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

Year Number of Results
1968 1
1969 1
1970 3
1971 2
1973 1
1976 3
1979 1
1981 1
1985 1
1987 2
1988 4
1989 2
1990 1
1991 4
1992 2
1993 2
1994 2
1995 3
1996 5
1997 4
1998 5
1999 5
2000 4
2001 3
2002 7
2003 4
2004 8
2005 5
2006 12
2007 6
2008 11
2009 11
2010 6
2011 6
2012 7
2013 13
2014 11
2015 9
2016 12
2017 9
2018 15
2019 7
2020 14
2021 16
2022 12
2023 14
2024 9

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256 results

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Page 1
Retinitis Pigmentosa (Non-syndromic).
Tsang SH, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:125-130. doi: 10.1007/978-3-319-95046-4_25. Adv Exp Med Biol. 2018. PMID: 30578498 Review.
Most of the genes causing autosomal recessive retinitis pigmentosa (AR-RP) are rare and cause 1% of all cases. Some of the genes, like PDE6 (PDE6A, PDE6B, PDE6G), RP25, and RPE65, have higher prevalence, about 2-5% of all cases. ...Clinically, it shows all the class …
Most of the genes causing autosomal recessive retinitis pigmentosa (AR-RP) are rare and cause 1% of all cases. Some of the gen …
Ciliopathies and the Kidney: A Review.
McConnachie DJ, Stow JL, Mallett AJ. McConnachie DJ, et al. Am J Kidney Dis. 2021 Mar;77(3):410-419. doi: 10.1053/j.ajkd.2020.08.012. Epub 2020 Oct 9. Am J Kidney Dis. 2021. PMID: 33039432 Free article. Review.
ER stress-induced cell death mechanisms.
Sano R, Reed JC. Sano R, et al. Biochim Biophys Acta. 2013 Dec;1833(12):3460-3470. doi: 10.1016/j.bbamcr.2013.06.028. Epub 2013 Jul 10. Biochim Biophys Acta. 2013. PMID: 23850759 Free PMC article. Review.
Retinitis pigmentosa.
Hartong DT, Berson EL, Dryja TP. Hartong DT, et al. Lancet. 2006 Nov 18;368(9549):1795-809. doi: 10.1016/S0140-6736(06)69740-7. Lancet. 2006. PMID: 17113430 Review.
Hereditary degenerations of the human retina are genetically heterogeneous, with well over 100 genes implicated so far. This Seminar focuses on the subset of diseases called retinitis pigmentosa, in which patients typically lose night vision in adolescence, side vis …
Hereditary degenerations of the human retina are genetically heterogeneous, with well over 100 genes implicated so far. This Seminar focuses …
A Global Assessment of Eye Health and Quality of Life: A Systematic Review of Systematic Reviews.
Assi L, Chamseddine F, Ibrahim P, Sabbagh H, Rosman L, Congdon N, Evans J, Ramke J, Kuper H, Burton MJ, Ehrlich JR, Swenor BK. Assi L, et al. JAMA Ophthalmol. 2021 May 1;139(5):526-541. doi: 10.1001/jamaophthalmol.2021.0146. JAMA Ophthalmol. 2021. PMID: 33576772 Free PMC article. Review.
FINDINGS: Nine systematic reviews evaluated the association between quality of life and vision impairment, age-related macular degeneration, glaucoma, diabetic retinopathy, or mendelian eye conditions (including retinitis pigmentosa). Of these, 5 were reviews of qua …
FINDINGS: Nine systematic reviews evaluated the association between quality of life and vision impairment, age-related macular degeneration, …
Nerve Growth Factor: Early Studies and Recent Clinical Trials.
Rocco ML, Soligo M, Manni L, Aloe L. Rocco ML, et al. Curr Neuropharmacol. 2018;16(10):1455-1465. doi: 10.2174/1570159X16666180412092859. Curr Neuropharmacol. 2018. PMID: 29651949 Free PMC article. Review.
NGF is the first discovered member of a family of neurotrophic factors, collectively indicated as neurotrophins, (which include brain-derived neurotrophic factor, neurotrophin-3 and neurotrophin 4/5). NGF was discovered for its action on the survival and differentiation of …
NGF is the first discovered member of a family of neurotrophic factors, collectively indicated as neurotrophins, (which include brain-derive …
Inherited retinal diseases: Therapeutics, clinical trials and end points-A review.
Georgiou M, Fujinami K, Michaelides M. Georgiou M, et al. Clin Exp Ophthalmol. 2021 Apr;49(3):270-288. doi: 10.1111/ceo.13917. Epub 2021 Mar 20. Clin Exp Ophthalmol. 2021. PMID: 33686777 Review.
The scope of this review is to familiarise clinicians and scientists with the current management and the prospects for novel therapies for: (1) macular dystrophies, (2) cone and cone-rod dystrophies, (3) cone dysfunction syndromes, (4) Leber congenital amaurosis, (5) rod-c …
The scope of this review is to familiarise clinicians and scientists with the current management and the prospects for novel therapies for: …
The genetic and phenotypic landscapes of Usher syndrome: from disease mechanisms to a new classification.
Delmaghani S, El-Amraoui A. Delmaghani S, et al. Hum Genet. 2022 Apr;141(3-4):709-735. doi: 10.1007/s00439-022-02448-7. Epub 2022 Mar 30. Hum Genet. 2022. PMID: 35353227 Free PMC article. Review.
The traditional clinical classification of Usher syndrome defines three major subtypes-USH1, 2 and 3-according to hearing loss severity and onset, the presence or absence of vestibular dysfunction, and age at onset of retinitis pigmentosa. ...
The traditional clinical classification of Usher syndrome defines three major subtypes-USH1, 2 and 3-according to hearing loss severi …
Retinal Plasticity.
Strettoi E, Di Marco B, Orsini N, Napoli D. Strettoi E, et al. Int J Mol Sci. 2022 Jan 20;23(3):1138. doi: 10.3390/ijms23031138. Int J Mol Sci. 2022. PMID: 35163059 Free PMC article. Review.
Ciliopathy: Usher Syndrome.
Tsang SH, Aycinena ARP, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:167-170. doi: 10.1007/978-3-319-95046-4_32. Adv Exp Med Biol. 2018. PMID: 30578505 Review.
Because nearly every cell in the body (including the photoreceptors) contains cilia, defects in ciliary proteins typically affect multiple organ systems. Usher syndrome is the most common syndromic cause of retinitis pigmentosa (RP) and accounts for 10-20% of cases …
Because nearly every cell in the body (including the photoreceptors) contains cilia, defects in ciliary proteins typically affect multiple o …
256 results