Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Françoise, Bouhour"'
Autor:
Sylvie Gerber, Lola Lessard, Cécile Rouzier, Samira Ait‐el‐Mkadem Saadi, Roxana Ameli, Stéphane Thobois, Lucie Abouaf, Françoise Bouhour, Josseline Kaplan, Audrey Putoux, Antoine Pegat, Jean‐Michel Rozet
Publikováno v:
EMBO Molecular Medicine, Vol 15, Iss 8, Pp 1-6 (2023)
Graphical Abstract Gerber et al report 2 autosomal recessive pathogenic Misato homolog 1 (MSTO1) variants causing hereditary optic atrophy and raise concerns about a previously identified dominant variant of MSTO1 by Gal et al (2017).
Externí odkaz:
https://doaj.org/article/0a7e7570d3ec48889ab6d74d61b6f5a7
Autor:
Lucie Isoline Pisella, Sara Fernandes, Guilhem Solé, Tanya Stojkovic, Céline Tard, Jean-Baptiste Chanson, Françoise Bouhour, Emmanuelle Salort-Campana, Guillemette Beaudonnet, Louise Debergé, Fanny Duval, Aude-Marie Grapperon, Marion Masingue, Aleksandra Nadaj-Pakleza, Yann Péréon, Frédérique Audic, Anthony Behin, Diane Friedman, Armelle Magot, Jean-Baptiste Noury, Sarah Souvannanorath, Karim Wahbi, Jean-Christophe Antoine, Kévin Bigaut, Jean-Philippe Camdessanché, Pascal Cintas, Rabab Debs, Caroline Espil-Taris, Laurent Kremer, Thierry Kuntzer, Pascal Laforêt, Vincent Laugel, Martial Mallaret, Maud Michaud, Sylvain Nollet, Juliette Svahn, Savine Vicart, Rocio Nur Villar-Quiles, Isabelle Desguerre, David Adams, Sandrine Segovia-Kueny, Géraldine Merret, Elhadi Hammouda, Annamaria Molon, Shahram Attarian
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Background Due to their health condition, patients with neuromuscular diseases (NMD) are at greater risk of developing serious complications with COVID-19. The objective of this study was to analyze the prevalence of COVID-19 among NMD patie
Externí odkaz:
https://doaj.org/article/1f852d93563d40c5ad7e18eea6212e9c
Autor:
Chafké Belmokhtar, Pierre Lozeron, David Adams, Jérôme Franques, Arnaud Lacour, Etienne Godet, Mathieu Bataille, Odile Dubourg, Gilles Angibaud, Emilien Delmont, Françoise Bouhour, Philippe Corcia, Jean Pouget
Publikováno v:
Neurology and Therapy, Vol 8, Iss 1, Pp 69-78 (2019)
Abstract Introduction Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a debilitating autoimmune neuropathy that is treated with intravenous immunoglobulin (IVIG). The aim of this retrospective study was to investigate the efficacy
Externí odkaz:
https://doaj.org/article/eb21329c854842d99e62bbf82e6c17b9
Autor:
Nicolas Pons, Gorka Fernández‐Eulate, Antoine Pegat, Marie Théaudin, Régis Guieu, Paolo Ripellino, Manon Devedjian, Patrick Mace, Marion Masingue, Sarah Léonard‐Louis, Philipe Petiot, Pauline Roche, Emilien Bernard, Françoise Bouhour, Jean‐Marc Good, Annie Verschueren, Aude‐Marie Grapperon, Emmanuelle Salort, Anaïs Grosset, Jean‐Baptiste Chanson, Aleksandra Nadaj‐Pakleza, Anne‐Laure Bédat‐Millet, Ariane Choumert, Anne Barnier, Ghassen Hamdi, Gaëtan Lesca, Fabienne Prieur, Arnaud Bruneel, Philippe Latour, Tanya Stojkovic, Shahram Attarian, Nathalie Bonello‐Palot
Publikováno v:
European Journal of Neurology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7159cc223fe3b6844433bc66560368d3
https://doi.org/10.1111/ene.15793
https://doi.org/10.1111/ene.15793
Autor:
Arnaud Jacquier, Julian Theuriet, Fanny Fontaine, Valentine Mosbach, Nicolas Lacoste, Shams Ribault, Valérie Risson, Julien Carras, Laurent Coudert, Thomas Simonet, Philippe Latour, Tanya Stojkovic, Juliette Piard, Anne Cosson, Gaëtan Lesca, Françoise Bouhour, Stéphane Allouche, Hélène Puccio, Antoine Pegat, Laurent Schaeffer
Publikováno v:
Brain.
