Red blood cell deformability is reduced in homozygous sickle cell disease patients with leg ulcers
Author:
Affiliation:
1. Sickle Cell Unit, Tropical Medicine Research Institute, University of the West Indies, Mona, Kingston 7, Jamaica, W.I.
2. Physiology Section, Department of Basic Medical Sciences, University of the West Indies, Mona, Kingston 7, Jamaica, W.I.
Publisher
IOS Press
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine,Hematology,Physiology
Reference36 articles.
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4. Sickle cell anemia with few painful crises is characterized by decreased red cell deformability and increased number of dense cells;Ballas;Am J Hematol,1991
5. Ballas S.K. and Connes P, The paradox of the serrated sickle erythrocyte: The importance of the red blood cell membrane topography, Clin Hemorheol Microcirc (2015), in press.
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