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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1963 1
1968 1
1969 1
1971 1
1972 1
1973 1
1974 1
1975 3
1976 1
1977 2
1978 1
1979 1
1980 2
1981 1
1982 2
1983 1
1984 1
1986 2
1987 2
1988 2
1989 7
1990 9
1991 2
1992 3
1993 5
1994 7
1995 5
1996 7
1997 8
1998 11
1999 6
2000 2
2001 4
2002 7
2003 13
2004 10
2005 7
2006 8
2007 14
2008 14
2009 7
2010 13
2011 9
2012 15
2013 11
2014 21
2015 20
2016 20
2017 19
2018 21
2019 9
2020 7
2021 18
2022 16
2023 19
2024 2

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366 results

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Page 1
Optic neuritis and autoimmune optic neuropathies: advances in diagnosis and treatment.
Bennett JL, Costello F, Chen JJ, Petzold A, Biousse V, Newman NJ, Galetta SL. Bennett JL, et al. Lancet Neurol. 2023 Jan;22(1):89-100. doi: 10.1016/S1474-4422(22)00187-9. Epub 2022 Sep 22. Lancet Neurol. 2023. PMID: 36155661 Review.
Optic neuritis is an inflammatory optic neuropathy that is commonly indicative of autoimmune neurological disorders including multiple sclerosis, myelin-oligodendrocyte glycoprotein antibody-associated disease, and neuromyelitis optica spectrum disorder. ...G …
Optic neuritis is an inflammatory optic neuropathy that is commonly indicative of autoimmune neurological disorders including multipl …
Acquired color vision deficiency.
Simunovic MP. Simunovic MP. Surv Ophthalmol. 2016 Mar-Apr;61(2):132-55. doi: 10.1016/j.survophthal.2015.11.004. Epub 2015 Nov 30. Surv Ophthalmol. 2016. PMID: 26656928 Review.
Acquired color vision deficiency occurs as the result of ocular, neurologic, or systemic disease. ...We also briefly review the types of color vision deficiencies encountered in ocular disease, with an emphasis placed on larger or more de …
Acquired color vision deficiency occurs as the result of ocular, neurologic, or systemic disease. ...We also briefly re …
Gene Therapy for Color Blindness.
Hassall MM, Barnard AR, MacLaren RE. Hassall MM, et al. Yale J Biol Med. 2017 Dec 19;90(4):543-551. eCollection 2017 Dec. Yale J Biol Med. 2017. PMID: 29259520 Free PMC article. Review.
Achromatopsia is a rare congenital cause of vision loss due to isolated cone photoreceptor dysfunction. The most common underlying genetic mutations are autosomal recessive changes in CNGA3, CNGB3, GNAT2, PDE6H, PDE6C, or ATF6. Animal models of Cnga3, Cngb3, and Gnat2 have …
Achromatopsia is a rare congenital cause of vision loss due to isolated cone photoreceptor dysfunction. The most common underlying ge …
Non-syndromic retinitis pigmentosa.
Verbakel SK, van Huet RAC, Boon CJF, den Hollander AI, Collin RWJ, Klaver CCW, Hoyng CB, Roepman R, Klevering BJ. Verbakel SK, et al. Prog Retin Eye Res. 2018 Sep;66:157-186. doi: 10.1016/j.preteyeres.2018.03.005. Epub 2018 Mar 27. Prog Retin Eye Res. 2018. PMID: 29597005 Free article. Review.
RP typically manifests with night blindness in adolescence, followed by concentric visual field loss, reflecting the principal dysfunction of rod photoreceptors; central vision loss occurs later in life due to cone dysfunction. Photoreceptor function measured with an elect …
RP typically manifests with night blindness in adolescence, followed by concentric visual field loss, reflecting the principal dysfunction o …
Oculocutaneous albinism.
Grønskov K, Ek J, Brondum-Nielsen K. Grønskov K, et al. Orphanet J Rare Dis. 2007 Nov 2;2:43. doi: 10.1186/1750-1172-2-43. Orphanet J Rare Dis. 2007. PMID: 17980020 Free PMC article. Review.
Clinical manifestations include various degrees of congenital nystagmus, iris hypopigmentation and translucency, reduced pigmentation of the retinal pigment epithelium, foveal hypoplasia, reduced visual acuity usually (20/60 to 20/400) and refractive errors, color visio
Clinical manifestations include various degrees of congenital nystagmus, iris hypopigmentation and translucency, reduced pigmentation of the …
[Signs, symptoms, and clinical forms of cataract in adults].
Delbarre M, Froussart-Maille F. Delbarre M, et al. J Fr Ophtalmol. 2020 Sep;43(7):653-659. doi: 10.1016/j.jfo.2019.11.009. Epub 2020 Jun 22. J Fr Ophtalmol. 2020. PMID: 32586638 Review. French.
The common symptom is loss of visual acuity, but other symptoms (photophobia, monocular diplopia, myopic shift, change in color vision, etc.) may be found depending on the anatomical distribution of the opacities (nuclear, posterior subcapsular, cortical). ...Catara …
The common symptom is loss of visual acuity, but other symptoms (photophobia, monocular diplopia, myopic shift, change in color vi
IMI Accommodation and Binocular Vision in Myopia Development and Progression.
Logan NS, Radhakrishnan H, Cruickshank FE, Allen PM, Bandela PK, Davies LN, Hasebe S, Khanal S, Schmid KL, Vera-Diaz FA, Wolffsohn JS. Logan NS, et al. Invest Ophthalmol Vis Sci. 2021 Apr 28;62(5):4. doi: 10.1167/iovs.62.5.4. Invest Ophthalmol Vis Sci. 2021. PMID: 33909034 Free PMC article. Review.
Specific topics reviewed included accommodation and myopia, role of spatial frequency, and contrast of the task of objects in the near environment, color cues to accommodation, lag of accommodation, accommodative-convergence ratio, and near phoria status. ...
Specific topics reviewed included accommodation and myopia, role of spatial frequency, and contrast of the task of objects in the near envir …
Uveal melanoma: relatively rare but deadly cancer.
Kaliki S, Shields CL. Kaliki S, et al. Eye (Lond). 2017 Feb;31(2):241-257. doi: 10.1038/eye.2016.275. Epub 2016 Dec 2. Eye (Lond). 2017. PMID: 27911450 Free PMC article. Review.
Although it is a relatively rare disease, primarily found in the Caucasian population, uveal melanoma is the most common primary intraocular tumor in adults with a mean age-adjusted incidence of 5.1 cases per million per year. ...These observations call attention to an unm …
Although it is a relatively rare disease, primarily found in the Caucasian population, uveal melanoma is the most common primary intr …
Achromatopsia: Genetics and Gene Therapy.
Michalakis S, Gerhardt M, Rudolph G, Priglinger S, Priglinger C. Michalakis S, et al. Mol Diagn Ther. 2022 Jan;26(1):51-59. doi: 10.1007/s40291-021-00565-z. Epub 2021 Dec 3. Mol Diagn Ther. 2022. PMID: 34860352 Free PMC article. Review.
Achromatopsia (ACHM), also known as rod monochromatism or total color blindness, is an autosomal recessively inherited retinal disorder that affects the cones of the retina, the type of photoreceptors responsible for high-acuity daylight vision. ...The loss o …
Achromatopsia (ACHM), also known as rod monochromatism or total color blindness, is an autosomal recessively inherited retinal dis
366 results