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Neuromuscular Disorders : NMD|December 3, 2014
Efficacy of intravenous immunoglobulin for treatment of Lambert-Eaton myasthenic syndrome without anti-presynaptic P/Q-type voltage-gated calcium channel antibodies: a case reportAkinori Okada, Haruki Koike, Tomohiko Nakamura, et al.
Neuromuscular Disorders : NMD|December 3, 2014
A novel m.7539C>T point mutation in the mt-tRNA(Asp) gene associated with multisystemic mitochondrial diseaseDiana Lehmann, Kathrin Schubert, Pushpa R Joshi, et al.
Neuromuscular Disorders : NMD|November 19, 2013
Outcome of children with acetylcholine receptor (AChR) antibody positive juvenile myasthenia gravis following thymectomyH S Heng, M Lim, M Absoud, et al.
Neuromuscular Disorders : NMD|November 19, 2013
Anoctamin 5 muscular dystrophy associated with a silent p.Leu115Leu mutation resulting in exon skippingPushpa Raj Joshi, Dieter Gläser, Carolin Dreßel, et al.
Neuromuscular Disorders : NMD|November 19, 2013
Novel TPM3 mutation in a family with cap myopathy and review of the literatureT Schreckenbach, J M Schröder, T Voit, et al.
Neuromuscular Disorders : NMD|November 28, 2017
Clinical phenotypes and trajectories of disease progression in type 1 spinal muscular atrophyRoberto De Sanctis, Marika Pane, Giorgia Coratti, et al.
Neuromuscular Disorders : NMD|December 6, 2017
A randomized placebo-controlled phase 3 trial of an antisense oligonucleotide, drisapersen, in Duchenne muscular dystrophyNathalie Goemans, Eugenio Mercuri, Elena Belousova, et al.
Neuromuscular Disorders : NMD|June 2, 2012
The multifaceted character of lymphotoxin β in inflammatory myopathies and muscular dystrophiesKim K Creus, Boel De Paepe, Joachim Weis, et al.
Neuromuscular Disorders : NMD|April 18, 2012
MPV17 mutation causes neuropathy and leukoencephalopathy with multiple mtDNA deletions in muscleEmma L Blakely, Anna Butterworth, Robert D M Hadden, et al.
Neuromuscular Disorders : NMD|August 11, 2015
Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1Giorgio Tasca, Adele D'Amico, Mauro Monforte, et al.
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