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Hematology/Oncology Clinics of North America|February 2, 2010
Hydroxyurea for children with sickle cell diseaseMatthew M Heeney, Russell E WareCurrent Opinion in Hematology|March 5, 2011
Hydroxyurea for sickle cell anemia: what have we learned and what questions still remain?Patrick T McGann, Russell E WareBritish Journal of Haematology|February 11, 2021
Absence of hydroxyurea-induced mutational effects supports higher utilisation for the treatment of sickle cell anaemiaRussell E Ware, Stephen D DertingerBlood|February 10, 2012
Stroke With Transfusions Changing to Hydroxyurea (SWiTCH)Russell E Ware, Ronald W Helms, International Journal of Neonatal Screening|February 20, 2026
Advances and Gaps in Global Newborn Screening for Sickle Cell DiseaseLisa Marie Shook, Russell E WareJournal of Pediatric Hematology/Oncology|January 29, 2022
Documented Viral Illness at the Time of Splenic Sequestration Does Not Affect the Odds of Recurrence in Children With Sickle Cell DiseaseOmoyeni Clement, Joanna Fishbein, Abena Appiah-Kubi, et al.Blood|November 14, 2022
Hydroxyurea treatment is associated with lower malaria incidence in children with sickle cell anemia in sub-Saharan AfricaPeter Olupot-Olupot, George Tomlinson, Thomas N Williams, et al.Blood|April 26, 2011
Genetic predictors for stroke in children with sickle cell anemiaJonathan M Flanagan, Denise M Frohlich, Thad A Howard, et al.Plos One|October 7, 2016
Genetic Modifiers of White Blood Cell Count, Albuminuria and Glomerular Filtration Rate in Children with Sickle Cell AnemiaBeverly A Schaefer, Jonathan M Flanagan, Ofelia A Alvarez, et al.Pediatrics|July 22, 2024
Health Supervision for Children and Adolescents With Sickle Cell Disease: Clinical ReportAmber M Yates, Banu Aygun, Rachelle Nuss, et al.Pageof 27