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Annals of Neurology|November 1, 1996
Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathyE Pegoraro, P Mancias, S H Swerdlow, et al.Neurobiology of Disease|October 11, 2001
Gene expression profiling in postmortem Rett Syndrome brain: differential gene expression and patient classificationC Colantuoni, O H Jeon, K Hyder, et al.Nature Genetics|November 1, 1995
Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complexC G Bönnemann, R Modi, S Noguchi, et al.Journal of Medical Genetics|September 1, 1991
Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17M C Koch, K Ricker, M Otto, et al.Human Genetics|November 1, 1991
Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17M C Koch, K Ricker, M Otto, et al.Cell|August 12, 1988
Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surfaceE Bonilla, C E Samitt, A F Miranda, et al.Neurology|August 26, 1998
Pilot study of myoblast transfer in the treatment of Becker muscular dystrophyA M Neumeyer, D Cros, D McKenna-Yasek, et al.Neurology|July 17, 1999
Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15F Martínez Murillo, H Kobayashi, E Pegoraro, et al.Neurology|December 13, 2000
A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathyP C Scacheri, E P Hoffman, J D Fratkin, et al.Muscle & Nerve|April 16, 1999
Heart involvement in muscular dystrophies due to sarcoglycan gene mutationsP Melacini, M Fanin, D J Duggan, et al.Pageof 19