EXPERIMENTAL DEFIBRINATION WITH BOTHROPASE. A STUDY ON THE FIBRINOLYTIC MECHANISM IN VIVO.KELEN EMA; ROSENFELD G; VAINZOF M et al.1978; HAEMOSTASIS; SWITZ.; DA. 1978; VOL. 7; NO 1; PP. 35-45; BIBL. 1 P. 1/2Article

Serum CK-MB activity in progressive muscular dystrophy: is it of nosologic value?VAINZOF, M; ZATZ, M; OTTO, P. A et al.American journal of medical genetics. 1985, Vol 22, Num 1, pp 81-87, issn 0148-7299Article

Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q : Analysis of muscle beta 1 syntrophinROCCO, P; VAINZOF, M; FROEHNER, S. C et al.American journal of medical genetics. 2000, Vol 92, Num 2, pp 122-127, issn 0148-7299Article

Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardationREED, U. C; TSANACLIS, A. M. C; VAINZOF, M et al.Brain & development (Tokyo. 1979). 1999, Vol 21, Num 4, pp 274-278, issn 0387-7604Article

Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population : From LGMD2A to LGMD2GPASSOS-BUENO, M. R; VAINZOF, M; MOREIRA, E. S et al.American journal of medical genetics. 1999, Vol 82, Num 5, pp 392-398, issn 0148-7299Article

Caveolin-3 in muscular dystrophyMCNALLY, E. M; DE SA MOREIRA, E; KUNKEL, L. M et al.Human molecular genetics (Print). 1998, Vol 7, Num 5, pp 871-877, issn 0964-6906Article

Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate regionPASSOS-BUENO, M. R; RAMAISA BASHIR; STRACHAN, T et al.Genomics (San Diego, Calif.). 1995, Vol 27, Num 1, pp 192-195, issn 0888-7543Article

Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapyPASSOS-BUENO, M. R; VAINZOF, M; MARIE, S. K et al.Human molecular genetics (Print). 1994, Vol 3, Num 6, pp 919-922, issn 0964-6906Article

A novel locus for late onset amyotrophic lateral sclerosis/motor neurone disease variant at 20q13NISHIMURA, A. L; MITNE-NETO, M; SILVA, H. C. A et al.Journal of medical genetics. 2004, Vol 41, Num 4, pp 315-320, issn 0022-2593, 6 p.Article

Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A)SPENCER, M. J; TIDBALL, J. G; ANDERSON, L. V. B et al.Journal of the neurological sciences. 1997, Vol 146, Num 2, pp 173-178, issn 0022-510XArticle

Mild and severe muscular dystrophy caused by a single γ-sarcoglycan mutationMCNALLY, E. M; PASSOS-BUENO, M. R; KUNKEL, L. M et al.American journal of human genetics. 1996, Vol 59, Num 5, pp 1040-1047, issn 0002-9297Article

assessment of t 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophyZATZ, M; MATSUMURA, K; VAINZOF, M et al.Journal of the neurological sciences. 1994, Vol 123, Num 1-2, pp 122-128, issn 0022-510XArticle

Familial occurrence of Duchenne dystrophy through paternal lines in four familiesZATZ, M; PASSOS-BUENO, M. R; RAPAPORT, D et al.American journal of medical genetics. 1991, Vol 38, Num 1, pp 80-84, issn 0148-7299, 5 p.Article

Serum creatine-kinase (CK) and pyruvate-kinase (PK) activities in Duchenne (DMD) as compared with Becker (BMD) muscular dystrophyZATZ, M; RAPAPORT, D; VAINZOF, M et al.Journal of the neurological sciences. 1991, Vol 102, Num 2, pp 190-196, issn 0022-510XArticle

Relation between height and clinical course in Duchenne muscular dystrophyZATZ, M; RAPAPORT, D; VAINZOF, M et al.American journal of medical genetics. 1988, Vol 29, Num 2, pp 405-410, issn 0148-7299Article

Mazindol and growth hormone inhibition in Duchenne muscular dystrophyZATZ, M; VAINZOF, M; RAPAPORT, D et al.American journal of medical genetics. 1987, Vol 27, Num 4, pp 993-995, issn 0148-7299Article

Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian populationVAINZOF, M; PASSOS-BUENO, M. R; PAVANELLO, R. C. M et al.Journal of the neurological sciences. 1999, Vol 164, Num 1, pp 44-49, issn 0022-510XArticle

Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriersSUMITA, D. R; VAINZOF, M; CAMPIOTTO, S et al.American journal of medical genetics. 1998, Vol 80, Num 4, pp 356-361, issn 0148-7299Article

Deficiency of α-actinin-3 (ACTN3) occurs in different forms of muscular dystrophyVAINZOF, M; COSTA, C. S; MARIE, S. K et al.Neuropediatrics. 1997, Vol 28, Num 4, pp 223-228, issn 0174-304XArticle

The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12MOREIRA, E. S; VAINZOF, M; MARIE, S. K et al.American journal of human genetics. 1997, Vol 61, Num 1, pp 151-159, issn 0002-9297Article

Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiencyREED, U. C; MARIE, S. K; VAINZOF, M et al.Brain & development (Tokyo. 1979). 1996, Vol 18, Num 1, pp 53-58, issn 0387-7604Article

Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian familiesPASSOS-BUENO, M. R; MOREIRA, E. S; STRACHAN, T et al.Journal of medical genetics. 1996, Vol 33, Num 2, pp 97-102, issn 0022-2593Article

A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophyRITA PASSOS BUENO, M; MOREIRA, E. S; VAINZOF, M et al.Human molecular genetics (Print). 1995, Vol 4, Num 7, pp 1163-1167, issn 0964-6906Article

Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysisPASSOS-BUENO, M. R; OLIVEIRA, J. R; BAKKER, E et al.Human molecular genetics (Print). 1993, Vol 2, Num 11, pp 1945-1947, issn 0964-6906Article

Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotypeVAINZOF, M; PASSOS-BUENO, M. R; TAKATA, R. I et al.Journal of the neurological sciences. 1993, Vol 119, Num 1, pp 38-42, issn 0022-510XArticle