Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1975 1
1976 1
1980 1
1981 1
1984 1
1985 1
1986 1
1987 1
1988 2
1989 2
1990 1
1992 2
1993 1
1994 2
1995 2
1996 1
1997 2
1998 3
1999 3
2000 3
2001 3
2003 3
2004 5
2005 2
2006 2
2007 4
2008 2
2009 2
2010 2
2011 3
2012 9
2013 7
2014 7
2015 11
2016 9
2017 6
2018 11
2019 7
2020 10
2021 10
2022 11
2023 11
2024 3

Text availability

Article attribute

Article type

Publication date

Search Results

147 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Retinitis pigmentosa 45"
Page 1
Thicknesses of the retina and choroid in children with retinitis pigmentosa.
Li C, Peng C, Zhang C, Li N. Li C, et al. BMC Ophthalmol. 2023 Jan 17;23(1):25. doi: 10.1186/s12886-023-02772-0. BMC Ophthalmol. 2023. PMID: 36650468 Free PMC article.
PURPOSE: To compare the retinal thicknesses (RT) and choroidal thicknesses (CT) in retinitis pigmentosa (RP) children with those of healthy children using enhanced depth imaging (EDI) optical coherence tomography (OCT). ...The mean temporal CT was smaller in the XLR …
PURPOSE: To compare the retinal thicknesses (RT) and choroidal thicknesses (CT) in retinitis pigmentosa (RP) children with tho …
Cataract surgery in retinitis pigmentosa.
Chatterjee S, Agrawal D, Agrawal D, Parchand SM, Sahu A. Chatterjee S, et al. Indian J Ophthalmol. 2021 Jul;69(7):1753-1757. doi: 10.4103/ijo.IJO_2916_20. Indian J Ophthalmol. 2021. PMID: 34146021 Free PMC article.
PURPOSE: The aim of this study was to evaluate visual outcomes of cataract surgery in patients with retinitis pigmentosa. METHODS: This retrospective case series includes a review of the medical records of all patients with retinitis pigmentosa undergo …
PURPOSE: The aim of this study was to evaluate visual outcomes of cataract surgery in patients with retinitis pigmentosa. METH …
Genetic and Clinical Findings in an Ethnically Diverse Cohort with Retinitis Pigmentosa Associated with Pathogenic Variants in CERKL.
Downes SM, Nguyen T, Tai V, Broadgate S, Shah M, Al-Khuzaei S, MacLaren RE, Shanks M, Clouston P, Halford S. Downes SM, et al. Genes (Basel). 2020 Dec 12;11(12):1497. doi: 10.3390/genes11121497. Genes (Basel). 2020. PMID: 33322828 Free PMC article. Clinical Trial.
Autosomal recessive retinitis pigmentosa is caused by mutations in over 40 genes, one of which is the ceramide kinase-like gene (CERKL). ...All but one had central visual loss as one of their main presenting symptoms. Four patients had features of retinitis …
Autosomal recessive retinitis pigmentosa is caused by mutations in over 40 genes, one of which is the ceramide kinase-like gen …
Hyperautofluorescent Ring Pattern in Retinitis Pigmentosa: Clinical Implications and Modifications Over Time.
Antropoli A, Arrigo A, Bianco L, Cavallari E, Bandello F, Battaglia Parodi M. Antropoli A, et al. Invest Ophthalmol Vis Sci. 2023 Sep 1;64(12):8. doi: 10.1167/iovs.64.12.8. Invest Ophthalmol Vis Sci. 2023. PMID: 37669062 Free PMC article.
PURPOSE: The purpose of this study was to investigate the relation among hyperautofluorescent ring patterns, visual acuity (VA), and optical coherence tomography (OCT) features in patients with retinitis pigmentosa (RP), and to describe its modifications over time. …
PURPOSE: The purpose of this study was to investigate the relation among hyperautofluorescent ring patterns, visual acuity (VA), and optical …
New Insight into the Genotype-Phenotype Correlation of PRPH2-Related Diseases Based on a Large Chinese Cohort and Literature Review.
Wang Y, Wang J, Jiang Y, Zhu D, Ouyang J, Yi Z, Li S, Jia X, Xiao X, Sun W, Wang P, Zhang Q. Wang Y, et al. Int J Mol Sci. 2023 Apr 4;24(7):6728. doi: 10.3390/ijms24076728. Int J Mol Sci. 2023. PMID: 37047703 Free PMC article. Review.
In our cohort, the most frequent variant was p.G305Afs*19, accounting for 33.3% (5/15) of alleles, in contrast to the literature, where p.R172G (11.6%, 119/1028) was the most common variant. Nine in-house families (63.8%) were diagnosed with retinitis pigmentosa (RP …
