Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sébastien Alphandéry"'
Autor:
Raul Juntas-Morales, Nicolas Pageot, Abdelkarim Bendarraz, Sébastien Alphandéry, Frédéric Sedel, Stéphanie Seigle, William Camu
Publikováno v:
EClinicalMedicine, Vol 19, Iss , Pp - (2020)
Background: Oligodendrocytes (OGs) provide metabolic support to motor neurons (MNs) and are implicated in the pathophysiology of amyotrophic lateral sclerosis (ALS). MD1003, or high-dose Pharmaceutical grade Biotin (hdPB), may improve disability in p
Externí odkaz:
https://doaj.org/article/808df3a8ac1b42b99b763bfd9e5f5b3c
Autor:
Raul Juntas-Morales, Nicolas Pageot, Gregory Marin, Anne-Marie Dupuy, Sébastien Alphandery, Laura Labar, Florence Esselin, Marie Christine Picot, William Camu
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Background: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by progressive degeneration of upper and lower motor neurons. Prognosis is highly variable, ranging from few months to more than 30 years. 25OH vitami
Externí odkaz:
https://doaj.org/article/00607de86b244069b791e75283c0a98e
Autor:
Florence Esselin, Kevin Mouzat, Anne Polge, Raul Juntas-Morales, Nicolas Pageot, Elisa De la Cruz, Emilien Bernard, Emmeline Lagrange, Véronique Danel, Sébastien Alphandery, Laura Labar, Erika Nogué, Marie-Christine Picot, Serge Lumbroso, William Camu
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2020)
BackgroundIn familial amyotrophic lateral sclerosis (ALS) cases, the presence of an abnormal C9ORF72 repeat expansion (C9RE) is the most frequent genetic cause identified. Various clinical phenotypes have been described in relation to the presence of
Externí odkaz:
https://doaj.org/article/6806aa5c2f4d48209e98685564e94abd