skip to main content
Language:
Results 1 2 3 4 5 next page
Refined by: creation date: 2001To2008 remove
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Achados histológicos em biópsia muscular de eqüino com alterações neuromusculares
Achados histológicos em biópsia muscular de eqüino com alterações neuromusculares
Material Type:
Conference Paper 		Add to e-Shelf

Achados histológicos em biópsia muscular de eqüino com alterações neuromusculares

Luciana Luchesi Quintanilha Fogaça L. G Miyazato; H. C. A Silva; F. H. F D'Angeles; J. E. R Moraes; Jose Correa Lacerda Neto; Mariz Vainzof; Congresso Brasileiro de Genética (49. 2003 Águas de Lindóia, SP)

Resumo Águas de Lindóia, 2003

Águas de Lindóia 2003

Check holdings(GetIt)

2
Análise multiplex de mutações nos genes das proteínas sarcoglicanas
Análise multiplex de mutações nos genes das proteínas sarcoglicanas
Material Type:
Conference Paper 		Add to e-Shelf

Análise multiplex de mutações nos genes das proteínas sarcoglicanas

T. L. F. Gouveia E. S Moreira; Maria Rita Passos-Bueno; Mayana Zatz; Mariz Vainzof; Congresso Nacional de Genética (47. 2001 Águas de Lindóia, SP)

A genética no século XXI: desafios Águas de Lindóia, 2001

Águas de Lindóia Sociedade Brasileira de Genética 2001

Check holdings(GetIt)

3
Animal models for genetic neuromuscular diseases
Animal models for genetic neuromuscular diseases
Material Type:
Article 		Add to e-Shelf

Animal models for genetic neuromuscular diseases

Mariz Vainzof Danielle Ayub-Guerrieri; Paula C. G Onofre; Poliana C. M Martins; Vanessa F Lopes; Dinorah Zilberztajn; Lucas S Maia; Karen Sell; Lydia U Yamamoto

Journal of Molecular Neuroscience Totowa v. 34, n. 3, p. 241-248, Mar. 2008

Totowa 2008

Check holdings(GetIt)

4
Asymptomatic carriers for homozygous novel mutations in the FKRP gene the other end of the spectrum
Asymptomatic carriers for homozygous novel mutations in the FKRP gene the other end of the spectrum
Material Type:
Article 		Add to e-Shelf

Asymptomatic carriers for homozygous novel mutations in the FKRP gene the other end of the spectrum

Flavia de Paula Natassia Vieira; Alessandra Starling; Lydia Uraco Yamamoto; Bruno Lima; Rita de Cássia Pavanello; Mariz Vainzof; Vincenzo Nigro; Mayana Zatz

European Journal of Human Genetics London v. 11, p. 923-930, 2003

London 2003

Check holdings(GetIt)

5
Aplicação de RMN no estudo da distrofia muscular mdx em camundongos
Aplicação de RMN no estudo da distrofia muscular mdx em camundongos
Material Type:
Conference Paper 		Add to e-Shelf

Aplicação de RMN no estudo da distrofia muscular mdx em camundongos

Aurea Beatriz Martins Antonio Carlos Bloise Junior; S. R Rabbani (Said Rahnamaye); Mariz Vainzof; Encontro Nacional de Física da Matéria Condensada (30. 2007 São Lourenço)

São Paulo : SBF, 2007

São Paulo SBF 2007

Online access

6
Calpain-3 mutations in atypical limb-girdle muscular dystrophy patients
Calpain-3 mutations in atypical limb-girdle muscular dystrophy patients
Material Type:
Conference Paper 		Add to e-Shelf

Calpain-3 mutations in atypical limb-girdle muscular dystrophy patients

F de Paula H. A. C Silva; C Esteves; T Jazedje; A Starling; Rita de Cássia M Pavanello; Mariz Vainzof; Mayana Zatz; International Congress of the World Muscle Society (8. 2003 Szeged)

Neuromuscular Disorders Oxford v. 13, n. 7-8, p. 648, 2003

Oxford 2003

Check holdings(GetIt)

7
Calpainopathy how broad is the spectrum of clinical variability?
Calpainopathy how broad is the spectrum of clinical variability?
Material Type:
Article 		Add to e-Shelf

Calpainopathy how broad is the spectrum of clinical variability?

Alessandra Starling Flavia de Paula; Helga Cristina Almeida da Silva; Mariz Vainzof; Mayana Zatz

Journal of Molecular Neuroscience v. 21, n. 3, p. 233-236, 2003

Totowa, N.J. 2003

Check holdings(GetIt)

8
Calpainopathy how broad is the spectrum of clinical variability?
Calpainopathy how broad is the spectrum of clinical variability?
Material Type:
Article 		Add to e-Shelf

Calpainopathy how broad is the spectrum of clinical variability?

Alessandra Starling Flavia de Paula; Helga Cristina Almeida da Silva; Mariz Vainzof; Mayana Zatz

Journal of Molecular Neuroscience v. 21, n. 3, p. 233-236, 2003

Totowa, N.J. 2003

Check holdings(GetIt)

9
Calpainopatia surpresas nos estudos de correlação genótipo: fenótipo
Calpainopatia surpresas nos estudos de correlação genótipo: fenótipo
Material Type:
Conference Paper 		Add to e-Shelf

Calpainopatia surpresas nos estudos de correlação genótipo: fenótipo

Flavia de Paula Cyntia E Lima; Helga da Silva; Mariz Vainzof; Mayana Zatz; Congresso Brasileiro de Genética (49. 2003 Águas de Lindóia, SP)

Resumo Águas de Lindóia, 2003

Águas de Lindóia 2003

Check holdings(GetIt)

10
Central core disease due to recessive mutations in RYR1 gene is it more common than described?
Central core disease due to recessive mutations in RYR1 gene is it more common than described?
Material Type:
Article 		Add to e-Shelf

Central core disease due to recessive mutations in RYR1 gene is it more common than described?

Patricia Mayumi Kossugue Julia F Paim; Monica M Navarro; Helga Cristina Almeida da Silva; Rita de Cássia M Pavanello; Juliana Gurgel-Giannetti; Mayana Zatz; Mariz Vainzof

Muscle & Nerve v. 35, n. 5, p. 670-674, 2007

Hoboken 2007

Check holdings(GetIt)

Results 1 2 3 4 5 next page

Personalize your results

  1. Edit

Refine Search Results

Refine My Results

Resource Type 

  1. Articles  (119)
  2. Academic Productions  (7)
  3. Books  (4)
  4. Text Resources  (2)
  5. More options open sub menu

Creation Date 

From To
Refine
  1. Before2002  (22)
  2. 2002To2002  (24)
  3. 2003To2003  (31)
  4. 2004To2005  (17)
  5. After 2005  (38)
  6. More options open sub menu

Language 

  1. English  (86)
  2. Portuguese  (46)
  3. More options open sub menu

Suggested New Searches

Ignore my query and look for everything

by this author/creator:

  1. Vainzof, M
  2. Zatz, M
  3. Pavanello, R
  4. Paula, F
  5. Passos-Bueno, M

on this subject:

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

  • Implemented by: ABCD-USP USP   Social Network Logos: Freepik

Searching Remote Databases, Please Wait