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Neuromuscular Disorders : NMD|October 29, 2000
Mitochondrial DNA variants in inclusion body myositisC C Kok, A Boyt, S Gaudieri, et al.
Neuromuscular Disorders : NMD|September 21, 2000
Phenotypic expression of late-onset glycogen storage disease type II: identification of asymptomatic adults through family studies and review of reported familiesM G Ausems, K ten Berg, F A Beemer, et al.
Neuromuscular Disorders : NMD|September 21, 2000
Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2)W Kress, B Mueller-Myhsok, K Ricker, et al.
Neuromuscular Disorders : NMD|September 21, 2000
A mitochondrial tRNA(Lys) gene mutation (T8316C) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodesY Campos, G Lorenzo, M A Martín, et al.
Neuromuscular Disorders : NMD|September 21, 2000
Hereditary spastic paraplegia associated with peripheral neuropathy: a distinct clinical and genetic entityM L Mostacciuolo, L Rampoldi, E Righetti, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Autosomal dominant distal myopathy: further evidence of a chromosome 14 locusT Voit, P Kutz, B Leube, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle alpha-actin (ACTA1) geneH Jungbluth, C A Sewry, S C Brown, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Cationic channels in normal and dystrophic human myotubesC Vandebrouck, G Duport, C Cognard, et al.
Neuromuscular Disorders : NMD|January 3, 2026
Monoclonal Gammopathy - the common denominator of sporadic late-onset nemaline myopathy and paraproteinemic neuropathyEleonora Torchia, Frauke Stascheit, Felix Kleefeld, et al.
Neuromuscular Disorders : NMD|July 1, 1995
Abnormal expression of intermediate filament proteins in X-linked myotubular myopathy is not reproduced in vitroP F Van der Ven, P H Jap, P G Barth, et al.
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