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Neuromuscular Disorders : NMD|April 12, 2026
Severe neonatal-onset PYROXD1-related myopathy with a novel homozygous missense variant: expanding the phenotypic spectrumZahra A Aleisa, Grace Yoon, Sylvie Friant, et al.
Neuromuscular Disorders : NMD|March 29, 2000
Oculopharyngeal muscular dystrophy in a Japanese family with a short GCG expansion (GCG)(11) in PABP2 geneT Nagashima, H Kato, M Kase, et al.
Neuromuscular Disorders : NMD|December 6, 2016
Advance care discussions with young people affected by life-limiting neuromuscular diseases: A systematic literature review and narrative synthesisAndy Hiscock, Isla Kuhn, Stephen Barclay
Neuromuscular Disorders : NMD|June 12, 2003
Reduction in excess daytime sleepiness by modafinil in patients with myotonic dystrophyK Talbot, J Stradling, J Crosby, et al.
Neuromuscular Disorders : NMD|December 18, 2021
mRNA intramuscular vaccination produces a robust IgG antibody response in advanced neuromuscular diseaseAlexis R Demonbreun, Matthew P Velez, Rana Saber, et al.
Neuromuscular Disorders : NMD|June 24, 2026
A portrait of facioscapulohumeral muscular dystrophy through history: past milestones and future challenges on the road to understanding and treatmentAnna Greco, George W Padberg, Kees van de Graaf, et al.
Neuromuscular Disorders : NMD|October 29, 2021
Incidence and clinical spectrum of rhabdomyolysis in general neurology: a retrospective cohort studyChiara Paternostro, Lorina Gopp, Matthias Tomschik, et al.
Neuromuscular Disorders : NMD|July 29, 2026
Characterizing obsessive-compulsive features in Duchenne muscular dystrophy: a DSM-5 approachFrancesca Cumbo, Michele Tosi, Michela Catteruccia, et al.
Neuromuscular Disorders : NMD|August 5, 2026
Gastrointestinal manifestations are common and highly burdensome in patients with adult-onset myotonic dystrophy type 1Louise Iterbeke, Bente Ponsaerts, Ingrid Demedts, et al.
Neuromuscular Disorders : NMD|August 7, 2026
Evaluation of antibody reactivity to dystrophin products: does Dp40 really exist?Takahiro Fujimoto, Kyoko Itoh
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