorial for: | Carr JC | J Magn Reson Imaging | 2020 |
| Clinical outcomes following bone marrow transplantation in patients with sickle cell disease: A cohort study of US Medicaid enrollees. | Mahesri M, Schneeweiss S, Globe D, Mutebi A, Bohn R, Achebe M, Levin R, Desai RJ | Eur J Haematol | 2020 |
| Delayed repair of aortic dissection in sickle cell anaemia as a combined cardiac and vascular surgical approach. | Capoccia M, Mireskandari M, Cheshire NJ, Rosendahl UP | J Saudi Heart Assoc | 2020 |
| Right ventricular functions in subphenotypes of sickle cell disease. | Youssry I, Shaltout MF, AbdelMassih AF, Ghobrial C, Nabih M, Doss R, Fouda R, El-Sisi A | J Saudi Heart Assoc | 2020 |
| Hemolysis Inhibits Humoral B Cell Responses and Modulates Alloimmunization Risk in Patients with Sickle Cell Disease. | Pal M, Bao W, Wang R, Liu Y, An X, Mitchell WB, Lobo C, Minniti CP, Shi P, Manwani D, Yazdanbakhsh K, Zhong H | Blood | 2020 |
| Trends in Sickle Cell Trait and Disease Screening in the Republic of Uganda, 2014-2019. | Hernandez AG, Kiyaga C, Howard TA, Ssewanyana I, Ndeezi G, Aceng JR, Ware RE | Trop Med Int Health | 2020 |
| NT-proBNP Levels and Cardiopulmonary Function in Children with Sickle Cell Disease. | Feld L, Fiorino EK, Aygun B, Appiah-Kubi A, Mitchell EC, Jackson S, Mehran R, Fishbein J, Santiago MT | Pediatr Pulmonol | 2020 |
| Weight status and health behaviors of adolescents and young adults with sickle cell disease: The emerging risk for obesity. | Strong H, Harry O, Westcott E, Kidwell KM, Couch SC, Peairs A, Britto MT, Crosby LE | Pediatr Hematol Oncol | 2020 |
| MTHFR C677T, Prothrombin G20210A, and Factor V Leiden (G1691A) Polymorphism and Beta-Thalassemia Risk: A Meta-Analysis. | Nigam N, Singh PK, Agrawal M, Nigam S, Gupta H, Saxena S | Cureus | 2020 |
| Development of a Severity Classification System for Sickle Cell Disease. | Shah N, Beenhouwer D, Broder MS, Bronte-Hall L, De Castro LM, Gibbs SN, Gordeuk VR, Kanter J, Klings ES, Lipato T, Manwani D, Scullin B, Yermilov I, Smith WR | Clinicoecon Outcomes Res | 2020 |
| Hydroxyurea treatment is associated with reduced degree of oxidative perturbation in children and adolescents with sickle cell anemia. | Vinhaes CL, Teixeira RS, Monteiro-Júnior JAS, Tibúrcio R, Cubillos-Angulo JM, Arriaga MB, Sabarin AG, de Souza AJ, Silva JJ, Lyra IM, Ladeia AM, Andrade BB | Sci Rep | 2020 |
| Detection of an α-Globin Fusion Gene Using Real-Time Polymerase Chain Reaction-Based Multicolor Melting Curve. | Ju AP, Jiang F, Li J, Tang XW, Li DZ | Hemoglobin | 2020 |
| Randomized controlled trial of effect of N-acetylcysteine as an antioxidant on iron overload in children with thalassemia major. | Mohamed YA, Meabed MH, Ashraf A, Morgan DS, Abdul Latif MG, Abd-Elkareem RM, Ahmed HM | Clin Exp Pediatr | 2020 |
| An Investigation of Structure-Activity Relationships of Azolylacryloyl Derivatives Yielded Potent and Long-Acting Hemoglobin Modulators for Reversing Erythrocyte Sickling. | Omar AM, Abdulmalik O, Ghatge MS, Muhammad YA, Paredes SD, El-Araby ME, Safo MK | Biomolecules | 2020 |
| Unusual Presentation of Renal Medullary Carcinoma With Undiagnosed Sickle Cell Trait. | Basher F, Dutcher G, England JS, Lopes G | Cureus | 2020 |
| DXA and pQCT derived parameters in Indian children with beta thalassemia major - A case controlled study. | Shah N, Khadilkar A, Ekbote V, Mughal Z, Gondhalekar K, Khadilkar S, Ramanan V, Khadilkar V, Padidela R | Bone | 2020 |
| Monoterpenes as therapeutic candidates to induce fetal hemoglobin synthesis and up-regulation of gamma-globin gene: An in vitro and in vivo investigation. | Iftikhar F, Khan MBN, Musharraf SG | Eur J Pharmacol | 2020 |
| Priapism in Sickle Cell Trait With High Sensitivity to Multiple Psychotropic Medications. | Satodiya R, Yacoub A | J Clin Psychopharmacol | 2020 |
| Molecular Characterization and Disease-Related Morbidities of β-Thalassemia Patients from the Northeastern Part of Iraq. | Amin S, Jalal S, Ali K, Rasool L, Osman T, Ali O, M-Saeed A | Int J Gen Med | 2020 |
| Assessing the atria in pediatric sickle cell disease: Beyond the dilation. | Loar RW, George A, Varghese NP, Liu AM, Colquitt JL, Pignatelli RH | Echocardiography | 2020 |
| Editorial to | Lee JZ, Deshmukh AJ | J Arrhythm | 2020 |
| Sickle cell disease-associated arrhythmias and in-hospital outcomes: Insights from the National Inpatient Sample. | Patel U, Desai R, Hanna B, Patel D, Akbar S, Zubair M, Kumar G, Sachdeva R | J Arrhythm | 2020 |
| Sickle cell disease in Grenada: Quality of life and barriers to care. | Grygiel A, Ikolo F, Stephen R, Bleasdille D, Robbins-Furman P, Nelson B, Sobering AK, Elsea SH | Mol Genet Genomic Med | 2020 |
