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6. Cone electroretinograms in congenital nyctalopia with myopia. Hill DA; Arbel KF; Berson EL Am J Ophthalmol; 1974 Jul; 78(1):127-36. PubMed ID: 4546161 [No Abstract] [Full Text] [Related]
7. Recovery of the human early receptor potential during dark adaptation in hereditary retinal disease. Berson EL; Goldstein EB Vision Res; 1970 Mar; 10(3):219-26. PubMed ID: 5311448 [No Abstract] [Full Text] [Related]
8. 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]
9. Electroretinographic studies of families with dominant retinitis pigmentosa. Andréasson S Acta Ophthalmol (Copenh); 1991 Apr; 69(2):162-8. PubMed ID: 1872134 [TBL] [Abstract][Full Text] [Related]
10. [Pseudoretinopathia pigmentosa following measles]. Jünemann G; Damaske E Med Klin; 1968 Oct; 63(42):1687-90. PubMed ID: 5725567 [No Abstract] [Full Text] [Related]
11. Light deprivation and retinitis pigmentosa. Berson EL Vision Res; 1980; 20(12):1179-84. PubMed ID: 7269274 [No Abstract] [Full Text] [Related]
12. X-linked retinitis pigmentosa: functional phenotype of an RP2 genotype. Jacobson SG; Roman AJ; Cideciyan AV; Robey MG; Iwata T; Inana G Invest Ophthalmol Vis Sci; 1992 Dec; 33(13):3481-92. PubMed ID: 1464493 [TBL] [Abstract][Full Text] [Related]
13. The early receptor potential in sex-linked retinitis pigmentosa. Berson EL; Goldstein EB Invest Ophthalmol; 1970 Jan; 9(1):58-63. PubMed ID: 5411252 [No Abstract] [Full Text] [Related]
14. 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]
15. A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa. Rosenfeld PJ; Cowley GS; McGee TL; Sandberg MA; Berson EL; Dryja TP Nat Genet; 1992 Jun; 1(3):209-13. PubMed ID: 1303237 [TBL] [Abstract][Full Text] [Related]
16. Dominant retinitis pigmentosa with reduced penetrance. Further studies of the electroretinogram. Berson EL; Simonoff EA Arch Ophthalmol; 1979 Jul; 97(7):1286-91. PubMed ID: 454264 [TBL] [Abstract][Full Text] [Related]
17. Two forms of autosomal dominant primary retinitis pigmentosa. Massof RW; Finkelstein D Doc Ophthalmol; 1981 Nov; 51(4):289-346. PubMed ID: 6975710 [TBL] [Abstract][Full Text] [Related]
18. Progressive generalized cone dysfunction. François J; de Rouck A; Verriest G; de Laey JJ; Cambie E Ophthalmologica; 1974; 169(4):255-84. PubMed ID: 4547582 [No Abstract] [Full Text] [Related]
19. Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study. Moore AT; Fitzke F; Jay M; Arden GB; Inglehearn CF; Keen TJ; Bhattacharya SS; Bird AC Br J Ophthalmol; 1993 Aug; 77(8):473-9. PubMed ID: 8025041 [TBL] [Abstract][Full Text] [Related]
20. Rod and cone activity in patients with dominantly inherited retinitis pigmentosa: comparisons between psychophysical and electroretinographic measurements. Arden GB; Carter RM; Hogg CR; Powell DJ; Ernst WJ; Clover GM; Lyness AL; Quinlan MP Br J Ophthalmol; 1983 Jul; 67(7):405-18. PubMed ID: 6860608 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]