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Pediatric Hematology and Oncology|August 3, 2010
Transfusion and chelation practices in sickle cell disease: a regional perspectiveElliott P Vichinsky, Kwaku Ohene-Frempong, Swee Lay Thein, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 26, 2022
Phenotypic screening of the ReFRAME drug repurposing library to discover new drugs for treating sickle cell diseaseBelhu Metaferia, Troy Cellmer, Emily B Dunkelberger, et al.
Haematologica|March 19, 2026
Variations in mitochondrial genome as potential prognostic markers in sickle cell diseaseRudra Ray, Haiou Li, Shijinqiu Gao, et al.
Rheumatology (Oxford, England)|June 25, 2026
Is clonal haematopoiesis the missing link between lupus and cardiovascular disease?Aamir Shamsi, Chris Wincup, Charis Pericleous, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 27, 2007
Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adultsSwee Lay Thein, Stephan Menzel, Xu Peng, et al.
JCI Insight|January 20, 2026
Pyruvate kinase deficiency modifies sickle hemoglobin carrier and sickle cell disease phenotypes in miceXunde Wang, Meghann Smith, Sayuri Kamimura, et al.
British Journal of Haematology|February 19, 2016
Reduced rate of sickle-related complications in Brazilian patients carrying HbF-promoting alleles at the BCL11A and HMIP-2 lociFlávia C Leonardo, Ana F Brugnerotto, Igor F Domingos, et al.
Blood Advances|January 28, 2020
American Society of Hematology 2020 guidelines for sickle cell disease: transfusion supportStella T Chou, Mouaz Alsawas, Ross M Fasano, et al.
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