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Molecular Aspects of Medicine|April 30, 1998
Diseases caused by voltage-gated ion channelsB Fontaine, E Plassart-Schiess, S NicoleThe Journal of Physiology|May 23, 1998
Functional expression of the Ile693Thr Na+ channel mutation associated with paramyotonia congenita in a human cell lineE Plassart-Schiess, L Lhuillier, A L George, et al.Brain Research. Brain Research Reviews|December 18, 2001
Neurosteroids: recent findingsE Plassart-Schiess, E E BaulieuJournal of Neurology|October 20, 1999
Novel mutations in the muscle chloride channel CLCN1 gene causing myotonia congenita in Spanish familiesC de Diego, J Gámez, E Plassart-Schiess, et al.Neurology|May 5, 1998
Novel muscle chloride channel (CLCN1) mutations in myotonia congenita with various modes of inheritance including incomplete dominance and penetranceE Plassart-Schiess, A Gervais, B Eymard, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Schwartz-Jampel syndrome and perlecan deficiencyM Stum, C S Davoine, B Fontaine, et al.Human Genetics|September 10, 1999
The human CDC42 gene: genomic organization, evidence for the existence of a putative pseudogene and exclusion as a SJS1 candidate geneS Nicole, P S White, H Topaloglu, et al.Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|June 28, 2005
[Smoking and breastfeeding: how can we help mothers stop smoking?]B FontaineRevue Neurologique|September 11, 2012
[Will multiple sclerosis (MS) susceptibility genes one day become biomarkers for MS diagnosis?]B FontaineRevue Neurologique|July 23, 2004
[Muscular genetic disorders caused by abnormal membrane excitability]B FontainePageof 50