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Philippe Connes

Showing results (91-100 of 305) with videos related to

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British Journal of Haematology|June 28, 2017
Decrease of externalized phosphatidylserine density on red blood cell-derived microparticles in SCA patients treated with hydroxycarbamideYohann Garnier, Séverine Ferdinand, Philippe Connes, et al.
Blood Reviews|September 6, 2015
The role of blood rheology in sickle cell diseasePhilippe Connes, Tamas Alexy, Jon Detterich, et al.
Scientific Reports|May 3, 2019
Impact of surface-area-to-volume ratio, internal viscosity and membrane viscoelasticity on red blood cell deformability measured in isotonic conditionCéline Renoux, Magalie Faivre, Amel Bessaa, et al.
Frontiers in Physiology|June 30, 2020
Mechanical Signature of Red Blood Cells Flowing Out of a Microfluidic Constriction Is Impacted by Membrane Elasticity, Cell Surface-to-Volume Ratio and DiseasesMagalie Faivre, Céline Renoux, Amel Bessaa, et al.
Frontiers in Physiology|August 10, 2019
Receptor for Advanced Glycation End Products Antagonism Blunts Kidney Damage in Transgenic Townes Sickle MiceEmmanuelle Charrin, Camille Faes, Amandine Sotiaux, et al.
American Journal of Hematology|August 30, 2012
Increased blood viscosity and red blood cell aggregation in a patient with sickle cell anemia and smoldering myelomaNathalie Lemonne, Philippe Connes, Marc Romana, et al.
British Journal of Haematology|June 13, 2024
Controversies in the pathophysiology of leg ulcers in sickle cell diseaseJudith Catella, Nicolas Guillot, Elie Nader, et al.
British Journal of Haematology|April 24, 2014
Effects of oxidative stress on red blood cell rheology in sickle cell patientsRégine Hierso, Xavier Waltz, Pierre Mora, et al.
British Journal of Haematology|February 10, 2022
Comment on: Oxygen gradient ektacytometry does not predict pain in children with sickle cell anaemiaVivien A Sheehan, Eduard J van Beers, Philippe Connes, et al.
Blood Cells, Molecules & Diseases|July 6, 2010
Alpha-thalassemia is associated with a decreased occurrence and a delayed age-at-onset of albuminuria in sickle cell anemia patientsDanitza Nebor, Cédric Broquere, Karine Brudey, et al.
Pageof 31

Showing results (91-100 of 305) with videos related to

Sort By:
Pageof 31
British Journal of Haematology|June 28, 2017
Decrease of externalized phosphatidylserine density on red blood cell-derived microparticles in SCA patients treated with hydroxycarbamideYohann Garnier, Séverine Ferdinand, Philippe Connes, et al.
Blood Reviews|September 6, 2015
The role of blood rheology in sickle cell diseasePhilippe Connes, Tamas Alexy, Jon Detterich, et al.
Scientific Reports|May 3, 2019
Impact of surface-area-to-volume ratio, internal viscosity and membrane viscoelasticity on red blood cell deformability measured in isotonic conditionCéline Renoux, Magalie Faivre, Amel Bessaa, et al.
Frontiers in Physiology|June 30, 2020
Mechanical Signature of Red Blood Cells Flowing Out of a Microfluidic Constriction Is Impacted by Membrane Elasticity, Cell Surface-to-Volume Ratio and DiseasesMagalie Faivre, Céline Renoux, Amel Bessaa, et al.
Frontiers in Physiology|August 10, 2019
Receptor for Advanced Glycation End Products Antagonism Blunts Kidney Damage in Transgenic Townes Sickle MiceEmmanuelle Charrin, Camille Faes, Amandine Sotiaux, et al.
American Journal of Hematology|August 30, 2012
Increased blood viscosity and red blood cell aggregation in a patient with sickle cell anemia and smoldering myelomaNathalie Lemonne, Philippe Connes, Marc Romana, et al.
British Journal of Haematology|June 13, 2024
Controversies in the pathophysiology of leg ulcers in sickle cell diseaseJudith Catella, Nicolas Guillot, Elie Nader, et al.
British Journal of Haematology|April 24, 2014
Effects of oxidative stress on red blood cell rheology in sickle cell patientsRégine Hierso, Xavier Waltz, Pierre Mora, et al.
British Journal of Haematology|February 10, 2022
Comment on: Oxygen gradient ektacytometry does not predict pain in children with sickle cell anaemiaVivien A Sheehan, Eduard J van Beers, Philippe Connes, et al.
Blood Cells, Molecules & Diseases|July 6, 2010
Alpha-thalassemia is associated with a decreased occurrence and a delayed age-at-onset of albuminuria in sickle cell anemia patientsDanitza Nebor, Cédric Broquere, Karine Brudey, et al.
Pageof 31