Distal hereditary motor neuropathy represents a group of motor inherited neuropathies leading to distal weakness. We report a family of two brothers and a sister affected by distal hereditary motor neuropathy in whom a homozygous variant c.3G>T (p.1M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1d652fe34314795bbeb799f54171f52
https://doi.org/10.1093/brain/awac453
https://doi.org/10.1093/brain/awac453
Autor:
Laure Gallay, Lola Lessard, G. Bassez, Sabrina Sacconi, Frederic Berard, Emmanuelle Salort-Campana, David Orlikowski, Françoise Bouhour, Céline Tard, Pascal Laforêt, Philippe Merle, Anthony Béhin, Sylvain Nollet
Publikováno v:
Les Cahiers de Myologie. :32-37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12e4c981bdac7e59f8d75f8d60cc65ff
https://doi.org/10.1051/myolog/202123012
https://doi.org/10.1051/myolog/202123012
Autor:
Claire Peillet, David Adams, Shahram Attarian, Françoise Bouhour, Cécile Cauquil, Julien Cassereau, Jean‐Baptiste Chanson, Pascal Cintas, Alain Creange, Emilien Delmont, Guillaume Fargeot, Steeve Genestet, Antoine Gueguen, Anne Laure Kaminsky, Thierry Kuntzer, Céline Labeyrie, Maud Michaud, Yann Pereon, Angela Puma, Karine Viala, Pascale Chretien, Clovis Adam, Andoni Echaniz‐Laguna
Publikováno v:
European journal of neurologyREFERENCES. 29(12)
In this retrospective study involving 14 university hospitals from France and Switzerland, the aim was to define the clinicopathological features of chronic neuropathies with anti-disialosyl ganglioside immunoglobulin M (IgM) antibodies (CNDA).Fifty-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4f16544d8234965569016046ab4ec96
https://pubmed.ncbi.nlm.nih.gov/35969369
https://pubmed.ncbi.nlm.nih.gov/35969369
Autor:
Lola Lessard, Céline Tard, Emmanuelle Salort-Campana, Sabrina Sacconi, Anthony Béhin, Guillaume Bassez, David Orlikowski, Philippe Merle, Sylvain Nollet, Laure Gallay, Frédéric Bérard, Philip Robinson, Françoise Bouhour, Pascal Laforêt
Publikováno v:
Molecular Genetics and Metabolism. :107611
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7cf6ad80bc25917b805065d06772f27
https://doi.org/10.1016/j.ymgme.2023.107611
https://doi.org/10.1016/j.ymgme.2023.107611
Autor:
Françoise Bouhour, P. Roche
Publikováno v:
Revue Neurologique. 177:215-219
Myasthenia gravis is an autoimmune disease characterised by fluctuating muscle weakness, which worsens during activity. It affects particularly scapular and pelvic girdles, axial and bulbar muscles. Myasthenia gravis is twice more frequent in women a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21b0069e5f832c5b26d1d0cc5ffd619d
https://doi.org/10.1016/j.neurol.2020.09.015
https://doi.org/10.1016/j.neurol.2020.09.015
Autor:
Diane Friedman, Djillali Annane, Guillemette Beaudonnet, Emmanuelle Salort-Campana, Bernard Clair, Jean-Baptiste Chanson, Frédérique Audic, Tiphaine Saulnier, Marco Spinazzi, Louis Carla, Gwendal Le Masson, Stéphane Mathis, Alexandra Foubert-Samier, Aleksandra Nadaj-Pakleza, Antoine Soulages, Shahram Attarian, Fanny Duval, Laurent Kremer, Tanya Stojkovic, Françoise Bouhour, Jean-Christophe Antoine, Pascal Cintas, Céline Tard, Sandrine Segovia-Kueny, Marie-Hélène Violleau, Guilhem Solé, Léa Kern, Armelle Magot
Publikováno v:
Neurology. 96:e2109-e2120
ObjectiveTo describe the clinical characteristics and outcomes of coronavirus disease 2019 (COVID-19) among patients with myasthenia gravis (MG) and identify factors associated with COVID-19 severity in patients with MG.MethodsThe CO-MY-COVID registr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fec8b0a6c39bc5a64644d29ab8f7cf01
https://doi.org/10.1212/wnl.0000000000011669
https://doi.org/10.1212/wnl.0000000000011669