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Gene Therapy|February 3, 2021
Genome editing for Duchenne muscular dystrophy: a glimpse of the future?Christian Kupatt, Alina Windisch, Alessandra Moretti, et al.
Neuromuscular Disorders : NMD|April 18, 2019
Charcot-Marie-Tooth disease type 2CC due to a frameshift mutation of the neurofilament heavy polypeptide gene in an Austrian familyElena Ikenberg, Peter Reilich, Angela Abicht, et al.
Orphanet Journal of Rare Diseases|October 26, 2023
Cost of illness in inclusion body myositis: results from a cross-sectional study in GermanyKatja C Senn, Simone Thiele, Karsten Kummer, et al.
European Radiology|July 24, 2008
Involvement patterns in myotilinopathy and desminopathy detected by a novel neuromuscular whole-body MRI protocolNicolai Schramm, Christine Born, Sabine Weckbach, et al.
BMC Medical Genetics|September 18, 2013
Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A - evidence for "double trouble" overlapping syndromesOlivia Schreiber, Peter Schneiderat, Wolfram Kress, et al.
Neuromuscular Disorders : NMD|January 27, 2009
Eosinophilic myositis as presenting symptom in gamma-sarcoglycanopathySarah K Baumeister, Slobodanka Todorovic, Vedrana Milić-Rasić, et al.
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