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Brain : a Journal of Neurology|February 4, 2006
Shared blood and muscle CD8+ T-cell expansions in inclusion body myositisDalia Dimitri, Olivier Benveniste, Odile Dubourg, et al.Journal of Inherited Metabolic Disease|November 26, 2019
A high prevalence of arterial hypertension in patients with mitochondrial diseasesCaroline Chong-Nguyen, Caroline Stalens, Yves Goursot, et al.Neuromuscular Disorders : NMD|January 24, 2015
Abnormal sodium current properties contribute to cardiac electrical and contractile dysfunction in a mouse model of myotonic dystrophy type 1Vincent Algalarrondo, Karim Wahbi, Frédéric Sebag, et al.Neuromuscular 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.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.The American Journal of Pathology|April 17, 2010
DNAJB2 expression in normal and diseased human and mouse skeletal muscleKristl G Claeys, Magdalena Sozanska, Jean-Jacques Martin, et al.Annals of Clinical and Translational Neurology|April 16, 2016
Natural history of LGMD2A for delineating outcome measures in clinical trialsIsabelle Richard, Jean-Yves Hogrel, Daniel Stockholm, et al.Neuromuscular Disorders : NMD|October 25, 2008
Truncating mutations in C-terminal titin may cause more severe tibial muscular dystrophy (TMD)Peter Hackman, Sylvie Marchand, Jaakko Sarparanta, et al.European Journal of Heart Failure|April 1, 2015
Reduced inotropic reserve is predictive of further degradation in left ventricular ejection fraction in patients with Duchenne muscular dystrophyFrançois-Xavier Goudot, Karim Wahbi, Linda Aïssou, et al.Developmental Medicine and Child Neurology|August 7, 2012
Psychiatric and cognitive phenotype of childhood myotonic dystrophy type 1Marie Douniol, Aurélia Jacquette, David Cohen, et al.Pageof 21