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Neuropediatrics|June 26, 2015
Long-Term Observations in an Affected Family with Neurogenic Scapuloperoneal Syndrome Caused by Mutation R269C in the TRPV4 GeneKatharina Vill, Marius Kuhn, Dieter Gläser, et al.Journal of Neurology|May 6, 2011
The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 genePeter Reilich, Rita Horvath, Sabine Krause, et al.Journal of Clinical Medicine|August 12, 2023
Patient-Reported Health-Related Quality of Life, Anxiety and Depression in Patients with Inclusion Body Myositis: A Register-Based Cross-Sectional Study in GermanyKatja C Senn, Simone Thiele, Karsten Kummer, et al.Gene Therapy|February 3, 2021
Genome editing for Duchenne muscular dystrophy: a glimpse of the future?Christian Kupatt, Alina Windisch, Alessandra Moretti, 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.Neuromuscular Disorders : NMD|September 18, 2012
Muscle MRI findings in limb girdle muscular dystrophy type 2LAnna Sarkozy, Marcus Deschauer, Robert-Yves Carlier, et al.Neuromuscular Disorders : NMD|December 23, 2021
Cutaneous T-cell lymphoma mimicking myopathy with lipoatrophyMiriam Hiebeler, Markus Reinholz, Michael Flaig, et al.Plos One|October 30, 2019
Measurement of structural integrity of the spinal cord in patients with amyotrophic lateral sclerosis using diffusion tensor magnetic resonance imagingMaximilian Patzig, Katja Bochmann, Jürgen Lutz, et al.Brain : a Journal of Neurology|September 13, 2022
Methylation of the 4q35 D4Z4 repeat defines disease status in facioscapulohumeral muscular dystrophyHannes Erdmann, Florentine Scharf, Stefanie Gehling, et al.Neuromuscular Disorders : NMD|July 22, 2020
Utility of maximum inspiratory and expiratory pressures as a screening method for respiratory insufficiency in slowly progressive neuromuscular disordersStephan Wenninger, Kristina Stahl, Corinna Wirner, et al.Pageof 17