| Crizanlizumab in vaso-occlusive crisis caused by sickle cell disease. | Gardner RV | Drugs Today (Barc) | 2020 |
| A case of hyperhaemolysis syndrome in a pregnant Chinese woman with β-thalassemia during perinatal transfusion. | Wu Y, Ji Y, Dai B, Guo F, Wu Y, He Z, Mo C, Wu S, Hu Y | Transfus Med | 2020 |
| No differences in hemostatic and endothelial activations between haploidentical and matched-donor hematopoietic stem cell transplantation in thalassemia disease. | Lertthammakiat S, Sitthirat P, Anurathapan U, Songdej D, Pakakasama S, Chuansumrit A, Putawornsub N, Sirasittikarn S, Wantanawijarn S, Kadegasem P, Hongeng S, Sirachainan N | Thromb J | 2020 |
| Exploration of Barriers and Facilitators to Optimal Emergency Department Care of Sickle Cell Disease: Opportunities for Patient-Physician Partnerships to Improve Care. | Liederman Z, Quartey NK, Ward R, Papadakos J | Hemoglobin | 2020 |
| Developmental Profile of Sleep and Its Potential Impact on Daytime Functioning from Childhood to Adulthood in Sickle Cell Anaemia. | Kölbel M, Kirkham FJ, Dimitriou D | Brain Sci | 2020 |
| A cross-sectional, case-control study of intracranial arterial wall thickness and complete blood count measures in sickle cell disease. | Yuan S, Jordan LC, Davis LT, Cogswell PM, Lee CA, Patel NJ, Waddle SL, Juttukonda M, Sky Jones R, Griffin A, Donahue MJ | Br J Haematol | 2020 |
| Parvovirus B19 infection as a potential trigger for fat embolism syndrome in patients with sickle cell disease. | Lampejo T | J Med Virol | 2020 |
| Assessment of Ventricular Repolarization in Sickle Cell Anemia Patients: The Role of QTc Interval, Tp-e Interval and Tp-e/QTc Ratio and Its Gender Implication. | Ajibare AO, Olabode OP, Fagbemiro EY, Akinlade OM, Akintunde AA, Akinpelu OO, Olatunji LA, Soladoye AO, Opadijo OG | Vasc Health Risk Manag | 2020 |
| [50 years of the Neonatal Screening Program in Catalonia.] | Marín Soria JL, López Galera RM, Argudo Ramírez A, González de Aledo JM, Pajares García S, Navarro Sastre A, Hernandez Pérez JM, Ribes Rubio A, Gort Mas L, García Villoria J, Gartner Tizano S, Rovira Amigo S, Asensio de la Cruz O, García González M, Cols Roig M, Costa Colomer J, Bádenas Orquin C, Yeste Fernández D, Campos Martorell A, Clemente León M, Mogas Viñals E, Ferrer Costa R, Giralt Arnaiz M, Campistol Plana J, García Cazorla Á, Beneitez Pastor D, Ortuño Cabrero A, Blanco Álvarez A, Tazón Vega B, Roué G, Velasco Puyo P, Murciano Carrillo T, Murillo Sanjuan L, Díaz de Heredia Rubio C, Mañú Pereira MDM, Vives Corrons JL, Arranz Amo JA, Carnicer Cáceres C, Del Toro Riera M, Ormazábal Herrero A, Artuch Iriberri R, García-Volpe C, de Los Santos MM, Sierra March C, Ruiz Hernández CJ, Meavilla Olivas SM, Martín Nalda A, Rivière JG, Parra Martínez A, Soler Palacín P, Martínez Gallo M, Colobran R, Casals Senent T, Armelles Sebastia M, Vidal Benede MJ, Jané Checa M, Fernández Bordón RM, Asso Ministral L, Prats Viedma B, Cabezas Peña C | Rev Esp Salud Publica | 2020 |
| [Results of the neonatal screening on Western Andalusia after a decade of experience.] | Delgado-Pecellín C, Álvarez Ríos I, Bueno Delgado MDA, Jiménez Jambrina MM, Quintana Gallego ME, Ruiz Salas P, Marcos Luque I, Melguizo Madrid E | Rev Esp Salud Publica | 2020 |
| Annual Academy of Sickle Cell and Thalassaemia (ASCAT) conference: a summary of the proceedings. | Strunk C, Campbell A, Colombatti R, Andemariam B, Kesse-Adu R, Treadwell M, Inusa BPD | BMC Proc | 2020 |
| Patterns and patient factors associated with loss to follow-up in the Muhimbili sickle cell cohort, Tanzania. | Masamu U, Sangeda RZ, Kandonga D, Ondengo J, Ndobho F, Mmbando B, Nkya S, Msami K, Makani J | BMC Health Serv Res | 2020 |
| β-Thalassemia Major and Coronavirus-19, Mortality and Morbidity: a Systematic Review Study. | Zafari M, Rad MTS, Mohseni F, Nikbakht N | Hemoglobin | 2020 |
| Addressing the psychosocial needs of young people with thalassaemia undergoing bone marrow transplantation. | Fyfe-Taylor L, Cockett A | Nurs Child Young People | 2020 |
| Repeated CD45RA-depleted DLI successfully increases donor chimerism in a patient with beta-thalassemia major after haploidentical stem cell transplant. | Chan WYK, Kwok JSY, Chiang AKS, Chan GCF, Lee PPW, Ha SY, Cheuk DKL | Pediatr Transplant | 2020 |
| Dielectric spectroscopy of red blood cells in sickle cell disease. | Liu J, Qiang Y, Du E | Electrophoresis | 2020 |
| Intraoperative Periprosthetic Fractures in Total Hip Arthroplasty in Patients With Sickle Cell Disease at King Fahad Hospital Hofuf: A Cross-Sectional Study. | Alsaleem MK, Alalwan HA, Alkhars AM, Al Huwaiyshil AH, Alamri WM | Cureus | 2020 |
