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Journal Abstract Search

122 related items for PubMed ID: 8223046

  • 1. [A study of spectral electroretinograms of color vision defects due to macular diseases].
    Tian N.
    Zhonghua Yan Ke Za Zhi; 1993 May; 29(3):166-8. PubMed ID: 8223046
    [Abstract] [Full Text] [Related]

  • 2. A study of spectral electroretinogram of color vision defects due to macular diseases.
    Tian N, Wu DZ, Liang J.
    Yan Ke Xue Bao; 1994 Sep; 10(3):163-7. PubMed ID: 7744208
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  • 3. Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases.
    Nishiguchi KM, Sandberg MA, Gorji N, Berson EL, Dryja TP.
    Hum Mutat; 2005 Mar; 25(3):248-58. PubMed ID: 15712225
    [Abstract] [Full Text] [Related]

  • 4. Psychophysical flicker thresholds and ERG flicker responses in congenital and acquired vision deficiencies.
    Meyer JJ, Korol S, Gramoni R, Tupling R.
    Mod Probl Ophthalmol; 1978 Mar; 19():33-49. PubMed ID: 310055
    [Abstract] [Full Text] [Related]

  • 5. [Disorders of color vision in central serous chorio-retinopathies].
    Coscas G, Legras M.
    Arch Ophtalmol Rev Gen Ophtalmol; 1970 Mar; 30(6-7):491-6. PubMed ID: 4247459
    [No Abstract] [Full Text] [Related]

  • 6. The effect of illuminance on colour discrimination in senile macular degeneration.
    Bowman KJ.
    Mod Probl Ophthalmol; 1978 Mar; 19():71-6. PubMed ID: 364298
    [No Abstract] [Full Text] [Related]

  • 7. [Evaluation of 3 chromatic mechanisms in the acquired pathology of color vision].
    Maione M, Carta F, Barberini E, Pitino G, Scoccianti L.
    Bull Soc Ophtalmol Fr; 1975 Nov; 75(11):967-72. PubMed ID: 1084793
    [No Abstract] [Full Text] [Related]

  • 8. Color matching and Stiles-Crawford effect in central serous choroidopathy.
    Smith VC, Pokorny J, Diddie KR.
    Mod Probl Ophthalmol; 1978 Nov; 19():284-95. PubMed ID: 310046
    [Abstract] [Full Text] [Related]

  • 9. [A study on examination of color vision with pattern-visual evoked potential].
    Liu H, Guo J.
    Zhonghua Yan Ke Za Zhi; 2002 Jun; 38(6):355-9. PubMed ID: 12139813
    [Abstract] [Full Text] [Related]

  • 10. [Color vision in a family with Stargardt's disease].
    Malbrel C, Foltz A.
    Bull Soc Ophtalmol Fr; 1980 Jun; 80(8-9):675-7. PubMed ID: 6969127
    [No Abstract] [Full Text] [Related]

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  • 12. Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy.
    Tyni T, Kivelä T, Lappi M, Summanen P, Nikoskelainen E, Pihko H.
    Ophthalmology; 1998 May; 105(5):810-24. PubMed ID: 9593380
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  • 15. Blue-on-yellow perimetry in the complete type of congenital stationary night blindness.
    Terasaki H, Miyake Y, Nomura R, Horiguchi M, Suzuki S, Kondo M.
    Invest Ophthalmol Vis Sci; 1999 Oct; 40(11):2761-4. PubMed ID: 10509678
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  • 19. Colour contrast sensitivity in patients with age-related Bruch's membrane changes.
    Holz FG, Gross-Jendroska M, Eckstein A, Hogg CR, Arden GB, Bird AC.
    Ger J Ophthalmol; 1995 Nov; 4(6):336-41. PubMed ID: 8751098
    [Abstract] [Full Text] [Related]

  • 20. The early receptor potential in the human eye. III. ERP in dichromats.
    Okamoto M, Okajima O, Tanino T.
    Jpn J Ophthalmol; 1982 Nov; 26(1):23-8. PubMed ID: 6981014
    [Abstract] [Full Text] [Related]

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