Showing results (1061-1070 of 3,396) with videos related to

Sort By:
Pageof 340
Neuromuscular Disorders : NMD|July 19, 2000
Cerebrotendinous xanthomatosis. Controversies about nerve and muscle: observations in ten patientsA Verrips, B G van Engelen, H ter Laak, et al.
Neuromuscular Disorders : NMD|June 26, 1999
Proximal myotonic myopathy (PROMM) presenting as myotonia during pregnancyB Newman, G Meola, D G O'Donovan, et al.
Neuromuscular Disorders : NMD|June 26, 1999
Severe clinical expression in X-linked Emery-Dreifuss muscular dystrophyM Hoeltzenbein, T Karow, J A Zeller, et al.
Neuromuscular Disorders : NMD|June 26, 1999
A new mutation in the myophosphorylase gene (Asn684Tyr) in a Spanish patient with McArdle's diseaseA L Andreu, C Bruno, L Tamburino, et al.
Neuromuscular Disorders : NMD|June 26, 1999
Molecular analysis of 4q35 rearrangements in fascioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the diseaseG Galluzzi, G Deidda, S Cacurri, et al.
Neuromuscular Disorders : NMD|March 11, 2000
Amyotrophic lateral sclerosis: copper/zinc superoxide dismutase (SOD1) gene mutationsR W Orrell
Neuromuscular Disorders : NMD|January 5, 2000
Expression, regulation and localisation of dystrophin isoforms in human foetal skeletal and cardiac muscleS Torelli, A Ferlini, L Obici, et al.
Neuromuscular Disorders : NMD|January 5, 2000
Deletion patterns of dystrophin gene in Hungarian patients with Duchenne/Becker muscular dystrophiesA Herczegfalvi, G Tóth, P Gyürüs, et al.
Neuromuscular Disorders : NMD|January 5, 2000
Association of monoamine oxidase B alleles with age at onset in amyotrophic lateral sclerosisS Orrù, V Mascia, M Casula, et al.
Neuromuscular Disorders : NMD|January 5, 2000
Immunosuppressive treatment of rippling muscles in patients with myasthenia gravisW Müller-Felber, C F Ansevin, K Ricker, et al.
Pageof 340