In our cohort, the most frequent variant was p.G305Afs*19, accounting for 33.3% (5/15) of alleles, in contrast to the literature, where p.R1 …
Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa.
Liu X, Li J, Lin S, Xiao X, Luo J, Wei W, Ling Y, Fang L, Xiao H, Chen L, Huang J, Zhong Y, Zhang Q. Liu X, et al. Exp Eye Res. 2020 Aug;197:108118. doi: 10.1016/j.exer.2020.108118. Epub 2020 Jun 17. Exp Eye Res. 2020. PMID: 32562694
Primary angle-closure glaucoma (PACG) and retinitis pigmentosa (RP) can co-occur, but the mechanism of their association is not yet established. ...The 326 genes included 10 PACG-associated genes from two genome wide association studies; 45 genes associated w …
Primary angle-closure glaucoma (PACG) and retinitis pigmentosa (RP) can co-occur, but the mechanism of their association is no …
Frequency of cystoid macular edema and vitreomacular interface disorders in genetically solved syndromic and non-syndromic retinitis pigmentosa.
Marques JP, Neves E, Geada S, Carvalho AL, Murta J, Saraiva J, Silva R. Marques JP, et al. Graefes Arch Clin Exp Ophthalmol. 2022 Sep;260(9):2859-2866. doi: 10.1007/s00417-022-05649-y. Epub 2022 Apr 7. Graefes Arch Clin Exp Ophthalmol. 2022. PMID: 35389060
PURPOSE: Retinitis pigmentosa (RP) corresponds to a group of inherited retinal disorders where progressive rod-cone degeneration is observed. ...CME was found in 17.1% of eyes, while ERM was found in 54.3% of eyes. The frequency of CME (p = 0.45) and ERM (p = …
PURPOSE: Retinitis pigmentosa (RP) corresponds to a group of inherited retinal disorders where progressive rod-cone degenerati …
Clinical and Molecular Features of a Chinese Cohort With Syndromic and Nonsyndromic Retinal Dystrophies Related to the CEP290 Gene.
Zhu T, Shen Y, Sun Z, Han X, Wei X, Li W, Lu C, Cheng T, Zou X, Li H, Cao Z, Gao H, Ma X, Luo M, Sui R. Zhu T, et al. Am J Ophthalmol. 2023 Apr;248:96-106. doi: 10.1016/j.ajo.2022.11.023. Epub 2022 Dec 7. Am J Ophthalmol. 2023. PMID: 36493848
Four retinal dystrophy phenotypes were confirmed: Leber congenital amaurosis (LCA, 46/61), early-onset severe retinal dystrophy (EOSRD, 4/61), retinitis pigmentosa (RP, 10/61), and cone-rod dystrophy (CORD, 1/61). The SCP phenotypes included Joubert syndrome (JS) (2 …
Four retinal dystrophy phenotypes were confirmed: Leber congenital amaurosis (LCA, 46/61), early-onset severe retinal dystrophy (EOSRD, 4/61 …
Spectral-Domain Optical Coherence Tomography Analysis in Syndromic and Nonsyndromic Forms of Retinitis Pigmentosa due to USH2A Genetic Variants.
Colombo L, Maltese PE, Romano D, Fogagnolo P, Castori M, Marceddu G, Cristofoli F, Percio M, Piteková B, Modarelli AM, Bertelli M, Rossetti L. Colombo L, et al. Ophthalmic Res. 2022;65(2):180-195. doi: 10.1159/000520329. Epub 2021 Nov 15. Ophthalmic Res. 2022. PMID: 34781295 Free article.
INTRODUCTION: This study aimed to analyze macular structure by using spectral-domain optical coherence tomography (SD-OCT) in a cohort of patients affected by autosomal recessive retinitis pigmentosa and Usher syndrome, due to genetic variants in USH2A gene, and to …
INTRODUCTION: This study aimed to analyze macular structure by using spectral-domain optical coherence tomography (SD-OCT) in a cohort of pa …
OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY IN PATIENTS WITH RETINITIS PIGMENTOSA.
Alnawaiseh M, Schubert F, Heiduschka P, Eter N. Alnawaiseh M, et al. Retina. 2019 Jan;39(1):210-217. doi: 10.1097/IAE.000000000000190. Retina. 2019. PMID: 30570620
PURPOSE: To evaluate the correlation between the flow density measured by optical coherence tomography angiography and functional parameters in patients with retinitis pigmentosa. METHODS: Twenty eyes of 20 patients with retinitis pigmentosa and 21 eye …
PURPOSE: To evaluate the correlation between the flow density measured by optical coherence tomography angiography and functional parameters …
147 results