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JAMA Network Open|December 9, 2025
Role of Menstrual Bleeding Assessments in Sickle Cell ClinicsGillian Rush, Rania E Mohamed, Kimberly Moffatt-Bazile, et al.
British Journal of Haematology|July 31, 2025
Grandchildren of GRNDaD: Shifts in disease-modifying therapy at the adolescent transition in sickle cell diseaseMatthew Chang, Daniel Semakula, Jane A Little, et al.
MMWR. Morbidity and Mortality Weekly Report|March 28, 2024
Birth Prevalence of Sickle Cell Disease and County-Level Social Vulnerability - Sickle Cell Data Collection Program, 11 States, 2016-2020Mariam Kayle, Audrey L Blewer, Wei Pan, 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.
Blood Advances|October 29, 2024
Hematopoietic cell transplant compared with standard care in adolescents and young adults with sickle cell diseaseMark C Walters, Mary Eapen, Yiwen Liu, et al.
Blood|November 19, 2011
Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, sex, and relative high systolic blood pressureMichael R DeBaun, Sharada A Sarnaik, Mark J Rodeghier, et al.
American Journal of Hematology|July 2, 2024
Hydroxyurea to prevent brain injury in children with sickle cell disease (HU Prevent)-A randomized, placebo-controlled phase II feasibility/pilot studyJames F Casella, Dana K Furstenau, Robert J Adams, et al.
The New England Journal of Medicine|August 21, 2014
Controlled trial of transfusions for silent cerebral infarcts in sickle cell anemiaMichael R DeBaun, Mae Gordon, Robert C McKinstry, et al.
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