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Clinical Hemorheology and Microcirculation|November 20, 2020
HbF-promoting polymorphisms may specifically reduce the residual risk of cerebral vasculopathy in SCA children with alpha-thalassemiaPhilippe Joly, Nathalie Bonello-Palot, Catherine Badens, et al.
Blood Cells, Molecules & Diseases|May 7, 2026
In vitro effects of voxelotor on red blood cell senescence and rheological behavior in sickle cell anemiaBita Asghariastanehei, Philippe Connes, Romain Carin, et al.
Blood Cells, Molecules & Diseases|June 19, 2017
Moderate exercise training decreases inflammation in transgenic sickle cell miceEmmanuelle Charrin, John J Dubé, Philippe Connes, et al.
Biorheology|May 22, 2009
Relationships between hemodynamic, hemorheological and metabolic responses during exercisePhilippe Connes, Julien Tripette, Martin Mukisi-Mukaza, et al.
Frontiers in Physiology|July 25, 2022
Physical Properties of Blood and their Relationship to Clinical ConditionsTamas Alexy, Jon Detterich, Philippe Connes, et al.
Plos One|December 16, 2014
Blood thixotropy in patients with sickle cell anaemia: role of haematocrit and red blood cell rheological propertiesJens Vent-Schmidt, Xavier Waltz, Marc Romana, et al.
Clinical Hemorheology and Microcirculation|January 14, 2012
Abnormal flow adhesion of sickle red blood cells to human placental trophoblast extracellular matrixYann Lamarre, Stéphane Petres, Marie-Dominique Hardy-Dessources, et al.
Clinical Hemorheology and Microcirculation|March 26, 2009
Effects of storage duration and temperature of human blood on red cell deformability and aggregationMehmet Uyuklu, Melike Cengiz, Pinar Ulker, et al.
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