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Annals of Hematology|November 18, 2017
Simultaneous point-of-care detection of anemia and sickle cell disease in Tanzania: the RAPID studyLuke R Smart, Emmanuela E Ambrose, Kevin C Raphael, et al.Environmental and Molecular Mutagenesis|February 26, 2023
Lack of hydroxyurea-associated mutagenesis in pediatric sickle cell disease patientsDorothea K Torous, Svetlana Avlasevich, Jeffrey C Bemis, et al.The Lancet. Haematology|March 4, 2023
Hydroxyurea with dose escalation for primary stroke risk reduction in children with sickle cell anaemia in Tanzania (SPHERE): an open-label, phase 2 trialEmmanuela E Ambrose, Teresa S Latham, Primrose Songoro, et al.Blood|January 3, 2024
Hydroxyurea reduces infections in children with sickle cell anemia in UgandaRuth Namazzi, Caitlin Bond, Andrea L Conroy, et al.JMIR Research Protocols|June 25, 2016
Novel Use of Hydroxyurea in an African Region With Malaria: Protocol for a Randomized Controlled Clinical TrialJuliana N Anyanwu, Olatundun Williams, Casey L Sautter, et al.Blood|October 21, 2017
Novel use Of Hydroxyurea in an African Region with Malaria (NOHARM): a trial for children with sickle cell anemiaRobert O Opoka, Christopher M Ndugwa, Teresa S Latham, et al.American Journal of Hematology|February 23, 2026
Artificial Intelligence-Based Analysis of Central Nervous System Vasculopathy in Pediatric Sickle Cell AnemiaMeredith E Fay, Raghav Tandon, Teresa Latham, et al.Pediatric Blood & Cancer|December 9, 2008
A pilot study of hydroxyurea to prevent chronic organ damage in young children with sickle cell anemiaCourtney D Thornburg, Natalia Dixon, Shelly Burgett, 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.Blood Advances|January 4, 2018
Hemoglobin variants identified in the Uganda Sickle Surveillance StudyBeverly A Schaefer, Charles Kiyaga, Thad A Howard, et al.Pageof 27