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Journal of Neurology|January 17, 2003
Creatine monohydrate in myotonic dystrophy: a double-blind, placebo-controlled clinical studyMaggie C Walter, Peter Reilich, Hanns Lochmüller, et al.Neurology|March 29, 2019
Cost of illness in Charcot-Marie-Tooth neuropathy: Results from GermanyElisabeth Schorling, Simone Thiele, Laura Gumbert, et al.European Neurology|July 11, 2009
Lower limb radiology of distal myopathy due to the S60F myotilin mutationAlisdair McNeill, Daniel Birchall, Volker Straub, et al.Journal of Neurology|February 22, 2011
A novel mutation in the myotilin gene (MYOT) causes a severe form of limb girdle muscular dystrophy 1A (LGMD1A)Peter Reilich, Sabine Krause, Nicolai Schramm, et al.Neuromuscular Disorders : NMD|January 11, 2005
Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophyMaggie C Walter, Thomas N Witt, Beate Schlotter Weigel, et al.Journal of Neuromuscular Diseases|May 31, 2021
Health-related Quality of Life and Satisfaction with German Health Care Services in Patients with Charcot-Marie-Tooth NeuropathyElisabeth Schorling, Katja C Senn, Simone Thiele, et al.Neuromuscular Disorders : NMD|May 30, 2006
Novel splice site mutation in the caveolin-3 gene leading to autosomal recessive limb girdle muscular dystrophyJuliane S Müller, Henriett Piko, Benedikt G H Schoser, et al.Fortschritte Der Neurologie-Psychiatrie|September 14, 2022
[Adult Spinal Muscular Atrophy]Maggie C Walter, Miriam HiebelerJournal of Neurology|February 11, 2010
Facioscapulohumeral muscular dystrophy presenting with unusual phenotypes and atypical morphological features of vacuolar myopathyPeter Reilich, Nicolai Schramm, Benedikt Schoser, et al.Fortschritte Der Neurologie-Psychiatrie|September 25, 2018
[Spinal muscular atrophy - clinical spectrum and therapy]Maggie C Walter, Anne Julia StauberPageof 17