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5. Ocular manifestations in autosomal dominant retinitis pigmentosa with a Lys-296-Glu rhodopsin mutation at the retinal binding site. Owens SL; Fitzke FW; Inglehearn CF; Jay M; Keen TJ; Arden GB; Bhattacharya SS; Bird AC Br J Ophthalmol; 1994 May; 78(5):353-8. PubMed ID: 8025068 [TBL] [Abstract][Full Text] [Related]
6. Retinitis pigmentosa: accelerated course of visual loss secondary to exogenous thyroid administration. Pearlman JT; Saxton J; Van Herle A Adv Exp Med Biol; 1977; 77():223-32. PubMed ID: 300551 [TBL] [Abstract][Full Text] [Related]
7. Report of a case of retinitis pigmentosa follow-up from 7 months to 27 years of age. Zetterström B Acta Ophthalmol (Copenh); 1974; 52(3):349-52. PubMed ID: 4546901 [No Abstract] [Full Text] [Related]
8. Snowflake degeneration: an independent entity or a variant of retinitis pigmentosa? Chen CJ; Everett TK; Marascalco D South Med J; 1986 Oct; 79(10):1216-23. PubMed ID: 3489996 [TBL] [Abstract][Full Text] [Related]
9. Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene. Bessant DA; Holder GE; Fitzke FW; Payne AM; Bhattacharya SS; Bird AC Arch Ophthalmol; 2003 Jun; 121(6):793-802. PubMed ID: 12796249 [TBL] [Abstract][Full Text] [Related]
11. Low incidence of retinitis pigmentosa among heterozygous carriers of a specific rhodopsin splice site mutation. Rosenfeld PJ; Hahn LB; Sandberg MA; Dryja TP; Berson EL Invest Ophthalmol Vis Sci; 1995 Oct; 36(11):2186-92. PubMed ID: 7558711 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Retinitis pigmentosa and allied diseases: applications of electroretinographic testing. Berson EL Int Ophthalmol; 1981 Aug; 4(1-2):7-22. PubMed ID: 7028651 [TBL] [Abstract][Full Text] [Related]
14. Electroretinographic findings in retinitis pigmentosa. Berson EL Jpn J Ophthalmol; 1987; 31(3):327-48. PubMed ID: 2448510 [TBL] [Abstract][Full Text] [Related]
15. No pigment deposition in a patient with advanced retinitis punctata albescens. Fujii M; Hayasaka S Ophthalmologica; 1994; 208(6):339-41. PubMed ID: 7845653 [TBL] [Abstract][Full Text] [Related]
16. Clinical features of Japanese family with autosomal dominant retinitis pigmentosa caused by point mutation in codon 347 of rhodopsin gene. Shiono T; Hotta Y; Noro M; Sakuma T; Tamai M; Hayakawa M; Hashimoto T; Fujiki K; Kanai A; Nakajima A Jpn J Ophthalmol; 1992; 36(1):69-75. PubMed ID: 1635298 [TBL] [Abstract][Full Text] [Related]
17. Clinical investigation of retinitis pigmentosa. Bird AC Aust N Z J Ophthalmol; 1988 Aug; 16(3):189-98. PubMed ID: 3052528 [TBL] [Abstract][Full Text] [Related]
19. Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypes. Neidhardt J; Barthelmes D; Farahmand F; Fleischhauer JC; Berger W Invest Ophthalmol Vis Sci; 2006 Apr; 47(4):1630-5. PubMed ID: 16565402 [TBL] [Abstract][Full Text] [Related]
20. A clinical, psychophysical, and electroretinographic survey of patients with autosomal dominant retinitis pigmentosa. Lyness AL; Ernst W; Quinlan MP; Clover GM; Arden GB; Carter RM; Bird AC; Parker JA Br J Ophthalmol; 1985 May; 69(5):326-39. PubMed ID: 3873253 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]