Zobrazeno 1 - 10
of 120
pro vyhledávání: '"Jean-Antoine Ribeil"'
Autor:
Rahal Ihlem, Ambroise Marçais, Clarisse Cazelles, Sandra Manceau, Jean-Antoine Ribeil, Jean-Benoît Arlet, Benoit Meunier, Alice Corsia, Marina Cavazzana, Felipe Suarez, Laure Joseph
Publikováno v:
HemaSphere, Vol 7, p e75086e6 (2023)
Externí odkaz:
https://doaj.org/article/df24c82806854d55bd9dcecb021d8f64
Autor:
Margaux Chauvet, Cerina Chhuon, Joanna Lipecka, Sébastien Dechavanne, Célia Dechavanne, Murielle Lohezic, Margherita Ortalli, Damien Pineau, Jean-Antoine Ribeil, Sandra Manceau, Caroline Le Van Kim, Adrian J. F. Luty, Florence Migot-Nabias, Slim Azouzi, Ida Chiara Guerrera, Anaïs Merckx
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 11 (2021)
The high prevalence of sickle cell disease in some human populations likely results from the protection afforded against severe Plasmodium falciparum malaria and death by heterozygous carriage of HbS. P. falciparum remodels the erythrocyte membrane a
Externí odkaz:
https://doaj.org/article/832879f0770b47558930f1715e2b7709
Autor:
James G. McArthur, Niels Svenstrup, Chunsheng Chen, Aurelie Fricot, Caroline Carvalho, Julia Nguyen, Phong Nguyen, Anna Parachikova, Fuad Abdulla, Gregory M. Vercellotti, Olivier Hermine, Dave Edwards, Jean-Antoine Ribeil, John D. Belcher, Thiago T. Maciel
Publikováno v:
Haematologica, Vol 105, Iss 3 (2020)
The most common treatment for patients with sickle cell disease (SCD) is the chemotherapeutic hydroxyurea, a therapy with pleiotropic effects, including increasing fetal hemoglobin (HbF) in red blood cells and reducing adhesion of white blood cells t
Externí odkaz:
https://doaj.org/article/d6ee0ba0f7734291aed299d4622bb466
Autor:
Maria Domenica Cappellini, John Porter, Raffaella Origa, Gian Luca Forni, Ersi Voskaridou, Frédéric Galactéros, Ali T. Taher, Jean-Benoît Arlet, Jean-Antoine Ribeil, Maciej Garbowski, Giovanna Graziadei, Chantal Brouzes, Michaela Semeraro, Abderrahmane Laadem, Dimana Miteva, Jun Zou, Victoria Sung, Tatiana Zinger, Kenneth M. Attie, Olivier Hermine
Publikováno v:
Haematologica, Vol 104, Iss 3 (2019)
β-thalassemia, a hereditary blood disorder caused by defective synthesis of hemoglobin β globin chains, leads to ineffective erythropoiesis and chronic anemia that may require blood transfusions. Sotatercept (ACE-011) acts as a ligand trap to inhib
Externí odkaz:
https://doaj.org/article/42143f447b874874951469d891959391
Autor:
Elsa Denoix, Charlène Bomahou, Lorraine Clavier, Jean-Antoine Ribeil, François Lionnet, Pablo Bartolucci, Marie Courbebaisse, Jacques Pouchot, Jean-Benoît Arlet
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 2, p 308 (2020)
Primary hyperparathyroidism (pHPT) is the third most common endocrine disorder and usually affects patients between 60 and 70 years of age. To our knowledge, this condition has never been studied in young patients with sickle cell disease (SCD). Our
Externí odkaz:
https://doaj.org/article/7cf6323db30c42b699eb4caf8819a08f
Autor:
Chantal Lagresle-Peyrou, François Lefrère, Elisa Magrin, Jean-Antoine Ribeil, Oriana Romano, Leslie Weber, Alessandra Magnani, Hanem Sadek, Clémence Plantier, Aurélie Gabrion, Brigitte Ternaux, Tristan Félix, Chloé Couzin, Aurélie Stanislas, Jean-Marc Tréluyer, Lionel Lamhaut, Laure Joseph, Marianne Delville, Annarita Miccio, Isabelle André-Schmutz, Marina Cavazzana
Publikováno v:
Haematologica, Vol 103, Iss 5 (2018)
Sickle cell disease is characterized by chronic anemia and vaso-occlusive crises, which eventually lead to multi-organ damage and premature death. Hematopoietic stem cell transplantation is the only curative treatment but it is limited by toxicity an
Externí odkaz:
https://doaj.org/article/38e6828b68394087a1a5f54437c70e29
Autor:
Marie Courbebaisse, Hind Mehel, Camille Petit-Hoang, Jean-Antoine Ribeil, Laurent Sabbah, Véronique Tuloup-Minguez, David Bergerat, Jean-Benoit Arlet, Aurélie Stanislas, Jean-Claude Souberbielle, Hervé Le Clésiau, Rodolphe Fischmeister, Gérard Friedlander, Dominique Prié
Publikováno v:
Haematologica, Vol 102, Iss 2 (2017)
Externí odkaz:
https://doaj.org/article/5d2edf7d6a6b4cc5a529817b87a04944
Autor:
Mariane de Montalembert, Jean-Antoine Ribeil, Valentine Brousse, Agnes Guerci-Bresler, Aspasia Stamatoullas, Jean-Pierre Vannier, Cécile Dumesnil, Agnès Lahary, Mohamed Touati, Krimo Bouabdallah, Marina Cavazzana, Emmanuelle Chauzit, Amandine Baptiste, Thibaud Lefebvre, Hervé Puy, Caroline Elie, Zoubida Karim, Olivier Ernst, Christian Rose
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0172147 (2017)
The risk and clinical significance of cardiac iron overload due to chronic transfusion varies with the underlying disease. Cardiac iron overload shortens the life expectancy of patients with thalassemia, whereas its effect is unclear in those with my
Externí odkaz:
https://doaj.org/article/002d532590b14061a3fc1d1939ec6a2d
Autor:
Jean-Antoine Ribeil, Jean-Benoit Arlet, Michael Dussiot, Ivan Cruz Moura, Geneviève Courtois, Olivier Hermine
Publikováno v:
The Scientific World Journal, Vol 2013 (2013)
In humans, β-thalassemia dyserythropoiesis is characterized by expansion of early erythroid precursors and erythroid progenitors and then ineffective erythropoiesis. This ineffective erythropoiesis is defined as a suboptimal production of mature ery
Externí odkaz:
https://doaj.org/article/76f900d08c044fda95f25a901e894d0e
Autor:
Yannis Hara, Viktor T. Lemgart, Nis Halland, Kiana Mahdaviani, Jean-Antoine Ribeil, Samuel Lessard, Alexandra Hicks, David R. Light
Publikováno v:
Blood Advances. 7:2317-2323