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Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|April 26, 2003
Protein defects in neuromuscular diseasesM Vainzof, M ZatzAmerican Journal of Medical Genetics|September 1, 1985
Serum CK-MB activity in progressive muscular dystrophy: is it of nosologic value?M Vainzof, M Zatz, P A OttoCurrent Opinion in Neurology|November 10, 2000
Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genesM Zatz, M Vainzof, M R Passos-BuenoActa Geneticae Medicae Et Gemellologiae|January 1, 1991
Estimates of genetic and environmental components of serum isocitrate dehydrogenase (ICDH) in normal twinsD Rapaport, G M Colletto, M Vainzof, et al.Journal of Clinical Pathology|August 2, 2003
The effect of calpain 3 deficiency on the pattern of muscle degeneration in the earliest stages of LGMD2AM Vainzof, F de Paula, A M Tsanaclis, et al.American Journal of Medical Genetics|September 25, 1995
Absence of correlation between utrophin localization and quantity and the clinical severity in Duchenne/Becker dystrophiesM Vainzof, M R Passos-Bueno, N Man, et al.American Journal of Medical Genetics|January 1, 1991
Familial occurrence of Duchenne dystrophy through paternal lines in four familiesM Zatz, M R Passos-Bueno, D Rapaport, et al.American Journal of Medical Genetics|March 9, 1999
Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2GM R Passos-Bueno, M Vainzof, E S Moreira, et al.Human Molecular Genetics|June 1, 1994
Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapyM R Passos-Bueno, M Vainzof, S K Marie, et al.Journal of the Neurological Sciences|July 1, 1995
Is dystrophin always altered in Becker muscular dystrophy patients?M Vainzof, M R Passos-Bueno, R C Pavanello, et al.Pageof 26