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Neuromuscular Disorders : NMD|July 19, 2022
Transcriptome analysis from muscle biopsy tissues in late-onset myopathies identifies potential biomarkers correlating to muscle pathologyMatthew M Joel, Carly Pontifex, Kristina Martens, et al.
Neuromuscular Disorders : NMD|July 22, 2022
A validated WAIS-IV short-form to estimate intellectual functioning in myotonic dystrophy type 1Joana Garmendia, Garazi Labayru, Jone Aliri, et al.
Neuromuscular Disorders : NMD|August 22, 2018
Steroid therapy in an alpha-dystroglycanopathy due to GMPPB gene mutations: A case reportS Fecarotta, V Gragnaniello, R Della Casa, et al.
Neuromuscular Disorders : NMD|August 23, 2018
ECEL1 gene related contractural syndrome: Long-term follow-up and update on clinical and pathological aspectsUrielle Ullmann, Luigi D'Argenzio, Shrey Mathur, et al.
Neuromuscular Disorders : NMD|December 17, 2009
Ca2+ sensitizers: An emerging class of agents for counterbalancing weakness in skeletal muscle diseases?Julien Ochala
Neuromuscular Disorders : NMD|December 19, 2009
A novel mitochondrial MTND5 frameshift mutation causing isolated complex I deficiency, renal failure and myopathyCharlotte L Alston, Monika Morak, Christopher Reid, et al.
Neuromuscular Disorders : NMD|May 16, 2018
Uniparental disomy unveils a novel recessive mutation in POMT2Brianna N Brun, Tobias Willer, Benjamin W Darbro, et al.
Neuromuscular Disorders : NMD|January 25, 2014
Approach to the diagnosis of congenital myopathiesKathryn N North, Ching H Wang, Nigel Clarke, et al.
Neuromuscular Disorders : NMD|January 27, 2023
Impact of restricted access to, and low awareness of, mexiletine on people with myotonia: a real-world European surveyJordi Díaz-Manera, J Andoni Urtizberea, Carina Schey, et al.
Neuromuscular Disorders : NMD|August 16, 2022
Feasibility, safety, and efficacy of 12-week side-to-side vibration therapy in children and adolescents with congenital myopathy in New ZealandAlena Adaikina, José G B Derraik, Lisa C Power, et al.
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