Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Virginie Guillet"'
Autor:
Isabelle Journe-Mallet, Frédérique Etcharry-Bouyx, Valérie Chauviré, Virginie Guillet-Pichon, Christophe Verny, Franck Letournel, Philippe Codron
Publikováno v:
Revue Neurologique. 179:S72-S74
Autor:
Isabelle Journe‐Mallet, Julien Gouju, Frédérique Etcharry‐Bouyx, Valérie Chauvire, Virginie Guillet‐Pichon, Clarisse Scherer‐Gagou, Adriana Prundean, Sophie Godard, Aldéric Lecluse, Julien Cassereau, Christophe Verny, Franck Letournel, Philippe Codron
Publikováno v:
Brain Pathology. 33
The diagnosis of neurodegenerative diseases is made complex by the heterogenous phenotype of the patients and the regular occurrence of concomitant pathology. Studying clinicopathological correlations in autopsy series is a central approach to improv
Publikováno v:
Revue Neurologique. 178:S46-S47
Publikováno v:
Revue Neurologique. 178:S45
Autor:
Valérie Desquiret, Arnaud Chevrollier, Virginie Guillet, Patrizia Amati-Bonneau, Claire Angebault, Naïg Gueguen, Romain Cartoni, Vincent Procaccio, Jean-Claude Martinou, Dominique Bonneau, Pascal Reynier
Publikováno v:
FASEB Journal
FASEB Journal, Federation of American Society of Experimental Biology, 2011, 25 (5), pp.1618-27. ⟨10.1096/fj.10-173609⟩
FASEB Journal, Vol. 25, No 5 (2011) pp. 1618-27
FASEB Journal, Federation of American Society of Experimental Biology, 2011, 25 (5), pp.1618-27. ⟨10.1096/fj.10-173609⟩
FASEB Journal, Vol. 25, No 5 (2011) pp. 1618-27
International audience; Charcot-Marie-Tooth disease type 2A (CMT2A) is an autosomal dominant axonal form of peripheral neuropathy caused by mutations in the mitofusin 2 gene (MFN2), which encodes a mitochondrial outer membrane protein that promotes m
Autor:
Frédéric Dubas, Clarisse Scherer, Pascal Reynier, Patrizia Amati-Bonneau, Christophe Verny, Virginie Guillet, Dominique Bonneau, Marc Ferré, Vincent Procaccio
Publikováno v:
Revue Neurologique
Revue Neurologique, Elsevier Masson, 2010, 166 (12), pp.959-65. ⟨10.1016/j.neurol.2010.07.033⟩
Revue Neurologique, Elsevier Masson, 2010, 166 (12), pp.959-65. ⟨10.1016/j.neurol.2010.07.033⟩
International audience; IntroductionLes atrophies optiques héréditaires forment un groupe hétérogène de maladies responsables d’une dégénérescence des cellules ganglionnaires de la rétine avec une expression phénotypique variable, allant
Autor:
Patrizia Amati-Bonneau, Dominique Bonneau, Laurence Richard, Valérie Desquiret, Arnaud Chevrollier, Naïg Gueguen, Pascal Reynier, Vincent Procaccio, Franck Letournel, Christophe Verny, Virginie Guillet, Julien Cassereau
Publikováno v:
Mitochondrion
Mitochondrion, Elsevier, 2010, 10 (2), pp.115-124. ⟨10.1016/j.mito.2009.11.004⟩
Mitochondrion, Elsevier, 2010, 10 (2), pp.115-124. ⟨10.1016/j.mito.2009.11.004⟩
International audience; Ethambutol (EMB), widely used in the treatment of tuberculosis, has been reported to cause Leber’s hereditary optic neuropathy in patients carrying mitochondrial DNA mutations. We study the effect of EMB on mitochondrial met
Autor:
Arnaud Chevrollier, Marc Ferré, Marie-Anne Pou de Crescenzo, Pascal Reynier, Dominique Loiseau, Naïg Gueguen, Agnès Guichet, Yves Malthièry, Marie-Claire Malinge, Dominique Bonneau, Guillaume Nicolas, Patrizia Amati-Bonneau, Christophe Verny, Virginie Guillet
Publikováno v:
Annals of Neurology. 61:315-323
Objective Mutations of the mitofusin 2 gene (MFN2) may account for at least a third of the cases of Charcot–Marie–Tooth disease type 2 (CMT2). This study investigates mitochondrial cellular bioenergetics in MFN2-related CMT2A. Methods Mitochondri
Publikováno v:
Revue Neurologique. 172:A67-A68
Introduction Nous rapportons un cas de syndrome de vasoconstriction cerebrale reversible (SVCR), secondaire a une endarteriectomie carotidienne, complique d’un infarctus cerebral. Observation Une femme âgee de 61 ans, hypertendue, dyslipidemique,
Autor:
Patrizia Amati-Bonneau, Julien Cassereau, Dominique Loiseau, Dominique Bonneau, Naïg Gueguen, Christophe Verny, Marc Ferré, Virginie Guillet, Dan Milea, Claire Angebault, Pascal Reynier, Arnaud Chevrollier, Vincent Procaccio, Valérie Desquiret-Dumas
Publikováno v:
BMC Research Notes
BMC Research Notes, 2011, 4 (1), pp.557. ⟨10.1186/1756-0500-4-557⟩
BMC Research Notes, BioMed Central, 2011, 4 (1), pp.557. ⟨10.1186/1756-0500-4-557⟩
BMC Research Notes, Vol 4, Iss 1, p 557 (2011)
BMC Research Notes, 2011, 4 (1), pp.557. ⟨10.1186/1756-0500-4-557⟩
BMC Research Notes, BioMed Central, 2011, 4 (1), pp.557. ⟨10.1186/1756-0500-4-557⟩
BMC Research Notes, Vol 4, Iss 1, p 557 (2011)
Background Leber's hereditary optic neuropathy (LHON) is caused by mutations in the complex I subunits of the respiratory chain. Although patients have been treated with idebenone since 1992, the efficacy of the drug is still a matter of debate. Meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c415f0d9bd34577e98c366a0f8f1824
https://www.hal.inserm.fr/inserm-00673659/document
https://www.hal.inserm.fr/inserm-00673659/document