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9. Compound heterozygous RDH5 mutations in familial fleck retina with night blindness. Hayashi T; Goto-Omoto S; Takeuchi T; Gekka T; Ueoka Y; Kitahara K Acta Ophthalmol Scand; 2006 Apr; 84(2):254-8. PubMed ID: 16637847 [TBL] [Abstract][Full Text] [Related]
10. [Electroretinographic and electroencephalographic studies in Stargardt's disease]. François J; De Rouck A Klin Monbl Augenheilkd; 1965 Dec; 147(5):654-62. PubMed ID: 5869305 [No Abstract] [Full Text] [Related]
11. [Congenital stationary night blindness]. Kocyła-Karczmarewicz B; Grałek M; Juszko J; Trzebicka A; Sarti G Klin Oczna; 2004; 106(3 Suppl):509-11. PubMed ID: 15636252 [TBL] [Abstract][Full Text] [Related]
12. Electro-retino-encephalography in Leber's tapeto-retinal dystrophy. Firat T Turk J Pediatr; 1969 Apr; 11(2):51-6. PubMed ID: 5369924 [No Abstract] [Full Text] [Related]
13. On very short wavelength electroretinography. An original technique of diagnosis in infraclinical synthetic antimalarial retinopathies. Alfieri R; Sole P Ophthalmologica; 1969; 158 Suppl():661-8. PubMed ID: 5359763 [No Abstract] [Full Text] [Related]
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17. [Congenital stationary night blindness]. Svĕrák J; Jebavá R; Peregrin J; Zizka J; Hartmann M Cesk Slov Oftalmol; 1996 Jul; 52(3):135-42. PubMed ID: 8768469 [TBL] [Abstract][Full Text] [Related]
18. Novel CACNA1F mutations in Japanese patients with incomplete congenital stationary night blindness. Nakamura M; Ito S; Terasaki H; Miyake Y Invest Ophthalmol Vis Sci; 2001 Jun; 42(7):1610-6. PubMed ID: 11381068 [TBL] [Abstract][Full Text] [Related]
19. The ERG in amblyopia. Ruedemann AD Trans Am Ophthalmol Soc; 1966; 64():163-84. PubMed ID: 5964921 [No Abstract] [Full Text] [Related]
20. The electroretinographic and electrooculographic findings in patients with macular lesions. Krill AE Trans Am Acad Ophthalmol Otolaryngol; 1966; 70(6):1063-83. PubMed ID: 5971470 [No Abstract] [Full Text] [Related] [Next] [New Search]