| Self-Report for Assessment of Pain and Quality of Life in Children with Sickle Cell Anemia in a Developing Country. | Brito da Cunha V, Freitas de Andrade Rodrigues C, Alves Rodrigues T, Silva Gomes de Oliveira EJ, Santos Garcia JB | J Pain Res | 2020 |
| Association of FOXO3 polymorphism (rs3800231) and clinical subphenotypes of beta thalassemic individuals. | Torres FF, Bernardo VS, Silva DGH, Okumura JV, Bonini-Domingos CR | Hematol Transfus Cell Ther | 2020 |
| Hemoglobin Target and Transfusion Modality for Adult Patients With Sickle Cell Disease Acute Chest Syndrome. | Simonson JL, Rosentsveyg JA, Schwartz NG, Agrawal A, Koenig S, Zaidi GZ | J Intensive Care Med | 2020 |
| Differences in Gut Microbiome in Hospitalized Immunocompetent vs. Immunocompromised Children, Including Those With Sickle Cell Disease. | Mohandas S, Soma VL, Tran TDB, Sodergren E, Ambooken T, Goldman DL, Weinstock G, Herold BC | Front Pediatr | 2020 |
| Retinal Nerve Fibre Layer Thinning in Patients with Thalassaemia, Iron Deficiency Anaemia, and Anaemia of Chronic Diseases. | Datta S, Baidya K, Banerjee M, Mahapatra S, Mukherjee S | J Ophthalmol | 2020 |
| Bradycardia associated with antithymocyte globulin treatment of a pediatric patient with sickle cell disease: a case report and literature review. | Elazhary S, Alawyat HA | Hematol Transfus Cell Ther | 2020 |
| Spectrum of pathogenic alterations identified after two decades of HBB gene sequencing for molecular diagnosis of beta-thalassaemias and haemoglobinopathies. | Poon KS, Tan KM | Pathology | 2020 |
| A study of red blood cell alloimmunization and autoimmunization among 200 multitransfused Egyptian β thalassemia patients. | El-Beshlawy A, Salama AA, El-Masry MR, El Husseiny NM, Abdelhameed AM | Sci Rep | 2020 |
| Moderate to severe liver siderosis and raised AST are independent risk factors for vitamin D insufficiency in β-thalassemia patients. | Darvishi-Khezri H, Karami H, Naderisorki M, Zahedi M, Razavi A, Kosaryan M, Aliasgharian A | Sci Rep | 2020 |
| DNA methylation patterns of β-globin cluster in β-thalassemia patients. | Bao X, Zuo Y, Chen D, Zhao C | Clin Epigenetics | 2020 |
| Academic Challenges and School Service Utilization in Children with Sickle Cell Disease. | Karkoska KA, Haber K, Elam M, Strong S, McGann PT | J Pediatr | 2020 |
| Challenges in chronic transfusion for patients with thalassemia. | Lal A | Hematology Am Soc Hematol Educ Program | 2020 |
| Neuropathic pain in sickle cell disease: measurement and management. | Glaros A, Brandow AM | Hematology Am Soc Hematol Educ Program | 2020 |
| Inherited microcytic anemias. | Cappellini MD, Russo R, Andolfo I, Iolascon A | Hematology Am Soc Hematol Educ Program | 2020 |
| Optimizing the management of chronic pain in sickle cell disease. | Osunkwo I, O'Connor HF, Saah E | Hematology Am Soc Hematol Educ Program | 2020 |
| Prevalence and Predictive Factors for Leg Ulcers in Sickle Cell Disease Patients in Saudi Arabia: A Cross-Sectional Observational Study. | Kaliyadan F, Alkhars AZ, Albaqshi AA, AlHajri HM, Albaqshi NK, Aldihnayn RM, Almarzooq ZY | Cureus | 2020 |
| Chronic Disease Management in Sickle Cell Trait Patients in the Primary Care Setting: A Case Report. | Fields RN, Minor S | Cureus | 2020 |
| COVID-19 Pandemic and Thalassemia Major Patients: Transfusion Practice and Treatment Assessment. | Oymak Y, Karapinar TH | J Pediatr Hematol Oncol | 2020 |
| Considerations for Cannabis Use to Treat Pain in Sickle Cell Disease. | Argueta DA, Aich A, Muqolli F, Cherukury H, Sagi V, DiPatrizio NV, Gupta K | J Clin Med | 2020 |
| Feasibility and acceptability of early infant screening for sickle cell disease in Lagos, Nigeria-A pilot study. | Oluwole EO, Adeyemo TA, Osanyin GE, Odukoya OO, Kanki PJ, Afolabi BB | PLoS One | 2020 |
| Preventive measures for the critical post-exercise period in sickle cell trait and disease. | Messonnier LA, Bartolucci P, d'Humières T, Dalmais E, Lacour JR, Freund H, Galactéros F, Féasson L | J Appl Physiol (1985) | 2020 |
| Case Series and Review of Hematological and Non-Hematological Malignancies in Aging Patients with Sickle Cell Disease in the Hydroxyurea Era. | Rizk S, Axelrod DJ, Olaosebikan R, Ballas SK | Hemoglobin | 2020 |
| Xanthine Oxidase Drives Hemolysis and Vascular Malfunction in Sickle Cell Disease. | Schmidt HM, Wood KC, Lewis SE, Hahn SA, Williams XM, McMahon B, Baust JJ, Yuan S, Bachman TN, Wang Y, Oh JY, Ghosh S, Ofori-Acquah SF, Lebensburger JD, Patel RP, Du J, Vitturi DA, Kelley EE, Straub AC | Arterioscler Thromb Vasc Biol | 2020 |
| First Report of a Coincidental Discovery of Hb Antibes-Juan-Les-Pins (: c.349_350insGTGTGCTGGCCC) in a Greek Woman. | Theodoridou S, Boutou E, Vyzantiadis TA, Balassopoulou A, Vlachaki E | Hemoglobin | 2020 |
