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Neuromuscular Disorders : NMD|September 1, 1993
Desmin-lacZ transgene, a marker of regenerating skeletal muscleL Lescaudron, Z Li, D Paulin, et al.Neuromuscular Disorders : NMD|September 1, 1993
Genetic heterogeneity of familial hypertrophic cardiomyopathyE Dausse, K SchwartzNeuromuscular Disorders : NMD|September 1, 1993
Molecular genetics of facioscapulohumeral muscular dystrophyC Wijmenga, R R Frants, J E Hewitt, et al.Neuromuscular Disorders : NMD|September 1, 1993
Myotonic dystrophy: over-expression or/and under-expression? A critical review on a controversial pointH Hofmann-Radvanyi, C JunienNeuromuscular Disorders : NMD|September 1, 1993
Inclusions in familial cytoplasmic body myopathy are stained by anti-dystrophin antibodiesA Caron, F Chapon, C Berthelin, et al.Neuromuscular Disorders : NMD|September 1, 1993
Malignant hyperthermia and central core disease: analysis of two families with heterogeneous clinical expressionN B Romero, Y Nivoche, J Lunardi, et al.Neuromuscular Disorders : NMD|September 1, 1993
Pathological findings in 165 patients explored for malignant hyperthermia susceptibilityD Figarella-Branger, G Kozak-Ribbens, L Rodet, et al.Neuromuscular Disorders : NMD|September 1, 1993
Morphological analyses of paraspinal muscles: comparison of progressive lumbar kyphosis (camptocormia) and narrowing of lumbar canal by disc protrusionsM B Delisle, M Laroche, H Dupont, et al.Neuromuscular Disorders : NMD|May 1, 1997
Spinal muscular atrophy--clinical and genetic correlationsK Zerres, B Wirth, S Rudnik-SchönebornNeuromuscular Disorders : NMD|November 26, 2009
Adult course in dynamin 2 dominant centronuclear myopathy with neonatal onsetAtle Melberg, Christine Kretz, Hannu Kalimo, et al.Pageof 340