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Philippe Connes

Showing results (241-250 of 305) with videos related to

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Plos One|February 16, 2019
Evaluation of agreement between hemoglobin A1c, fasting glucose, and fructosamine in Senegalese individuals with and without sickle-cell traitSarah Skinner, Mor Diaw, Maïmouna Ndour Mbaye, et al.
Clinical Hemorheology and Microcirculation|March 31, 2012
Relationship between acute chest syndrome and the sympatho-vagal balance in adults with hemoglobin SS disease; a case control studyJennifer M Knight-Madden, Philippe Connes, Andre Bowers, et al.
Clinical Hemorheology and Microcirculation|March 15, 2012
Delayed beneficial effect of acute exercise on red blood cell aggregate strength in patients with sickle cell anemiaXavier Waltz, Mona Hedreville, Stéphane Sinnapah, et al.
American Journal of Hematology|August 23, 2012
Hemorheological alterations, decreased cerebral microvascular oxygenation and cerebral vasomotion compensation in sickle cell patientsXavier Waltz, Aurélien Pichon, Danièle Mougenel, et al.
Acta Pharmaceutica Sinica. B|July 18, 2022
Multiparametric characterization of red blood cell physiology after hypotonic dialysis based drug encapsulation processMélanie Robert, Bastien Laperrousaz, Diana Piedrahita, et al.
Frontiers in Medicine|January 10, 2022
Priming With Red Blood Cells Allows Red Blood Cell Exchange for Sickle Cell Disease in Low-Weight ChildrenOlivier Hequet, Camille Boisson, Philippe Joly, et al.
Blood|April 15, 2020
Plasma microparticles of sickle patients during crisis or taking hydroxyurea modify endothelium inflammatory propertiesYohann Garnier, Séverine Ferdinand, Marie Garnier, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|October 22, 2005
Faster lactate transport across red blood cell membrane in sickle cell trait carriersFagnété Sara, Sara Fagnété, Philippe Connes, et al.
Clinical Hemorheology and Microcirculation|December 28, 2020
Methodological aspects of oxygen gradient ektacytometry in sickle cell disease: Effects of sample storage on outcome parameters in distinct patient subgroupsCamille Boisson, Minke A E Rab, Elie Nader, et al.
Haematologica|March 30, 2013
Hematologic and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell diseaseXavier Waltz, Marc Romana, Marie-Laure Lalanne-Mistrih, et al.
Pageof 31

Showing results (241-250 of 305) with videos related to

Sort By:
Pageof 31
Plos One|February 16, 2019
Evaluation of agreement between hemoglobin A1c, fasting glucose, and fructosamine in Senegalese individuals with and without sickle-cell traitSarah Skinner, Mor Diaw, Maïmouna Ndour Mbaye, et al.
Clinical Hemorheology and Microcirculation|March 31, 2012
Relationship between acute chest syndrome and the sympatho-vagal balance in adults with hemoglobin SS disease; a case control studyJennifer M Knight-Madden, Philippe Connes, Andre Bowers, et al.
Clinical Hemorheology and Microcirculation|March 15, 2012
Delayed beneficial effect of acute exercise on red blood cell aggregate strength in patients with sickle cell anemiaXavier Waltz, Mona Hedreville, Stéphane Sinnapah, et al.
American Journal of Hematology|August 23, 2012
Hemorheological alterations, decreased cerebral microvascular oxygenation and cerebral vasomotion compensation in sickle cell patientsXavier Waltz, Aurélien Pichon, Danièle Mougenel, et al.
Acta Pharmaceutica Sinica. B|July 18, 2022
Multiparametric characterization of red blood cell physiology after hypotonic dialysis based drug encapsulation processMélanie Robert, Bastien Laperrousaz, Diana Piedrahita, et al.
Frontiers in Medicine|January 10, 2022
Priming With Red Blood Cells Allows Red Blood Cell Exchange for Sickle Cell Disease in Low-Weight ChildrenOlivier Hequet, Camille Boisson, Philippe Joly, et al.
Blood|April 15, 2020
Plasma microparticles of sickle patients during crisis or taking hydroxyurea modify endothelium inflammatory propertiesYohann Garnier, Séverine Ferdinand, Marie Garnier, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|October 22, 2005
Faster lactate transport across red blood cell membrane in sickle cell trait carriersFagnété Sara, Sara Fagnété, Philippe Connes, et al.
Clinical Hemorheology and Microcirculation|December 28, 2020
Methodological aspects of oxygen gradient ektacytometry in sickle cell disease: Effects of sample storage on outcome parameters in distinct patient subgroupsCamille Boisson, Minke A E Rab, Elie Nader, et al.
Haematologica|March 30, 2013
Hematologic and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell diseaseXavier Waltz, Marc Romana, Marie-Laure Lalanne-Mistrih, et al.
Pageof 31