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Curing Sickle Cell Disease by Allogeneic Hematopoietic Stem Cell (HSC) Transplantation Toward In Vivo HSC Gene Therapy. [PDF]
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Iron, Oxidative Stress, and Haptoglobin Gene Polymorphism in Sickle Cell Disease Patients With Inflammation in Cameroon: An Analytical Cross-Sectional Study. [PDF]
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Physiologic impact of circulating RBC microparticles upon blood-vascular interactions [PDF]
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End points for sickle cell disease clinical trials: Renal and cardiopulmonary, cure, and low-resource settings [PDF]
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Impact of telehealth on hydroxyurea adherence and clinical outcomes in sickle cell disease management: A systematic review and meta-analysis. [PDF]
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Intravascular hemolysis and the pathophysiology of sickle cell disease
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