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

Year Number of Results
1970 1
1988 1
1992 1
1993 2
1995 1
1996 1
1997 1
2003 3
2005 2
2008 3
2009 2
2010 1
2016 2
2017 1
2018 1
2020 1
2021 2
2022 5
2023 2
2024 0

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27 results

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Page 1
Choroidal vascularity index and choroidal thickness: potential biomarkers in retinitis pigmentosa.
Abdolrahimzadeh S, Di Pippo M, Ciancimino C, Di Staso F, Lotery AJ. Abdolrahimzadeh S, et al. Eye (Lond). 2023 Jun;37(9):1766-1773. doi: 10.1038/s41433-022-02270-5. Epub 2022 Oct 7. Eye (Lond). 2023. PMID: 36207507 Free PMC article. Review.
Retinitis pigmentosa (RP) is the commonest inherited retinal dystrophy. ...
Retinitis pigmentosa (RP) is the commonest inherited retinal dystrophy. ...
Genetic obesity syndromes.
Goldstone AP, Beales PL. Goldstone AP, et al. Front Horm Res. 2008;36:37-60. doi: 10.1159/000115336. Front Horm Res. 2008. PMID: 18230893 Review.
Progression Rate of Visual Function and Affecting Factors at Different Stages of Retinitis Pigmentosa.
Ito N, Miura G, Shiko Y, Kawasaki Y, Baba T, Yamamoto S. Ito N, et al. Biomed Res Int. 2022 Jul 14;2022:7204954. doi: 10.1155/2022/7204954. eCollection 2022. Biomed Res Int. 2022. PMID: 35872870 Free PMC article. Review.
We reviewed medical records of 121 patients/235 eyes of typical retinitis pigmentosa (RP) patients who could be followed up for at least 5 years with the aim of investigating the long-term course of visual function progression at each RP stage and appropriate assess …
We reviewed medical records of 121 patients/235 eyes of typical retinitis pigmentosa (RP) patients who could be followed up fo …
Retinitis pigmentosa: genes, proteins and prospects.
Hims MM, Diager SP, Inglehearn CF. Hims MM, et al. Dev Ophthalmol. 2003;37:109-25. doi: 10.1159/000072042. Dev Ophthalmol. 2003. PMID: 12876833 Review.
The name retinitis pigmentosa (RP) describes a heterogeneous group of inherited progressive retinal dystrophies, primarily affecting the peripheral retina. ...
The name retinitis pigmentosa (RP) describes a heterogeneous group of inherited progressive retinal dystrophies, primarily aff …
Gene therapy for inherited retinal and optic nerve degenerations.
Moore NA, Morral N, Ciulla TA, Bracha P. Moore NA, et al. Expert Opin Biol Ther. 2018 Jan;18(1):37-49. doi: 10.1080/14712598.2018.1389886. Epub 2017 Oct 23. Expert Opin Biol Ther. 2018. PMID: 29057663 Free article. Review.
AREAS COVERED: This review covers Leber's congenital amaurosis, choroideremia, retinitis pigmentosa, Usher syndrome, Stargardt disease, Leber's hereditary optic neuropathy, Achromatopsia, and X-linked retinoschisis. ...
AREAS COVERED: This review covers Leber's congenital amaurosis, choroideremia, retinitis pigmentosa, Usher syndrome, Stargardt …
Argus II retinal prosthesis system: An update.
Rachitskaya AV, Yuan A. Rachitskaya AV, et al. Ophthalmic Genet. 2016 Sep;37(3):260-6. doi: 10.3109/13816810.2015.1130152. Epub 2016 Feb 8. Ophthalmic Genet. 2016. PMID: 26855177 Review.
This review focuses on a description of the Argus II retinal prosthesis system (Argus II; Second Sight Medical Products, Sylmar, CA) that was approved for humanitarian use by the FDA in 2013 in patients with retinitis pigmentosa with bare or no light perception visi …
This review focuses on a description of the Argus II retinal prosthesis system (Argus II; Second Sight Medical Products, Sylmar, CA) that wa …
Pluripotent Stem Cell-Based Organoid Technologies for Developing Next-Generation Vision Restoration Therapies of Blindness.
Singh RK, Binette F, Seiler M, Petersen-Jones SM, Nasonkin IO. Singh RK, et al. J Ocul Pharmacol Ther. 2021 Apr;37(3):147-156. doi: 10.1089/jop.2020.0016. Epub 2020 Oct 14. J Ocul Pharmacol Ther. 2021. PMID: 33052761 Free PMC article. Review.
In addition, a large number of orphan inherited (mostly monogenic) conditions, such as retinitis pigmentosa and Leber Congenital Amaurosis, add to the overall number of patients with blinding retinal degenerative diseases. ...
In addition, a large number of orphan inherited (mostly monogenic) conditions, such as retinitis pigmentosa and Leber Congenit …
The application and progression of CRISPR/Cas9 technology in ophthalmological diseases.
Hu X, Zhang B, Li X, Li M, Wang Y, Dan H, Zhou J, Wei Y, Ge K, Li P, Song Z. Hu X, et al. Eye (Lond). 2023 Mar;37(4):607-617. doi: 10.1038/s41433-022-02169-1. Epub 2022 Aug 1. Eye (Lond). 2023. PMID: 35915232 Free PMC article. Review.
Thus far, applications of CRISPR/Cas9 genome editing technology in ophthalmology have included gene therapy for corneal dystrophy, glaucoma, congenital cataract, Leber's congenital amaurosis, retinitis pigmentosa, Usher syndrome, fundus neovascular disease, prolifer …
Thus far, applications of CRISPR/Cas9 genome editing technology in ophthalmology have included gene therapy for corneal dystrophy, glaucoma, …
The roles of microglia in neural remodeling during retinal degeneration.
Gao H, Huang X, He J, Zou T, Chen X, Xu H. Gao H, et al. Histol Histopathol. 2022 Jan;37(1):1-10. doi: 10.14670/HH-18-384. Epub 2021 Oct 25. Histol Histopathol. 2022. PMID: 34693982 Review.
Analogously, microglia have been found to participate in the clearance of synaptic elements in a complement-dependent manner in the classic retinitis pigmentosa (RP) model, Royal College of Surgeons (RCS) rats, and retard the formation of ectopic neuritogenesis and …
Analogously, microglia have been found to participate in the clearance of synaptic elements in a complement-dependent manner in the classic …
Epidemiology of Mutations in the 65-kDa Retinal Pigment Epithelium (RPE65) Gene-Mediated Inherited Retinal Dystrophies: A Systematic Literature Review.
Sallum JMF, Kaur VP, Shaikh J, Banhazi J, Spera C, Aouadj C, Viriato D, Fischer MD. Sallum JMF, et al. Adv Ther. 2022 Mar;39(3):1179-1198. doi: 10.1007/s12325-021-02036-7. Epub 2022 Jan 30. Adv Ther. 2022. PMID: 35098484 Free PMC article. Review.
Adult and paediatric patients with vision loss due to IRD caused by biallelic mutations in the 65-kDa retinal pigment epithelium (RPE65) gene are often clinically diagnosed as retinitis pigmentosa (RP), and Leber congenital amaurosis (LCA). This study aimed to under …
Adult and paediatric patients with vision loss due to IRD caused by biallelic mutations in the 65-kDa retinal pigment epithelium (RPE65) gen …
27 results