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Experimental Neurology|February 11, 2004
Inducible expression of FGF2 by a rat oligodendrocyte precursor cell line promotes CNS myelination in vitroLaurent Magy, Caroline Mertens, Virginia Avellana-Adalid, et al.Scientific Reports|February 3, 2018
Substitutions of the S4DIV R2 residue (R1451) in NaV1.4 lead to complex forms of paramyotonia congenita and periodic paralysesHugo Poulin, Pascal Gosselin-Badaroudine, Savine Vicart, et al.Archives of Neurology|August 20, 2003
Subtle cognitive impairment but no dementia in patients with spastin mutationsChantal M E Tallaksen, Elodie Guichart-Gomez, Patrice Verpillat, et al.The Journal of Physiology|April 16, 2005
In vivo and in vitro functional characterization of Andersen's syndrome mutationsSaïd Bendahhou, Emmanuel Fournier, Damien Sternberg, et al.Respiratory Medicine and Research|June 11, 2026
Determinants of diaphragm ultrasound and its diagnostic performance for predicting respiratory status in myotonic dystrophy type 1Abdallah Fayssoil, Marie De Antonio, Helene Prigent, et al.European Journal of Human Genetics : EJHG|November 17, 2011
Determination of the real effect of genes identified in GWAS: the example of IL2RA in multiple sclerosisMarie-Claude Babron, Hervé Perdry, Adam E Handel, et al.Annals of Neurology|June 21, 2006
Cold extends electromyography distinction between ion channel mutations causing myotoniaEmmanuel Fournier, Karine Viala, Hélène Gervais, et al.Journal of Inherited Metabolic Disease|December 1, 2012
Krabbe disease in adults: phenotypic and genotypic update from a series of 11 cases and a reviewRabab Debs, Roseline Froissart, Patrick Aubourg, et al.American Journal of Human Genetics|March 19, 2002
Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60Jens Jacob Hansen, Alexandra Dürr, Isabelle Cournu-Rebeix, et al.Archives of Neurology|December 15, 2004
Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegiaAlexandra Dürr, Agnès Camuzat, Emilie Colin, et al.Pageof 15