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Blood Advances|October 20, 2022
The Consortium on Newborn Screening in Africa for sickle cell disease: study rationale and methodologyNancy S Green, Andrew Zapfel, Obiageli E Nnodu, et al.
Blood|January 12, 2026
Long-term efficacy and safety results of betibeglogene autotemcel gene therapy for transfusion-dependent β-thalassemiaJanet L Kwiatkowski, Alexis A Thompson, Jennifer Schneiderman, et al.
The New England Journal of Medicine|April 3, 2026
Base Editing of HBG1 and HBG2 Promoters for Sickle Cell DiseaseAshish O Gupta, Akshay Sharma, Haydar Frangoul, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 9, 2023
Secondary Neoplasms After Hematopoietic Cell Transplant for Sickle Cell DiseaseMary Eapen, Ruta Brazauskas, David A Williams, et al.
Pediatric Blood & Cancer|March 7, 2025
Engaging Parents of Children With Sickle Cell Disease in Shared Decision-Making for Hydroxyurea: The ENGAGE-HU StudyAimee K Hildenbrand, Constance A Mara, Bridget Murphy, et al.
American Journal of Hematology|November 5, 2025
Hospital Variations in Time-To-Crisis-Resolution Among Children and Adolescents With Sickle Cell DiseaseChris A Rees, Dunia Hatabah, Rawan Korman, et al.
The New England Journal of Medicine|August 10, 2007
Prophylaxis versus episodic treatment to prevent joint disease in boys with severe hemophiliaMarilyn J Manco-Johnson, Thomas C Abshire, Amy D Shapiro, et al.
Haematologica|April 6, 2019
Immunosuppressive therapy for pediatric aplastic anemia: a North American Pediatric Aplastic Anemia Consortium studyZora R Rogers, Taizo A Nakano, Timothy S Olson, et al.
American Journal of Hematology|July 22, 2014
Silent cerebral infarction, income, and grade retention among students with sickle cell anemiaAllison A King, Mark J Rodeghier, Julie Ann Panepinto, et al.
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