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Neuromuscular Disorders : NMD|July 2, 2017
Rare diagnosis of telethoninopathy (LGMD2G) in a Turkish patientElena Ikenberg, Ivan Karin, Birgit Ertl-Wagner, et al.Molecular Genetics and Metabolism|May 22, 2012
In vitro supplementation with deoxynucleoside monophosphates rescues mitochondrial DNA depletionStefanie Bulst, Elke Holinski-Feder, Brendan Payne, et al.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 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.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|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.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.Pageof 16