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Neuromuscular Disorders : NMD|December 3, 2014
Left ventricular non-compaction cardiomyopathy associated with epidermolysis bullosa simplex with muscular dystrophy and PLEC1 mutationChet R Villa, Thomas D Ryan, James J Collins, et al.
Neuromuscular Disorders : NMD|December 3, 2014
Suitability of North Star Ambulatory Assessment in young boys with Duchenne muscular dystrophyRoberto De Sanctis, Marika Pane, Serena Sivo, et al.
Neuromuscular Disorders : NMD|December 3, 2014
Muscle ultrasound in classic infantile and adult Pompe disease: a useful screening tool in adults but not in infantsK Vill, J Schessl, V Teusch, et al.
Neuromuscular Disorders : NMD|December 3, 2014
Eosinophilic myositis as first manifestation in a patient with type 2 myotonic dystrophy CCTG expansion mutation and rheumatoid arthritisAlain Meyer, Béatrice Lannes, Raphaël Carapito, et al.
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.
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