| Impact of sickle cell disease on patients' daily lives, symptoms reported, and disease management strategies: Results from the international Sickle Cell World Assessment Survey (SWAY). | Osunkwo II, Andemariam B, Inusa BPD, El Rassi F, Francis-Gibson B, Nero A, Minniti CP, Trimnell C, Abboud MR, Arlet JB, Colombatti R, de Montalembert M, Jain S, Jastaniah W, Nur E, Pita M, DeBonnett L, Ramscar N, Bailey T, Rajkovic-Hooley O, James J | Am J Hematol | 2020 |
| Beneficial effects of adenotonsillectomy in children with sickle cell disease. | Liguoro I, Arigliani M, Singh B, Van Geyzel L, Chakravorty S, Bossley C, Pelidis M, Rees D, Inusa BPD, Gupta A | ERJ Open Res | 2020 |
| Total hip arthroplasty for osteonecrosis of the femoral head in sickle cell disease: a case series from our African experience. | Rossi G, Maffulli N, Lombardo MDM, Manfroni F, Bassani R, Petrachi BV, Sirtori P, Brugnoli A, Cuccuru T, Brambilla L, Domenicucci M, Marmotti A, Dzissah OEK, Mangiavini L, Kombate NK, Peretti GM | J Biol Regul Homeost Agents | 2020 |
| One-stage Bilateral Total Hip Arthroplasty in patient with sickle cell disease and previous Girdlestone procedure on the right side: First presentation in Togo. | Manfroni F, Maffulli N, Lombardo MDM, Rossi G, Sirtori P, Petrachi BV, Bassani R, Agnoletto M, Brambilla L, Marmotti A, Mangiavini L, Edem Kwashivi Dzissah O, Kombate NK, Peretti GM | J Biol Regul Homeost Agents | 2020 |
| Bilateral THA in the same sitting for avascular necrosis of the head of the femur in sickle cell patient: our African experience. | Lombardo MDM, Maffulli N, Bassani R, Petrachi BV, Rossi G, Manfroni F, Sirtori P, Brambilla L, Agnoletto M, Marmotti A, Edem Kwashivi Dzissah O, Mangiavini L, Kombate NK, Peretti GM | J Biol Regul Homeost Agents | 2020 |
| Hydroxyurea does not affect the spermatogonial pool in prepubertal patients with sickle cell disease. | Gille AS, Pondarre C, Dalle JH, Bernaudin F, Chalas C, Fahd M, Jean C, Lezeau H, Riou L, Drouineaud V, Paye-Jaouen A, Kamdem A, Neven B, Arnaud C, Azarnoush S, Yakouben K, Sarnacki S, De Montalembert M, Comperat EM, Lenaour G, Sibony M, Dhedin N, Vaiman D, Wolf JP, Patrat C, Fouchet P, Poirot C, Barraud-Lange V | Blood | 2020 |
| Restoration of β-globin expression with optimally designed lentiviral vector for β-thalassemia treatment in Chinese patients. | Ouyang W, Dong G, Zhao W, Li J, Zhou Z, Yang G, Liu R, Li Y, Zhang Q, Du X, Sun H, Gu Y, Lai Y, Liu S, Liu C | Hum Gene Ther | 2020 |
| Eculizumab for complement mediated thrombotic microangiopathy in sickle cell disease. | Chonat S, Graciaa S, Shin HS, Newton JG, Quarmyne MO, Boudreaux J, Tang A, Zerra PE, Rollins MR, Josephson CD, Brown C, Joiner CH, Fasano RM, Stowell SR | Haematologica | 2020 |
| The proteome of neutrophils in sickle cell disease reveals an unexpected activation of interferon alpha signaling pathway. | Hermand P, Azouzi S, Gautier EF, Guillonneau F, Bondet V, Duffy D, Dechavanne S, Tharaux PL, Mayeux P, Le Van Kim C, Koehl B | Haematologica | 2020 |
| Gap Junctions between Endothelial Cells Are Disrupted by Circulating Extracellular Vesicles from Sickle Cell Patients with Acute Chest Syndrome. | Gemel J, Mao Y, Lapping-Carr G, Beyer EC | Int J Mol Sci | 2020 |
| The impact of ferritin on the disassociation of HbA1c and mean plasma glucose. | Li Y, Zhang F, Zhang X, Fu Z, Wang L, Zhao C, Guo G, Zhou X, Ji L | J Diabetes | 2020 |
| Empirically Derived Profiles of Health-Related Quality of Life in Youth and Young Adults with Sickle Cell Disease. | Keenan ME, Loew M, Berlin KS, Hodges J, Alberts NM, Hankins JS, Porter JS | J Pediatr Psychol | 2020 |
| Loss of alpha-globin genes in human subjects is associated with improved nitric oxide-mediated vascular perfusion. | Denton CC, Shah P, Suriany S, Liu H, Thuptimdang W, Sunwoo J, Chalacheva P, Veluswamy S, Kato R, Wood JC, Detterich JA, Khoo MCK, Coates TD | Am J Hematol | 2020 |
| Positive effects of ultrasound-guided peripheral IV insertion on pediatric sickle cell anemia/thalassemia patients receiving automated red cell exchange procedures or chronic transfusion therapy. | Mahon P, Grouchy K, McCartney H, Douglas K, Wu JK | J Clin Apher | 2020 |
| Hydroxyurea Optimization through Precision Study (HOPS): study protocol for a randomized, multicenter trial in children with sickle cell anemia. | Meier ER, Creary SE, Heeney MM, Dong M, Appiah-Kubi AO, Nelson SC, Niss O, Piccone C, Quarmyne MO, Quinn CT, Saving KL, Scott JP, Talati R, Latham TS, Pfeiffer A, Shook LM, Vinks AA, Lane A, McGann PT | Trials | 2020 |
