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American Journal of Medical Genetics|January 1, 1991
Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequenceM R Passos-Bueno, J Terwilliger, J Ott, et al.Journal of the Neurological Sciences|May 1, 1991
Limb-girdle syndrome: a genetic study of 22 large Brazilian families. Comparison with X-linked Duchenne and Becker dystrophiesM R Passos-Bueno, M Vainzof, R de C Pavanello, et al.Neuromuscular Disorders : NMD|July 16, 2002
Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye?M M O Tonini, M R Passos-Bueno, A Cerqueira, et al.Brain & Development|January 1, 1996
Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiencyU C Reed, S K Marie, M Vainzof, et al.Neuromuscular Disorders : NMD|December 1, 1996
The phenotype of chromosome 2p-linked limb-girdle muscular dystrophyI Mahjneh, M R Passos-Bueno, M Zatz, et al.American Journal of Medical Genetics|August 15, 1994
Knobloch syndrome in a large Brazilian consanguineous family: confirmation of autosomal recessive inheritanceM R Passos-Bueno, S K Marie, M Monteiro, et al.Human Mutation|January 1, 1997
Novel point mutations in the dystrophin geneR Sitnik, S Campiotto, M Vainzof, et al.American Journal of Medical Genetics|December 1, 1988
Effect of mazindol on growth hormone levels in patients with Duchenne muscular dystrophyM Zatz, D Rapaport, M Vainzof, et al.American Journal of Medical Genetics|February 1, 1988
Relation between height and clinical course in Duchenne muscular dystrophyM Zatz, D Rapaport, M Vainzof, et al.Journal of the Neurological Sciences|September 1, 1990
Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a Brazilian studyM Vainzof, R C Pavanello, I Pavanello Filho, et al.Pageof 26