End-of-Life Care in Sickle Cell Disease and Transfusion-Dependent β-Thalassemia: Clinical, Psychosocial, and Ethical Considerations. [PDF]
Mediterr J Hematol Infect DisDelicou S +3 more
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Pregnancy-Triggered Vaso-Occlusive Crises in Hemoglobin SE Disease Complicated by Glucose-6-Phosphate Dehydrogenase Deficiency: A Case Report. [PDF]
CureusAlzahrani LM, Altassan FF, Althubaity W.
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Bilateral Peripheral Neovascularization in Hemoglobin C Trait Retinopathy. [PDF]
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Atypical Overt Hemorrhagic Stroke in an Adult With Sickle Cell-Hemoglobin C Disease: A Report of a Rare Case. [PDF]
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Engraftment Outcome of CRISPR/Cas9-Edited Hematopoietic Stem Cells for Genetic Diseases: A Systematic Review and Meta-Analysis of Preclinical Evidence. [PDF]
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Diagnostic Limitations of Hemoglobin A1c in the Setting of Compound Hemoglobinopathy: A Case Report of Sickle Cell Disease, Alpha Thalassemia, and Occult Diabetes. [PDF]
CureusToperzer K, Moon A.
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Distribution of Hemoglobinopathy Disorders in Al-Kharj Province Based on Data from the Premarital Screening and Genetic Counseling Program. [PDF]
Medicina (Kaunas)Al-Dayan N.
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Prenatal hemoglobinopathy screening in India: Enhancing coverage, counselling, & continuity. [PDF]
Indian J Med ResAphale P, Dokania S, Shekhar H.
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Correction to: Association between HLA-DRB1*04, HLA-DQB1*03, and HLA-DQB1*06 with alloimmunization in transfusion-dependent patients with thalassemia: the first case-control study in Iran. [PDF]
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