S
Stéphane Mathis
Researcher at University of Bordeaux
Publications - 132
Citations - 2164
Stéphane Mathis is an academic researcher from University of Bordeaux. The author has contributed to research in topics: Nerve biopsy & Polyradiculoneuropathy. The author has an hindex of 21, co-authored 122 publications receiving 1678 citations. Previous affiliations of Stéphane Mathis include University of Limoges & Centre Hospitalier Universitaire de Bordeaux.
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Journal ArticleDOI
Genetics of amyotrophic lateral sclerosis: A review.
TL;DR: Since the first identification of a causative gene in the 1990s and with recent advances in genetics, more than twenty genes have now been linked to FALS, this increased number of genes led to a tremendous amount of research and contributed to a better understanding of the pathophysiology of this disorder.
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Guillain-Barré Syndrome (42 Cases) Occurring During a Zika Virus Outbreak in French Polynesia.
TL;DR: This epidemic raises several questions, such as the potential existence of interactions between Zika virus and Polynesian HLA system and/or the consequences of several recombination events of this virus, which should call for increased vigilance, especially in countries where Aedes mosquitoes are present.
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Paranodal lesions in chronic inflammatory demyelinating polyneuropathy associated with anti-Neurofascin 155 antibodies.
Jean-Michel Vallat,Nobuhiro Yuki,Kenji Sekiguchi,Norito Kokubun,Nobuyuki Oka,Stéphane Mathis,Laurent Magy,Diane L. Sherman,Peter J. Brophy,Jérôme Devaux +9 more
TL;DR: It is found that patients with anti-Nfasc155 antibodies presented a selective loss of the septate-like junctions at all paranodes examined, and cellular processes penetrated into the expanded spaces between the paranodal myelin loops and the axolemma in these patients with important nerve conduction slowing and demyelination.
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Charcot–Marie–Tooth diseases: an update and some new proposals for the classification
Stéphane Mathis,Cyril Goizet,Meriem Tazir,Corinne Magdelaine,Anne-Sophie Lia,Laurent Magy,Jean-Michel Vallat +6 more
TL;DR: The aim was to review the various CMT subtypes identified at the present time and suggest a modification of the current classification and explain why such a change is needed.
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Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases: an update.
TL;DR: This work proposes a simplified classification of Charcot-Marie-Tooth diseases, and stresses that next generation sequencing techniques, now considered to be the most efficient methods of genetic testing in CMT, will be helpful in molecular diagnosis and research of new genes involved.