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Neuromuscular Disorders : NMD|September 11, 2002
Dystrophin and functionally related proteins in the nematode Caenorhabditis elegansLaurent Ségalat
Neuromuscular Disorders : NMD|September 11, 2002
Dystrobrevin dynamics in muscle-cell signalling: a possible target for therapeutic intervention in Duchenne muscular dystrophy?Derek J Blake
Neuromuscular Disorders : NMD|September 11, 2002
Steroids in Duchenne muscular dystrophy: from clinical trials to genomic researchFrancesco Muntoni, Ivan Fisher, Jennifer E Morgan, et al.
Neuromuscular Disorders : NMD|October 12, 2001
Three mouse models of muscular dystrophy: the natural history of strength and fatigue in dystrophin-, dystrophin/utrophin-, and laminin alpha2-deficient miceA M Connolly, R M Keeling, S Mehta, et al.
Neuromuscular Disorders : NMD|October 12, 2001
Valproic acid triggers acute rhabdomyolysis in a patient with carnitine palmitoyltransferase type II deficiencyM Kottlors, M Jaksch, U P Ketelsen, et al.
Neuromuscular Disorders : NMD|October 12, 2001
Oculopharyngodistal myopathy is genetically heterogeneous and most cases are distinct from oculopharyngeal muscular dystrophyN Minami, K Ikezoe, H Kuroda, et al.
Neuromuscular Disorders : NMD|October 12, 2001
Normal innervation and differentiation of X-linked myotubular myopathy muscle cells in a nerve-muscle coculture systemO M Dorchies, J Laporte, S Wagner, et al.
Neuromuscular Disorders : NMD|October 12, 2001
A discrepancy resolved: human satellite cells are not preprogrammed to fast and slow lineagesS Bonavaud, O Agbulut, R Nizard, et al.
Neuromuscular Disorders : NMD|June 19, 2001
Proximal myotonic myopathy and proximal myotonic dystrophy: two different entities? The phenotypic variability of proximal myotonic syndromesC Schneider, C Wessig, C R Müller, et al.
Neuromuscular Disorders : NMD|June 19, 2001
Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomatic carrier with 'de novo' duplication of dystrophin geneN B Romero, P De Lonlay, S Llense, et al.
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