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British Journal of Haematology|February 19, 2009
Pharmacotherapy in sickle cell disease--state of the art and future prospectsJane Hankins, Banu AygunPediatric Blood & Cancer|April 27, 2012
A global perspective on sickle cell diseaseBanu Aygun, Isaac OdameEuropean Journal of Haematology|May 7, 2014
Predictors of splenic function preservation in children with sickle cell anemia treated with hydroxyureaKerri A Nottage, Russell E Ware, Bryan Winter, et al.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.American Journal of Hematology|September 16, 2017
A clinically meaningful fetal hemoglobin threshold for children with sickle cell anemia during hydroxyurea therapyJeremie H Estepp, Matthew P Smeltzer, Guolian Kang, et al.Hematology. American Society of Hematology. Education Program|December 6, 2015
Optimizing hydroxyurea therapy for sickle cell anemiaRussell E WareBlood|March 13, 2010
How I use hydroxyurea to treat young patients with sickle cell anemiaRussell E WareBlood|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.The Lancet. Haematology|May 3, 2024
Hydroxyurea dose optimisation for children with sickle cell anaemia in sub-Saharan Africa (REACH): extended follow-up of a multicentre, open-label, phase 1/2 trialBanu Aygun, Adam Lane, Luke R Smart, et al.Pageof 27