Filtros : "Neitz, M" Limpar

Filtros



Refine with date range


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

    Subjects: DIABETES MELLITUS, RETINA, GENÉTICA

    Acesso à fonteHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      BONCI, Daniela Maria Oliveira et al. Color vision and spatial contrast sensitivity in patients with the risk allele for Diabetes proliferative retinopathy: preliminary data. 2010, Anais.. Lauderdale, Florida: Association for Research in Vision and Ophthalmology, 2010. Disponível em: http://abstracts.iovs.org/cgi/content/abstract/51/5/120?maxtoshow=&hits=10&RESULTFORMAT=1&author1=Bonci&andorexacttitle=and&andorexacttitleabs=and&andorexactfulltext=and&searchid=1&FIRSTINDEX=0&sortspec=relevance&resourcetype=HWCIT,HWELTR. Acesso em: 08 maio 2024.
    • APA

      Bonci, D. M. O., Gualtieri, M., Neitz, M., Neitz, J., Moura, A. L. A., Damico, F. M., & Ventura, D. S. F. (2010). Color vision and spatial contrast sensitivity in patients with the risk allele for Diabetes proliferative retinopathy: preliminary data. In Anais. Lauderdale, Florida: Association for Research in Vision and Ophthalmology. Recuperado de http://abstracts.iovs.org/cgi/content/abstract/51/5/120?maxtoshow=&hits=10&RESULTFORMAT=1&author1=Bonci&andorexacttitle=and&andorexacttitleabs=and&andorexactfulltext=and&searchid=1&FIRSTINDEX=0&sortspec=relevance&resourcetype=HWCIT,HWELTR
    • NLM

      Bonci DMO, Gualtieri M, Neitz M, Neitz J, Moura ALA, Damico FM, Ventura DSF. Color vision and spatial contrast sensitivity in patients with the risk allele for Diabetes proliferative retinopathy: preliminary data [Internet]. Anais. 2010 ;[citado 2024 maio 08 ] Available from: http://abstracts.iovs.org/cgi/content/abstract/51/5/120?maxtoshow=&hits=10&RESULTFORMAT=1&author1=Bonci&andorexacttitle=and&andorexacttitleabs=and&andorexactfulltext=and&searchid=1&FIRSTINDEX=0&sortspec=relevance&resourcetype=HWCIT,HWELTR
    • Vancouver

      Bonci DMO, Gualtieri M, Neitz M, Neitz J, Moura ALA, Damico FM, Ventura DSF. Color vision and spatial contrast sensitivity in patients with the risk allele for Diabetes proliferative retinopathy: preliminary data [Internet]. Anais. 2010 ;[citado 2024 maio 08 ] Available from: http://abstracts.iovs.org/cgi/content/abstract/51/5/120?maxtoshow=&hits=10&RESULTFORMAT=1&author1=Bonci&andorexacttitle=and&andorexacttitleabs=and&andorexactfulltext=and&searchid=1&FIRSTINDEX=0&sortspec=relevance&resourcetype=HWCIT,HWELTR
  • Source: Anais. Conference titles: Internacional Colour Vision Society Symposium. Unidade: IP

    Subjects: OFTALMOLOGIA, DIABETES MELLITUS, VISÃO

    Acesso à fonteHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      GUALTIERI, Mirella et al. Association between color vision ACV8 loss and risk genotype for vascular proliferation in type 2 diabetics. 2009, Anais.. Braga, Portugal: Universidade do Ninho, 2009. Disponível em: http://labcolour.fisica.uminho.pt/icvs/files/abstract_book_icvs09.pdf. Acesso em: 08 maio 2024.
    • APA

      Gualtieri, M., Bonci, D. M. O., Neitz, M., Neitz, J., Moura, A. L. A., Damico, F. M., & Ventura, D. S. F. (2009). Association between color vision ACV8 loss and risk genotype for vascular proliferation in type 2 diabetics. In Anais. Braga, Portugal: Universidade do Ninho. Recuperado de http://labcolour.fisica.uminho.pt/icvs/files/abstract_book_icvs09.pdf
    • NLM

      Gualtieri M, Bonci DMO, Neitz M, Neitz J, Moura ALA, Damico FM, Ventura DSF. Association between color vision ACV8 loss and risk genotype for vascular proliferation in type 2 diabetics [Internet]. Anais. 2009 ;[citado 2024 maio 08 ] Available from: http://labcolour.fisica.uminho.pt/icvs/files/abstract_book_icvs09.pdf
    • Vancouver

      Gualtieri M, Bonci DMO, Neitz M, Neitz J, Moura ALA, Damico FM, Ventura DSF. Association between color vision ACV8 loss and risk genotype for vascular proliferation in type 2 diabetics [Internet]. Anais. 2009 ;[citado 2024 maio 08 ] Available from: http://labcolour.fisica.uminho.pt/icvs/files/abstract_book_icvs09.pdf
  • Source: Reduce Disparites in eye disease and treatment. Conference titles: Meeting of the Association for Research in Vision and Ophthalmology (ARVO). Unidade: IP

    Subjects: NEUROFTALMOLOGIA, VISÃO, GENÉTICA, DEFICIÊNCIA VISUAL

    Acesso à fonteHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      BONCI, Daniela Maria Oliveira et al. Genetic analysis of color vision defects in Duchenne Muscular Dystrophy and leber's hereditary optic neuropathy. 2009, Anais.. Fort Lauderdale: ARVO - Association for Researg in Vision and Ophthalmology, 2009. p. A609. Disponível em: http://arvo.abstractsonline.com/Plan/ViewAbstract.aspx?mID=2281&sKey=152d5fda-4593-4605-825a-7220562ee371&cKey=651b1a79-cbb3-43c3-a977-8fcac4347725. Acesso em: 08 maio 2024.
    • APA

