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Items: 1 to 20 of 241

1.
Prevalence and Determinants of Color Vision Defects among Preparatory University Students at Makkah, Saudi Arabia
Osama Abdulqadir Khairoalsindi, Bayan Mutlaq Almasoudi, Ashjan Yousef Bamahfouz, Abdullah Atiah Alghamdi, Muhammad Irfanullah Siddiqui
Middle East Afr J Ophthalmol. 2019 Jul-Sep; 26(3): 133–137. Published online 2019 Sep 30. doi: 10.4103/meajo.MEAJO_29_19
PMCID:
PMC6788315
AbstractArticle
2.
Genotype-phenotype relationships in human red/green color-vision defects: molecular and psychophysical studies.
S S Deeb, D T Lindsey, Y Hibiya, E Sanocki, J Winderickx, D Y Teller, A G Motulsky
Am J Hum Genet. 1992 Oct; 51(4): 687–700.
PMCID:
PMC1682812
SummaryPage BrowsePDF–2.2M
3.
A Novel Smartphone-Based Color Test for Detection of Color Vision Defects in Age Related Macular Degeneration
Vassilios Karampatakis, Diamantis Almaliotis, Leonidas Karamitopoulos, George Kalliris, Stavroula Almpanidou
J Ophthalmol. 2022; 2022: 9744065. Published online 2022 Mar 31. doi: 10.1155/2022/9744065
PMCID:
PMC8991385
AbstractArticlePDF–913K
4.
Prevalence of Red-Green Color Vision Defects among Muslim Males and Females of Manipur, India
Ahsana SHAH, Ruqaiya HUSSAIN, Mohd FAREED, Mohammad AFZAL
Iran J Public Health. 2013; 42(1): 16–24. Published online 2013 Jan 1.
PMCID:
PMC3595632
AbstractArticlePDF–380K
5.
High visibility colored fabrics for normal trichromats and individuals with color vision defects in a sunset-simulated environment
Tatsuya Iizuka, Takushi Kawamorita, Hajime Tsuji, Hiroyuki Kanai, Toshihiro Hirai, Hiroo Suzuki, Tomoya Handa, Hitoshi Ishikawa
PLoS One. 2022; 17(9): e0274824. Published online 2022 Sep 16. doi: 10.1371/journal.pone.0274824
PMCID:
PMC9480988
AbstractArticlePDF–2.3M
6.
Cone pigments in human deutan colour vision defects.
M Alpern, T Wake
J Physiol. 1977 Apr; 266(3): 595–612. doi: 10.1113/jphysiol.1977.sp011784
PMCID:
PMC1283582
SummaryPage BrowsePDF–1.8M
7.
Molecular basis of abnormal red-green color vision: a family with three types of color vision defects.
M Drummond-Borg, S Deeb, A G Motulsky
Am J Hum Genet. 1988 Nov; 43(5): 675–683.
PMCID:
PMC1715545
SummaryPage BrowsePDF–1.3M
8.
Color vision defects in adrenomyeloneuropathy.
G H Sack, Jr, M B Raven, H W Moser
Am J Hum Genet. 1989 Jun; 44(6): 794–798.
PMCID:
PMC1715662
SummaryPage BrowsePDF–793K
9.
Impact of congenital colour vision defects on occupation
P Cumberland, J Rahi, C Peckham
Arch Dis Child. 2005 Sep; 90(9): 906–908. Published online 2005 May 24. doi: 10.1136/adc.2004.062067
PMCID:
PMC1720587
SummaryPDF–56K
10.
Acquired Color Vision Defects and Hexane Exposure: A Study of San Francisco Bay Area Automotive Mechanics
Stella Beckman, Ellen A. Eisen, Michael N. Bates, Sa Liu, Gunilla Haegerstrom-Portnoy, S. Katharine Hammond
Am J Epidemiol. 2016 Jun 1; 183(11): 969–976. Published online 2016 May 17. doi: 10.1093/aje/kwv328
PMCID:
PMC4887581
AbstractArticlePDF–123K
11.
