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Revue Neurologique|November 9, 2023
Epidemiology of myasthenia gravis in France: A retrospective claims database study (STAMINA)E Salort-Campana, P Laforet, G de Pouvourville, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 1, 2007
[Early detection of myocardial disease in young patients with Becker's muscular dystrophy asymptomatic from the cardiac point of view: value of myocardial doppler tissue imaging]C Meune, K Wahbi, H M Bécane, et al.
Journal of Inherited Metabolic Disease|June 10, 2006
Potential of fibrates in the treatment of fatty acid oxidation disorders: revival of classical drugs?F Djouadi, F Aubey, D Schlemmer, et al.
La Revue De Medecine Interne|July 28, 1999
[Macrophagic myofasciitis: description and etiopathogenic hypotheses. Study and Research Group on Acquired and Dysimmunity-related Muscular Diseases (GERMMAD) of the French Association against Myopathies (AFM)]P Chérin, P Laforet, R K Ghérardi, et al.
Circulation|March 2, 1999
Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophyA Lazarus, J Varin, Z Ounnoughene, et al.
Neurology|January 13, 2012
Muscle phosphorylase kinase deficiency: a neutral metabolic variant or a disease?N Preisler, M C Orngreen, A Echaniz-Laguna, et al.
Revue Neurologique|January 10, 2022
Nusinersen treatment in adults with severe spinal muscular atrophy: A real-life retrospective observational cohort studyC Lefeuvre, M Brisset, M Sarlon, et al.
Revue Neurologique|May 2, 2020
Guidance for the care of neuromuscular patients during the COVID-19 pandemic outbreak from the French Rare Health Care for Neuromuscular Diseases NetworkG Solé, E Salort-Campana, Y Pereon, et al.
Clinical Genetics|November 6, 2007
Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decayM Krahn, C Pécheux, F Chapon, et al.
Revue Neurologique|January 29, 2005
[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations]R Ben Yaou, H-M Bécane, L Demay, et al.
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