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1
Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families
Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Study of 4q dna markers in brazilian fascioscapulohumeral muscular dystrophy (fshd) families

Maria Rita Passos-Bueno C Wijmenga; R I Takata; Suely Kazue Nagahashi Marie; M Vainzof; R C M Pavanello; J E Hewitt; E Bakker; A A S Carvalho; J Akiyama; R R Frants; World Congress of Neurology (15. 1993 Vancouver)

Calgary v.20, n.suppl.4, p.s30, aug. 1993 Canadian Journal of Neurological Sciences

Calgary 1993

Localização: FM - Fac. Medicina    (BCSEP 1993 038 ) e outros locais(Acessar)

2
Autosomal recessive limb-girdle muscular dystrophies
Autosomal recessive limb-girdle muscular dystrophies
Material Type:
Livro 		Adicionar ao Meu Espaço

Autosomal recessive limb-girdle muscular dystrophies

M Zatz M Vainzof; Maria Rita Passos-Bueno; J Akiyama; Suely Kazue Nagahashi Marie

Lane, R J M (*), Ed New York : Marcel Dekker, 1996 Handbook of Muscle Disease

New York Marcel Dekker 1996

Item não circula. Consulte sua biblioteca.(Acessar)

3
Mesma mutacao no gene da adalina pode causar formas graves e leves de distrofia muscular tipo cinturas
Mesma mutacao no gene da adalina pode causar formas graves e leves de distrofia muscular tipo cinturas
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Mesma mutacao no gene da adalina pode causar formas graves e leves de distrofia muscular tipo cinturas

Maria Rita Passos-Bueno E S Moreira; Mariz Vainzof; L Pereira; Suely Kazue Nagahashi Marie; J Akiyama; Mayana Zatz; Congresso Nacional de Genetica (41. 1995 Caxambu)

v.13, n.3 suppl., p.557, sep. 1995 Revista Brasileira de Genetica = Brazilian Journal of Genetics

1995

Item não circula. Consulte sua biblioteca.(Acessar)

4
Becker and limb-girdle muscular dystrophies a psychiatric and intellectual level comparative study
Becker and limb-girdle muscular dystrophies a psychiatric and intellectual level comparative study
Material Type:
Artigo 		Adicionar ao Meu Espaço

Becker and limb-girdle muscular dystrophies a psychiatric and intellectual level comparative study

M. Melo V Lauriano; V Gentil; S Eggers; S S Bianco; P R Gimenez; J Akiyama; H Okabaiashi; O Frota-Pessoa; Maria Rita Passos-Bueno; M Zatz

New York v.60, n.1 , p.33-8, feb. 1995 American Journal of Medical Genetics (Neuropsychiatric Genetics)

New York 1995

Item não circula. Consulte sua biblioteca.(Acessar)

5
Becker and limb-girdle muscular dystrophies a psychiatric and intellectual level comparative study
Becker and limb-girdle muscular dystrophies a psychiatric and intellectual level comparative study
Material Type:
Artigo 		Adicionar ao Meu Espaço

Becker and limb-girdle muscular dystrophies a psychiatric and intellectual level comparative study

M. Melo V Lauriano; V Gentil; S Eggers; S S Bianco; P R Gimenez; J Akiyama; H Okabaiashi; O Frota-Pessoa; Maria Rita Passos-Bueno; Mayana Zatz

New York v.60, n.1 , p.33-8, feb. 1995 American Journal of Medical Genetics (Neuropsychiatric Genetics)

New York 1995

Item não circula. Consulte sua biblioteca.(Acessar)

6
Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy
Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy
Material Type:
Artigo 		Adicionar ao Meu Espaço

Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy

Maria Rita Passos-Bueno E S Moreira; M Vainzof; J Chamberlain; Suely Kazue Nagahashi Marie; L Pereira; J Akiyama; S L Roberds; K P Campbell; M Zatz

Oxford v.4 , n.7 , p.1163-7, 1995 Human Molecular Genetics

Oxford 1995

Item não circula. Consulte sua biblioteca.(Acessar)

7
Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy
Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy
Material Type:
Artigo 		Adicionar ao Meu Espaço

Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy

Maria Rita Passos-Bueno E S Moreira; Mariz Vainzof; J Chamberlain; Suely Kazue Nagahashi Marie; L Pereira; J Akiyama; S L Roberds; K P Campbell; Mayana Zatz

Oxford v.4 , n.7 , p.1163-7, 1995 Human Molecular Genetics

Oxford 1995

Item não circula. Consulte sua biblioteca.(Acessar)

8
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?
Material Type:
Artigo 		Adicionar ao Meu Espaço

Why is the reproductive performance lower in becker (bmd) as compared to limb girdle (lgmd) muscular dystrophy male patients?

S. Eggers V. A. F Lauriano; M. A. S Melo; R. I Takata; J. Y Akiyama; Maria Rita Passos-Bueno; Valentim Gentil Filho; O Frota-Pessoa; M Zatz

New York v. 60, n. 1, p. 27-32, feb. 1995 American Journal of Medical Genetics (Neuropsychiatric Genetics)

New York 1995

Item não circula. Consulte sua biblioteca.(Acessar)

9
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?
Material Type:
Artigo 		Adicionar ao Meu Espaço

Why is the reproductive performance lower in becker (bmd) as compared to limb girdle (lgmd) muscular dystrophy male patients?

S. Eggers V. A. F Lauriano; M. A. S Melo; R. I Takata; J. Y Akiyama; Maria Rita Passos-Bueno; Valentim Gentil Filho; O Frota-Pessoa; Mayana Zatz

New York v. 60, n. 1, p. 27-32, feb. 1995 American Journal of Medical Genetics (Neuropsychiatric Genetics)

New York 1995

Item não circula. Consulte sua biblioteca.(Acessar)

10
No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers
No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers
Material Type:
Artigo 		Adicionar ao Meu Espaço

No evidence of genetic heterogeneity in brazilian facioscapulohumeral muscular dystrophy familes (fshd) with 4q markers

Maria Rita Passos-Bueno C Wijmenga; R I Takata; Suely Kazue Nagahashi Marie; M Vainzof; R C M Pavanello; J E Hewitt; E Bakker; A Carvalho; J Akiyama; R R Frants

Oxford v.2 , n.5 , p.557-62, 1993 Human Molecular Genetics

Oxford 1993

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Passos-Bueno, M
  2. Akiyama, J
  3. Vainzof, M
  4. Marie, S
  5. Zatz, M

Neste Assunto:

  1. Genética Médica
  2. Neurologia
  3. Psiquiatria

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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