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British Journal of Haematology|May 29, 2020
The pyruvate kinase (PK) to hexokinase enzyme activity ratio and erythrocyte PK protein level in the diagnosis and phenotype of PK deficiencyHanny Al-Samkari, Kathryn Addonizio, Bertil Glader, et al.
British Journal of Haematology|April 25, 2015
Dysregulated arginine metabolism and cardiopulmonary dysfunction in patients with thalassaemiaClaudia R Morris, Hae-Young Kim, Elizabeth S Klings, et al.
The New England Journal of Medicine|December 13, 2021
Biologic and Clinical Efficacy of LentiGlobin for Sickle Cell DiseaseJulie Kanter, Mark C Walters, Lakshmanan Krishnamurti, et al.
Pediatric Blood & Cancer|June 16, 2011
Response to steroids predicts response to rituximab in pediatric chronic immune thrombocytopeniaRachael F Grace, Carolyn M Bennett, A Kim Ritchey, et al.
European Journal of Haematology|April 24, 2023
Health-related quality of life in patients with β-thalassemia: Data from the phase 3 BELIEVE trial of luspaterceptMaria Domenica Cappellini, Ali T Taher, Antonio Piga, et al.
Molecular Genetics and Metabolism|June 9, 2016
A framework for assessing outcomes from newborn screening: on the road to measuring its promiseCynthia F Hinton, Charles J Homer, Alexis A Thompson, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|January 29, 2018
Unrelated Donor Transplantation in Children with Thalassemia using Reduced-Intensity Conditioning: The URTH TrialShalini Shenoy, Mark C Walters, Alex Ngwube, et al.
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