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Handbook of Clinical Neurology|April 30, 2013
Congenital myasthenic syndromesBruno Eymard, Daniel Hantaï, Brigitte EstournetCurrent Opinion in Neurology|September 3, 2013
Congenital myasthenic syndromes: an updateDaniel Hantaï, Sophie Nicole, Bruno EymardCurrent Opinion in Neurology|September 16, 2004
Congenital myasthenic syndromesDaniel Hantaï, Pascale Richard, Jeanine Koenig, et al.Bulletin De L'Academie Nationale De Medecine|August 13, 2015
[Congenital myasthenic syndromes; French experience]Bruno Eymard, Daniel Hantaï, Emmanuel Fournier, et al.Neuromuscular Disorders : NMD|March 1, 2003
Two novel mutations in the COLQ gene cause endplate acetylcholinesterase deficiencyKeiko Ishigaki, Delphine Nicolle, Eric Krejci, et al.The Journal of Pathology|September 24, 2005
The origin of tubular aggregates in human myopathiesFrédéric Chevessier, Stéphanie Bauché-Godard, Jean-Paul Leroy, et al.Neuromuscular Disorders : NMD|March 17, 2007
A synonymous CHRNE mutation responsible for an aberrant splicing leading to congenital myasthenic syndromePascale Richard, Karen Gaudon, Emmanuel Fournier, et al.Presse Medicale (Paris, France : 1983)|November 25, 2003
[Polymyositis, dermatomyositis and inclusion body myositis, nosological aspects]Bruno EymardNeuromuscular Disorders : NMD|December 9, 2003
Electrophysiological and morphological characterization of a case of autosomal recessive congenital myasthenic syndrome with acetylcholine receptor deficiency due to a N88K rapsyn homozygous mutationEriko Yasaki, Cassandra Prioleau, Julien Barbier, et al.Pageof 26