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Philippe Joly

Showing results (111-120 of 120) with videos related to

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Pediatric Blood & Cancer|January 19, 2017
Alpha-thalassaemia promotes frequent vaso-occlusive crises in children with sickle cell anaemia through haemorheological changesCéline Renoux, Philippe Connes, Elie Nader, et al.
Frontiers in Immunology|November 30, 2020
Association Between Nitric Oxide, Oxidative Stress, Eryptosis, Red Blood Cell Microparticles, and Vascular Function in Sickle Cell AnemiaElie Nader, Marc Romana, Nicolas Guillot, et al.
Blood Advances|November 17, 2023
Oxygen gradient ektacytometry-derived biomarkers are associated with acute complications in sickle cell diseaseMinke A E Rab, Celeste K Kanne, Camille Boisson, et al.
Haematologica|December 7, 2014
A genetic score for the prediction of beta-thalassemia severityFabrice Danjou, Marcella Francavilla, Franco Anni, et al.
Plos One|June 30, 2016
Effect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional StudyCéline Renoux, Marc Romana, Philippe Joly, et al.
Cells|April 30, 2021
Effects of Genotypes and Treatment on Oxygenscan Parameters in Sickle Cell DiseaseCamille Boisson, Minke A E Rab, Elie Nader, et al.
British Journal of Haematology|January 16, 2016
The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotesZhihua Jiang, Hong-Yuan Luo, Shengwen Huang, et al.
Orphanet Journal of Rare Diseases|November 22, 2025
Characterization of a novel SERPINA1 variant carrying two missense mutations: molecular mechanisms and functional impactCeline Leon, Marie-Françoise Odou, Bertrand Roquelaure, et al.
Clinical Chemistry and Laboratory Medicine|August 20, 2020
Appropriate thresholds for accurate screening for β-thalassemias in the newborn period: results from a French center for newborn screeningBichr Allaf, Corinne Pondarre, Slimane Allali, et al.
Nature Genetics|March 23, 2011
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approachBelinda Giardine, Joseph Borg, Douglas R Higgs, et al.
Pageof 12

Showing results (111-120 of 120) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 120 results.
Pediatric Blood & Cancer|January 19, 2017
Alpha-thalassaemia promotes frequent vaso-occlusive crises in children with sickle cell anaemia through haemorheological changesCéline Renoux, Philippe Connes, Elie Nader, et al.
Frontiers in Immunology|November 30, 2020
Association Between Nitric Oxide, Oxidative Stress, Eryptosis, Red Blood Cell Microparticles, and Vascular Function in Sickle Cell AnemiaElie Nader, Marc Romana, Nicolas Guillot, et al.
Blood Advances|November 17, 2023
Oxygen gradient ektacytometry-derived biomarkers are associated with acute complications in sickle cell diseaseMinke A E Rab, Celeste K Kanne, Camille Boisson, et al.
Haematologica|December 7, 2014
A genetic score for the prediction of beta-thalassemia severityFabrice Danjou, Marcella Francavilla, Franco Anni, et al.
Plos One|June 30, 2016
Effect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional StudyCéline Renoux, Marc Romana, Philippe Joly, et al.
Cells|April 30, 2021
Effects of Genotypes and Treatment on Oxygenscan Parameters in Sickle Cell DiseaseCamille Boisson, Minke A E Rab, Elie Nader, et al.
British Journal of Haematology|January 16, 2016
The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotesZhihua Jiang, Hong-Yuan Luo, Shengwen Huang, et al.
Orphanet Journal of Rare Diseases|November 22, 2025
Characterization of a novel SERPINA1 variant carrying two missense mutations: molecular mechanisms and functional impactCeline Leon, Marie-Françoise Odou, Bertrand Roquelaure, et al.
Clinical Chemistry and Laboratory Medicine|August 20, 2020
Appropriate thresholds for accurate screening for β-thalassemias in the newborn period: results from a French center for newborn screeningBichr Allaf, Corinne Pondarre, Slimane Allali, et al.
Nature Genetics|March 23, 2011
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approachBelinda Giardine, Joseph Borg, Douglas R Higgs, et al.
Pageof 12