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Neuromuscular Disorders : NMD|March 1, 2003
Two novel mutations in the COLQ gene cause endplate acetylcholinesterase deficiencyKeiko Ishigaki, Delphine Nicolle, Eric Krejci, et al.
Neuromuscular Disorders : NMD|June 12, 2003
Inhibition of dystroglycan cleavage causes muscular dystrophy in transgenic miceVianney Jayasinha, Holly H Nguyen, Bing Xia, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Experimental regeneration in canine muscular dystrophy--1. Immunocytochemical evaluation of dystrophin and beta-spectrin expressionC A Sewry, L A Wilson, L Dux, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosumF Hentati, C Ben Hamida, M Zeghal, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Cognitive functions in Duchenne muscular dystrophy: a reappraisal and comparison with spinal muscular atrophyC Billard, P Gillet, J L Signoret, et al.
Neuromuscular Disorders : NMD|January 1, 1992
A randomized controlled trial of early surgery in Duchenne muscular dystrophyA Y Manzur, S A Hyde, E Rodillo, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Variability of the expression of muscle mitochondrial damage in ocular mitochondrial myopathyG Siciliano, B Rossi, C Angelini, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Polyglucosan body myopathy: a new caseP Tonin, G Tomelleri, M Vio, et al.
Neuromuscular Disorders : NMD|May 1, 1994
Age-related changes in collagen gene expression in the muscles of mdx dystrophic and normal miceG Goldspink, K Fernandes, P E Williams, et al.
Neuromuscular Disorders : NMD|May 1, 1994
Immunohistochemical analysis of perforin and granzyme A in inflammatory myopathiesS Orimo, R Koga, K Goto, et al.
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