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Journal of the Neurological Sciences|October 1, 1993
Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotypeM Vainzof, M R Passos-Bueno, R I Takata, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complexM Vainzof, E S Moreira, G Ferraz, et al.
Human Molecular Genetics|March 1, 1995
Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?M Zatz, M R Passos-Bueno, A Cerqueira, et al.
Muscle & Nerve|May 8, 2002
Lack of the C-terminal domain of nebulin in a patient with nemaline myopathyJ Gurgel-Giannetti, M-L Bang, U Reed, et al.
Journal of Medical Genetics|December 1, 1998
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathiesE S Moreira, M Vainzof, S K Marie, et al.
American Journal of Medical Genetics|May 30, 1998
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than femalesM Zatz, S K Marie, A Cerqueira, et al.
American Journal of Medical Genetics|August 26, 1998
Paternal inheritance or different mutations in maternally related patients occur in about 3% of Duchenne familial casesM Zatz, D Sumita, S Campiotto, et al.
American Journal of Human Genetics|July 1, 1997
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12E S Moreira, M Vainzof, S K Marie, et al.
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.
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.
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