Zobrazeno 1 - 10
of 74
pro vyhledávání: '"Stéphane Moutereau"'
Autor:
Antoine Jobbé‐Duval, Mélanie Bézard, Stéphane Moutereau, Mounira Kharoubi, Silvia Oghina, Amira Zaroui, Arnault Galat, Coraline Chalard, Elisabeth Hugon‐Vallet, Francois Lemonnier, Damien Eyharts, Elsa Poulot, Pascale Fanen, Benoit Funalot, Valérie Molinier‐Frenkel, Vincent Audard, Luc Hittinger, Marc Antoine Delbarre, Emmanuel Teiger, Thibaud Damy
Publikováno v:
ESC Heart Failure, Vol 9, Iss 2, Pp 1314-1327 (2022)
Abstract Aims Iron deficiency (ID) is common in patient with chronic heart failure (HF) and has been widely studied. In contrast, data concerning ID in cardiac amyloidosis (CA) are limited. Amyloidosis is a severe and fatal systemic disease, characte
Externí odkaz:
https://doaj.org/article/1655f7014e624439b01d1f60dddf39e8
Autor:
Camille Cohen, Séverine Coulon, Kanit Bhukhai, Antoine Neuraz, Michael Dussiot, Guillemette Fouquet, Marie-Bénédicte Le Stang, Martin Flamant, François Vrtovsnik, Aurélie Hummel, Bertrand Knebelmann, Laurent Mesnard, Eric Rondeau, Thiago T. Maciel, Fabrizia Favale, Nicole Casadevall, Thao Nguyen-Khoa, Stéphane Moutereau, Christophe Legendre, Marc Benhamou, Renato C. Monteiro, Olivier Hermine, Khalil El Karoui, Ivan C. Moura
Publikováno v:
EBioMedicine, Vol 75, Iss , Pp 103785- (2022)
Summary: Background: Erythrocytosis is a hematological disorder usually related to hematopoietic stem cell somatic mutations. However, unexplained erythrocytosis remains frequent. In this study, we evaluated the involvement of IgA1, a regulator of er
Externí odkaz:
https://doaj.org/article/736d119de1ba4bb9b49d07811c31cf55
Autor:
Lamisse Mansour-Hendili, Abdelrazak Aissat, Bouchra Badaoui, Mehdi Sakka, Christine Gameiro, Valérie Ortonne, Orianne Wagner-Ballon, Serge Pissard, Véronique Picard, Khaldoun Ghazal, Michel Bahuau, Corinne Guitton, Ziad Mansour, Mylène Duplan, Arnaud Petit, Nathalie Costedoat-Chalumeau, Marc Michel, Pablo Bartolucci, Stéphane Moutereau, Benoît Funalot, Frédéric Galactéros
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-15 (2020)
Abstract Background Congenital hemolytic anemia constitutes a heterogeneous group of rare genetic disorders of red blood cells. Diagnosis is based on clinical data, family history and phenotypic testing, genetic analyses being usually performed as a
Externí odkaz:
https://doaj.org/article/6f893e2c9cf14483b312306ba68dde60
Autor:
Arnault Galat, Aziz Guellich, Diane Bodez, Larissa Lipskaia, Stéphane Moutereau, Eric Bergoend, Sophie Hüe, Julien Ternacle, Dania Mohty, Jean‐Luc Monin, Geneviève Derumeaux, Costin Radu, Thibaud Damy
Publikováno v:
ESC Heart Failure, Vol 6, Iss 4, Pp 649-657 (2019)
Abstract Aims Cardiac fibrosis is associated with left ventricular (LV) remodelling and contractile dysfunction in aortic stenosis (AS). The fibrotic process in this condition is still unclear. The aim of this study was to determine the role of both
Externí odkaz:
https://doaj.org/article/722f973c96654411ad512a702da31516
Autor:
Keyvan Razazi, Ségolène Gendreau, Elise Cuquemelle, Mehdi Khellaf, Constance Guillaud, Bertrand Godeau, Giovanna Melica, Stéphane Moutereau, Camille Gomart, Slim Fourati, Nicolas De Prost, Guillaume Carteaux, Christian Brun-Buisson, Pablo Bartolucci, Anoosha Habibi, Armand Mekontso Dessap
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 11, p 3718 (2020)
Acute chest syndrome (ACS) is a major complication of sickle-cell disease. Bacterial infection is one cause of ACS, so current guidelines recommend the routine use of antibiotics. We performed a prospective before–after study in medical wards and a
Externí odkaz:
https://doaj.org/article/c2c0f96109bd4e7ba391b098167af5c4
Autor:
Pablo Bartolucci, Anoosha Habibi, Mehdi Khellaf, Françoise Roudot-Thoraval, Giovanna Melica, Anne-Sophie Lascaux, Stéphane Moutereau, Sylvain Loric, Orianne Wagner-Ballon, Jugurtha Berkenou, Aline Santin, Marc Michel, Bertrand Renaud, Yves Lévy, Frédéric Galactéros, Bertrand Godeau
Publikováno v:
EBioMedicine, Vol 10, Iss C, Pp 305-311 (2016)
Background: Vaso-occlusive crisis (VOC), hallmark of sickle-cell disease (SCD), is the first cause of patients' Emergency-Room admissions and hospitalizations. Acute chest syndrome (ACS), a life-threatening complication, can occur during VOC, be fata
Externí odkaz:
https://doaj.org/article/c167de1897764b6c91e0cef125127e65
Autor:
Linda Salem, Nadine Saleh, Gaelle Désaméricq, Katia Youssov, Guillaume Dolbeau, Laurent Cleret, Marie-Laure Bourhis, Jean-Philippe Azulay, Pierre Krystkowiak, Christophe Verny, Françoise Morin, Stéphane Moutereau, French Huntington Study Group, Anne-Catherine Bachoud-Lévi, Patrick Maison
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0162890 (2016)
BACKGROUND:Huntington's disease (HD) is one of several neurodegenerative disorders that have been associated with metabolic alterations. Changes in Insulin Growth Factor 1 (IGF-1) and/or insulin input to the brain may underlie or contribute to the pr
Externí odkaz:
https://doaj.org/article/d458497426e74f66a74221c9d2cbfd54
Autor:
Nadine Saleh, Stéphane Moutereau, Alexandra Durr, Pierre Krystkowiak, Jean-Philippe Azulay, Christine Tranchant, Emmanuel Broussolle, Françoise Morin, Anne-Catherine Bachoud-Lévi, Patrick Maison
Publikováno v:
PLoS ONE, Vol 4, Iss 3, p e4962 (2009)
BACKGROUND: Huntington's disease (HD) is a severe inherited neurodegenerative disorder characterized, in addition to neurological impairment, by weight loss suggesting endocrine disturbances. The aims of this study were to look for neuroendocrine dis
Externí odkaz:
https://doaj.org/article/eaeac266ac574cb79351e5aeb6e7d769
Autor:
Alix Millet, Stéphane Moutereau, Pascal Boileau, Frédéric Galacteros, Emmanuelle Motte‐Signoret
Publikováno v:
Pediatric Blood and Cancer
Pediatric Blood and Cancer, Wiley, 2022, ⟨10.1002/pbc.29570⟩
Pediatric Blood and Cancer, Wiley, 2022, ⟨10.1002/pbc.29570⟩
International audience
Autor:
Alix, Millet, Stéphane, Moutereau, Pascal, Boileau, Frédéric, Galacteros, Emmanuelle, Motte-Signoret
Publikováno v:
Pediatric bloodcancer. 69(7)