| β-Hemoglobinopathies in the Lao People's Democratic Republic: Molecular diagnostics and implication for a prevention and control program. | Singha K, Chaibunruang A, Souvanlasy B, Srivorakun H, Yamsri S, Fucharoen G, Fucharoen S | Int J Lab Hematol | 2020 |
| Hereditary methaemoglobinemia caused by haemoglobin M Boston. | Chen J, Zhao H, Deng X, Zhao C, Xia M, Zhang R, Cui F, Shuang WB | Lancet Haematol | 2020 |
| The role of haematopoietic stem cell transplantation for sickle cell disease in the era of targeted disease-modifying therapies and gene editing. | de la Fuente J, Gluckman E, Makani J, Telfer P, Faulkner L, Corbacioglu S, | Lancet Haematol | 2020 |
| Lung clearance index in children with sickle cell disease. | Machogu EM, Khurana M, Kaericher J, Clem CC, Slaven JE, Hatch JE, Davis SD, Peterson-Carmichael S | Pediatr Pulmonol | 2020 |
| Splenectomy in Jamaican children with sickle cell disease: Outcome of selective blood transfusion. | Steele O, Duncan AL, Simms LN, Duncan SA, Byles SED, Duncan ND | Trop Doct | 2020 |
| A Patient in Need of a Red Cell Exchange? | Perez-Alvarez I, Crews BO, Woo JS, Rezk S, Tran MH | J Appl Lab Med | 2020 |
| Association between haematological parameters and sickle cell genotypes in children with Plasmodium falciparum malaria resident in Kisumu County in Western Kenya. | Kosiyo P, Otieno W, Gitaka J, Munde EO, Ouma C | BMC Infect Dis | 2020 |
| Fetal Hemoglobin in Sickle Hemoglobinopathies: High HbF Genotypes and Phenotypes. | Steinberg MH | J Clin Med | 2020 |
| Primary prevention of stroke in children with sickle cell anemia in sub-Saharan Africa: rationale and design of phase III randomized clinical trial. | Abdullahi SU, Wudil BJ, Bello-Manga H, Musa AB, Gambo S, Galadanci NA, Aminu H, Tijjani Gaya A, Sanusi S, Tabari MA, Galadanci A, Borodo A, Abba MS, Dambatta AH, Haliru L, Gambo A, Cassell H, Rodeghier M, Ghafuri DL, Covert Greene BV, Neville K, Kassim AA, Kirkham F, Trevathan E, Jordan LC, Aliyu MH, DeBaun MR | Pediatr Hematol Oncol | 2020 |
| Challenges in transfusion and the role of Thalidomide in E-β-Thalassemia-A case report. | Javed R, Radhakrishnan V, Basu S, Chandy M | Clin Case Rep | 2020 |
| Changes in Care Delivery for Children With Sickle Cell Anemia During the COVID-19 Pandemic. | Noisette ML, Phillips S, Schlenz AM, Mueller M, Kanter J | J Pediatr Hematol Oncol | 2020 |
| Navigating decisional conflict as a family when facing the decision of stem cell transplant for a child or adolescent with sickle cell disease. | Schulz GL, Kelly KP, Holtmann M, Armer JM | Patient Educ Couns | 2020 |
| Definitive hematopoietic stem/progenitor cells from human embryonic stem cells through serum/feeder-free organoid-induced differentiation. | Demirci S, Haro-Mora JJ, Leonard A, Drysdale C, Malide D, Keyvanfar K, Essawi K, Vizcardo R, Tamaoki N, Restifo NP, Tisdale JF, Uchida N | Stem Cell Res Ther | 2020 |
| Management of Iron Overload in Beta-Thalassemia Patients: Clinical Practice Update Based on Case Series. | Pinto VM, Forni GL | Int J Mol Sci | 2020 |
| Relation of hepcidin gene expression in blood mononuclear cells with iron overload severity among β-thalassemia major patients. | Ayatollahi H, Mousavi Nezhad SF, Talebpour A, Badiei Z, Nezami H | Mol Biol Rep | 2020 |
| Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed Program. | Dinardo CL, Oliveira TGM, Kelly S, Ashley-Koch A, Telen M, Schmidt LC, Castilho S, Melo K, Dezan MR, Wheeler MM, Johnsen JM, Nickerson DA, Jain D, Custer B, Pereira AC, Sabino EC, | Transfusion | 2020 |
| COVID-19 and the pulmonary complications of sickle cell disease. | Sivalingam T, Inusa B, Doyle P, Oteng-Ntim E | EJHaem | 2020 |
| Vitamin and mineral supplementation for β-thalassemia during COVID-19 pandemic. | d'Arqom A, G Putri M, Savitri Y, Rahul Alfaidin AM | Future Sci OA | 2020 |
| Hemoglobin C Trait Presenting with Bilateral Central Retinal Vein Occlusion. | Neuhouser AJ, Sanders RN, Konda M, Uwaydat SH | Retin Cases Brief Rep | 2020 |
| [Advances in gene therapy for β-thalassemia and hemophilia based on the CRISPR/Cas9 technology]. | Bao LW, Zhou YY, Zeng FY | Yi Chuan | 2020 |
| Genotyping analysis of the MNS blood group system of thalassemia patients with alloantibodies in Iran. | Gholamrezazade A, Amirizadeh N, Oodi A | Transfus Apher Sci | 2020 |
| Prevalence of sickle cell disorders and malaria infection in children aged 1-12 years in the Volta Region, Ghana: a community-based study. | Oppong M, Lamptey H, Kyei-Baafour E, Aculley B, Ofori EA, Tornyigah B, Kweku M, Ofori MF | Malar J | 2020 |
