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Neuromuscular Disorders : NMD|April 20, 2012
Cardiomyopathy is common in patients with the mitochondrial DNA m.3243A>G mutation and correlates with mutation loadKieren G Hollingsworth, Grainne S Gorman, Michael I Trenell, et al.Neuromuscular Disorders : NMD|April 10, 2012
X inactivation in females with X-linked Charcot-Marie-Tooth diseaseSinéad M Murphy, Richard Ovens, James Polke, et al.Neuromuscular Disorders : NMD|February 7, 2012
Paroxysmal neuromyotonia: a new sporadic channelopathyTeeratorn Pulkes, Charungthai Dejthevaporn, Metha Apiwattanakul, et al.Neuromuscular Disorders : NMD|November 22, 2011
Myopathy in a woman and her daughter associated with a novel splice site MTM1 mutationCarola Hedberg, Christopher Lindberg, Gyöngyvér Máthé, et al.Neuromuscular Disorders : NMD|March 14, 2000
Genetic heterogeneity in three Chinese children with Fukuyama congenital muscular dystrophyY J Jong, K Kobayashi, T Toda, et al.Neuromuscular Disorders : NMD|March 14, 2000
A clinical and genetic study of a manifesting heterozygote with X-linked myotubular myopathyS R Hammans, D O Robinson, C Moutou, et al.Neuromuscular Disorders : NMD|March 21, 2001
Novel dystrophin mutations revealed by analysis of dystrophin mRNA: alternative splicing suppresses the phenotypic effect of a nonsense mutationL Fajkusová, Z Lukás, M Tvrdíková, et al.Neuromuscular Disorders : NMD|March 21, 2001
Nebulin expression in patients with nemaline myopathyJ Gurgel-Giannetti, U Reed, M L Bang, et al.Neuromuscular Disorders : NMD|March 21, 2001
Force and power output of diaphragm muscle strips from mdx and control mice after clenbuterol treatmentG S Lynch, R T Hinkle, J A FaulknerNeuromuscular Disorders : NMD|September 21, 2000
Perineurial cell hyperplasia in early-onset polyneuropathy with multiple cranial neuropathiesG I Wolfe, R D Brower, D K BurnsPageof 340