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Plos One|January 4, 2013
Normal muscle oxygen consumption and fatigability in sickle cell patients despite reduced microvascular oxygenation and hemorheological abnormalitiesXavier Waltz, Aurélien Pichon, Nathalie Lemonne, et al.
The Journal of Physiology|December 26, 2023
Expedition 5300: limits of human adaptations in the highest city in the worldBenoit Champigneulle, Julien V Brugniaux, Emeric Stauffer, et al.
Diabetes Care|September 2, 2015
Sickle Cell Trait Worsens Oxidative Stress, Abnormal Blood Rheology, and Vascular Dysfunction in Type 2 DiabetesMor Diaw, Vincent Pialoux, Cyril Martin, et al.
Microvascular Research|December 5, 2018
Altered blood rheology and impaired pressure-induced cutaneous vasodilation in a mouse model of combined type 2 diabetes and sickle cell traitSarah Skinner, Philippe Connes, Dominique Sigaudo-Roussel, et al.
European Journal of Haematology|June 16, 2015
G6PD deficiency and absence of α-thalassemia increase the risk for cerebral vasculopathy in children with sickle cell anemiaPhilippe Joly, Nathalie Garnier, Kamila Kebaili, et al.
Oxidative Medicine and Cellular Longevity|August 21, 2019
Effects of Individualized Treadmill Endurance Training on Oxidative Stress in Skeletal Muscles of Transgenic Sickle MiceEtienne Gouraud, Emmanuelle Charrin, John J Dubé, et al.
Plos One|November 14, 2013
Decreased hematocrit-to-viscosity ratio and increased lactate dehydrogenase level in patients with sickle cell anemia and recurrent leg ulcersPhilippe Connes, Yann Lamarre, Marie-Dominique Hardy-Dessources, et al.
Frontiers in Physiology|November 22, 2019
Blood Rheology: Key Parameters, Impact on Blood Flow, Role in Sickle Cell Disease and Effects of ExerciseElie Nader, Sarah Skinner, Marc Romana, et al.
Blood|December 6, 2012
Abnormal properties of red blood cells suggest a role in the pathophysiology of Gaucher diseaseMelanie Franco, Emmanuel Collec, Philippe Connes, et al.
Blood Cells, Molecules & Diseases|March 25, 2017
Micro- and macrovascular function in children with sickle cell anaemia and sickle cell haemoglobin C diseaseBerenike Möckesch, Keyne Charlot, Stéphane Jumet, et al.
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