Skip to main page content
U.S. flag

An official website of the United States government

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

1975
2025

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

Year Number of Results
1975 1
1989 1
1994 1
1996 1
1998 1
2000 2
2002 3
2007 1
2008 2
2011 2
2012 2
2013 1
2014 1
2015 2
2016 2
2018 2
2019 3
2020 4
2021 3
2022 3
2023 5
2024 8
2025 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Search Results

46 results

Results by year

Filters applied: . Clear all
Your search was processed without automatic term mapping because it retrieved zero results.
Page 1
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes.
Georgiou M, Robson AG, Fujinami K, de Guimarães TAC, Fujinami-Yokokawa Y, Daich Varela M, Pontikos N, Kalitzeos A, Mahroo OA, Webster AR, Michaelides M. Georgiou M, et al. Prog Retin Eye Res. 2024 May;100:101244. doi: 10.1016/j.preteyeres.2024.101244. Epub 2024 Jan 24. Prog Retin Eye Res. 2024. PMID: 38278208 Review.
Herein we present in a comprehensive and concise manner: (i) macular dystrophies (Stargardt disease (ABCA4), X-linked retinoschisis (RS1), Best disease (BEST1), PRPH2-associated pattern dystrophy, Sorsby fundus dystrophy (TIMP3), and autosomal dominant drusen (EFEMP1)), (ii) cone …
Herein we present in a comprehensive and concise manner: (i) macular dystrophies (Stargardt disease (ABCA4), X-linked retinoschisis (RS1), B …
Diagnostic accuracy of artificial intelligence in detecting retinitis pigmentosa: A systematic review and meta-analysis.
Musleh AM, AlRyalat SA, Abid MN, Salem Y, Hamila HM, Sallam AB. Musleh AM, et al. Surv Ophthalmol. 2024 May-Jun;69(3):411-417. doi: 10.1016/j.survophthal.2023.11.010. Epub 2023 Dec 1. Surv Ophthalmol. 2024. PMID: 38042377 Review.
Retinitis pigmentosa (RP) is often undetected in its early stages. Artificial intelligence (AI) has emerged as a promising tool in medical diagnostics. ...We included studies in the English language that used any ophthalmic imaging modality, such as OCT or fundus ph
Retinitis pigmentosa (RP) is often undetected in its early stages. Artificial intelligence (AI) has emerged as a promising too
Oxidative Stress and Microglial Response in Retinitis Pigmentosa.
Murakami Y, Nakabeppu Y, Sonoda KH. Murakami Y, et al. Int J Mol Sci. 2020 Sep 28;21(19):7170. doi: 10.3390/ijms21197170. Int J Mol Sci. 2020. PMID: 32998461 Free PMC article. Review.
An imbalance between the production of reactive oxygen species (ROS) and anti-oxidant capacity results in oxidative injury to cellular components and molecules, which in turn disturbs the homeostasis of cells and organs. Although retinitis pigmentosa (RP) is a hered …
An imbalance between the production of reactive oxygen species (ROS) and anti-oxidant capacity results in oxidative injury to cellular compo …
A review of the immunologic findings observed in retinitis pigmentosa.
McMurtrey JJ, Tso MOM. McMurtrey JJ, et al. Surv Ophthalmol. 2018 Nov-Dec;63(6):769-781. doi: 10.1016/j.survophthal.2018.03.002. Epub 2018 Mar 16. Surv Ophthalmol. 2018. PMID: 29551596 Review.
Most patients suffering from retinitis pigmentosa (RP) inherit the disorder; however, the immune-pathologic features associated with this disease have yet to be extensively studied. ...Twenty-one percent to 51% of RP patients display antiretinal antibodies, whereas …
Most patients suffering from retinitis pigmentosa (RP) inherit the disorder; however, the immune-pathologic features associate …
PHARC syndrome: an overview.