      Bonci, D. M. O., Ventura, D. S. F., Salomão, S. R., Berezovsky, A., Sadun, A. A., Zatz, M., et al. (2009). Genetic analysis of color vision defects in Duchenne Muscular Dystrophy and leber's hereditary optic neuropathy. In Reduce Disparites in eye disease and treatment (p. A609). Fort Lauderdale: ARVO - Association for Researg in Vision and Ophthalmology. Recuperado de http://arvo.abstractsonline.com/Plan/ViewAbstract.aspx?mID=2281&sKey=152d5fda-4593-4605-825a-7220562ee371&cKey=651b1a79-cbb3-43c3-a977-8fcac4347725
    • NLM

      Bonci DMO, Ventura DSF, Salomão SR, Berezovsky A, Sadun AA, Zatz M, Costa MF da, CArelli V, Neitz J, Neitz M. Genetic analysis of color vision defects in Duchenne Muscular Dystrophy and leber's hereditary optic neuropathy [Internet]. Reduce Disparites in eye disease and treatment. 2009 ;( 50): A609.[citado 2024 maio 08 ] Available from: http://arvo.abstractsonline.com/Plan/ViewAbstract.aspx?mID=2281&sKey=152d5fda-4593-4605-825a-7220562ee371&cKey=651b1a79-cbb3-43c3-a977-8fcac4347725
    • Vancouver

      Bonci DMO, Ventura DSF, Salomão SR, Berezovsky A, Sadun AA, Zatz M, Costa MF da, CArelli V, Neitz J, Neitz M. Genetic analysis of color vision defects in Duchenne Muscular Dystrophy and leber's hereditary optic neuropathy [Internet]. Reduce Disparites in eye disease and treatment. 2009 ;( 50): A609.[citado 2024 maio 08 ] Available from: http://arvo.abstractsonline.com/Plan/ViewAbstract.aspx?mID=2281&sKey=152d5fda-4593-4605-825a-7220562ee371&cKey=651b1a79-cbb3-43c3-a977-8fcac4347725
  • Source: Reduce Disparites in eye disease and treatment. Conference titles: Meeting of the Association for Research in Vision and Ophthalmology (ARVO). Unidade: IP

    Subjects: DIABETES MELLITUS, VISÃO, FÁRMACOS, PERCEPÇÃO DE COR

    Acesso à fonteHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      GUALTIERI, Mirella et al. Color vision is worse in the diabetics with risk genotype for retinopathy as shown by erythropoietin expression markers: preliminary data. 2009, Anais.. Fort Lauderdale: ARVO - Association for Researg in Vision and Ophthalmology, 2009. p. A608. Disponível em: http://arvo.abstractsonline.com/Plan/ViewAbstract.aspx?mID=2281&sKey=152d5fda-4593-4605-825a-7220562ee371&cKey=f8cea986-d718-4ab7-b64e-a349d88c8cf3. Acesso em: 08 maio 2024.
    • APA

      Gualtieri, M., Bonci, D. M. O., Neitz, M., Moura, A. L. A., Damico, F. M., & Ventura, D. S. F. (2009). Color vision is worse in the diabetics with risk genotype for retinopathy as shown by erythropoietin expression markers: preliminary data. In Reduce Disparites in eye disease and treatment (p. A608). Fort Lauderdale: ARVO - Association for Researg in Vision and Ophthalmology. Recuperado de http://arvo.abstractsonline.com/Plan/ViewAbstract.aspx?mID=2281&sKey=152d5fda-4593-4605-825a-7220562ee371&cKey=f8cea986-d718-4ab7-b64e-a349d88c8cf3
    • NLM

      Gualtieri M, Bonci DMO, Neitz M, Moura ALA, Damico FM, Ventura DSF. Color vision is worse in the diabetics with risk genotype for retinopathy as shown by erythropoietin expression markers: preliminary data [Internet]. Reduce Disparites in eye disease and treatment. 2009 ;( 50): A608.[citado 2024 maio 08 ] Available from: http://arvo.abstractsonline.com/Plan/ViewAbstract.aspx?mID=2281&sKey=152d5fda-4593-4605-825a-7220562ee371&cKey=f8cea986-d718-4ab7-b64e-a349d88c8cf3
    • Vancouver

      Gualtieri M, Bonci DMO, Neitz M, Moura ALA, Damico FM, Ventura DSF. Color vision is worse in the diabetics with risk genotype for retinopathy as shown by erythropoietin expression markers: preliminary data [Internet]. Reduce Disparites in eye disease and treatment. 2009 ;( 50): A608.[citado 2024 maio 08 ] Available from: http://arvo.abstractsonline.com/Plan/ViewAbstract.aspx?mID=2281&sKey=152d5fda-4593-4605-825a-7220562ee371&cKey=f8cea986-d718-4ab7-b64e-a349d88c8cf3
  • Source: Anais. Conference titles: Internacional Colour Vision Society Symposium. Unidade: IP

    Subjects: OFTALMOLOGIA, TESTES VISUAIS, DOENÇAS HEREDITÁRIAS

    Acesso à fonteHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • 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: 08 maio 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 maio 08 ] 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 maio 08 ] Available from: http://labcolour.fisica.uminho.pt/icvs/files/abstract_book_icvs09.pdf

Digital Library of Intellectual Production of Universidade de São Paulo     2012 - 2024