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Muscle & Nerve|October 13, 2007
Complete fatty degeneration of lumbar erector spinae muscles caused by a primary dysferlinopathyP Seror, M Krahn, P Laforet, et al.Revue Neurologique|June 9, 2001
[A case of mitochondrial cytopathy (MERFF) without ragged red fibers at the onset]L Gignoux, T Maisonobe, P Laforet, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2009
Clinical and mutational spectrum of limb-girdle muscular dystrophy type 2I in 11 French patientsH Bourteel, P Vermersch, J-M Cuisset, et al.Revue Neurologique|March 14, 2007
[Phenotypic aspects of FKRP-linked muscular dystrophy type 2I in a series of eleven patients]H Bourteel, T Stojkovic, J M Cuisset, et al.Revue Neurologique|April 29, 2008
[A retrospective study of six patients with late-onset Pompe disease]A Saux, P Laforet, A M Pagès, et al.The European Respiratory Journal|December 2, 2005
Respiratory insufficiency and limb muscle weakness in adults with Pompe's diseaseN Pellegrini, P Laforet, D Orlikowski, et al.Journal of Neurology|October 10, 2024
Treatment of myasthenia gravis in france: A retrospective claims database study (STAMINA)C Tard, P Laforet, G de Pouvourville, et al.Neurology|December 15, 2004
New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysisS Vicart, D Sternberg, E Fournier, et al.Arthritis and Rheumatism|February 13, 2002
Results and long-term followup of intravenous immunoglobulin infusions in chronic, refractory polymyositis: an open study with thirty-five adult patientsPatrick Cherin, S Pelletier, A Teixeira, et al.Pageof 3