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American Journal of Medical Genetics|March 1, 1989
Estimate of the proportion of Duchenne muscular dystrophy with autosomal recessive inheritanceM Zatz, M R Passos-Bueno, D RapaportAmerican 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|June 15, 1991
Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophyD Rapaport, M R Passos-Bueno, L Brandão, 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 Medical Genetics|July 1, 1993
Facioscapulohumeral muscular dystrophy: aspects of genetic counselling, acceptance of preclinical diagnosis, and fitnessS Eggers, M R Passos-Bueno, M ZatzCurrent 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-BuenoJournal of Medical Genetics|March 1, 1990
Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115M R Passos-Bueno, D Rapaport, D Love, 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.Journal of the Neurological Sciences|February 1, 1991
Immunofluorescence dystrophin study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal region of the proteinM Vainzof, E E Zubrzycka-Gaarn, D Rapaport, et al.Journal of the Neurological Sciences|April 1, 1991
Serum creatine-kinase (CK) and pyruvate-kinase (PK) activities in Duchenne (DMD) as compared with Becker (BMD) muscular dystrophyM Zatz, D Rapaport, M Vainzof, et al.Pageof 33