• Publications
  • Influence

Claim Your Author Page
Ensure your research is discoverable on Semantic Scholar. Claiming your author page allows you to personalize the information displayed and manage publications (all current information on this profile has been aggregated automatically from publisher and metadata sources).
  • Shahram Attarian, Jean-michel Vallat, +29 authors Daniel Cohen
  • Biology, Medicine
  • Orphanet Journal of Rare Diseases
  • 1 December 2014
  • BackgroundCharcot-Marie-Tooth type 1A disease (CMT1A) is a rare orphan inherited neuropathy caused by an autosomal dominant duplication of a gene encoding for the structural myelin protein PMP22,Continue Reading
  • Ilya Chumakov, Aude Milet, +16 authors Daniel Cohen
  • Biology, Medicine
  • Orphanet Journal of Rare Diseases
  • 1 December 2014
  • Charcot-Marie-Tooth disease type 1A (CMT1A) is the most common inherited sensory and motor peripheral neuropathy. It is caused by PMP22 overexpression which leads to defects of peripheralContinue Reading
  • Shahram Attarian, Jean-michel Vallat, +29 authors Daniel Cohen
  • Medicine
  • Orphanet Journal of Rare Diseases
  • 2016
  • Erratum to: An exploratory randomised double-blind and placebo-controlled phase 2 study of a combination of baclofen, naltrexone and sorbitol (PXT3003) in patients with Charcot-Marie-Tooth diseaseContinue Reading
    Описана методика непараметрического оценивания показателей надежности уникального высокона-дежного оборудования. Отмечено, что в условиях малых выборок статистических данных об отказах необ-ходимоContinue Reading