Zobrazeno 1 - 10
of 187
pro vyhledávání: '"Christophe, Verny"'
Autor:
Cinzia Bocca, Judith Kouassi-Nzoughet, Juan Manuel Chao de la Barca, Dominique Bonneau, Christophe Verny, Philippe Gohier, Christophe Orssaud, Pascal Reynier
Publikováno v:
Acta Neuropathologica Communications, Vol 12, Iss 1, Pp 1-3 (2024)
Externí odkaz:
https://doaj.org/article/4f745d54585a4808a18b008b47ac493d
Autor:
Jean-Francois Mangin, Denis Rivière, Edouard Duchesnay, Yann Cointepas, Véronique Gaura, Christophe Verny, Philippe Damier, Pierre Krystkowiak, Anne-Catherine Bachoud-Lévi, Philippe Hantraye, Philippe Remy, Gwenaëlle Douaud
Publikováno v:
NeuroImage: Clinical, Vol 26, Iss , Pp - (2020)
Huntington's disease (HD) is an inherited, autosomal dominant disorder that is characteristically thought of as a degenerative disorder. Despite cellular and molecular grounds suggesting HD could also impact normal development, there has been scarce
Externí odkaz:
https://doaj.org/article/aa8f8d6e4cc84a6aaa449c2ac2538ff0
Autor:
Philippe Allain, Martin Hamon, Virginie Saoût, Christophe Verny, Mickaël Dinomais, Jeremy Besnard
Publikováno v:
Frontiers in Neurology, Vol 10 (2020)
Background: In view of the recent literature, the negative impact of traumatic brain injury (TBI) on social cognition remains a debated issue. On one hand, a considerable number of studies reported significant impairments in emotion recognition, empa
Externí odkaz:
https://doaj.org/article/197c8c8506b544b088b3ac43104f2292
Autor:
Stéphanie Leruez, Christophe Verny, Dominique Bonneau, Vincent Procaccio, Guy Lenaers, Patrizia Amati-Bonneau, Pascal Reynier, Clarisse Scherer, Adriana Prundean, Christophe Orssaud, Xavier Zanlonghi, Marie-Bénédicte Rougier, Caroline Tilikete, Dan Miléa
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-9 (2018)
Abstract Backrground Evaluation of the efficacy of oral cyclosporine A as a prophylactic agent in preventing second-eye involvement in Leber’s hereditary optic neuropathy (LHON) in a prospective, open-label, non-randomized, multicenter pilot study.
Externí odkaz:
https://doaj.org/article/b5c070273686438d8909deeeb7d9a15a
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1ec48d098d6982dc39ac28be03e8199
https://doi.org/10.1016/j.neurol.2023.01.421
https://doi.org/10.1016/j.neurol.2023.01.421
Autor:
Aude, Rocatcher, Valérie, Desquiret-Dumas, Majida, Charif, Marc, Ferré, Philippe, Gohier, Delphine, Mirebeau-Prunier, Christophe, Verny, Dan, Milea, Guy, Lenaers, Dominique, Bonneau, Pascal, Reynier, Patrizia, Amati-Bonneau
Publikováno v:
Brain. 146:455-460
Hereditary optic neuropathies are caused by the degeneration of retinal ganglion cells whose axons form the optic nerves, with a consistent genetic heterogeneity. As part of our diagnostic activity, we retrospectively evaluated the combination of Leb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::683c43fd0c4c392f4969205a9de628a9
https://doi.org/10.1093/brain/awac395
https://doi.org/10.1093/brain/awac395
Autor:
Anne-Catherine Bachoud-Lévi, Joaquim Ferreira, Renaud Massart, Katia Youssov, Anne Rosser, Monica Busse, David Craufurd, Ralf Reilmann, Giuseppe De Michele, Daniela Rae, Ferdinando Squitieri, Klaus Seppi, Charles Perrine, Clarisse Scherer-Gagou, Olivier Audrey, Christophe Verny, Jean-Marc Burgunder
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
The European Huntington's Disease Network (EHDN) commissioned an international task force to provide global evidence-based recommendations for everyday clinical practice for treatment of Huntington's disease (HD). The objectives of such guidelines ar
Externí odkaz:
https://doaj.org/article/d0adb6bc86654d5aac5758ac339767dd
Publikováno v:
The Journal of Neuropsychiatry and Clinical Neurosciences. 34:100-112
Although apathy is commonly reported among patients with Huntington's disease (HD), this psychiatric symptom has not yet been clearly defined or extensively studied in HD. Most researchers have adopted descriptive approaches, showing that apathy is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e028d524655741b4b62d6c14b2159afd
https://doi.org/10.1176/appi.neuropsych.21060154
https://doi.org/10.1176/appi.neuropsych.21060154
Autor:
Juan Manuel Chao de la Barca, Delphine Prunier-Mirebeau, Patrizia Amati-Bonneau, Marc Ferré, Emmanuelle Sarzi, Céline Bris, Stéphanie Leruez, Arnaud Chevrollier, Valérie Desquiret-Dumas, Naïg Gueguen, Christophe Verny, Christian Hamel, Dan Miléa, Vincent Procaccio, Dominique Bonneau, Guy Lenaers, Pascal Reynier
Publikováno v:
Neurobiology of Disease, Vol 90, Iss , Pp 20-26 (2016)
Mutations in the Optic Atrophy 1 gene (OPA1) were first identified in 2000 as the main cause of Dominant Optic Atrophy, a disease specifically affecting the retinal ganglion cells and the optic nerve. Since then, an increasing number of symptoms invo
Externí odkaz:
https://doaj.org/article/7a66761b919e48789ee9bffc3c58a9b2
Autor:
Mohamad El Haj, Marie Caillaud, Ahmed Moustafa, Adriana Prundean, Clarisse Scherer, Christophe Verny, Philippe Allain
Publikováno v:
Neurological Sciences.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6a1a44f239a2131723d47782a0f9325
https://doi.org/10.1007/s10072-023-06775-z
https://doi.org/10.1007/s10072-023-06775-z