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M Vainzof

Showing results (31-40 of 85) with videos related to

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Human Heredity|January 1, 1991
Estimate of the intrafamilial correlation for serum creatine kinase and pyruvate kinase in females at risk for Duchenne and Becker muscular dystrophiesE Rabbi-Bortolini, G M Dal Colletto, M R Passos-Bueno, et al.
Neuromolecular Medicine|February 25, 2012
Differential expression of genes involved in the degeneration and regeneration pathways in mouse models for muscular dystrophiesP C G Onofre-Oliveira, A L F Santos, P M Martins, et al.
Journal of the Neurological Sciences|June 29, 1999
Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian populationM Vainzof, M R Passos-Bueno, R C Pavanello, 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|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.
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.
Pageof 9

Showing results (31-40 of 85) with videos related to

Sort By:
Pageof 9
Human Heredity|January 1, 1991
Estimate of the intrafamilial correlation for serum creatine kinase and pyruvate kinase in females at risk for Duchenne and Becker muscular dystrophiesE Rabbi-Bortolini, G M Dal Colletto, M R Passos-Bueno, et al.
Neuromolecular Medicine|February 25, 2012
Differential expression of genes involved in the degeneration and regeneration pathways in mouse models for muscular dystrophiesP C G Onofre-Oliveira, A L F Santos, P M Martins, et al.
Journal of the Neurological Sciences|June 29, 1999
Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian populationM Vainzof, M R Passos-Bueno, R C Pavanello, 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|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.
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.
Pageof 9