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3. [Electrophysiological study on the retinitis pigmentosa]. Imaizumi K Nippon Ganka Gakkai Zasshi; 1969 Nov; 73(11):2347-496. PubMed ID: 5391946 [No Abstract] [Full Text] [Related]
4. Clinical measures of visual function in familial retinitis pigmentosa. Williams TD; Lovasik JV Am J Optom Physiol Opt; 1985 Jan; 62(1):45-51. PubMed ID: 3976835 [TBL] [Abstract][Full Text] [Related]
5. Temporal aspects of the electroretinogram in sector retinitis pigmentosa. Berson EL; Howard J Arch Ophthalmol; 1971 Dec; 86(6):653-65. PubMed ID: 5128159 [No Abstract] [Full Text] [Related]
6. [Histology of retinopathia pigmentosa cum et sine pigmento (author's transl)]. Eichholtz W Klin Monbl Augenheilkd; 1974 Apr; 164(4):467-75. PubMed ID: 4843831 [No Abstract] [Full Text] [Related]
7. Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutation. Moore AT; Fitzke FW; Kemp CM; Arden GB; Keen TJ; Inglehearn CF; Bhattacharya SS; Bird AC Br J Ophthalmol; 1992 Aug; 76(8):465-9. PubMed ID: 1390527 [TBL] [Abstract][Full Text] [Related]
8. Statistical evaluation of visual functions in dominant and recessive autosomal pigmentary retinopathy. De Rouck A; de Bie S; Kayembe D Doc Ophthalmol; 1986 Mar; 62(3):265-80. PubMed ID: 3698795 [TBL] [Abstract][Full Text] [Related]
9. Sector retinitis pigmentosa. Electrophysiological and psychophysical study of the visual system. Abraham FA Doc Ophthalmol; 1975 Nov; 39(1):13-28. PubMed ID: 1201696 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Clinical features of autosomal dominant retinitis pigmentosa with rhodopsin gene codon 17 mutation and retinal neovascularization in a Japanese patient. Hayakawa M; Hotta Y; Imai Y; Fujiki K; Nakamura A; Yanashima K; Kanai A Am J Ophthalmol; 1993 Feb; 115(2):168-73. PubMed ID: 7679248 [TBL] [Abstract][Full Text] [Related]
13. The clinical significance of retinitis pigmentosa without pigment: a computer assisted analysis. Pearlman JT; Saxton J; Flood TP; Seiff SR Adv Exp Med Biol; 1977; 77():31-5. PubMed ID: 322461 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. The natural history of retinitis pigmentosa. Weinstein GW Adv Exp Med Biol; 1977; 77():3-23. PubMed ID: 848398 [No Abstract] [Full Text] [Related]
16. Clinical symptoms at different ages in autosomal dominant retinitis pigmentosa. A family study in three generations. Mäntyjärvi M; Tuppurainen K Ophthalmologica; 1994; 208(1):23-8. PubMed ID: 8145980 [TBL] [Abstract][Full Text] [Related]
17. [The electroretinogram in central retinitis pigmentosa]. Hommer K Albrecht Von Graefes Arch Klin Exp Ophthalmol; 1969; 178(1):30-43. PubMed ID: 5306791 [No Abstract] [Full Text] [Related]