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Philippe Connes

Showing results (221-230 of 305) with videos related to

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British Journal of Sports Medicine|March 8, 2019
Association between physical activity and sedentary behaviour on carotid atherosclerotic plaques: an epidemiological and histological study in 90 asymptomatic patientsPauline Mury, Mathilde Mura, Nellie Della-Schiava, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|August 12, 2006
Effects of progressive and maximal exercise on plasma levels of adhesion molecules in athletes with sickle cell trait with or without alpha-thalassemiaGeraldine Monchanin, Laura D Serpero, Philippe Connes, et al.
American Journal of Hematology|March 27, 2014
Association between relative systemic hypertension and otologic disorders in patients with sickle cell-hemoglobin C disorderNathalie Lemonne, Marc Romana, Yann Lamarre, et al.
British Journal of Haematology|February 6, 2016
Effects of Poloxamer 188 on red blood cell membrane properties in sickle cell anaemiaBarbara Sandor, Mickaël Marin, Claudine Lapoumeroulie, et al.
Frontiers in Physiology|October 11, 2021
Nocturnal Hypoxemia Rather Than Obstructive Sleep Apnea Is Associated With Decreased Red Blood Cell Deformability and Enhanced Hemolysis in Patients With Sickle Cell DiseaseEmeric Stauffer, Solène Poutrel, Giovanna Cannas, et al.
Clinical Hemorheology and Microcirculation|April 18, 2018
Pulse wave velocity is lower in trained than in untrained sickle cell trait carriersValentin Ouédraogo, Philippe Connes, Julien Tripette, et al.
Vox Sanguinis|September 23, 2020
Automated RBC Exchange has a greater effect on whole blood viscosity than manual whole blood exchange in adult patients with sickle cell diseaseNassim Ait Abdallah, Philippe Connes, Gaetana Di Liberto, et al.
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.
Haematologica|March 18, 2014
Impaired blood rheology plays a role in the chronic disorders associated with sickle cell-hemoglobin C diseaseNathalie Lemonne, Yann Lamarre, Marc Romana, 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.
Pageof 31

Showing results (221-230 of 305) with videos related to

Sort By:
Pageof 31
British Journal of Sports Medicine|March 8, 2019
Association between physical activity and sedentary behaviour on carotid atherosclerotic plaques: an epidemiological and histological study in 90 asymptomatic patientsPauline Mury, Mathilde Mura, Nellie Della-Schiava, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|August 12, 2006
Effects of progressive and maximal exercise on plasma levels of adhesion molecules in athletes with sickle cell trait with or without alpha-thalassemiaGeraldine Monchanin, Laura D Serpero, Philippe Connes, et al.
American Journal of Hematology|March 27, 2014
Association between relative systemic hypertension and otologic disorders in patients with sickle cell-hemoglobin C disorderNathalie Lemonne, Marc Romana, Yann Lamarre, et al.
British Journal of Haematology|February 6, 2016
Effects of Poloxamer 188 on red blood cell membrane properties in sickle cell anaemiaBarbara Sandor, Mickaël Marin, Claudine Lapoumeroulie, et al.
Frontiers in Physiology|October 11, 2021
Nocturnal Hypoxemia Rather Than Obstructive Sleep Apnea Is Associated With Decreased Red Blood Cell Deformability and Enhanced Hemolysis in Patients With Sickle Cell DiseaseEmeric Stauffer, Solène Poutrel, Giovanna Cannas, et al.
Clinical Hemorheology and Microcirculation|April 18, 2018
Pulse wave velocity is lower in trained than in untrained sickle cell trait carriersValentin Ouédraogo, Philippe Connes, Julien Tripette, et al.
Vox Sanguinis|September 23, 2020
Automated RBC Exchange has a greater effect on whole blood viscosity than manual whole blood exchange in adult patients with sickle cell diseaseNassim Ait Abdallah, Philippe Connes, Gaetana Di Liberto, et al.
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.
Haematologica|March 18, 2014
Impaired blood rheology plays a role in the chronic disorders associated with sickle cell-hemoglobin C diseaseNathalie Lemonne, Yann Lamarre, Marc Romana, 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.
Pageof 31