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Neuromuscular Disorders : NMD|December 24, 2016
Ephedrine treatment for autoimmune myasthenia gravisAlexander F Lipka, Charlotte Vrinten, Erik W van Zwet, et al.
Neuromuscular Disorders : NMD|November 19, 2016
"The Certified Duchenne Care Center Program"Kathi Kinnett, James J Dowling, Jerry R Mendell
Neuromuscular Disorders : NMD|November 7, 2016
Pilot phenotype and natural history study of hereditary neuropathies caused by mutations in the HSPB1 geneAlexander M Rossor, Jasper M Morrow, James M Polke, et al.
Neuromuscular Disorders : NMD|December 6, 2016
Cardiac autophagic vacuolation in severe X-linked myopathy with excessive autophagyIulia Munteanu, Hannu Kalimo, Antti Saraste, et al.
Neuromuscular Disorders : NMD|February 21, 2019
Various effects of AAV9-mediated βARKct gene therapy on the heart in dystrophin-deficient (mdx) mice and δ-sarcoglycan-deficient (Sgcd-/-) miceRalf Bauer, Helene Enns, Andreas Jungmann, et al.
Neuromuscular Disorders : NMD|March 12, 2019
"The impact of European Neuromuscular Centre (ENMC) workshops on the neuromuscular field; 25 years on …"Alexandra Breukel, Raffaella Willmann, George Padberg, et al.
Neuromuscular Disorders : NMD|February 16, 2019
Respiratory dysfunction in myotonic dystrophy type 1: A systematic reviewA M Hawkins, C L Hawkins, K Abdul Razak, et al.
Neuromuscular Disorders : NMD|February 17, 2019
Safety, tolerability, pharmacokinetics, pharmacodynamics, and exploratory efficacy of the novel enzyme replacement therapy avalglucosidase alfa (neoGAA) in treatment-naïve and alglucosidase alfa-treated patients with late-onset Pompe disease: A phase 1, open-label, multicenter, multinational, ascending dose studyLoren D M Pena, Richard J Barohn, Barry J Byrne, et al.
Neuromuscular Disorders : NMD|May 1, 2014
Influence of a two-year steroid treatment on body composition as measured by dual X-ray absorptiometry in boys with Duchenne muscular dystrophyCarole Vuillerot, Pierre Braillon, Stephanie Fontaine-Carbonnel, et al.
Neuromuscular Disorders : NMD|May 6, 2014
Distal weakness with respiratory insufficiency caused by the m.8344A > G "MERRF" mutationEmma L Blakely, Charlotte L Alston, Bryan Lecky, et al.
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