114 related articles for article (PubMed ID: 23521034)
1. Retinitis pigmentosa and granular dystrophy: a rare and unique combination in one patient.
Crawford C
Binocul Vis Strabolog Q Simms Romano; 2013; 28(1):36-8. PubMed ID: 23521034
[TBL] [Abstract][Full Text] [Related]
2. IMPG2-associated retinitis pigmentosa displays relatively early macular involvement.
van Huet RA; Collin RW; Siemiatkowska AM; Klaver CC; Hoyng CB; Simonelli F; Khan MI; Qamar R; Banin E; Cremers FP; Theelen T; den Hollander AI; van den Born LI; Klevering BJ
Invest Ophthalmol Vis Sci; 2014 May; 55(6):3939-53. PubMed ID: 24876279
[TBL] [Abstract][Full Text] [Related]
3. Unilateral retinitis pigmentosa.
Bhattarai D; Paudel N; Adhikari P; Gnyawali S; Joshi SN
Nepal J Ophthalmol; 2015; 7(1):56-9. PubMed ID: 26695607
[TBL] [Abstract][Full Text] [Related]
4. [Long-term follow-up of a case of unilateral retinitis pigmentosa].
Kato K; Miyake Y; Matsubara H; Uji Y
Nippon Ganka Gakkai Zasshi; 2012 Nov; 116(11):1086-93. PubMed ID: 23316657
[TBL] [Abstract][Full Text] [Related]
5. Unilateral retinitis pigmentosa with amblyopia in the fellow eye.
Chen H; Wu D; Huang S; Jiang F
Graefes Arch Clin Exp Ophthalmol; 2006 Dec; 244(12):1701-4. PubMed ID: 16598464
[TBL] [Abstract][Full Text] [Related]
6. Nonclassic retinitis pigmentosa: A challenging clinical diagnosis solved by pedigree analysis and electrodiagnostic testing.
Lanier KT; Joy JT; Morris RW
Optometry; 2010 Apr; 81(4):181-7. PubMed ID: 20346889
[TBL] [Abstract][Full Text] [Related]
7. Retinitis pigmentosa and bilateral cystoid macular oedema in a patient heterozygous for the RIM1 mutation previously associated with cone-rod dystrophy 7.
Warwick AN; Shawkat F; Lotery AJ
Ophthalmic Genet; 2017; 38(2):178-182. PubMed ID: 27176872
[TBL] [Abstract][Full Text] [Related]
8. Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 gene.
Hugosson T; Friedman JS; Ponjavic V; Abrahamson M; Swaroop A; Andréasson S
Arch Ophthalmol; 2010 Jun; 128(6):772-8. PubMed ID: 20547956
[TBL] [Abstract][Full Text] [Related]
9. Wide-field fundus autofluorescence abnormalities and visual function in patients with cone and cone-rod dystrophies.
Oishi M; Oishi A; Ogino K; Makiyama Y; Gotoh N; Kurimoto M; Yoshimura N
Invest Ophthalmol Vis Sci; 2014 May; 55(6):3572-7. PubMed ID: 24845635
[TBL] [Abstract][Full Text] [Related]
10. ERG and other discriminators between advanced hydroxychloroquine retinopathy and retinitis pigmentosa.
Nair AA; Marmor MF
Doc Ophthalmol; 2017 Jun; 134(3):175-183. PubMed ID: 28451987
[TBL] [Abstract][Full Text] [Related]
11. [A case of monocular retinitis pigmentosa (author's transl)].
Grüntzig J; Leide E; Tillmann W
Klin Monbl Augenheilkd; 1975 Nov; 167(5):737-41. PubMed ID: 1206957
[TBL] [Abstract][Full Text] [Related]
12. Clinical characteristics of rod and cone photoreceptor dystrophies in patients with mutations in the C8orf37 gene.
van Huet RA; Estrada-Cuzcano A; Banin E; Rotenstreich Y; Hipp S; Kohl S; Hoyng CB; den Hollander AI; Collin RW; Klevering BJ
Invest Ophthalmol Vis Sci; 2013 Jul; 54(7):4683-90. PubMed ID: 23788369
[TBL] [Abstract][Full Text] [Related]
13. Coats-type retinitis pigmentosa in a 4-year-old child.
Kim RY; Kearney JJ
Am J Ophthalmol; 1997 Dec; 124(6):846-8. PubMed ID: 9402836
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. 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]
16. Intravitreal injection of autologous bone marrow-derived mononuclear cells for hereditary retinal dystrophy: a phase I trial.
Siqueira RC; Messias A; Voltarelli JC; Scott IU; Jorge R
Retina; 2011 Jun; 31(6):1207-14. PubMed ID: 21293313
[TBL] [Abstract][Full Text] [Related]
17. Asymmetric retinitis pigmentosa, luetic retinopathy and the question of unilateral retinitis pigmentosa.
Skalka HW
Acta Ophthalmol (Copenh); 1979 Jun; 57(3):351-7. PubMed ID: 474081
[TBL] [Abstract][Full Text] [Related]
18. Full-field ERG, multifocal ERG and multifocal VEP in patients with retinitis pigmentosa and residual central visual fields.
Gränse L; Ponjavic V; Andréasson S
Acta Ophthalmol Scand; 2004 Dec; 82(6):701-6. PubMed ID: 15606467
[TBL] [Abstract][Full Text] [Related]
19. SPATA7: Evolving phenotype from cone-rod dystrophy to retinitis pigmentosa.
Matsui R; McGuigan Iii DB; Gruzensky ML; Aleman TS; Schwartz SB; Sumaroka A; Koenekoop RK; Cideciyan AV; Jacobson SG
Ophthalmic Genet; 2016 Sep; 37(3):333-8. PubMed ID: 26854980
[TBL] [Abstract][Full Text] [Related]
20. Unilateral retinitis pigmentosa. A case report.
Nazar C; Feldman M; González R; Espinoza R
Arch Soc Esp Oftalmol; 2017 Jun; 92(6):287-290. PubMed ID: 27793487
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]