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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.Neuromuscular Disorders : NMD|March 13, 2022
A population-based follow-up study of maximal muscle strength and mobility in patients with myasthenia gravisJan Lykke Scheel Thomsen, Lotte Vinge, Thomas Harbo, et al.Neuromuscular Disorders : NMD|March 6, 2022
Upper body involvement in GNE myopathy assessed by muscle imagingE Torchia, M Lucchini, S Bortolani, et al.Neuromuscular Disorders : NMD|March 2, 2022
BMI-z scores of boys with Duchenne muscular dystrophy already begin to increase before losing ambulation: a longitudinal exploration of BMI, corticosteroids and caloric intakeSaskia L S Houwen-van Opstal, Laura Rodwell, Daphne Bot, et al.Neuromuscular Disorders : NMD|March 4, 1999
Higher content of insulin-like growth factor-I in dystrophic mdx mouse: potential role in the spontaneous regeneration through an electrophysiological investigation of muscle functionA De Luca, S Pierno, C Camerino, et al.Neuromuscular Disorders : NMD|March 4, 1999
Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2)J W Day, R Roelofs, B Leroy, et al.Neuromuscular Disorders : NMD|March 4, 1999
Transforming growth factor-beta1 and fibrosis in congenital muscular dystrophiesP Bernasconi, C Di Blasi, M Mora, et al.Neuromuscular Disorders : NMD|March 4, 1999
IgM paraproteinemia in a patient with primary lateral sclerosisJ Desai, M SwashNeuromuscular Disorders : NMD|March 27, 1999
Mutual interference of myotonia and muscular dystrophy in the mouse: a study on ADR-MDX double mutantsP Heimann, M Augustin, S Wieneke, et al.Neuromuscular Disorders : NMD|March 27, 1999
Scapulothoracic arthrodesis for patients with facioscapulohumeral muscular dystrophyC T Andrews, T C Taylor, V H PattersonPageof 341