| Procalcitonin to Reduce Antibiotic Exposure during Acute Chest Syndrome in Adult Patients with Sickle-Cell Disease. | Razazi K, Gendreau S, Cuquemelle E, Khellaf M, Guillaud C, Godeau B, Melica G, Moutereau S, Gomart C, Fourati S, De Prost N, Carteaux G, Brun-Buisson C, Bartolucci P, Habibi A, Mekontso Dessap A | J Clin Med | 2020 |
| A natural DNMT1 mutation elevates the fetal hemoglobin via epigenetic de-repression of γ-globin gene in β-thalassemia. | Gong Y, Zhang X, Zhang Q, Zhang Y, Ye Y, Yu W, Shao C, Yan T, Huang J, Zhong J, Wang L, Li Y, Wang L, Xu X | Blood | 2020 |
| Correlation Of Serum Ferritin With Haemoglobin A2 Level In Beta Thalassemia Traits. | Hameed M, Raziq F, Mir A | J Ayub Med Coll Abbottabad | 2020 |
| Predictors of dental complications post-dental treatment in patients with sickle cell disease. | Gusmini MADS, De Sa AC, Feng C, Arany S | Clin Exp Dent Res | 2020 |
| An exploratory study of the effects of strenuous exercise on markers of coagulation activation, circulating microparticles, and inflammation in sickle cell trait. | Skinner S, Ryan ED, Stafford HC, McMurray RG, Key NS, Mooberry MJ | EJHaem | 2020 |
| Predictors of musculoskeletal manifestations in paediatric patients presenting with sickle cell disease at a tertiary teaching hospital in Lusaka, Zambia. | Musowoya RM, Kaonga P, Bwanga A, Chunda-Lyoka C, Lavy C, Munthali J | Bone Jt Open | 2020 |
| HV2 fragment mutations in β-thalassemia patients and a new base pair insertion of high-altitude cases. | Al Thwiby NM, Hussien NA, Bayoumy ES, Shokary M | Am J Blood Res | 2020 |
| Mortality trends in sickle cell patients. | Cintron-Garcia J, Ajebo G, Kota V, Guddati AK | Am J Blood Res | 2020 |
| Effect of immigration on mortality trends in sickle cell patients. | Cintron-Garcia J, Guddati AK | Am J Blood Res | 2020 |
| [>Femoral bone infarction revealing compound heterozygous SC sickle cell disease in a Moroccan patient]. | Bennis FZ, Biaz A, Zkik A, Rachid A, Bouhsain S, Dami A, Samira EI | Pan Afr Med J | 2020 |
| Quality of life assessments in a cohort of Mozambican children with sickle cell disease. | Issa F, Dang BN, Buck WC, Chicumbe S, Nicolau N, Virate C, Cassamo N, Dias A, Amodo F | Pan Afr Med J | 2020 |
| Genetic epidemiology of hemoglobinopathies among Iraqi Kurds. | Al-Allawi N, Al Allawi S, Jalal SD | J Community Genet | 2020 |
| Attitudes and impact among people with abnormal premarital screening test results in Muscat governorate's primary healthcare centers in 2018. | Al Zeedi MASA, Al Abri ZG | J Community Genet | 2020 |
| A rare complication of Sickle Cell Anemia. | Surapaneni PK, Mills K, Renelus BD | Gastroenterology | 2020 |
| Genotyping of blood groups in alloimmunized patients with β-thalassemia major by T-ARMS-PCR and multiplex-aso-pcr. | Gholami MS, Shahidi M, Tabibian S, Naderi M, Dorgalaleh A | Transfus Apher Sci | 2020 |
| Management of non-transfusion-dependent β-thalassemia (NTDT): The next 5 years. | Musallam KM, Rivella S, Taher AT | Am J Hematol | 2020 |
| VZHE-039, a novel antisickling agent that prevents erythrocyte sickling under both hypoxic and anoxic conditions. | Abdulmalik O, Pagare PP, Huang B, Xu GG, Ghatge MS, Xu X, Chen Q, Anabaraonye N, Musayev FN, Omar AM, Venitz J, Zhang Y, Safo MK | Sci Rep | 2020 |
| Hb Angers: A new α2-globin variant [α2 (140)(HC2) Tyr → Ser; HBA2: C.422 A>C] with increased oxygen affinity leading to erythrocytosis. | Orvain C, Kiger L, Peronet I, Peron A, Galacteros F, Wajcman H, Pissard S | Int J Lab Hematol | 2020 |
| Impact of renal function on hydroxyurea exposure in sickle-cell disease patients. | Pressiat C, Rakotoson MG, Habibi A, Barau C, Arrouasse R, Galactéros F, Stehlé T, Audard V, Hulin A, Bartolucci P | Br J Clin Pharmacol | 2020 |
| A complication risk score to evaluate clinical severity of thalassaemia syndromes. | Vitrano A, Meloni A, Addario Pollina W, Karimi M, El-Beshlawy A, Hajipour M, Di Marco V, Hussain Ansari S, Filosa A, Ricchi P, Ceci A, Daar S, Titi Singer S, Naserullah ZA, Pepe A, Scondotto S, Dardanoni G, Bonifazi F, Vichinsky E, Maggio A | Br J Haematol | 2020 |
| Improved stenosis outcome in stroke-free sickle cell anemia children after transplantation compared to chronic transfusion. | Verlhac S, Gabor F, Paillard C, Chateil JF, Jubert C, Petras M, Grevent D, Brousse V, Petit P, Thuret I, Arnaud C, Kamdem A, Pondarré C, Gauthier A, de Montalembert M, Divialle-Doumdo L, Elmaleh M, Missud F, Guitton C, Bernaudin F, | Br J Haematol | 2020 |
| Engulfment and cell motility 1 (ELMO1) and apolipoprotein A1 (APOA1) as candidate genes for sickle cell nephropathy. | Saraf SL, Zhang X, Shah BN, Raslan R, Tayo BO, Lash JP, Franceschini N, Gordeuk VR | Br J Haematol | 2020 |
