Christophe Marcel
University of Strasbourg
12 Papers
97 Citations
Christophe Marcel is an academic researcher from University of Strasbourg. The author has contributed to research in topics: Neuromyelitis optica & Medicine. The author has an hindex of 7, co-authored 12 publications.
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Papers
Magnetic resonance spectroscopy evaluation in patients with neuromyelitis optica
Jérôme De Seze,Frédéric Blanc,Stéphane Kremer,Nicolas Collongues,Marie Fleury,Christophe Marcel,Izzie Jacques Namer +6 more
TL;DR: The results are clearly different from those found in MS, where NAA is frequently decreased and choline increased, even in NAWM, and could have an impact on the differentiation between MS and NMO.
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Diffusion-weighted imaging in noncompressive myelopathies: a 33-patient prospective study
Christophe Marcel,Stéphane Kremer,J. Jeantroux,Frédéric Blanc,Jean-Louis Dietemann,Jérôme De Seze +5 more
TL;DR: The aim of this study was to evaluate the diagnostic value of DWI and the measurement of the apparent diffusion coefficient (ADC) in noncompressive myelopathy explorations and results are similar to those described in cerebral explorations.
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Electrophysiological studies in a mouse model of Schwartz–Jampel syndrome demonstrate muscle fiber hyperactivity of peripheral nerve origin
Andoni Echaniz-Laguna,Frédérique René,Christophe Marcel,Marie Bangratz,Marie Bangratz,Bertrand Fontaine,Bertrand Fontaine,Jean-Philippe Loeffler,Sophie Nicole,Sophie Nicole +9 more
TL;DR: An electrophysiological investigation of an SJS mouse model with a missense mutation in the HSPG2 gene demonstrates that perlecan deficiency in SJS provokes a neuromyotonic syndrome and suggests a distal axonal localization of the generator of neuromyOTonic discharges.
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Moindre réactivité émotionnelle aux stimuli négatifs dans la sclérose en plaques, résultats préliminaires
L. Di Bitonto,Nadine Longato,Barbara Jung,Marie-Céline Fleury,Christophe Marcel,Nicolas Collongues,J. de Seze,Frédéric Blanc +7 more
TL;DR: In this paper, les patients of a sclerose en plaques remittente (SEP-R) were evaluated with respect to the evaluation of their visages and their emotions faciales.
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L-2-hydroxyglutaric aciduria diagnosed in a young adult with progressive cerebellar ataxia and facial dyskinesia.
Christophe Marcel,Martial Mallaret,Ouhaid Lagha-Boukbiza,Stéphane Kremer,Andoni Echaniz-Laguna,Christine Tranchant +5 more
TL;DR: In this paper, a 19-year-old woman presented with ataxia, facial dyskinesia, and mild cognitive impairment, and was confirmed by increased 2-hydroxyglutaric acid in urine and a genetic study.
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