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Results by year

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

Year Number of Results
1968 1
1969 1
1975 1
1979 4
1980 3
1982 2
1983 7
1984 5
1985 2
1986 7
1987 5
1988 5
1989 5
1990 7
1991 5
1992 4
1993 9
1994 3
1995 9
1996 8
1997 1
1998 7
1999 9
2000 13
2001 10
2002 18
2003 13
2004 11
2005 17
2006 9
2007 12
2008 11
2009 12
2010 19
2011 23
2012 21
2013 14
2014 16
2015 21
2016 20
2017 14
2018 18
2019 25
2020 15
2021 15
2022 18
2023 17
2024 3

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Search Results

443 results

Results by year

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Page 1
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.
Although the majority of RP cases are non-syndromic, 20-30% of patients with RP also have an associated non-ocular condition. RP typically manifests with night blindness in adolescence, followed by concentric visual field loss, reflecting the principal dysfunction o …
Although the majority of RP cases are non-syndromic, 20-30% of patients with RP also have an associated non-ocular condition. RP typically m …
Melanoma-associated retinopathy.
Elsheikh S, Gurney SP, Burdon MA. Elsheikh S, et al. Clin Exp Dermatol. 2020 Mar;45(2):147-152. doi: 10.1111/ced.14095. Epub 2019 Nov 19. Clin Exp Dermatol. 2020. PMID: 31742740 Review.
Melanoma-associated retinopathy (MAR) is a rare paraneoplastic autoimmune manifestation of cutaneous malignant melanoma. Patients classically present with acute onset night blindness, positive visual phenomena and visual field defects, and typically have significant …
Melanoma-associated retinopathy (MAR) is a rare paraneoplastic autoimmune manifestation of cutaneous malignant melanoma. Patients classicall …
An Update on Gene Therapy for Inherited Retinal Dystrophy: Experience in Leber Congenital Amaurosis Clinical Trials.
Chiu W, Lin TY, Chang YC, Isahwan-Ahmad Mulyadi Lai H, Lin SC, Ma C, Yarmishyn AA, Lin SC, Chang KJ, Chou YB, Hsu CC, Lin TC, Chen SJ, Chien Y, Yang YP, Hwang DK. Chiu W, et al. Int J Mol Sci. 2021 Apr 26;22(9):4534. doi: 10.3390/ijms22094534. Int J Mol Sci. 2021. PMID: 33926102 Free PMC article. Review.
Retinal degradation progress is often irreversible, with clinical manifestations including color or night blindness, peripheral visual defects and subsequent vision loss. ...
Retinal degradation progress is often irreversible, with clinical manifestations including color or night blindness, periphera …
Vitamin A supplementation for preventing morbidity and mortality in children from six months to five years of age.
Imdad A, Mayo-Wilson E, Haykal MR, Regan A, Sidhu J, Smith A, Bhutta ZA. Imdad A, et al. Cochrane Database Syst Rev. 2022 Mar 16;3:CD008524. doi: 10.1002/14651858.CD008524.pub4. Cochrane Database Syst Rev. 2022. PMID: 35294044 Free PMC article. Review.
VAS reduced the incidence of diarrhoea (RR 0.85, 95% CI 0.82 to 0.87; 15 studies, 77,946 children; low-certainty evidence), measles (RR 0.50, 95% CI 0.37 to 0.67; 6 studies, 19,566 children; moderate-certainty evidence), Bitot's spots (RR 0.42, 95% CI 0.33 to 0.53; 5 studies, 1,0 …
VAS reduced the incidence of diarrhoea (RR 0.85, 95% CI 0.82 to 0.87; 15 studies, 77,946 children; low-certainty evidence), measles (RR 0.50 …
TRPM1.
Irie S, Furukawa T. Irie S, et al. Handb Exp Pharmacol. 2014;222:387-402. doi: 10.1007/978-3-642-54215-2_15. Handb Exp Pharmacol. 2014. PMID: 24756714 Review.
Furthermore, human TRPM1 mutations are associated with congenital stationary night blindness (CSNB), whose patients lack rod function and suffer from night blindness starting in early childhood. ...
Furthermore, human TRPM1 mutations are associated with congenital stationary night blindness (CSNB), whose patients lack rod f …
Isotretinoin and night blindness.
Teo K, Yazdabadi A. Teo K, et al. Australas J Dermatol. 2014 Aug;55(3):222-4. doi: 10.1111/ajd.12107. Epub 2013 Oct 8. Australas J Dermatol. 2014. PMID: 25117163 Review.
Isotretinoin is an effective and increasingly popular treatment for acne vulgaris. There have been reports of night blindness as a side-effect of treatment although the evidence does not demonstrate a clear causal relationship between isotretinoin therapy and the ri …
Isotretinoin is an effective and increasingly popular treatment for acne vulgaris. There have been reports of night blindness …
Cone rod dystrophies.
Hamel CP. Hamel CP. Orphanet J Rare Dis. 2007 Feb 1;2:7. doi: 10.1186/1750-1172-2-7. Orphanet J Rare Dis. 2007. PMID: 17270046 Free PMC article. Review.
CRD is characterized by primary cone involvement, or, sometimes, by concomitant loss of both cones and rods that explains the predominant symptoms of CRDs: decreased visual acuity, color vision defects, photoaversion and decreased sensitivity in the central visual field, later fo …
CRD is characterized by primary cone involvement, or, sometimes, by concomitant loss of both cones and rods that explains the predominant sy …
Mechanism of Cone Degeneration in Retinitis Pigmentosa.
Song DJ, Bao XL, Fan B, Li GY. Song DJ, et al. Cell Mol Neurobiol. 2023 Apr;43(3):1037-1048. doi: 10.1007/s10571-022-01243-2. Epub 2022 Jul 6. Cell Mol Neurobiol. 2023. PMID: 35792991 Review.
The various mechanisms underlying rod degeneration primarily rely on genetic mutations, leading to night blindness initially. Cones gradually degenerate after rods are almost eliminated, resulting in varying degrees of visual disability and blindness. ...
The various mechanisms underlying rod degeneration primarily rely on genetic mutations, leading to night blindness initially. …
Congenital stationary night blindness: an update and review of the disease spectrum in Saudi Arabia.
Almutairi F, Almeshari N, Ahmad K, Magliyah MS, Schatz P. Almutairi F, et al. Acta Ophthalmol. 2021 Sep;99(6):581-591. doi: 10.1111/aos.14693. Epub 2020 Dec 26. Acta Ophthalmol. 2021. PMID: 33369259 Free article. Review.
Congenital stationary night blindness (CSNB) is a group of rare, mainly stationary disorders of the retina, resulting from dysfunction of several specific and essential visual processing mechanisms. ...
Congenital stationary night blindness (CSNB) is a group of rare, mainly stationary disorders of the retina, resulting from dys …
443 results