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Refinado por: Nome da Publicação: Journal of the Neurological Sciences remover
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1
Partial telethonin deficiency in severely affected north american LGMD patients
Partial telethonin deficiency in severely affected north american LGMD patients
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Partial telethonin deficiency in severely affected north american LGMD patients

Ronnie Houston David Muirhead; Nora Elmonoufy; Reuel Cornelia; Georgine Faulkner; Giorgio Valle; Mayana Zatz; Mariz Vainzof; Susan Iannaccone; International Congress on Neuromuscular Diseases (10. 2002 Vancouver)

Abstracts Journal of the Neurological Sciences Amsterdam v. 199, supl., p. S58, 2002

Amsterdam 2002

Item não circula. Consulte sua biblioteca.(Acessar)

2
Looking for one more autosomal recessive limb girdle muscular dystrophy gene
Looking for one more autosomal recessive limb girdle muscular dystrophy gene
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Looking for one more autosomal recessive limb girdle muscular dystrophy gene

A. Starling Mariz Vainzof; Marta Canovas; Rita de Cássia M Pavanello; Maria Rita Passos-Bueno; Mayana Zatz; International Congress on Neuromuscular Diseases (10. 2002 Vancouver)

Abstracts Journal of the Neurological Sciences Amsterdam v. 199, supl., p. S57, 2002

Amsterdam 2002

Item não circula. Consulte sua biblioteca.(Acessar)

3
Sarcomeric myopalladin study in limb girdle muscular dystrophies
Sarcomeric myopalladin study in limb girdle muscular dystrophies
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Sarcomeric myopalladin study in limb girdle muscular dystrophies

Mariz Vainzof Marta Canovas; Siegfried Labeit; Marie Louise Bang; Georgine Faulkner; G Valle; Mayana Zatz; International Congress on Neuromuscular Diseases (10. 2002 Vancouver)

Abstracts Journal of the Neurological Sciences Amsterdam v. 199, supl., p. S33, 2002

Amsterdam 2002

Item não circula. Consulte sua biblioteca.(Acessar)

4
Clinical variability in calpainopathy what makes the difference?
Clinical variability in calpainopathy what makes the difference?
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Clinical variability in calpainopathy what makes the difference?

F de Paula Mariz Vainzof; Edson Dias Moreira; Maria Rita Passos-Bueno; Rita de Cássia M Pavanello; Sérgio Russo Matioli; Vicenzo Nigro; Mayana Zatz; International Congress on Neuromuscular Diseases (10. 2002 Vancouver)

Abstracts Journal of the Neurological Sciences Amsterdam v. 199, supl., p. S57, 2002

Amsterdam 2002

Item não circula. Consulte sua biblioteca.(Acessar)

5
Is dystrophin always altered in becker muscular dystrophy patients?
Is dystrophin always altered in becker muscular dystrophy patients?
Material Type:
Artigo 		Adicionar ao Meu Espaço

Is dystrophin always altered in becker muscular dystrophy patients?

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

Amsterdam v.131, p.99-104, 1995 Journal of the Neurological Sciences

Amsterdam 1995

Item não circula. Consulte sua biblioteca.(Acessar)

6
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

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)

7
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
Material Type:
Artigo 		Adicionar ao Meu Espaço

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)

8
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
Material Type:
Artigo 		Adicionar ao Meu Espaço

Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the brazilian population

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

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

Estados Unidos 1999

Localização: FM - Fac. Medicina    (BCSEP 253 1999 )(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

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)

10
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)

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Deste Autor:

  1. Vainzof, M
  2. Zatz, M
  3. Passos-Bueno, M
  4. Pavanello, R
  5. Marie, S

Neste Assunto:

  1. Genética Médica
  2. Distrofia Muscular
  3. Neurologia
  4. Mutação Genética
  5. Doenças Neuromusculares

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

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