178 related articles for article (PubMed ID: 37198560)
1. Asymmetric presentation with a novel RP2 gene mutation in X-Linked retinitis pigmentosa: a case report.
Lee HW; Lee EK
BMC Ophthalmol; 2023 May; 23(1):221. PubMed ID: 37198560
[TBL] [Abstract][Full Text] [Related]
2. Evaluation of multimodal imaging in carriers of X-linked retinitis pigmentosa.
Acton JH; Greenberg JP; Greenstein VC; Marsiglia M; Tabacaru M; Theodore Smith R; Tsang SH
Exp Eye Res; 2013 Aug; 113():41-8. PubMed ID: 23669302
[TBL] [Abstract][Full Text] [Related]
3. Mutational analysis of RPGR and RP2 genes in Japanese patients with retinitis pigmentosa: identification of four mutations.
Jin ZB; Liu XQ; Hayakawa M; Murakami A; Nao-i N
Mol Vis; 2006 Oct; 12():1167-74. PubMed ID: 17093403
[TBL] [Abstract][Full Text] [Related]
4. RP2 phenotype and pathogenetic correlations in X-linked retinitis pigmentosa.
Jayasundera T; Branham KE; Othman M; Rhoades WR; Karoukis AJ; Khanna H; Swaroop A; Heckenlively JR
Arch Ophthalmol; 2010 Jul; 128(7):915-23. PubMed ID: 20625056
[TBL] [Abstract][Full Text] [Related]
5. RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History in a Large Cohort of Female Carriers.
Georgiou M; Robson AG; Uwaydat SH; Ji MH; Shakarchi AF; Pontikos N; Mahroo OA; Cheetham ME; Webster AR; Hardcastle AJ; Michaelides M
Am J Ophthalmol; 2024 May; 261():112-120. PubMed ID: 37977507
[TBL] [Abstract][Full Text] [Related]
6. Early-Onset X-Linked Retinitis Pigmentosa in a Heterozygous Female Harboring an Intronic Donor Splice Site Mutation in the Retinitis Pigmentosa GTPase Regulator Gene.
Shifera AS; Kay CN
Ophthalmic Genet; 2015; 36(3):251-6. PubMed ID: 24428633
[TBL] [Abstract][Full Text] [Related]
7. Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype.
Ponjavic V; Andréasson S; Abrahamson M; Ehinger B; Gieser L; Fujita R; Swaroop A
Ophthalmic Genet; 1998 Dec; 19(4):187-96. PubMed ID: 9895243
[TBL] [Abstract][Full Text] [Related]
8. X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60.
Fishman GA; Grover S; Jacobson SG; Alexander KR; Derlacki DJ; Wu W; Buraczynska M; Swaroop A
Ophthalmology; 1998 Dec; 105(12):2286-96. PubMed ID: 9855162
[TBL] [Abstract][Full Text] [Related]
9. Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa.
Churchill JD; Bowne SJ; Sullivan LS; Lewis RA; Wheaton DK; Birch DG; Branham KE; Heckenlively JR; Daiger SP
Invest Ophthalmol Vis Sci; 2013 Feb; 54(2):1411-6. PubMed ID: 23372056
[TBL] [Abstract][Full Text] [Related]
10. RP2 X-LINKED RETINITIS PIGMENTOSA CARRIER STATE PRESENTING WITH VASCULAR LEAKAGE AND UNILATERAL MACULAR ATROPHY.
Raparia E; Ballios BG; Place EM; Husain D; Huckfeldt RM
Retin Cases Brief Rep; 2023 Sep; 17(5):533-537. PubMed ID: 37643038
[TBL] [Abstract][Full Text] [Related]
11. RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosa.
Sharon D; Sandberg MA; Rabe VW; Stillberger M; Dryja TP; Berson EL
Am J Hum Genet; 2003 Nov; 73(5):1131-46. PubMed ID: 14564670
[TBL] [Abstract][Full Text] [Related]
12. Single-Exome sequencing identified a novel RP2 mutation in a child with X-linked retinitis pigmentosa.
Lim H; Park YM; Lee JK; Taek Lim H
Can J Ophthalmol; 2016 Oct; 51(5):326-330. PubMed ID: 27769321
[TBL] [Abstract][Full Text] [Related]
13. Phenotypic Features of Oguchi Disease and Retinitis Pigmentosa in Patients with S-Antigen Mutations: A Long-Term Follow-up Study.
Nishiguchi KM; Ikeda Y; Fujita K; Kunikata H; Akiho M; Hashimoto K; Hosono K; Kurata K; Koyanagi Y; Akiyama M; Suzuki T; Kawasaki R; Wada Y; Hotta Y; Sonoda KH; Murakami A; Nakazawa M; Nakazawa T; Abe T
Ophthalmology; 2019 Nov; 126(11):1557-1566. PubMed ID: 31257036
[TBL] [Abstract][Full Text] [Related]
14. X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers.
Kurata K; Hosono K; Hayashi T; Mizobuchi K; Katagiri S; Miyamichi D; Nishina S; Sato M; Azuma N; Nakano T; Hotta Y
Int J Mol Sci; 2019 Mar; 20(6):. PubMed ID: 30917587
[TBL] [Abstract][Full Text] [Related]
15. Phenotype in two families with RP3 associated with RPGR mutations.
Lorenz B; Andrassi M; Kretschmann U
Ophthalmic Genet; 2003 Jun; 24(2):89-101. PubMed ID: 12789573
[TBL] [Abstract][Full Text] [Related]
16. X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual function.
Sharon D; Bruns GA; McGee TL; Sandberg MA; Berson EL; Dryja TP
Invest Ophthalmol Vis Sci; 2000 Aug; 41(9):2712-21. PubMed ID: 10937588
[TBL] [Abstract][Full Text] [Related]
17. Reappearance of the tapetal-like reflex after prolonged dark adaptation in a female carrier of RPGR ORF15 X-linked retinitis pigmentosa.
Bregnhøj J; Al-Hamdani S; Sander B; Larsen M; Schatz P
Mol Vis; 2014; 20():852-63. PubMed ID: 24959064
[TBL] [Abstract][Full Text] [Related]
18. Mutations in RPGR and RP2 of Chinese patients with X-linked retinitis pigmentosa.
Ji Y; Wang J; Xiao X; Li S; Guo X; Zhang Q
Curr Eye Res; 2010 Jan; 35(1):73-9. PubMed ID: 20021257
[TBL] [Abstract][Full Text] [Related]
19. Clinical and genetic findings of a Japanese patient with RP1-related autosomal recessive retinitis pigmentosa.
Kurata K; Hosono K; Hotta Y
Doc Ophthalmol; 2018 Aug; 137(1):47-56. PubMed ID: 30027431
[TBL] [Abstract][Full Text] [Related]
20. Novel variants of RPGR in X-linked retinitis pigmentosa families and genotype-phenotype correlation.
Parmeggiani F; Barbaro V; Migliorati A; Raffa P; Nespeca P; De Nadai K; Del Vecchio C; Palù G; Parolin C; Di Iorio E
Eur J Ophthalmol; 2017 Mar; 27(2):240-248. PubMed ID: 27768226
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
