Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Deutan"'
Autor:
Giuseppe Giovanni Nardone, Beatrice Spedicati, Maria Pina Concas, Aurora Santin, Anna Morgan, Lorenzo Mazzetto, Maurizio Battaglia-Parodi, Giorgia Girotto
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Introduction: Color vision defects (CVDs) are conditions characterized by the alteration of normal trichromatic vision. CVDs can arise as the result of alterations in three genes (OPN1LW, OPN1MW, OPN1SW) or as a combination of genetic predisposition
Externí odkaz:
https://doaj.org/article/4b0714f7de2c4bca80ef9878c948145e
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 20, p 15247 (2023)
This study aimed to investigate the prevalence of color vision deficiencies (CVDs) and determine whether carriers could be detected by analyzing the visual pigment genes. Materials and Methods: The data of students who underwent routine CVD screening
Externí odkaz:
https://doaj.org/article/a4fed496c60e4059a918da4536a79abd
Publikováno v:
Journal of the Egyptian Public Health Association, Vol 95, Iss 1, Pp 1-6 (2020)
Abstract Background The prevalence of congenital colour vision deficiency (CCVD) varies from race to race and differs in different geographic regions. Colour vision deficiency or colour blindness, is the inability or decreased ability of discriminati
Externí odkaz:
https://doaj.org/article/4154ddbb68e24ad0b0542fda55fb7b85
Publikováno v:
Clinical Ophthalmology, Vol Volume 12, Pp 1121-1124 (2018)
Viola Andin Dohvoma, Stève Robert Ebana Mvogo, Giles Kagmeni, Nathalie Rosine Emini, Emilienne Epee, Côme Ebana Mvogo Department of Ophthalmology and ENT, Faculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroon Pur
Externí odkaz:
https://doaj.org/article/259e24f72a0644c8a3a13043ec494186
Akademický článek
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Publikováno v:
Glasnik Antropološkog Društva Srbije, Vol 2014, Iss 49, Pp 103-110 (2014)
The absence of one or more receptor types in the eye leads to colour blindness. The frequency of this anomaly varies between populations but also within different regions of a country. The aim of the study is to determine the frequency of colour blin
Externí odkaz:
https://doaj.org/article/c107ca41d8014495a7d1feac14e15c0d
Akademický článek
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Publikováno v:
Iranian Journal of Public Health, Vol 42, Iss 1, Pp 16-24 (2013)
Background: Color blindness is a common X-linked genetic disorder. However, most of color blinds remain undetected due to absence of proper screening. Our study was to determine the prevalence of red-green color vision defects among Manipuri Muslim m
Externí odkaz:
https://doaj.org/article/7251c725a9594c6cace0a907bd725f57
Autor:
Nabeela Hasrod, Alan Rubin
Publikováno v:
African Vision and Eye Health, Vol 75, Iss 1, Pp e1-e6 (2016)
Colour vision deficiencies (CVDs) can be categorised as being congenital or acquired. Some CVDs are already present at birth, as inherited conditions that are the result of changes at the photo-pigment level and are non-pathological, incurable and do
Externí odkaz:
https://doaj.org/article/15becfe164114d758c54941aaaab79ae
Autor:
Nabeela Hasrod, Alan Rubin
Publikováno v:
African Vision and Eye Health, Vol 74, Iss 1, Pp e1-e7 (2015)
The evaluation of colour vision and discrimination of an individual forms an integral part of a routine eye and vision examination. With the increasing prevalence of inherited colour vision deficiencies, defects of colour vision can be detected in an
Externí odkaz:
https://doaj.org/article/b0f2372b661d4bb889af24c00b8bd6a0