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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 2, 2020
Coagulation disorders in Duchenne muscular dystrophy? Results of a registry-based online surveyDavid C Schorling, Cornelia K Müller, Astrid Pechmann, et al.Journal of Child Neurology|April 3, 2009
Myofascial trigger points in children with tension-type headache: a new diagnostic and therapeutic optionCelina von Stülpnagel, Peter Reilich, Andreas Straube, et al.Journal of Neuromuscular Diseases|June 27, 2022
Slowly Progressive Limb-Girdle Weakness and HyperCKemia - Limb Girdle Muscular Dystrophy or Anti-3-Hydroxy-3-Methylglutaryl-CoA-Reductase-Myopathy?Miriam Hiebeler, Raimo Franke, Maria Ingenerf, et al.Neuromuscular Disorders : NMD|October 16, 2009
Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblastsJouni Vesa, Hailing Su, Giles D Watts, et al.Human Molecular Genetics|August 4, 2009
Evaluation of the therapeutic potential of carbonic anhydrase inhibitors in two animal models of dystrophin deficient muscular dystrophyJean Giacomotto, Cordula Pertl, Caroline Borrel, et al.Neuromuscular Disorders : NMD|November 20, 2020
Tasks and interfaces in primary and specialized palliative care for Duchenne muscular dystrophy - A patients' perspectiveMaria Janisch, Kristin Boehme, Simone Thiele, et al.Neuromuscular Disorders : NMD|December 18, 2003
A novel homozygous missense mutation in the GNE gene of a patient with quadriceps-sparing hereditary inclusion body myopathy associated with muscle inflammationSabine Krause, Beate Schlotter-Weigel, Maggie C Walter, et al.Journal of Neuromuscular Diseases|December 18, 2023
Self-Reported Health-Related Quality of Life of Children with Spinal Muscular Atrophy: Preliminary Insights from a Nationwide Patient Registry in GermanyErik Landfeldt, Berenike Leibrock, Justine Hussong, et al.Journal of Neuropathology and Experimental Neurology|May 8, 2010
Divergent molecular effects of desmin mutations on protein assembly in myofibrillar myopathyJohannes Levin, Stefanie Bulst, Christian Thirion, et al.Neuromuscular Disorders : NMD|May 9, 2015
50 years to diagnosis: Autosomal dominant tubular aggregate myopathy caused by a novel STIM1 mutationMaggie C Walter, Martina Rossius, Manuela Zitzelsberger, et al.Pageof 17