These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
118 related articles for article (PubMed ID: 4042819)
41. [C-wave changes in macular diseases]. Moschos M; Brouza D; Panagakis E J Fr Ophtalmol; 1989; 12(10):651-6. PubMed ID: 2638360 [TBL] [Abstract][Full Text] [Related]
42. L- and M-cone-driven electroretinograms in Stargardt's macular dystrophy-fundus flavimaculatus. Scholl HP; Kremers J; Vonthein R; White K; Weber BH Invest Ophthalmol Vis Sci; 2001 May; 42(6):1380-9. PubMed ID: 11328755 [TBL] [Abstract][Full Text] [Related]
43. Cross-sectional study of visual acuity and electroretinogram in two types of dominant drusen. Gerber DM; Munier FL; Niemeyer G Invest Ophthalmol Vis Sci; 2003 Feb; 44(2):493-6. PubMed ID: 12556373 [TBL] [Abstract][Full Text] [Related]
44. Electrophysiological and microperimetry changes in vitamin A deficiency retinopathy. Saker S; Morales M; Jhittay H; Wen Y; Amoaku W Doc Ophthalmol; 2015 Jun; 130(3):231-40. PubMed ID: 25626405 [TBL] [Abstract][Full Text] [Related]
45. Electrophysiology and inherited retinal disorders. Fishman GA Doc Ophthalmol; 1985 Aug; 60(2):107-19. PubMed ID: 3899558 [TBL] [Abstract][Full Text] [Related]
46. [From the symptom to electroretinography diagnosis]. Niemeyer G Klin Monbl Augenheilkd; 1999 May; 214(5):328-31. PubMed ID: 10420379 [TBL] [Abstract][Full Text] [Related]
47. Macular dysfunction and morphology in spinocerebellar ataxia type 7 (SCA 7). Hugosson T; Gränse L; Ponjavic V; Andréasson S Ophthalmic Genet; 2009 Mar; 30(1):1-6. PubMed ID: 19172503 [TBL] [Abstract][Full Text] [Related]
48. Full-field ERG as a predictor of the natural course of Schroeder M; Kjellström U Mol Vis; 2018; 24():1-16. PubMed ID: 29386879 [TBL] [Abstract][Full Text] [Related]
49. Longitudinal characterisation of function and structure of Bietti crystalline dystrophy: report on a novel homozygous mutation in Lockhart CM; Smith TB; Yang P; Naidu M; Rettie AE; Nath A; Weleber R; Kelly EJ Br J Ophthalmol; 2018 Feb; 102(2):187-194. PubMed ID: 28698241 [TBL] [Abstract][Full Text] [Related]
50. Studies on the retina and the pigment epithelium in hereditary canine ceroid lipofuscinosis. IV. Changes in the electroretinogram and the standing potential of the eye. Nilsson SE; Armstrong D; Koppang N; Persson P; Milde K Invest Ophthalmol Vis Sci; 1983 Jan; 24(1):77-84. PubMed ID: 6681808 [TBL] [Abstract][Full Text] [Related]
51. Relationship of drusen and abnormalities of the retinal pigment epithelium to the prognosis of neovascular macular degeneration. The Macular Photocoagulation Study Group. Bressler SB; Maguire MG; Bressler NM; Fine SL Arch Ophthalmol; 1990 Oct; 108(10):1442-7. PubMed ID: 1699513 [TBL] [Abstract][Full Text] [Related]
52. Low b-wave amplitudes in a strain of rabbits with a pigment epithelium defect. Lichtenberger T; Karbaum R; Flade A; Hanitzsch R Vision Res; 2000; 40(1):129-36. PubMed ID: 10768047 [TBL] [Abstract][Full Text] [Related]
53. Hereditary retinal degeneration in the Abyssinian cat: correlation of ophthalmoscopic and electroretinographic findings. Narfström K; Nilsson SE Doc Ophthalmol; 1985 Aug; 60(2):183-7. PubMed ID: 4042824 [TBL] [Abstract][Full Text] [Related]
57. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation. Smith PR; Bain SC; Good PA; Hattersley AT; Barnett AH; Gibson JM; Dodson PM Ophthalmology; 1999 Jun; 106(6):1101-8. PubMed ID: 10366077 [TBL] [Abstract][Full Text] [Related]