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Haematologica|March 17, 2018
Proteomic analysis of plasma from children with sickle cell anemia and silent cerebral infarctionSanjay Tewari, George Renney, John Brewin, et al.Plos One|June 8, 2018
A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemiaTitilope A Adeyemo, Oyesola O Ojewunmi, Idat A Oyetunji, et al.Haematologica|December 23, 2020
Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC)John N Brewin, Helen Rooks, Kate Gardner, et al.British Journal of Haematology|September 28, 2007
Circulating DNA: a potential marker of sickle cell crisisNisha Vasavda, Pinar Ulug, Sheila Kondaveeti, et al.Frontiers in Physiology|April 28, 2022
Automating Pitted Red Blood Cell Counts Using Deep Neural Network Analysis: A New Method for Measuring Splenic Function in Sickle Cell AnaemiaAmina Nardo-Marino, Thomas H Braunstein, Jesper Petersen, et al.British Journal of Haematology|March 8, 2007
The associations between air quality and the number of hospital admissions for acute pain and sickle-cell disease in an urban environmentDeborah Yallop, Edward R Duncan, Elizabeth Norris, et al.The Journal of Biological Chemistry|December 20, 2018
Regulation of erythrocyte Na+/K+/2Cl- cotransport by an oxygen-switched kinase cascadeSuilan Zheng, Nathan A Krump, Mary M McKenna, et al.European Journal of Haematology|December 17, 2013
Cost-effectiveness analysis of preoperative transfusion in patients with sickle cell disease using evidence from the TAPS trialEldon Spackman, Mark Sculpher, Jo Howard, et al.Plos One|July 26, 2017
The significance of inadequate transcranial Doppler studies in children with sickle cell diseaseSimon Greenwood, Colin Deane, Oliver L Rees, et al.Scientific Reports|May 27, 2022
The erythrocyte membrane properties of beta thalassaemia heterozygotes and their consequences for Plasmodium falciparum invasionViola Introini, Alejandro Marin-Menendez, Guilherme Nettesheim, et al.Pageof 16