Diagnosis of Normal and Abnormal Color Vision with Cone-Specific VEPs
Jeff C. Rabin, Andrew C. Kryder, Dan Lam
Transl Vis Sci Technol. 2016 May; 5(3): 8. Published online 2016 May 17. doi: 10.1167/tvst.5.3.8
PMCID:
PMC4874451
AbstractArticlePDF–831K
12.
A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defect
Susanne Kohl, Pablo Llavona, Alexandra Sauer, Peggy Reuter, Nicole Weisschuh, Melanie Kempf, Florian Alexander Dehmelt, Aristides B Arrenberg, Ieva Sliesoraityte, Eberhart Zrenner, Mary J van Schooneveld, Günther Rudolph, Laura Kühlewein, Bernd Wissinger
Hum Mol Genet. 2021 Jul 1; 30(13): 1218–1229. Published online 2021 Apr 22. doi: 10.1093/hmg/ddab117
PMCID:
PMC8212766
AbstractArticlePDF–1.0M
13.
Colour vision defects in asymptomatic carriers of the Leber's hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case‐control study
P A Quiros, R J Torres, S Salomao, A Berezovsky, V Carelli, J Sherman, F Sadun, A De Negri, R Belfort, A A Sadun
Br J Ophthalmol. 2006 Feb; 90(2): 150–153. doi: 10.1136/bjo.2005.074526
PMCID:
PMC1860163
AbstractArticlePDF–125K
14.
The causal mutation in ARR3 gene for high myopia and progressive color vision defect
Lei Gu, Peikuan Cong, Qingyao Ning, Bo Jiang, Jianyong Wang, Hongguang Cui
Sci Rep. 2023; 13: 8986. Published online 2023 Jun 2. doi: 10.1038/s41598-023-36141-0
PMCID:
PMC10238396
AbstractArticlePDF–1.6M
15.
Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations
Giuseppe Giovanni Nardone, Beatrice Spedicati, Maria Pina Concas, Aurora Santin, Anna Morgan, Lorenzo Mazzetto, Maurizio Battaglia-Parodi, Giorgia Girotto
Front Genet. 2023; 14: 1161696. Published online 2023 Jun 9. doi: 10.3389/fgene.2023.1161696
PMCID:
PMC10288324
AbstractArticlePDF–1.1M
16.
Impact of congenital color vision defect on color-related tasks among schoolchildren in Durban, South Africa
Khathutshelo Percy Mashige
Clin Optom (Auckl) 2019; 11: 97–102. Published online 2019 Aug 13. doi: 10.2147/OPTO.S204332
PMCID:
PMC6698162
AbstractArticlePDF–277K
17.
Molecular genetics of X chromosome-linked color vision among populations of African and Japanese ancestry: high frequency of a shortened red pigment gene among Afro-Americans.
A L Jørgensen, S S Deeb, A G Motulsky
Proc Natl Acad Sci U S A. 1990 Sep; 87(17): 6512–6516. doi: 10.1073/pnas.87.17.6512
PMCID:
PMC54566
SummaryPage BrowsePDF–1.2M
18.
Hereditary and Clinical Features of Retinitis Pigmentosa in Koreans
Sun Ho Lee, Hyeong Gon Yu, Jong Mo Seo, Sang Woong Moon, Jun Woong Moon, Sang Jin Kim, Hum Chung
J Korean Med Sci. 2010 Jun; 25(6): 918–923. Published online 2010 May 24. doi: 10.3346/jkms.2010.25.6.918
PMCID:
PMC2877238
AbstractArticlePDF–147K
19.
Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1
Barend F.T. Hogewind, Ronald J.E. Pennings, Frans A. Hol, Henricus P.M. Kunst, Elisabeth H. Hoefsloot, Johannes R.M. Cruysberg, Cor W.R.J. Cremers
Mol Vis. 2010; 16: 26–35. Published online 2010 Jan 12.
PMCID:
PMC2805421
AbstractArticlePDF–1.6M
20.
The red-green visual pigment gene region in adrenoleukodystrophy.
P Aubourg, R Feil, S Guidoux, J C Kaplan, H Moser, A Kahn, J L Mandel
Am J Hum Genet. 1990 Mar; 46(3): 459–469.
PMCID:
PMC1683637
SummaryPage BrowsePDF–3.6M

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