Harutyunyan L, Callaerts P, Vermeer S. Harutyunyan L, et al. Orphanet J Rare Dis. 2024 Nov 5;19(1):416. doi: 10.1186/s13023-024-03418-0. Orphanet J Rare Dis. 2024. PMID: 39501272 Free PMC article. Review.
PHARC, polyneuropathy, hearing loss, cerebellar ataxia, retinitis pigmentosa and cataracts, or PHARC is a very rare progressive neurodegenerative autosomal recessive disease caused by biallelic mutations in the ABHD12 (a/b-hydrolase domain containing 12) gene, which …
PHARC, polyneuropathy, hearing loss, cerebellar ataxia, retinitis pigmentosa and cataracts, or PHARC is a very rare progressiv …
Hereditary retinal disease.
Goodwin P. Goodwin P. Curr Opin Ophthalmol. 2008 May;19(3):255-62. doi: 10.1097/ICU.0b013e3282fc27fc. Curr Opin Ophthalmol. 2008. PMID: 18408503 Review.
SUMMARY: A literature review of the recent discoveries and potential treatments for retinitis pigmentosa, Leber's congenital amaurosis, X-linked retinoschisis, Best's disease, Stargardt's disease, and congenital stationary night blindness is presented, along with a …
SUMMARY: A literature review of the recent discoveries and potential treatments for retinitis pigmentosa, Leber's congenital a …
Mechanisms of Photoreceptor Death in Retinitis Pigmentosa.
Newton F, Megaw R. Newton F, et al. Genes (Basel). 2020 Sep 24;11(10):1120. doi: 10.3390/genes11101120. Genes (Basel). 2020. PMID: 32987769 Free PMC article. Review.
Retinitis pigmentosa (RP) is the most common cause of inherited blindness and is characterised by the progressive loss of retinal photoreceptors. ...
Retinitis pigmentosa (RP) is the most common cause of inherited blindness and is characterised by the progressive loss of reti
Targeting Necroptosis: A Novel Therapeutic Option for Retinal Degenerative Diseases.
Zhang Q, Hu XM, Zhao WJ, Ban XX, Li Y, Huang YX, Wan H, He Y, Liao LS, Shang L, Jiang B, Qing GP, Xiong K. Zhang Q, et al. Int J Biol Sci. 2023 Jan 1;19(2):658-674. doi: 10.7150/ijbs.77994. eCollection 2023. Int J Biol Sci. 2023. PMID: 36632450 Free PMC article. Review.
Retinal cell death is a leading cause of blindness and has been identified in most retinal diseases, e.g., age-related macular degeneration, glaucoma, retinal detachment, retinitis pigmentosa, etc. Increasing evidence demonstrates that retinal degenerative diseases …
Retinal cell death is a leading cause of blindness and has been identified in most retinal diseases, e.g., age-related macular degeneration, …
Cell-based Therapies for Corneal and Retinal Disorders.
Ajgaonkar BS, Kumaran A, Kumar S, Jain RD, Dandekar PP. Ajgaonkar BS, et al. Stem Cell Rev Rep. 2023 Nov;19(8):2650-2682. doi: 10.1007/s12015-023-10623-0. Epub 2023 Sep 14. Stem Cell Rev Rep. 2023. PMID: 37704835 Review.
Corneal disorders are mainly categorized mainly into corneal epithelial, stromal, and endothelial disorders. On the other hand, glaucoma, retinitis pigmentosa, age-related macular degeneration, diabetic retinopathy, Stargardt Disease, choroideremia, Leber congenital …
Corneal disorders are mainly categorized mainly into corneal epithelial, stromal, and endothelial disorders. On the other hand, glaucoma, …
Variant haploinsufficiency and phenotypic non-penetrance in PRPF31-associated retinitis pigmentosa.
Rose AM, Bhattacharya SS. Rose AM, et al. Clin Genet. 2016 Aug;90(2):118-26. doi: 10.1111/cge.12758. Epub 2016 Mar 4. Clin Genet. 2016. PMID: 26853529 Review.
Retinitis pigmentosa (RP) is a genetically heterogenous group of inherited disorders, characterized by death of the retinal photoreceptor cells, leading to progressive visual impairment. ...
Retinitis pigmentosa (RP) is a genetically heterogenous group of inherited disorders, characterized by death of the retinal ph
46 results