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Results: 1 to 20 of 616

1.

Color discrimination in carriers of color deficiency.

Hood SM, Mollon JD, Purves L, Jordan G.

Vision Res. 2006 Sep;46(18):2894-900. Epub 2006 May 11.

PMID:
16690099
[PubMed - indexed for MEDLINE]
Free Article
2.

Sex-related differences in chromatic sensitivity.

Rodríguez-Carmona M, Sharpe LT, Harlow JA, Barbur JL.

Vis Neurosci. 2008 May-Jun;25(3):433-40. doi: 10.1017/S095252380808019X.

PMID:
18598414
[PubMed - indexed for MEDLINE]
3.

The dimensionality of color vision in carriers of anomalous trichromacy.

Jordan G, Deeb SS, Bosten JM, Mollon JD.

J Vis. 2010 Jul 1;10(8):12. doi: 10.1167/10.8.12.

PMID:
20884587
[PubMed - indexed for MEDLINE]
Free Article
4.

Male prevalence of acquired color vision defects in asymptomatic carriers of Leber's hereditary optic neuropathy.

Ventura DF, Gualtieri M, Oliveira AG, Costa MF, Quiros P, Sadun F, de Negri AM, Salomão SR, Berezovsky A, Sherman J, Sadun AA, Carelli V.

Invest Ophthalmol Vis Sci. 2007 May;48(5):2362-70.

PMID:
17460303
[PubMed - indexed for MEDLINE]
Free Article
5.

Detection of female carriers of congenital color-vision deficiencies by visual pigment gene analysis.

Oda S, Ueyama H, Tanabe S, Tanaka Y, Yamade S, Kani K.

Curr Eye Res. 2000 Oct;21(4):767-73.

PMID:
11120566
[PubMed - indexed for MEDLINE]
6.

Color discrimination in heterozygous deutan carriers.

Lang A, Good GW.

Optom Vis Sci. 2001 Aug;78(8):584-8.

PMID:
11525549
[PubMed - indexed for MEDLINE]
7.

Colour-space distortion in women who are heterozygous for colour deficiency.

Bimler D, Kirkland J.

Vision Res. 2009 Mar;49(5):536-43. doi: 10.1016/j.visres.2008.12.015. Epub 2009 Jan 22.

PMID:
19167418
[PubMed - indexed for MEDLINE]
Free Article
8.

Chromatic discrimination losses in multiple sclerosis patients with and without optic neuritis using the Cambridge Colour Test.

Moura AL, Teixeira RA, Oiwa NN, Costa MF, Feitosa-Santana C, Callegaro D, Hamer RD, Ventura DF.

Vis Neurosci. 2008 May-Jun;25(3):463-8. doi: 10.1017/S0952523808080437.

PMID:
18598419
[PubMed - indexed for MEDLINE]
9.

Color naming and categorization in inherited color vision deficiencies.

Bonnardel V.

Vis Neurosci. 2006 May-Aug;23(3-4):637-43.

PMID:
16962007
[PubMed - indexed for MEDLINE]
10.

A study of women heterozygous for colour deficiencies.

Jordan G, Mollon JD.

Vision Res. 1993 Jul;33(11):1495-508.

PMID:
8351822
[PubMed - indexed for MEDLINE]
11.

Chromaticity discrimination in protan and deutan heterozygotes.

Verriest G.

Mod Probl Ophthalmol. 1974;13(0):262-4. No abstract available.

PMID:
4548142
[PubMed - indexed for MEDLINE]
12.

Color vision in two observers with highly biased LWS/MWS cone ratios.

Miyahara E, Pokorny J, Smith VC, Baron R, Baron E.

Vision Res. 1998 Feb;38(4):601-12.

PMID:
9536382
[PubMed - indexed for MEDLINE]
Free Article
13.

Relating color discrimination to photopigment genes in deutan observers.

Shevell SK, He JC, Kainz P, Neitz J, Neitz M.

Vision Res. 1998 Nov;38(21):3371-6.

PMID:
9893851
[PubMed - indexed for MEDLINE]
Free Article
14.

Diagnosing protan heterozygosity using the Medmont C-100 colour vision test.

Harris RW, Cole BL.

Clin Exp Optom. 2005 Jul;88(4):240-7.

PMID:
16083418
[PubMed - indexed for MEDLINE]
15.

Normality of colour vision in a compound heterozygous female carrying protan and deutan defects.

Tait DM, Carroll J.

Clin Exp Optom. 2009 Jul;92(4):356-61. doi: 10.1111/j.1444-0938.2009.00359.x. Epub 2009 Mar 17.

PMID:
19473349
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Rayleigh matches in carriers of inherited color vision defects: the contribution from the third L/M photopigment.

Sun Y, Shevell SK.

Vis Neurosci. 2008 May-Jun;25(3):455-62. doi: 10.1017/S0952523808080346.

PMID:
18598418
[PubMed - indexed for MEDLINE]
17.

[Individual variations in color vision and its molecular biology].

Kitahara K.

Nihon Ganka Gakkai Zasshi. 1998 Dec;102(12):837-49. Japanese.

PMID:
10025115
[PubMed - indexed for MEDLINE]
18.

Color vision in the tritan axis is predominantly affected at high altitude.

Tekavcic-Pompe M, Tekavcic I.

High Alt Med Biol. 2008 Spring;9(1):38-42. doi: 10.1089/ham.2008.1034.

PMID:
18331219
[PubMed - indexed for MEDLINE]
19.

Electroretinograms in carriers of blue cone monochromatism.

Berson EL, Sandberg MA, Maguire A, Bromley WC, Roderick TH.

Am J Ophthalmol. 1986 Aug 15;102(2):254-61.

PMID:
3488684
[PubMed - indexed for MEDLINE]
20.

Silent substitution tests like the OSCAR and the Medmont C100 can identify protan and deutan carriers of abnormal colour vision.

Robbins HG.

Clin Exp Optom. 2005 Nov;88(6):426-7. No abstract available.

PMID:
16329753
[PubMed - indexed for MEDLINE]
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