Filtros : "Sadun, A" Limpar

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  • Source: Anais. Conference titles: Annual Meeting of the Association for Research in Vision and Ophthalmology. Unidade: IP

    Subjects: NEUROFTALMOLOGIA (DIAGNÓSTICO), VISÃO, EPIDEMIOLOGIA ANALÍTICA

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    • ABNT

      CHICANI, C. F et al. Asymptomatic carriers with Leber’s Hereditary optic neuropathy often demonstrate visual field defects. 2010, Anais.. Lauderdale, Florida: Association for Research in Vision and Ophthalmology, 2010. Disponível em: http://abstracts.iovs.org/cgi/content/abstract/51/5/3258?maxtoshow=&hits=10&RESULTFORMAT=&author1=Damico&andorexactfulltext=and&searchid=1&FIRSTINDEX=10&sortspec=relevance&resourcetype=HWCIT. Acesso em: 31 out. 2024.
    • APA

      Chicani, C. F., Quiros, P. A., Barboni, P., Sadun, F., Moraes, M., Ventura, D. S. F., et al. (2010). Asymptomatic carriers with Leber’s Hereditary optic neuropathy often demonstrate visual field defects. In Anais. Lauderdale, Florida: Association for Research in Vision and Ophthalmology. Recuperado de http://abstracts.iovs.org/cgi/content/abstract/51/5/3258?maxtoshow=&hits=10&RESULTFORMAT=&author1=Damico&andorexactfulltext=and&searchid=1&FIRSTINDEX=10&sortspec=relevance&resourcetype=HWCIT
    • NLM

      Chicani CF, Quiros PA, Barboni P, Sadun F, Moraes M, Ventura DSF, Berezovsky A, Carelli V, Salomao SR, Sadun A. Asymptomatic carriers with Leber’s Hereditary optic neuropathy often demonstrate visual field defects [Internet]. Anais. 2010 ;[citado 2024 out. 31 ] Available from: http://abstracts.iovs.org/cgi/content/abstract/51/5/3258?maxtoshow=&hits=10&RESULTFORMAT=&author1=Damico&andorexactfulltext=and&searchid=1&FIRSTINDEX=10&sortspec=relevance&resourcetype=HWCIT
    • Vancouver

      Chicani CF, Quiros PA, Barboni P, Sadun F, Moraes M, Ventura DSF, Berezovsky A, Carelli V, Salomao SR, Sadun A. Asymptomatic carriers with Leber’s Hereditary optic neuropathy often demonstrate visual field defects [Internet]. Anais. 2010 ;[citado 2024 out. 31 ] Available from: http://abstracts.iovs.org/cgi/content/abstract/51/5/3258?maxtoshow=&hits=10&RESULTFORMAT=&author1=Damico&andorexactfulltext=and&searchid=1&FIRSTINDEX=10&sortspec=relevance&resourcetype=HWCIT
  • Source: Anais. Conference titles: Annual Meeting of the Association for Research in Vision and Ophthalmology. Unidade: IP

    Subjects: DEFICIÊNCIA VISUAL, RETINA, NEUROFTALMOLOGIA

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    • ABNT

      COSTA, Marcelo Fernandes da et al. Contrast sensitivity to achromatic spatial drifting gratings in asymptomatic carriers of the MtDNA 11778 mutation Leber's Hereditary Optic Neuropathy (LHON). 2010, Anais.. Lauderdale, Florida: Association for Research in Vision and Ophthalmology, 2010. Disponível em: http://abstracts.iovs.org/cgi/content/abstract/51/5/997?maxtoshow=&hits=10&RESULTFORMAT=1&author1=Costa%2C+MF&andorexacttitle=and&andorexacttitleabs=and&andorexactfulltext=and&searchid=1&FIRSTINDEX=0&sortspec=relevance&fdate=2/1/2010&resourcetype=HWCIT,HWELTR. Acesso em: 31 out. 2024.
    • APA

      Costa, M. F. da, Gualtieri, M., Oliveira, A. G. F., Moreira, S. M. C. F., Sadun, F., Berezovsky, A., et al. (2010). Contrast sensitivity to achromatic spatial drifting gratings in asymptomatic carriers of the MtDNA 11778 mutation Leber's Hereditary Optic Neuropathy (LHON). In Anais. Lauderdale, Florida: Association for Research in Vision and Ophthalmology. Recuperado de http://abstracts.iovs.org/cgi/content/abstract/51/5/997?maxtoshow=&hits=10&RESULTFORMAT=1&author1=Costa%2C+MF&andorexacttitle=and&andorexacttitleabs=and&andorexactfulltext=and&searchid=1&FIRSTINDEX=0&sortspec=relevance&fdate=2/1/2010&resourcetype=HWCIT,HWELTR
    • NLM

