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Neuromuscular Disorders : NMD|February 23, 2010
The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathyPeter Reilich, Benedikt Schoser, Nicolai Schramm, et al.
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.
Neuromuscular Disorders : NMD|March 16, 2013
Proteomic characterization of aggregate components in an intrafamilial variable FHL1-associated myopathySarah Feldkirchner, Maggie C Walter, Stefan Müller, et al.
Neurology|March 29, 2019
Cost of illness in Charcot-Marie-Tooth neuropathy: Results from GermanyElisabeth Schorling, Simone Thiele, Laura Gumbert, et al.
Journal of Neuroimmunology|May 6, 2011
Recombination mapping of the susceptibility region for sporadic inclusion body myositis within the major histocompatibility complexAdrian P Scott, Nigel G Laing, Frank Mastaglia, 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.
Neuromuscular Disorders : NMD|March 23, 2010
Reverse protein arrays as novel approach for protein quantification in muscular dystrophiesClaudia Escher, Hanns Lochmüller, Dirk Fischer, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|May 16, 2024
Health-related quality of life of adults with spinal muscular atrophy: insights from a nationwide patient registry in GermanyErik Landfeldt, Berenike Leibrock, Justine Hussong, et al.
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