| Development and clinical application of a preimplantation genetic testing for monogenic disease (PGT-M) for beta thalassemia in Vietnam. | Mai AD, Harton GL, Quang VN, Van HN, Thi NH, Thuy NP, Le Thi TH, Minh DN, Quoc QT | J Assist Reprod Genet | 2020 |
| Effects of three months of treatment with vitamin E and N-acetyl cysteine on the oxidative balance in patients with transfusion-dependent β-thalassemia. | Haghpanah S, Cohan N, Bordbar M, Bazrafshan A, Karimi M, Zareifar S, Safaei S, Aramesh A, Moghadam M, Fard SAZ, Zekavat OR | Ann Hematol | 2020 |
| HbF-promoting polymorphisms may specifically reduce the residual risk of cerebral vasculopathy in SCA children with alpha-thalassemia. | Joly P, Bonello-Palot N, Badens C, Pissard S, Chamouine A, Bernaudin F, Bertrand Y, Connes P, Renoux C | Clin Hemorheol Microcirc | 2020 |
| [Treatment of monogenic disorders with viral transduced haematopoietic stem cells]. | Ifversen MS, Masmas TN, Kornblit B, Rieneck K, Kaastrup EK, Lund AM, Fischer-Nielsen A, Glenthøj A | Ugeskr Laeger | 2020 |
| Implementation of a learning healthcare system for sickle cell disease. | Miller R, Coyne E, Crowgey EL, Eckrich D, Myers JC, Villanueva R, Wadman J, Jacobs-Allen S, Gresh R, Volchenboum SL, Kolb EA | JAMIA Open | 2020 |
| Haematological Profile of Children With Sickle Cell Anaemia in Steady State. | Aliu R, Iliya J, Quadri OR, Ibrahim OR, Daniel E | Cureus | 2020 |
| Respiratory Viral Infections in Sickle Cell Anemia: Special Emphasis on H1N1 Co-infection. | Alkindi S, Al-Yahyai T, Raniga S, Boulassel MR, Pathare A | Oman Med J | 2020 |
| Novel Pyrazoles as Hemoglobin Modulators for Treating Sickle Cell Disease. | Sabnis RW | ACS Med Chem Lett | 2020 |
| Compound heterozygosity for hemoglobin variant Hb-Broomhill and the Southeast Asian α-thalassemia deletion does not worsen outcome: a case report of two unrelated patients. | Qin D, Du L, Wang J, Yao C, Guo H, Yuan T, Liang J, Yin A | J Int Med Res | 2020 |
| Third-generation sequencing: any future opportunities for PGT? | Liu S, Wang H, Leigh D, Cram DS, Wang L, Yao Y | J Assist Reprod Genet | 2020 |
| Hereditary spherocytosis overlooked for 7 years in a pediatric patient with β-thalassemia trait and novel compound heterozygous mutations of SPTA1 gene. | Chen M, Ye YP, Liao L, Deng XL, Qiu YL, Lin FQ | Hematology | 2020 |
| Evaluation of Factors Affecting Awareness About Beta-Thalassemia in Western Rajasthan. | Kumar M, Purohit A, Pramanik S, Saini S | J Family Med Prim Care | 2020 |
| Yoda1 and phosphatidylserine exposure in red cells from patients with sickle cell anaemia. | Wadud R, Hannemann A, Rees DC, Brewin JN, Gibson JS | Sci Rep | 2020 |
| HEPATITIS C AND BETA-THALASSEMIA MAJOR IN CHILDREN: EXPERIENCE WITH GLECAPREVIR/PIBRENTASVIR. | Quintero García D, Sebastián Cuevas FJ, Crehuá Gaudiza E | Rev Esp Enferm Dig | 2020 |
| Executive function in children with sickle cell anemia on transfusion: NIH toolbox utility in the clinical context. | Downes M, Keenan L, Duane Y, Duffy K, Fortune G, Geoghegan R, Conroy H, McMahon C | Clin Neuropsychol | 2020 |
| Association of vitamin D and FGF23 with serum ferritin in hypoparathyroid thalassemia: a case control study. | Saki F, Salehifar A, Kassaee SR, Omrani GR | BMC Nephrol | 2020 |
| Compound Heterozygosity for a Novel Mutation Codon 104 (-A) (: c.313delA) and Codons 41/42 (-CTTT) (: c.126_129delCTTT) Leading to β-Thalassemia Major in a Chinese Family. | Qiu Y, Huang Y, Chen P, Wei S, Su Q, Zhang Z, Yang Z, Ye L, Huang J, Shen X, Mo W | Hemoglobin | 2020 |
| Changing patterns of thalassaemia in Italy: a WebThal perspective. | Longo F, Corrieri P, Origa R, Barella S, Sanna PMG, Bitti PP, Zuccarelli A, Commendatore FV, Vitucci A, Quarta A, Lisi R, Cappellini MD, Massei F, Forni GL, Piga A | Blood Transfus | 2020 |
| The relation between mitogen activated protein kinase (MAPK) pathway and different genes expression in patients with beta Thalassemia. | Elghobashy YA, Assar MF, Mahmoud AA, Monem A Eltorgoman A, Elmasry S | Biochem Biophys Rep | 2020 |
| Haematological indices of sickle cell patients with chronic leg ulcers on compression therapy. | Babalola OA, Ogunkeyede A, Odetunde AB, Fasola F, Oni AA, Babalola CP, Falusi AG | Afr J Lab Med | 2020 |
| Ambulatory Hypertension in Pediatric Patients With Sickle Cell Disease and Its Association With End-Organ Damage. | Ranabothu S, Hafeman M, Manwani D, Reidy K, Morrone K, Lorenzo J, Tria B, Kaskel F, Mahgerefteh J | Cureus | 2020 |
| Supplemental oxygen therapy recommendations in patients with sickle cell disease during air travel: A cross-sectional survey of North American health care providers. | Padda A, Corriveau-Bourque C, Belletrutti M, Bruce AAK | Paediatr Child Health | 2020 |
