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Muscle & Nerve|June 16, 2011
Epidermolysis bullosa with late-onset muscular dystrophy and plectin deficiencyEppie M Yiu, Alfred Klausegger, Leigh B Waddell, et al.Neurology|April 8, 2018
Unique clinical and neurophysiologic profile of a cohort of children with CMTX3Manoj Kanhangad, Kayla Cornett, Megan H Brewer, et al.Brain and Behavior|April 20, 2018
Dejerine-Sottas disease in childhood-Genetic and sonographic heterogeneitySanne M R Hobbelink, Cain R Brockley, Rachel A Kennedy, et al.Mitochondrion|August 1, 2016
Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial diseaseManoj P Menezes, Shamima Rahman, Kaustuv Bhattacharya, et al.Muscle & Nerve|February 14, 2024
Pilot study of a virtual weight management program for Duchenne muscular dystrophyNatassja Billich, Paula Bray, Helen Truby, et al.Journal of Paediatrics and Child Health|July 4, 2020
Benefits of powered standing wheelchair devices for adolescents with Duchenne muscular dystrophy in the first year of useKlair Bayley, Stephanie Parkinson, Peter Jacoby, et al.Journal of Neuromuscular Diseases|July 2, 2023
DEVOTE Study Exploring Higher Dose of Nusinersen in Spinal Muscular Atrophy: Study Design and Part A ResultsRichard S Finkel, John W Day, Samuel Ignacio Pascual Pascual, et al.Human Molecular Genetics|January 9, 2013
A new locus for X-linked dominant Charcot-Marie-Tooth disease (CMTX6) is caused by mutations in the pyruvate dehydrogenase kinase isoenzyme 3 (PDK3) geneMarina L Kennerson, Eppie M Yiu, David T Chuang, et al.Pharmacotherapy|May 14, 2025
Effect of creatine monohydrate on motor function in children with facioscapulohumeral muscular dystrophy: A multicenter, randomized, double-blind placebo-controlled crossover trialIan R Woodcock, Katy de Valle, Anita Cairns, et al.Annals of Neurology|July 6, 2004
Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutationsPankaj B Agrawal, Corinne D Strickland, Charles Midgett, et al.Pageof 16