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Neuromuscular Disorders : NMD|March 27, 2007
Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutationS Overeem, H J Schelhaas, P J Blijham, et al.
Neuromuscular Disorders : NMD|March 17, 2007
A novel mutation in the mitochondrial DNA tRNA Leu (UUR) gene associated with late-onset ocular myopathyE Maeso, A Rueda, S Jiménez, et al.
Neuromuscular Disorders : NMD|January 24, 2007
A congenital myopathy with diaphragmatic weakness not linked to the SMARD1 locusL Hartley, M Kinali, R Knight, et al.
Neuromuscular Disorders : NMD|January 24, 2007
Severe encephalomyopathy in a patient with homoplasmic A5814G point mutation in mitochondrial tRNACys geneCarmela Scuderi, Eugenia Borgione, Sebastiano Musumeci, et al.
Neuromuscular Disorders : NMD|December 13, 2006
Autosomal dominant nemaline myopathy: a new phenotype unlinked to previously known genetic lociP Y Jeannet, L Mittaz, M Dunand, et al.
Neuromuscular Disorders : NMD|December 13, 2006
Quantitative analysis of CAPN3 transcripts in LGMD2A patients: involvement of nonsense-mediated mRNA decayKristýna Stehlíková, Eva Zapletalová, Jana Sedlácková, et al.
Neuromuscular Disorders : NMD|November 30, 2006
Painful enlargement of the calf muscles in limb girdle muscular dystrophy type 2B (LGMD2B) with a novel compound heterozygous mutation in DYSFAlexander Diers, Miriam Carl, Gisela Stoltenburg-Didinger, et al.
Neuromuscular Disorders : NMD|November 23, 2006
Myosin storage (hyaline body) myopathy: a case reportMeena V Shingde, Penelope J Spring, Adam Maxwell, et al.
Neuromuscular Disorders : NMD|December 17, 2008
Upper motor neuron and extra-motor neuron involvement in amyotrophic lateral sclerosis: a clinical and brain imaging reviewM M van der Graaff, J M B V de Jong, F Baas, et al.
Neuromuscular Disorders : NMD|December 6, 2008
Characterization of a novel TYMP splice site mutation associated with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)Jan-Willem Taanman, Mariza Daras, Juliane Albrecht, et al.
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