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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.Neuromuscular Disorders : NMD|August 8, 2015
Atypical nuclear abnormalities in a patient with Brody diseaseJean-Marie Mussini, Armelle Magot, Daniel Hantaï, 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.Human Molecular Genetics|August 23, 2008
A mouse model for congenital myasthenic syndrome due to MuSK mutations reveals defects in structure and function of neuromuscular junctionsFrédéric Chevessier, Emmanuelle Girard, Jordi Molgó, 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 European Journal of Neuroscience|April 20, 2004
Thrombin reduces MuSK and acetylcholine receptor expression along with neuromuscular contact size in vitroBrice Faraut, Aymeric Ravel-Chapuis, Sylvie Bonavaud, 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.Pageof 3