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Nature|January 12, 1989
Conversion of mdx myofibres from dystrophin-negative to -positive by injection of normal myoblastsT A Partridge, J E Morgan, G R Coulton, et al.Muscle & Nerve|May 19, 1998
Homozygous alpha-sarcoglycan mutation in two siblings: one asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patientC Angelini, M Fanin, E Menegazzo, et al.Neurology|January 28, 1999
The clinical spectrum of sarcoglycanopathiesC Angelini, M Fanin, M P Freda, et al.Neuron|July 1, 1988
Cell and fiber-type distribution of dystrophinE P Hoffman, M S Hudecki, P A Rosenberg, et al.Neurology|August 1, 1989
Improved diagnosis of Becker muscular dystrophy by dystrophin testingE P Hoffman, L M Kunkel, C Angelini, et al.The Journal of Biological Chemistry|June 15, 1988
Evidence for the association of dystrophin with the transverse tubular system in skeletal muscleC M Knudson, E P Hoffman, S D Kahl, et al.Fetal Diagnosis and Therapy|May 1, 1995
Endoscopically assisted, ultrasound-guided fetal muscle biopsyM I Evans, R A Quintero, M King, et al.Neurogenetics|May 1, 1997
Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2)D J Duggan, D Manchester, K P Stears, et al.Human Molecular Genetics|April 1, 1995
Myotonic dystrophy: evidence for a possible dominant-negative RNA mutationJ Wang, E Pegoraro, E Menegazzo, et al.Annals of Neurology|October 1, 1991
Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of Duchenne muscular dystrophyE P Hoffman, C A Garcia, J S Chamberlain, et al.Pageof 19