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Blood Advances|July 14, 2026
Seroprotection after Measles Vaccination in Children with Sickle Cell Anemia Receiving HydroxyureaAlexandra Power-Hays, Abigail Leigh Kincaid, Kathryn E McElhinney, et al.Current Opinion in Hematology|March 25, 2020
Effective use of hydroxyurea for sickle cell anemia in low-resource countriesAlexandra Power-Hays, Russell E WarePediatric Blood & Cancer|July 28, 2020
Household material hardships impact emergency department reliance in pediatric patients with sickle cell diseaseAlexandra Power-Hays, Alyssa Patterson, Amy SobotaPediatric Blood & Cancer|October 2, 2019
Universal screening for social determinants of health in pediatric sickle cell disease: A quality-improvement initiativeAlexandra Power-Hays, Stephanie Li, Akosua Mensah, et al.American Journal of Hematology|March 14, 2026
Advancing Sickle Cell Disease Treatment in Sub-Saharan Africa: Challenges and Opportunities for Disease Modifying TherapiesYvonne Dei-Adomakoh, Emmanuela E Ambrose, Alexandra Power-HaysExperimental Biology and Medicine (Maywood, N.J.)|March 26, 2016
Minireview: Clinical severity in sickle cell disease: the challenges of definition and prognosticationCharles T QuinnSeminars in Hematology|May 11, 2026
More disease-modifying therapies for sickle cell disease: Are small molecules and drug repurposing the way forward?Charles T QuinnBritish Journal of Haematology|July 27, 2026
Predict less, prevent more: A familiar mantra for sickle cell anaemia?Charles T QuinnPediatric Clinics of North America|November 19, 2013
Sickle cell disease in childhood: from newborn screening through transition to adult medical careCharles T QuinnPageof 14