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Blood|August 24, 2012
Impact of hydroxyurea on clinical events in the BABY HUG trialCourtney D Thornburg, Beatrice A Files, Zhaoyu Luo, et al.
Blood|March 7, 2009
R2* magnetic resonance imaging of the liver in patients with iron overloadJane S Hankins, M Beth McCarville, Ralf B Loeffler, et al.
Pediatric Blood & Cancer|October 14, 2014
Humanism and professionalism education for pediatric hematology-oncology fellows: A model for pediatric subspecialty trainingJennifer C Kesselheim, Mark Atlas, Denise Adams, et al.
British Journal of Haematology|March 6, 2018
Transcranial Doppler velocity among Jamaican children with sickle cell anaemia: determining the significance of haematological values and nutritionAngela E Rankine-Mullings, Nadine Morrison-Levy, Deanne Soares, et al.
International Journal of Public Health|August 2, 2021
Prospective Newborn Screening for Sickle Cell Disease and Other Inherited Blood Disorders in Central MalawiGerald Tegha, Hillary M Topazian, Portia Kamthunzi, 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.
Blood|January 5, 2002
Predictors of fetal hemoglobin response in children with sickle cell anemia receiving hydroxyurea therapyRussell E Ware, Barry Eggleston, Rupa Redding-Lallinger, 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 Advances|April 9, 2026
Growth and puberty in African children with sickle cell anemia treated with hydroxyureaPhilippe Backeljauw, George Tomlinson, Luke R Smart, et al.
Blood Vessels, Thrombosis & Hemostasis|August 6, 2025
Angiopoietin-2 is associated with sickle cell complications, including stroke risk, and decreases with hydroxyurea therapyThomas F Siegert, Robert O Opoka, Maria Nakafeero, et al.
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