These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
124 related articles for article (PubMed ID: 37683184)
1. A SYSTEMATIC LITERATURE REVIEW OF DISEASE PROGRESSION REPORTED IN RPGR -ASSOCIATED X-LINKED RETINITIS PIGMENTOSA. Lam BL; Scholl HPN; Doub D; Sperling M; Hashim M; Li N Retina; 2024 Jan; 44(1):1-9. PubMed ID: 37683184 [TBL] [Abstract][Full Text] [Related]
2. Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations. Sandberg MA; Rosner B; Weigel-DiFranco C; Dryja TP; Berson EL Invest Ophthalmol Vis Sci; 2007 Mar; 48(3):1298-304. PubMed ID: 17325176 [TBL] [Abstract][Full Text] [Related]
4. Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus. Zito I; Thiselton DL; Gorin MB; Stout JT; Plant C; Bird AC; Bhattacharya SS; Hardcastle AJ Hum Genet; 1999; 105(1-2):57-62. PubMed ID: 10480356 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. AAV-RPGR Gene Therapy Rescues Opsin Mislocalisation in a Human Retinal Organoid Model of Sladen PE; Naeem A; Adefila-Ideozu T; Vermeule T; Busson SL; Michaelides M; Naylor S; Forbes A; Lane A; Georgiadis A Int J Mol Sci; 2024 Feb; 25(3):. PubMed ID: 38339118 [TBL] [Abstract][Full Text] [Related]
7. Multiprotein complexes of Retinitis Pigmentosa GTPase regulator (RPGR), a ciliary protein mutated in X-linked Retinitis Pigmentosa (XLRP). Murga-Zamalloa C; Swaroop A; Khanna H Adv Exp Med Biol; 2010; 664():105-14. PubMed ID: 20238008 [TBL] [Abstract][Full Text] [Related]
8. Detailed comparison of phenotype between male patients carrying variants in exons 1-14 and ORF15 of RPGR. Zou X; Fang S; Wu S; Li H; Sun Z; Zhu T; Wei X; Sui R Exp Eye Res; 2020 Sep; 198():108147. PubMed ID: 32702353 [TBL] [Abstract][Full Text] [Related]
9. Association of a Novel Intronic Variant in RPGR With Hypomorphic Phenotype of X-Linked Retinitis Pigmentosa. Cehajic-Kapetanovic J; McClements ME; Whitfield J; Shanks M; Clouston P; MacLaren RE JAMA Ophthalmol; 2020 Nov; 138(11):1151-1158. PubMed ID: 32970112 [TBL] [Abstract][Full Text] [Related]
10. Clinical characteristics of high myopia in female carriers of pathogenic Tran M; Kolesnikova M; Kim AH; Kowal T; Ning K; Mahajan VB; Tsang SH; Sun Y Ophthalmic Genet; 2023 Jun; 44(3):295-303. PubMed ID: 36017691 [TBL] [Abstract][Full Text] [Related]
11. Codon-Optimized RPGR Improves Stability and Efficacy of AAV8 Gene Therapy in Two Mouse Models of X-Linked Retinitis Pigmentosa. Fischer MD; McClements ME; Martinez-Fernandez de la Camara C; Bellingrath JS; Dauletbekov D; Ramsden SC; Hickey DG; Barnard AR; MacLaren RE Mol Ther; 2017 Aug; 25(8):1854-1865. PubMed ID: 28549772 [TBL] [Abstract][Full Text] [Related]
12. Disease course in patients with autosomal recessive retinitis pigmentosa due to the USH2A gene. Sandberg MA; Rosner B; Weigel-DiFranco C; McGee TL; Dryja TP; Berson EL Invest Ophthalmol Vis Sci; 2008 Dec; 49(12):5532-9. PubMed ID: 18641288 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Natural history and clinical biomarkers of progression in X-linked retinitis pigmentosa: a systematic review. Zada M; Cornish EE; Fraser CL; Jamieson RV; Grigg JR Acta Ophthalmol; 2021 Aug; 99(5):499-510. PubMed ID: 33258268 [TBL] [Abstract][Full Text] [Related]
15. Changes in Retinal Sensitivity Associated With Cotoretigene Toliparvovec in X-Linked Retinitis Pigmentosa With RPGR Gene Variations. von Krusenstiern L; Liu J; Liao E; Gow JA; Chen G; Ong T; Lotery AJ; Jalil A; Lam BL; MacLaren RE; JAMA Ophthalmol; 2023 Mar; 141(3):275-283. PubMed ID: 36757689 [TBL] [Abstract][Full Text] [Related]
16. Phenotypic high myopia in X-linked retinitis pigmentosa secondary to a novel mutation in the RPGR gene. Sanchez Tocino H; Diez Montero C; Villanueva Gómez A; Lobo Valentin R; Montero-Moreno JA Ophthalmic Genet; 2019 Apr; 40(2):170-176. PubMed ID: 31033374 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Rates of decline in regions of the visual field defined by frequency-domain optical coherence tomography in patients with RPGR-mediated X-linked retinitis pigmentosa. Birch DG; Locke KG; Felius J; Klein M; Wheaton DK; Hoffman DR; Hood DC Ophthalmology; 2015 Apr; 122(4):833-9. PubMed ID: 25556114 [TBL] [Abstract][Full Text] [Related]
19. A comparison of progressive loss of the ellipsoid zone (EZ) band in autosomal dominant and x-linked retinitis pigmentosa. Cai CX; Locke KG; Ramachandran R; Birch DG; Hood DC Invest Ophthalmol Vis Sci; 2014 Oct; 55(11):7417-22. PubMed ID: 25342618 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]