Publications by authors named "M Maillet-Vioud"

Background And Purpose: Dimethyl fumarate (DMF) and teriflunomide are approved oral disease-modifying treatments for relapsing-remitting multiple sclerosis (MS). Phase 3 trials established these agents to be effective and generally well tolerated, although comparative efficacy and discontinuation rates are still unknown. The aim of this study was to assess real-world efficacy and discontinuation of DMF and teriflunomide in patients with relapsing-remitting MS.

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Article Synopsis
  • Spinocerebellar ataxias (SCAs) are genetic neurodegenerative disorders linked to mutations in various genes, and SCA38 was specifically mapped to chromosome 6p in an Italian family through whole-genome analysis.
  • A single missense mutation in the ELOVL5 gene was found to be present in multiple SCA-affected families, indicating a common ancestry, while another variant was identified in a French family.
  • ELOVL5 plays a crucial role in producing essential fatty acids; affected individuals showed reduced levels of important fatty acids in their serum, highlighting the connection between fatty acid metabolism and neurological health.
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Enterovirus meningitis is well documented in children. However, there is a paucity of reports in adults, despite the availability of genome detection (RT-PCR) in cerebrospinal fluid (CSF), which provides a rapid and reliable diagnosis. The clinical course and management of 30 cases of entero-virus proven meningitis prospectively diagnosed between August 1999 and November 2000 in immunocompetent adults were analysed, and laboratory and clinical strategies evaluated.

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Two forms of neurofibromatosis are currently described. Von Reckinghausen Neurofibromatosis (NF 1) is the classic and common form, recently localised to chromosome 17. Neurofibromatosis type 2 (NF 2) or bilateral acoustic Neurofibromatosis, formerly the "central form" of von Reckinghausen disease, is characterized by multiple brain tumors, most often bilateral acoustic neuromas.

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