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British Journal of Haematology|February 25, 2012
Hydroxycarbamide alters erythroid gene expression in children with sickle cell anaemiaJonathan M Flanagan, Shirley Steward, Thad A Howard, et al.Journal of Clinical Pharmacology|October 8, 2020
Hydroxyurea Pharmacokinetics in Pediatric Patients After Total Pancreatectomy With Islet AutotransplantationAlexander A Boucher, Min Dong, Alexander A Vinks, et al.The Lancet. Global Health|February 3, 2016
Burden of sickle cell trait and disease in the Uganda Sickle Surveillance Study (US3): a cross-sectional studyGrace Ndeezi, Charles Kiyaga, Arielle G Hernandez, et al.Pediatric Blood & Cancer|May 17, 2019
Sickle cell screening in Uganda: High burden, human immunodeficiency virus comorbidity, and genetic modifiersCharles Kiyaga, Arielle G Hernandez, Isaac Ssewanyana, et al.Blood|February 21, 2013
Genetic mapping and exome sequencing identify 2 mutations associated with stroke protection in pediatric patients with sickle cell anemiaJonathan M Flanagan, Vivien Sheehan, Heidi Linder, et al.Blood Advances|January 4, 2018
Hemoglobin variants identified in the Uganda Sickle Surveillance StudyBeverly A Schaefer, Charles Kiyaga, Thad A Howard, et al.American Journal of Hematology|May 21, 2019
Robust clinical and laboratory response to hydroxyurea using pharmacokinetically guided dosing for young children with sickle cell anemiaPatrick T McGann, Omar Niss, Min Dong, et al.Bulletin of the World Health Organization|December 9, 2020
Surveillance for sickle cell disease, United Republic of TanzaniaEmmanuela E Ambrose, Luke R Smart, Mwesige Charles, 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.Pageof 4