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Neuromuscular Disorders : NMD|May 8, 2012
Inclusion body myositis coexisting with hypertrophic cardiomyopathy: an autopsy studyYukie Inamori, Itsuro Higuchi, Teruhiko Inoue, et al.
Neuromuscular Disorders : NMD|May 8, 2012
Congenital myopathy caused by a novel missense mutation in the CFL2 geneC W Ockeloen, H J Gilhuis, R Pfundt, et al.
Neuromuscular Disorders : NMD|June 2, 2012
Nerve, muscle and heart acute toxicity following oxaliplatin and capecitabine treatmentDaniele Orsucci, Chiara Pizzanelli, Greta Alì, et al.
Neuromuscular Disorders : NMD|October 8, 2013
Combined cap disease and nemaline myopathy in the same patient caused by an autosomal dominant mutation in the TPM3 geneEdoardo Malfatti, Ursula Schaeffer, Françoise Chapon, et al.
Neuromuscular Disorders : NMD|December 22, 2005
Rapidly progressive neurodegeneration in a case with the 7472insC mutation and the A7472C polymorphism in the mtDNA tRNA ser(UCN) geneElena Cardaioli, Paola Da Pozzo, Alfonso Cerase, et al.
Neuromuscular Disorders : NMD|December 22, 2005
Carbonic anhydrase inhibitors ameliorate the symptoms of hypokalaemic periodic paralysis in rats by opening the muscular Ca2+-activated-K+ channelsDomenico Tricarico, Antonietta Mele, Diana Conte Camerino
Neuromuscular Disorders : NMD|December 24, 2005
Temporal and spatial mRNA expression patterns of TGF-beta1, 2, 3 and TbetaRI, II, III in skeletal muscles of mdx miceLan Zhou, John D Porter, Georgiana Cheng, et al.
Neuromuscular Disorders : NMD|December 24, 2005
Clinical, electrophysiological and molecular genetic studies in a family with X-linked dominant Charcot-Marie-Tooth neuropathy presenting a novel mutation in GJB1 Promoter and a rare polymorphism in LITAF/SIMPLEKatell Beauvais, Alain Furby, Philippe Latour
Neuromuscular Disorders : NMD|October 27, 2009
Neuromuscular disease presentation with three genetic defects involving two genomesMazhor Al-Dosary, Roger G Whittaker, Joanna Haughton, et al.
Neuromuscular Disorders : NMD|October 27, 2009
Late-onset MNGIE without peripheral neuropathy due to incomplete loss of thymidine phosphorylase activityRoberto Massa, Alessandra Tessa, Maria Margollicci, et al.
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