      Costa MF da, Gualtieri M, Oliveira AGF, Moreira SMCF, Sadun F, Berezovsky A, Salomão SR, Carelli V, Sadun A, Ventura DSF. Contrast sensitivity to achromatic spatial drifting gratings in asymptomatic carriers of the MtDNA 11778 mutation Leber's Hereditary Optic Neuropathy (LHON) [Internet]. Anais. 2010 ;[citado 2024 out. 31 ] Available from: http://abstracts.iovs.org/cgi/content/abstract/51/5/997?maxtoshow=&hits=10&RESULTFORMAT=1&author1=Costa%2C+MF&andorexacttitle=and&andorexacttitleabs=and&andorexactfulltext=and&searchid=1&FIRSTINDEX=0&sortspec=relevance&fdate=2/1/2010&resourcetype=HWCIT,HWELTR
    • Vancouver

      Costa MF da, Gualtieri M, Oliveira AGF, Moreira SMCF, Sadun F, Berezovsky A, Salomão SR, Carelli V, Sadun A, Ventura DSF. Contrast sensitivity to achromatic spatial drifting gratings in asymptomatic carriers of the MtDNA 11778 mutation Leber's Hereditary Optic Neuropathy (LHON) [Internet]. Anais. 2010 ;[citado 2024 out. 31 ] Available from: http://abstracts.iovs.org/cgi/content/abstract/51/5/997?maxtoshow=&hits=10&RESULTFORMAT=1&author1=Costa%2C+MF&andorexacttitle=and&andorexacttitleabs=and&andorexactfulltext=and&searchid=1&FIRSTINDEX=0&sortspec=relevance&fdate=2/1/2010&resourcetype=HWCIT,HWELTR
  • Source: Anais. Conference titles: Internacional Colour Vision Society Symposium. Unidade: IP

    Subjects: OFTALMOLOGIA, TESTES VISUAIS, DOENÇAS HEREDITÁRIAS

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    • ABNT

      BONCI, Daniela Maria Oliveira et al. Genetic and psychophysical evaluation of P31 color vision in a large pedigree of Leber’s Hereditary Optical Neuropathy of the 11778/ND4 mtDNA mutation. 2009, Anais.. Braga, Portugal: Universidade do Ninho, 2009. Disponível em: http://labcolour.fisica.uminho.pt/icvs/files/abstract_book_icvs09.pdf. Acesso em: 31 out. 2024.
    • APA

      Bonci, D. M. O., Neitz, M., Neitz, J., Gualtieri, M., Oliveira, A. G. F., Moura, A. L. A., et al. (2009). Genetic and psychophysical evaluation of P31 color vision in a large pedigree of Leber’s Hereditary Optical Neuropathy of the 11778/ND4 mtDNA mutation. In Anais. Braga, Portugal: Universidade do Ninho. Recuperado de http://labcolour.fisica.uminho.pt/icvs/files/abstract_book_icvs09.pdf
    • NLM

      Bonci DMO, Neitz M, Neitz J, Gualtieri M, Oliveira AGF, Moura ALA, Barboni MT, Costa MF da, Salomão SR, Berezovsky A, Sadun A, Carelli V, Ventura DSF. Genetic and psychophysical evaluation of P31 color vision in a large pedigree of Leber’s Hereditary Optical Neuropathy of the 11778/ND4 mtDNA mutation [Internet]. Anais. 2009 ;[citado 2024 out. 31 ] Available from: http://labcolour.fisica.uminho.pt/icvs/files/abstract_book_icvs09.pdf
    • Vancouver

      Bonci DMO, Neitz M, Neitz J, Gualtieri M, Oliveira AGF, Moura ALA, Barboni MT, Costa MF da, Salomão SR, Berezovsky A, Sadun A, Carelli V, Ventura DSF. Genetic and psychophysical evaluation of P31 color vision in a large pedigree of Leber’s Hereditary Optical Neuropathy of the 11778/ND4 mtDNA mutation [Internet]. Anais. 2009 ;[citado 2024 out. 31 ] Available from: http://labcolour.fisica.uminho.pt/icvs/files/abstract_book_icvs09.pdf

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