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Proceedings of the National Academy of Sciences of the United States of America|October 19, 2004
Pleiotropic effects of the 8.1 HLA haplotype in patients with autoimmune myasthenia gravis and thymus hyperplasiaClaire Vandiedonck, Geneviève Beaurain, Matthieu Giraud, et al.Neuromuscular Disorders : NMD|June 2, 2009
Left ventricular dysfunction and cardiac arrhythmias are frequent in type 2 myotonic dystrophy: a case control studyKarim Wahbi, Christophe Meune, Henri Marc Bécane, et al.Clinical Therapeutics|October 8, 2009
Modafinil for the treatment of hypersomnia associated with myotonic muscular dystrophy in adults: a multicenter, prospective, randomized, double-blind, placebo-controlled, 4-week trialDavid Orlikowski, Sylvie Chevret, Maria Antonia Quera-Salva, et al.Neuromuscular Disorders : NMD|February 6, 2018
Genotype and other determinants of respiratory function in myotonic dystrophy type 1Ghilas Boussaïd, Karim Wahbi, Pascal Laforet, et al.Journal of Neurology|February 1, 2011
A novel MYH7 mutation occurring independently in French and Norwegian Laing distal myopathy families and de novo in one Finnish patientOdile Dubourg, Thierry Maisonobe, Anthony Behin, et al.Neuromuscular Disorders : NMD|April 25, 2008
Severe neonatal myasthenia due to maternal anti-MuSK antibodiesAnthony Béhin, Michèle Mayer, Bouchera Kassis-Makhoul, et al.Journal of Cellular Physiology|May 27, 2003
Thrombin downregulates muscle acetylcholine receptors via an IP3 signaling pathway by activating its G-protein-coupled protease-activated receptor-1Brice Faraut, Julien Barbier, Aymeric Ravel-Chapuis, et al.Journal of Neurology|July 17, 2017
Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathyStéphanie Bauché, Geoffroy Vellieux, Damien Sternberg, et al.American Heart Journal|August 28, 2007
Perindopril preventive treatment on mortality in Duchenne muscular dystrophy: 10 years' follow-upDenis Duboc, Christophe Meune, Bertrand Pierre, et al.Brain & Development|December 22, 2005
Brain MRI abnormalities in muscular dystrophy due to FKRP mutationsSusana Quijano-Roy, Itxaso Martí-Carrera, Samira Makri, et al.Pageof 26