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Trabalho de evento-resumo
Asymptomatic carriers with Leber’s Hereditary optic neuropathy often demonstrate visual field defects (2010)
Chicani, C. F; Quiros, P. A; Barboni, P; Sadun, F; Moraes, M; Ventura, Dora Selma Fix ; Berezovsky, A; Carelli, V; Salomao, S. R; Sadun, A
Source: Anais. Conference titles: Annual Meeting of the Association for Research in Vision and Ophthalmology. Unidade: IP
Subjects: NEUROFTALMOLOGIA (DIAGNÓSTICO), VISÃO, EPIDEMIOLOGIA ANALÍTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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
Trabalho de evento-resumo
Contrast sensitivity to achromatic spatial drifting gratings in asymptomatic carriers of the MtDNA 11778 mutation Leber's Hereditary Optic Neuropathy (LHON) (2010)
Costa, Marcelo Fernandes da ; Gualtieri, Mirella ; Oliveira, A. G. F; Moreira, S. M. C. F; Sadun, F; Berezovsky, A; Salomão, S. R; Carelli, V; Sadun, A; Ventura, Dora Selma Fix
Source: Anais. Conference titles: Annual Meeting of the Association for Research in Vision and Ophthalmology. Unidade: IP
Subjects: DEFICIÊNCIA VISUAL, RETINA, NEUROFTALMOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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
Trabalho de evento-resumo
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)
Bonci, Daniela Maria Oliveira ; Neitz, M; Neitz, J; Gualtieri, Mirella ; Oliveira, A. G. F; Moura, A. L. A; Barboni, M. T; Costa, Marcelo Fernandes da ; Salomão, S. R; Berezovsky, A; Sadun, A; Carelli, V; Ventura, Dora Selma Fix
Source: Anais. Conference titles: Internacional Colour Vision Society Symposium. Unidade: IP
Subjects: OFTALMOLOGIA, TESTES VISUAIS, DOENÇAS HEREDITÁRIAS
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: 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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