Zobrazeno 1 - 10
of 88
pro vyhledávání: '"M P, Chaunu"'
Autor:
Margaux Genevray, M.-P. Chaunu, Laurent Pierot, Ayman Tourbah, L. Daelman, Nathalie Caucheteux, Adil Maarouf, Jean Pelletier, Olivier Gout, Emmanuelle Leray, Gilles Edan, Jean-Christophe Ferré, Romain Deschamps
Publikováno v:
Journal of Neurology
Journal of Neurology, 2015, 262 (4), pp.979-987. ⟨10.1007/s00415-015-7668-9⟩
Journal of Neurology, Springer Verlag, 2015, 262 (4), pp.979-987. ⟨10.1007/s00415-015-7668-9⟩
Journal of Neurology, 2015, 262 (4), pp.979-987. ⟨10.1007/s00415-015-7668-9⟩
Journal of Neurology, Springer Verlag, 2015, 262 (4), pp.979-987. ⟨10.1007/s00415-015-7668-9⟩
International audience; The introduction of the McDonald criteria has enabled earlier diagnosis of multiple sclerosis (MS). However, even with the 2010 revised criteria, nearly 50 % of patients remain classified as “possible MS” following the fir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f30fd7346dfe1b81728529c991b0b393
https://doi.org/10.1007/s00415-015-7668-9
https://doi.org/10.1007/s00415-015-7668-9
Publikováno v:
Revue Neurologique. 169:345-349
Hashimoto's Encephalopathy (HE) is a rare condition defined by the association of encephalopathy and autoimmune thyroiditis with increased levels of antithyroid antibodies. Presenting symptoms of HE may be quite variable. Although seizures are rather
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72c87bacb5bcca717f2e70821809443e
https://doi.org/10.1016/j.neurol.2012.10.014
https://doi.org/10.1016/j.neurol.2012.10.014
Publikováno v:
Revue Neurologique. 168:852-860
Gerstmann's syndrome (GS) is defined by a clinical tetrad including acalculia, finger anomia, left-right disorientation and agraphia. In this article, we describe the case of a 42-year-old woman suffering from an aggressive relapsing-remitting multip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53160770f9f980d6677826abc9412bf4
https://doi.org/10.1016/j.neurol.2011.11.006
https://doi.org/10.1016/j.neurol.2011.11.006
Publikováno v:
Revue Neurologique. 170:48-50
Revue Neurologique - In Press.Proof corrected by the author Available online since mercredi 23 octobre 2013
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dde2507a2760aeab883ae0b046e4effb
https://doi.org/10.1016/j.neurol.2013.03.009
https://doi.org/10.1016/j.neurol.2013.03.009
Autor:
Jean Luc Novella, H. Mercier-Juttier, D. Gaillard, François Boyer, M P Chaunu, F. Carre-Pigeon
Publikováno v:
Annales de Réadaptation et de Médecine Physique. 49:105-112
Resume Objectifs. – (1) Etude descriptive et (2) analyse metrologique des scores de qualite de vie liee a la sante (QDVLS) issues du questionnaire Euroqol (EQ) recueillies aupres d'un echantillon specifique de personnes myopathes. Materiel et metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a2a0947a13d280cd56e6105e0847f74
https://doi.org/10.1016/j.annrmp.2006.01.007
https://doi.org/10.1016/j.annrmp.2006.01.007
Autor:
Sylvie Ughetto, Deborah Pugin, Eleonore Eymard-Pierre, Anne Fogli, Patricia Combes, Christine R. Kaneski, M. P. Chaunu, Graziella Uziel, M. Troncoso, Raphael Schiffmann, Diana Rodriguez, M. Pineda, Enrico Bertini, Odile Boespflug-Tanguy, Robert Surtees
Publikováno v:
Neurology. 62:1509-1517
Background: Recessive mutations in the five eucaryotic initiation factor 2B (eIF2B) subunits have been found in leukodystrophies of variable age at onset and severity.Objectives: To evaluate the clinical spectrum of eIF2B-related disorders and search
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4af3e0be7bef3934f0041162957a4bd
https://doi.org/10.1212/01.wnl.0000123259.67815.db
https://doi.org/10.1212/01.wnl.0000123259.67815.db
Autor:
Serge Bakchine, Nathalie Caucheteux, Audrey Henry, Michèle Montreuil, M.-P. Chaunu, Ayman Tourbah
Publikováno v:
Revue Neurologique. 173:S113
Introduction Plusieurs etudes ont mis en evidence une alteration de la cognition sociale dans la (SEP) mais aucune recherche n’a explore ces competences selon la forme de SEP. Objectifs L’objectif de cette recherche est d’evaluer les competence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ad284394247835137d21c30d634b495
https://doi.org/10.1016/j.neurol.2017.01.192
https://doi.org/10.1016/j.neurol.2017.01.192
Autor:
Desirée Lopis, Adil Maarouf, N. Gibelin, Audrey Henry, M.-P. Chaunu, Michèle Montreuil, Ayman Tourbah
Publikováno v:
Revue Neurologique. 171:A75-A76
Introduction La definition de la sclerose en plaques (SEP) dite benigne souffre de criteres trop restrictifs de duree de la maladie et de niveau de handicap physique, et ne tient pas compte des perturbations cognitives et thymiques. Objectifs Notre o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b87880e24a740a9d2a0791224c7180f0
https://doi.org/10.1016/j.neurol.2015.01.169
https://doi.org/10.1016/j.neurol.2015.01.169
Autor:
R. Wanono, M.-P. Chaunu, Nathalie Caucheteux, Adil Maarouf, Edwin Regrain, Gael Belassian, Ayman Tourbah
Publikováno v:
Revue Neurologique. 171:A82-A83
Introduction La fampridine est un traitement symptomatique des troubles de la marche chez les patients atteints de sclerose en plaques (SEP). Son efficacite, au long terme reste discutee. Objectifs Rapporter l’effet du traitement par fampridine sur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d65eba06b312ca20da501884bc557f7
https://doi.org/10.1016/j.neurol.2015.01.185
https://doi.org/10.1016/j.neurol.2015.01.185
Autor:
Isabelle Le Ber, Claude-Alain Maurage, Valérie Buée-Scherrer, Alexis Brice, Serge Bakchine, Khalid Hamid El Hachimi, Luc Buée, Vincent Deramecourt, M.-P. Chaunu, Nathalie Ehrlé, Michel Pluot
Publikováno v:
Journal of Alzheimer's disease : JAD. 37(4)
Frontotemporal lobe degeneration includes a large spectrum of neurodegenerative disorders. Patients with frontotemporal dementia with parkinsonism linked to chromosome 17 exhibit heterogeneity in both clinical and neuropathological features. Here, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8b856b1746ae8b7780813e8133e4c9a
https://pubmed.ncbi.nlm.nih.gov/23948919
https://pubmed.ncbi.nlm.nih.gov/23948919