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Neuromuscular Disorders : NMD|July 5, 2011
Nemaline myopathy caused by mutations in the nebulin gene may present as a distal myopathyVilma-Lotta Lehtokari, Katarina Pelin, Agnes Herczegfalvi, et al.
Neuromuscular Disorders : NMD|November 23, 2011
Current status of the congenital myasthenic syndromesAndrew G Engel
Neuromuscular Disorders : NMD|December 27, 2011
A Becker myotonia patient with compound heterozygosity for CLCN1 mutations and Prinzmetal angina pectorisDaniel Zielonka, Karin Jurkat-Rott, Paweł Stachowiak, et al.
Neuromuscular Disorders : NMD|December 27, 2011
PTPN22 and myasthenia gravis: replication in an Italian population and meta-analysis of literature dataCarlo Provenzano, Roberta Ricciardi, Flavia Scuderi, et al.
Neuromuscular Disorders : NMD|November 19, 2011
Screening for mutations in Spanish families with myotonia. Functional analysis of novel mutations in CLCN1 geneMaría J Mazón, Francisco Barros, Pilar De la Peña, et al.
Neuromuscular Disorders : NMD|September 13, 2011
Adult-onset multiple acyl CoA dehydrogenation deficiency associated with an abnormal isoenzyme pattern of serum lactate dehydrogenaseFuminobu Sugai, Kousuke Baba, Keiko Toyooka, et al.
Neuromuscular Disorders : NMD|June 11, 2011
The soy isoflavone genistein blunts nuclear factor kappa-B, MAPKs and TNF-α activation and ameliorates muscle function and morphology in mdx miceSonia Messina, Alessandra Bitto, M'hammed Aguennouz, et al.
Neuromuscular Disorders : NMD|December 31, 2011
N-Acetylcysteine treatment of dystrophic mdx mice results in protein thiol modifications and inhibition of exercise induced myofibre necrosisJessica R Terrill, Hannah G Radley-Crabb, Miranda D Grounds, et al.
Neuromuscular Disorders : NMD|March 9, 2012
Role of serotonergic system in the pathogenesis of fibrosis in canine idiopathic inflammatory myopathiesLuigi Michele Pavone, Silvana Rea, Francesca Trapani, et al.
Neuromuscular Disorders : NMD|February 24, 2012
A case of myelopathy, myopathy, peripheral neuropathy and subcortical grey matter degeneration associated with recessive compound heterozygous POLG1 mutationsP McKelvie, R Marotta, D R Thorburn, et al.
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