Maria Rita Passos-Bueno

Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population

Mariz Vainzof, Maria Rita Passos-Bueno, Rita C.M. Pavanello et al. · Journal of the Neurological Sciences · 1999 · 98 citations

Life Sciences, Genetics, Molecular Genetics +9

A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardation

Debora Rapaport, Maria Rita Passos-Bueno, Reinaldo Issao Takata et al. · Neuromuscular Disorders · 1992 · 44 citations

Life Sciences, Genetics, Molecular Genetics +11

Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers

Denilce R. Sumita, Mariz Vainzof, S Campiotto et al. · American Journal of Medical Genetics · 1998 · 39 citations

Life Sciences, Genetics, Molecular Genetics +16

Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype

Mariz Vainzof, Maria Rita Passos-Bueno, Reinaldo Issao Takata et al. · Journal of the Neurological Sciences · 1993 · 25 citations

Life Sciences, Genetics, Molecular Genetics +9

Novel point mutations in the dystrophin gene

Roberta Sitnik, S Campiotto, Mariz Vainzof et al. · Human Mutation · 1997 · 19 citations

Life Sciences, Genetics, Molecular Genetics +15