| Influence of hemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency on diagnosis of diabetes by HbA1c among Tanzanian adults with and without HIV: A cross-sectional study. | Kweka B, Lyimo E, Jeremiah K, Filteau S, Rehman AM, Friis H, Manjurano A, Faurholt-Jepsen D, Krogh-Madsen R, PrayGod G, Heimburger DC | PLoS One | 2020 |
| Choroidal Thickness Evaluation in a Transfusion-Dependent Beta-Thalassemia Greek Population. | Tsapardoni F, Makri OE, Lazaris V, Labropoulou V, Lygeros S, Mastronikolis S, Kouraklis A, Symeonidis A, Georgakopoulos CD | Clin Ophthalmol | 2020 |
| Α case of late diagnosis of compound heterozygosity for Hb Adana (HBA2:c.179G>A) in trans to an α+- thalassemia deletion: guilty or innocent. | Tampaki A, Theodoridou S, Apostolou C, Delaki EE, Vlachaki E | Hippokratia | 2020 |
| Left Atrial Strain Identifies Increased Atrial Ectopy in Patients with Beta-Thalassemia Major. | Vlachou M, Kamperidis V, Vlachaki E, Tziatzios G, Pantelidou D, Boutou A, Apostolou C, Papadopoulou D, Giannakoulas G, Karvounis H | Diagnostics (Basel) | 2020 |
| Association between inflammatory molecules, nitric oxide metabolites and leg ulcers in individuals with sickle cell anemia. | Belisário AR, Mendes-Oliveira F, de Souza VR, Bolina-Santos E, Mendes FG, Moreno EC, Franca AT, Sabino EC, Otta DA, de Faria ES, Coelho-Dos-Reis JGA, Martins-Filho OA, Carneiro-Proietti AB | Hematol Transfus Cell Ther | 2020 |
| Erythroferrone structure, function, and physiology: Iron homeostasis and beyond. | Srole DN, Ganz T | J Cell Physiol | 2020 |
| Sickle cell disease related mortality in Brazil, 2000-2018. | Santo AH | Hematol Transfus Cell Ther | 2020 |
| Denosumab versus zoledronic acid for patients with beta-thalassemia major-induced osteoporosis. | Yassin MA, Abdel Rahman MO, Hamad AA, Poil AR, Abdelrazek MT, Hussein RM, Kassem NA, Fadul AM, Elkourashy SA, Nashwan AJ | Medicine (Baltimore) | 2020 |
| Exploring self-management in adult sickle cell disease patients' at a Teaching Hospital in Ghana. | Amertil NP, Ayitey EK, Kpongboe DG, Attafuah PYA | Nurs Open | 2020 |
| The efficacy of voxelotor, 900 mg in patients with sickle cell anaemia: A meta-analysis of the randomised controlled trials. | Tanriverdi LH, Sarici A, Erkurt MA, Parlakpinar H | Int J Clin Pract | 2020 |
| MicroRNA-2355-5p regulates γ-globin expression in human erythroid cells by inhibiting KLF6. | Cheng Y, Shang X, Chen D, Pang D, Zhao C, Xu X | Br J Haematol | 2020 |
| Polycythemia Vera in a Patient With Heterozygous Beta-Thalassemia: Coincidence or Causal Relationship? | Kottas K, Marathonitis A, Nodarou A, Kanellis G, Christopoulos K | Cureus | 2020 |
| Hemochromatosis in a β-thalassemia minor patient with H63D homozygous mutation: A case report. | Pokhrel NB, Khanal S, Chapagain P, Pokhrel B, Shrestha A | Clin Case Rep | 2020 |
| Acute chest syndrome and COVID-19 in sickle cell disease pediatric patients. | Elia GM, Angel A, Regacini R, Nais RP, Santos ARAD, Vieira PPMG, Braga JAP | Hematol Transfus Cell Ther | 2020 |
| The role of red blood cell exchange in sickle cell disease in patient with COVID-19 infection and pulmonary infiltrates. | Okar L, Aldeeb M, Yassin MA | Clin Case Rep | 2020 |
| Access to health care for patients with thalassaemia in Greece: a cross-sectional study. | Souliotis K, Golna C, Nikolaidi S, Vatheia G, Hasurdjiev S | East Mediterr Health J | 2020 |
| Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC). | Brewin JN, Rooks H, Gardner K, Senior H, Morje M, Patel H, Calvet D, Bartolucci P, Thein SL, Menzel S, Rees DC | Haematologica | 2020 |
| Transferrin Receptors in Erythropoiesis. | Richard C, Verdier F | Int J Mol Sci | 2020 |
| Sickle cell trait: a cause of abdominal pain and pulmonary embolism. | Saad EJ, Tarditi Barra A, Monzoni G, Villegas C, Tabares AH | Rev Fac Cien Med Univ Nac Cordoba | 2020 |
| IL-6 levels are dramatically high in the sputum from children with sickle cell disease during acute chest syndrome. | Allali S, de Montalembert M, Rignault-Bricard R, Taylor M, Brice J, Brousse V, Talbot JM, Moulin F, Heilbronner C, Hermine O, Maciel TT | Blood Adv | 2020 |
| A RARE CASE OF RAPIDLY ENLARGING MYELOLIPOMA IN SICKLE CELL DISEASE. | Davari P, Lee CY, Lee JT | AACE Clin Case Rep | 2020 |
| Therapeutic gene editing strategies using CRISPR-Cas9 for the β-hemoglobinopathies. | Papizan JB, Porter SN, Sharma A, Pruett-Miller SM | J Biomed Res | 2020 |
| Silent cerebral infarcts in patients with sickle cell disease: a systematic review and meta-analysis. | Houwing ME, Grohssteiner RL, Dremmen MHG, Atiq F, Bramer WM, de Pagter APJ, Zwaan CM, White TJH, Vernooij MW, Cnossen MH | BMC Med | 2020 |
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