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Journal of Medical Genetics|October 9, 2010
Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencingKaren Gaudon, Isabelle Pénisson-Besnier, Brigitte Chabrol, et al.Nursing Ethics|February 11, 2012
Tracheotomy and children with spinal muscular atrophy type 1: ethical considerations in the French contextBrigitte Rul, Franco Carnevale, Brigitte Estournet, et al.Journal of Child Neurology|July 31, 2003
Evoked potentials in spinal muscular atrophyFawzia Cheliout-Heraut, Annie Barois, Andoni Urtizberea, et al.Neuromuscular Disorders : NMD|September 10, 2013
Peripheral nerve hyperexcitability with preterminal nerve and neuromuscular junction remodeling is a hallmark of Schwartz-Jampel syndromeStéphanie Bauché, Delphine Boerio, Claire-Sophie Davoine, et al.Chest|September 15, 2004
Respiratory capacity course in patients with infantile spinal muscular atrophyChristine Ioos, Danièle Leclair-Richard, Slah Mrad, et al.Muscle & Nerve|February 3, 2004
EMG and nerve conduction studies in children with congenital muscular dystrophySusana Quijano-Roy, Francis Renault, Norma Romero, et al.Bulletin De L'Academie Nationale De Medecine|May 2, 2008
[Jeune'disease (asphyxiating thoracic dystrophy) and respiratory failure: importance of early respiratory management with periodic hyperinsufflation]Claire Do Ngoc Thanh, Annie Barois, Brigitte Estournet-Mathiaud, et al.Journal of Autoimmunity|February 18, 2014
Diagnostic and clinical classification of autoimmune myasthenia gravisSonia Berrih-Aknin, Mélinée Frenkian-Cuvelier, Bruno EymardJournal of Neurology|June 14, 2017
Lambert-Eaton myasthenic syndrome (LEMS): a rare autoimmune presynaptic disorder often associated with cancerBenedikt Schoser, Bruno Eymard, Joe Datt, et al.European Journal of Pain (London, England)|December 24, 2003
Clinical study of chronic pain in hereditary myopathiesThierry Delorme, François Boureau, Bruno Eymard, et al.Pageof 26