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1
Analysis of contrast processing segregated into magnocellular and parvocellular system in unaffected carriers of 11778 LHON
Analysis of contrast processing segregated into magnocellular and parvocellular system in unaffected carriers of 11778 LHON
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Analysis of contrast processing segregated into magnocellular and parvocellular system in unaffected carriers of 11778 LHON

Mirella Gualtieri Marcelo Fernandes da Costa; A. G. F Oliveira; F Sadun; A. M De Negri; A Berezovsky; S. R Salomão; V Carelli; A. A Sadun; Dora Selma Fix Ventura; Annual Meeting Abstracts (2007 Rockville)

Rockville n. 48, p. E-Abstract 942-B917, 2007 Investigative Ophthalmology Visual Science

Rockville Association for Research in Vision and Ophthalmology 2007

Localização: IP - Instituto de Psicologia    ((AM=CMar/18) ) e outros locais(Acessar)

2
Psychophysical analysis of contrast processing segregated into magnocellular and parvocellular systems in asymptomatic carriers of 11778 Leber's hereditary optic neuropathy
Psychophysical analysis of contrast processing segregated into magnocellular and parvocellular systems in asymptomatic carriers of 11778 Leber's hereditary optic neuropathy
Material Type:
Artigo 		Adicionar ao Meu Espaço

Psychophysical analysis of contrast processing segregated into magnocellular and parvocellular systems in asymptomatic carriers of 11778 Leber's hereditary optic neuropathy

Mirella Gualtieri M Bandeira; R. D Hamer; Marcelo Fernandes da Costa; A. G. F Oliveira; A. L. A Moura; F Sadun; A. M De Negri; A Berezovsky; S. R Salomão; V Carelli; A. A Sadun; Dora Selma Fix Ventura

Visual Neuroscience New York v. 25, n. 3, p. 469-474, 2008

New York 2008

Acesso online. A biblioteca também possui exemplares impressos.

3
Psychophysical analysis of contrast processing segregated into magnocellular and parvocellular systems in asymptomatic carriers of 11778 Leber's hereditary optic neuropathy
Psychophysical analysis of contrast processing segregated into magnocellular and parvocellular systems in asymptomatic carriers of 11778 Leber's hereditary optic neuropathy
Material Type:
Artigo 		Adicionar ao Meu Espaço

Psychophysical analysis of contrast processing segregated into magnocellular and parvocellular systems in asymptomatic carriers of 11778 Leber's hereditary optic neuropathy

Mirella Gualtieri M Bandeira; R. D Hamer; Marcelo Fernandes da Costa; A. G. F Oliveira; A. L. A Moura; F Sadun; A. M De Negri; A Berezovsky; S. R Salomão; V Carelli; A. A Sadun; Dora Selma Fix Ventura

Visual Neuroscience New York v. 25, n. 3, p. 469-474, 2008

New York 2008

Acesso online. A biblioteca também possui exemplares impressos.

4
Genetic and psychophysical evaluation of P31 color vision in a large pedigree of Leber’s Hereditary Optical Neuropathy of the 11778/ND4 mtDNA mutation
Genetic and psychophysical evaluation of P31 color vision in a large pedigree of Leber’s Hereditary Optical Neuropathy of the 11778/ND4 mtDNA mutation
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Genetic and psychophysical evaluation of P31 color vision in a large pedigree of Leber’s Hereditary Optical Neuropathy of the 11778/ND4 mtDNA mutation

Daniela Maria Oliveira Bonci M Neitz; J Neitz; Mirella Gualtieri; A. G. F Oliveira; A. L. A Moura; M. T Barboni; Marcelo Fernandes da Costa; S. R Salomão; A Berezovsky; A Sadun; V Carelli; Dora Selma Fix Ventura; Internacional Colour Vision Society Symposium (20. 2009 Braga, Portugal)

Braga, Portugal: Universidade do Ninho, 2009 Anais

Braga, Portugal Universidade do Ninho 2009

Acesso online. A biblioteca também possui exemplares impressos.

5
Genetic and psychophysical evaluation of P31 color vision in a large pedigree of Leber’s Hereditary Optical Neuropathy of the 11778/ND4 mtDNA mutation
Genetic and psychophysical evaluation of P31 color vision in a large pedigree of Leber’s Hereditary Optical Neuropathy of the 11778/ND4 mtDNA mutation
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Genetic and psychophysical evaluation of P31 color vision in a large pedigree of Leber’s Hereditary Optical Neuropathy of the 11778/ND4 mtDNA mutation

D. M. O Bonci M Neitz; J Neitz; Mirella Gualtieri; A. G. F Oliveira; A. L. A Moura; M. T Barboni; Marcelo Fernandes da Costa; S. R Salomão; A Berezovsky; A Sadun; V Carelli; Dora Selma Fix Ventura; Internacional Colour Vision Society Symposium (20. 2009 Braga, Portugal)

Braga, Portugal: Universidade do Ninho, 2009 Anais

Braga, Portugal Universidade do Ninho 2009

Acesso online. A biblioteca também possui exemplares impressos.

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Deste Autor:

  1. Carelli, V
  2. Costa, M
  3. Gualtieri, M
  4. Oliveira, A
  5. Berezovsky, A

Neste Assunto:

  1. Oftalmopatias
  2. Testes Visuais
  3. Acuidade Visual
  4. Eletrofisiologia
  5. Oftalmologia

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

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