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1
American cutaneous leishmaniasis : Use of a skin test as a predictor of relapse after treatment
American cutaneous leishmaniasis : Use of a skin test as a predictor of relapse after treatment
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American cutaneous leishmaniasis : Use of a skin test as a predictor of relapse after treatment

PASSOS, V. M. A ; BARRETO, S. M ; ROMANHA, A. J ; KRETTLI, A. U ; VOLPINI, A. C ; LIMA E COSTA, M. F. F

Bulletin of the World Health Organization, 2000-01, Vol.78 (8), p.968-974 [Periódico revisado por pares]

Genève: Organisation mondiale de la santé

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2
Deficiency of α-Actinin-3 (ACTN3) Occurs in Different Forms of Muscular Dystrophy
Deficiency of α-Actinin-3 (ACTN3) Occurs in Different Forms of Muscular Dystrophy
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Deficiency of α-Actinin-3 (ACTN3) Occurs in Different Forms of Muscular Dystrophy

Vainzof, M. ; Costa, C. S. ; Marie, S. K. ; Moreira, E. S. ; Reed, U. ; Passos-Bueno, M. R. ; Beggs, A. H. ; Zatz, M.

Neuropediatrics, 1997-08, Vol.28 (4), p.223-228 [Periódico revisado por pares]

Stuttgart: Thieme

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3
Why is the reproductive performance lower in Becker (BMD) as compared to limb girdle (LGMD) muscular dystrophy male patients?
Why is the reproductive performance lower in Becker (BMD) as compared to limb girdle (LGMD) muscular dystrophy male patients?
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Why is the reproductive performance lower in Becker (BMD) as compared to limb girdle (LGMD) muscular dystrophy male patients?

Eggers, Sabine ; Lauriano, Valèria ; Melo, Marcio ; Takata, Reinaldo Issao ; Akiyama, Jeanne ; Passos-Bueno, Maria Rita ; Gentil, Valentim ; Frota-Pessoa, Oswaldo ; Zatz, Mayana

American journal of medical genetics, 1995-02, Vol.60 (1), p.27-32 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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4
Limb-girdle syndrome: a genetic study of 22 large Brazilian families comparison with X-linked Duchenne and Becker dystrophies
Limb-girdle syndrome: a genetic study of 22 large Brazilian families comparison with X-linked Duchenne and Becker dystrophies
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Limb-girdle syndrome: a genetic study of 22 large Brazilian families comparison with X-linked Duchenne and Becker dystrophies

Rita Passos-Bueno, M. ; Vainzof, Mariz ; de Cássia, Rita ; Pavanello, M. ; Pavanello-Filho, Ivo ; Lima, Martha A.B.O. ; Zatz, Mayana

Journal of the neurological sciences, 1991-05, Vol.103 (1), p.65-75 [Periódico revisado por pares]

Shannon: Elsevier B.V

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5
Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G
Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G
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Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G

Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Moreira, Eloisa S. ; Zatz, Mayana

American journal of medical genetics, 1999-02, Vol.82 (5), p.392-398

New York: Wiley Subscription Services, Inc., A Wiley Company

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6
Further evidence for a fourth gene causing X-linked pure spastic paraplegia
Further evidence for a fourth gene causing X-linked pure spastic paraplegia
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Further evidence for a fourth gene causing X-linked pure spastic paraplegia

Starling, A. ; Rocco, P. ; Cambi, F. ; Hobson, G.M. ; Passos Bueno, M.R. ; Zatz, M.

American journal of medical genetics, 2002-08, Vol.111 (2), p.152-156

New York: Wiley Subscription Services, Inc., A Wiley Company

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7
Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a Brazilian study
Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a Brazilian study
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Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a Brazilian study

Vainzof, Mariz ; Pavanello, Rita C.M. ; Filho, Ivo Pavanello ; Passos-Bueno, Maria Rita ; Rapaport, Debora ; Hsi, Chu T. ; Zatz, Mayana

Journal of the neurological sciences, 1990-09, Vol.98 (2), p.221-233 [Periódico revisado por pares]

Shannon: Elsevier B.V

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8
Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: Intragenic heterogeneity or a new form of X-linked mental retardation?
Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: Intragenic heterogeneity or a new form of X-linked mental retardation?
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Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: Intragenic heterogeneity or a new form of X-linked mental retardation?

Passos-Bueno, Maria Rita ; Byth, Barbara C. ; Rosenberg, Sergio ; Takata, Reinaldo I. ; Bakker, Egbert ; Beggs, Alan H. ; Pavanello, Rita C. ; Vainzof, Mariz ; Davies, Kay E. ; Zatz, Mayana

American journal of medical genetics, 1993-04, Vol.46 (2), p.172-175

New York: Wiley Subscription Services, Inc., A Wiley Company

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9
An epidemic of sporotrichosis in Rio de Janeiro, Brazil: epidemiological aspects of a series of cases
An epidemic of sporotrichosis in Rio de Janeiro, Brazil: epidemiological aspects of a series of cases
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An epidemic of sporotrichosis in Rio de Janeiro, Brazil: epidemiological aspects of a series of cases

BARROS, M. B. L. ; SCHUBACH, A. O. ; SCHUBACH, T. M. P. ; WANKE, B. ; LAMBERT-PASSOS, S. R.

Epidemiology and infection, 2008-09, Vol.136 (9), p.1192-1196 [Periódico revisado por pares]

Cambridge, UK: Cambridge University Press

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10
Suboptimal survival of male germ-cell tumors in southern Portugal—a population-based retrospective study for cases diagnosed in 1999 and 2000
Suboptimal survival of male germ-cell tumors in southern Portugal—a population-based retrospective study for cases diagnosed in 1999 and 2000
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Suboptimal survival of male germ-cell tumors in southern Portugal—a population-based retrospective study for cases diagnosed in 1999 and 2000

Passos-Coelho, J.L. ; Castro Ribeiro, M. ; Santos, E. ; Sousa Pontes, C. ; Brito, B. ; Miranda, A.C.

Annals of oncology, 2011-05, Vol.22 (5), p.1215-1220 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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