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Refinado por: Nome da Publicação: Journal of the Neurological Sciences remover
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1
Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population
Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population
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Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population

Mariz Vainzof Maria Rita Passos-Bueno; Rita de Cássia M Pavanello; Suely Kazue Nagahashi Marie; Acary B. S Oliveira; Mayana Zatz

Journal of the Neurological Sciences v. 164, p. 44-49, 1999

Amsterdam 1999

Item não circula. Consulte sua biblioteca.(Acessar)

2
Absence of calpain 3 in a form of limb-girdle muscular dystrophy (lgmd2a)
Absence of calpain 3 in a form of limb-girdle muscular dystrophy (lgmd2a)
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Absence of calpain 3 in a form of limb-girdle muscular dystrophy (lgmd2a)

M J Spencer J G Tidball; L V B Anderson; K M D Bushby; J B Harris; Maria Rita Passos-Bueno; H Somer; Mariz Vainzof; Mayana Zatz

Amsterdam v.146, p.173-8, 1997 Journal of the Neurological Sciences

Amsterdam 1997

Item não circula. Consulte sua biblioteca.(Acessar)

3
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

Mariz Vainzof R C M Pavanello; I Pavanello Filho; Maria Rita Passos-Bueno; D Rapaport; C T Hsi; Mayana Zatz

Amsterdam v.98, p.221-33, 1990 Journal of the Neurological Sciences

Amsterdam 1990

Item não circula. Consulte sua biblioteca.(Acessar)

4
Immunofluorescence dystrophin study in duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and amino-terminal region of the protein
Immunofluorescence dystrophin study in duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and amino-terminal region of the protein
Material Type:
Artigo 		Adicionar ao Meu Espaço

Immunofluorescence dystrophin study in duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and amino-terminal region of the protein

Mariz Vainzof E E Zubrzycka-Gaarn; D Rapaport; Maria Rita Passos-Bueno; R C M Pavanello; I Pavanello Filho; Mayana Zatz

Amsterdam v.101, p.141-7, 1991 Journal of the Neurological Sciences

Amsterdam 1991

Item não circula. Consulte sua biblioteca.(Acessar)

5
Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27
Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27
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Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy ( fsh ) at 6q23-q27

Maria Rita Passos-Bueno B Byth; D Love; J Terwilliger; J Ott; D Rapaport; Mariz Vainzof; Mayana Zatz; K E Davies

Amsterdam v.102, p.206-8, 1991 Journal of the Neurological Sciences

Amsterdam 1991

Item não circula. Consulte sua biblioteca.(Acessar)

6
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

Maria Rita Passos-Bueno Mariz Vainzof; R C M Pavanello; I Pavanello Filho; M A B O Lima; Mayana Zatz

Amsterdam v.103, p.65-75, 1991 Journal of the Neurological Sciences

Amsterdam 1991

Item não circula. Consulte sua biblioteca.(Acessar)

7
Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype
Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype
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Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype

Mariz Vainzof Maria Rita Passos-Bueno; R I Takata; R C M Pavanello; Mayana Zatz

Amsterdam v.119, p.38-42, 1993 Journal of the Neurological Sciences

Amsterdam 1993

Item não circula. Consulte sua biblioteca.(Acessar)

8
Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy
Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy
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Assessment of the 50-kda dystrophin-associated glycoprotein in brazilian patients with severe childhood autosomal recessive muscular dystrophy

Mayana Zatz K Matsumura; Mariz Vainzof; Maria Rita Passos-Bueno; R C M Pavanello; Suely Kazue Nagahashi Marie; K P Campbell

Amsterdam v.123, p.122-8, 1994 Journal of the Neurological Sciences

Amsterdam 1994

Item não circula. Consulte sua biblioteca.(Acessar)

9
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
Material Type:
Artigo 		Adicionar ao Meu Espaço

Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy a brazilian study

M Vainzof R C M Pavanello; I Pavanello Filho; Maria Rita Passos-Bueno; D Rapaport; C T Hsi; M Zatz

Amsterdam v.98, p.221-33, 1990 Journal of the Neurological Sciences

Amsterdam 1990

Item não circula. Consulte sua biblioteca.(Acessar)

10
Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype
Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype
Material Type:
Artigo 		Adicionar ao Meu Espaço

Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype

M Vainzof Maria Rita Passos-Bueno; R I Takata; R C M Pavanello; M Zatz

Amsterdam v.119, p.38-42, 1993 Journal of the Neurological Sciences

Amsterdam 1993

Item não circula. Consulte sua biblioteca.(Acessar)

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Autor/Criador 

  1. Pavanello, R  (14)
  2. Pavanello Filho, I  (6)
  3. Rapaport, D  (6)
  4. Marie, S  (4)
  5. Zubrzycka-Gaarn, E  (2)
  6. Tidball, J  (2)
  7. Campbell, K  (2)
  8. Byth, B  (2)
  9. Anderson, L  (2)
  10. Love, D  (2)
  11. Somer, H  (2)
  12. Oliveira, A  (2)
  13. Hsi, C  (2)
  14. Davies, K  (2)
  15. Bushby, K  (2)
  16. Takata, R  (2)
  17. Matsumura, K  (2)
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Deste Autor:

  1. Vainzof, M
  2. Passos-Bueno, M
  3. Zatz, M
  4. Pavanello, R
  5. Pavanello Filho, I

Neste Assunto:

  1. Genética Médica
  2. Neurologia

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

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