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Philippe Joly

Showing results (71-80 of 148) with videos related to

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Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|February 3, 2020
Goal-Oriented Monitoring of Cyclosporine Is Effective for Graft-versus-Host Disease Prevention after Hematopoietic Stem Cell Transplantation in Sickle Cell Disease and Thalassemia MajorAlexandra Gauthier, Nathalie Bleyzac, Nathalie Garnier, et al.
Clinical Hemorheology and Microcirculation|April 10, 2018
Blood rheology in children with the S/β+-thalassemia syndromeCéline Renoux, Philippe Joly, Alexandra Gauthier, et al.
Clinical Hemorheology and Microcirculation|July 8, 2025
Differences in oxygen-gradient ektacytometry parameters and blood viscosity between patients with sickle cell anemia and patients with sickle cell-hemoglobin C disorderPhilippe Connes, Marie Martin, Camille Boisson, et al.
American Journal of Hematology|July 26, 2017
Plasmapheresis may improve clinical condition in sickle cell disease through its effects on red blood cell rheologyElie Nader, Philippe Connes, Yann Lamarre, et al.
Haematologica|July 28, 2011
Variants in genetic modifiers of β-thalassemia can help to predict the major or intermedia type of the diseaseCatherine Badens, Philippe Joly, Imane Agouti, et al.
Journal of Synchrotron Radiation|January 5, 2022
The CirPAD, a circular 1.4 M hybrid pixel detector dedicated to X-ray diffraction measurements at Synchrotron SOLEILKewin Desjardins, Cristian Mocuta, Arkadiusz Dawiec, et al.
British Journal of Haematology|February 2, 2022
Determinants of the point of sickling measured by oxygen gradient ektacytometry in sickle cell anaemiaPhilippe Joly, Camille Boisson, Céline Renoux, et al.
British Journal of Haematology|August 16, 2022
Does G6PD deficiency cause further damage to red blood cells of patients with sickle cell anaemia?Sofia Esperti, Camille Boisson, Mélanie Robert, et al.
British Journal of Haematology|June 12, 2023
Mitochondria retention in mature RBCs from haemoglobin SC patientsSofia Esperti, Elie Nader, Camille Boisson, et al.
British Journal of Haematology|January 7, 2021
Impact of COVID-19 on red blood cell rheologyCéline Renoux, Romain Fort, Elie Nader, et al.
Pageof 15

Showing results (71-80 of 148) with videos related to

Sort By:
Pageof 15
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|February 3, 2020
Goal-Oriented Monitoring of Cyclosporine Is Effective for Graft-versus-Host Disease Prevention after Hematopoietic Stem Cell Transplantation in Sickle Cell Disease and Thalassemia MajorAlexandra Gauthier, Nathalie Bleyzac, Nathalie Garnier, et al.
Clinical Hemorheology and Microcirculation|April 10, 2018
Blood rheology in children with the S/β+-thalassemia syndromeCéline Renoux, Philippe Joly, Alexandra Gauthier, et al.
Clinical Hemorheology and Microcirculation|July 8, 2025
Differences in oxygen-gradient ektacytometry parameters and blood viscosity between patients with sickle cell anemia and patients with sickle cell-hemoglobin C disorderPhilippe Connes, Marie Martin, Camille Boisson, et al.
American Journal of Hematology|July 26, 2017
Plasmapheresis may improve clinical condition in sickle cell disease through its effects on red blood cell rheologyElie Nader, Philippe Connes, Yann Lamarre, et al.
Haematologica|July 28, 2011
Variants in genetic modifiers of β-thalassemia can help to predict the major or intermedia type of the diseaseCatherine Badens, Philippe Joly, Imane Agouti, et al.
Journal of Synchrotron Radiation|January 5, 2022
The CirPAD, a circular 1.4 M hybrid pixel detector dedicated to X-ray diffraction measurements at Synchrotron SOLEILKewin Desjardins, Cristian Mocuta, Arkadiusz Dawiec, et al.
British Journal of Haematology|February 2, 2022
Determinants of the point of sickling measured by oxygen gradient ektacytometry in sickle cell anaemiaPhilippe Joly, Camille Boisson, Céline Renoux, et al.
British Journal of Haematology|August 16, 2022
Does G6PD deficiency cause further damage to red blood cells of patients with sickle cell anaemia?Sofia Esperti, Camille Boisson, Mélanie Robert, et al.
British Journal of Haematology|June 12, 2023
Mitochondria retention in mature RBCs from haemoglobin SC patientsSofia Esperti, Elie Nader, Camille Boisson, et al.
British Journal of Haematology|January 7, 2021
Impact of COVID-19 on red blood cell rheologyCéline Renoux, Romain Fort, Elie Nader, et al.
Pageof 15