153 related articles for article (PubMed ID: 22605925)
1. A tapetal-like fundus reflex in a healthy male: evidence against a role in the pathophysiology of retinal degeneration?
Schatz P; Bregnhøj J; Arvidsson H; Sharon D; Mizrahi-Meissonnier L; Sander B; Grønskov K; Larsen M
Mol Vis; 2012; 18():1147-55. PubMed ID: 22605925
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. A longitudinal study of visual function in carriers of X-linked recessive retinitis pigmentosa.
Grover S; Fishman GA; Anderson RJ; Lindeman M
Ophthalmology; 2000 Feb; 107(2):386-96. PubMed ID: 10690843
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Visual Function in Carriers of X-Linked Retinitis Pigmentosa.
Comander J; Weigel-DiFranco C; Sandberg MA; Berson EL
Ophthalmology; 2015 Sep; 122(9):1899-906. PubMed ID: 26143542
[TBL] [Abstract][Full Text] [Related]
7. Structural and functional characteristics in carriers of X-linked retinitis pigmentosa with a tapetal-like reflex.
Genead MA; Fishman GA; Lindeman M
Retina; 2010; 30(10):1726-33. PubMed ID: 20829740
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. Clinical and Electrophysiologic Characteristics of a Large Kindred with X-Linked Retinitis Pigmentosa Associated with the RPGR Locus.
Tzu JH; Arguello T; Berrocal AM; Berrocal M; Weisman AD; Liu M; Hess D; Caputo M; Goldberg JL; Feuer WJ; Stone EM; Lam BL
Ophthalmic Genet; 2015; 36(4):321-6. PubMed ID: 24555744
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Phenotypic characterization of 3 families with autosomal dominant retinitis pigmentosa due to mutations in KLHL7.
Wen Y; Locke KG; Klein M; Bowne SJ; Sullivan LS; Ray JW; Daiger SP; Birch DG; Hughbanks-Wheaton DK
Arch Ophthalmol; 2011 Nov; 129(11):1475-82. PubMed ID: 22084217
[TBL] [Abstract][Full Text] [Related]
15. Fundus albipunctatus associated with compound heterozygous mutations in RPE65.
Schatz P; Preising M; Lorenz B; Sander B; Larsen M; Rosenberg T
Ophthalmology; 2011 May; 118(5):888-94. PubMed ID: 21211845
[TBL] [Abstract][Full Text] [Related]
16. [Clinical findings in members of a Czech family with retinitis pigmentosa caused by the c.2426_2427delAG mutation in RPGR].
Kousal B; Skalická P; Diblík P; Kuthan P; Langrová H; Lišková P
Cesk Slov Oftalmol; 2013 Mar; 69(1):8-15. PubMed ID: 23822596
[TBL] [Abstract][Full Text] [Related]
17. A new 2-base pair deletion in the RPGR gene in a black family with X-linked retinitis pigmentosa.
Fishman GA; Grover S; Buraczynska M; Wu W; Swaroop A
Arch Ophthalmol; 1998 Feb; 116(2):213-8. PubMed ID: 9488274
[TBL] [Abstract][Full Text] [Related]
18. Detection using the multifocal electroretinogram of mosaic retinal dysfunction in carriers of X-linked retinitis pigmentosa.
Vajaranant TS; Seiple W; Szlyk JP; Fishman GA
Ophthalmology; 2002 Mar; 109(3):560-8. PubMed ID: 11874762
[TBL] [Abstract][Full Text] [Related]
19. Severe retinal degeneration in women with a c.2543del mutation in ORF15 of the RPGR gene.
Kousal B; Skalicka P; Valesova L; Fletcher T; Hart-Holden N; O'Grady A; Chakarova CF; Michaelides M; Hardcastle AJ; Liskova P
Mol Vis; 2014; 20():1307-17. PubMed ID: 25352739
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
