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Neuromuscular Disorders : NMD|December 12, 2001
Intelligence and cognitive function in children and adolescents with spinal muscular atrophyA von Gontard, K Zerres, M Backes, et al.Neuromuscular Disorders : NMD|December 12, 2001
Stable motor and lung function throughout pregnancy in a patient with infantile spinal muscular atrophy type IISabine Rudnik-Schöneborn, Christian Breuer, Klaus ZerresNeuromuscular Disorders : NMD|December 12, 2001
Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathyKati Donner, Miina Ollikainen, Maaret Ridanpää, et al.Neuromuscular Disorders : NMD|December 12, 2001
Dysferlin expression after normal myoblast transplantation in SCID and in SJL miceK Leriche-Guérin, L V B Anderson, K Wrogemann, et al.Neuromuscular Disorders : NMD|December 12, 2001
Creatine supplementation reduces skeletal muscle degeneration and enhances mitochondrial function in mdx miceAnne-Catherine Passaquin, Mathilde Renard, Laurence Kay, et al.Neuromuscular Disorders : NMD|December 12, 2001
The muscle-specific marker desmin is expressed in a proportion of human dermal fibroblasts after their exposure to galectin-1K Goldring, G E Jones, C A Sewry, et al.Neuromuscular Disorders : NMD|September 11, 2002
The role of utrophin in the potential therapy of Duchenne muscular dystrophyKelly J Perkins, Kay E DaviesNeuromuscular Disorders : NMD|September 11, 2002
An effective, low-dosage, intermittent schedule of prednisolone in the long-term treatment of early cases of Duchenne dystrophyMaria Kinali, Eugenio Mercuri, Marion Main, et al.Neuromuscular Disorders : NMD|March 29, 2000
The Fukuyama congenital muscular dystrophy storyT Toda, K Kobayashi, E Kondo-Iida, et al.Neuromuscular Disorders : NMD|March 29, 2000
Hypothyroidism unmasking proximal myotonic myopathyV Sansone, R C Griggs, R T MoxleyPageof 340