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Journal Abstract Search

184 related items for PubMed ID: 14680778

  • 21. Rod photoreceptor function in children with mitochondrial disorders.
    Cooper LL, Hansen RM, Darras BT, Korson M, Dougherty FE, Shoffner JM, Fulton AB.
    Arch Ophthalmol; 2002 Aug; 120(8):1055-62. PubMed ID: 12149059
    [Abstract] [Full Text] [Related]

  • 22. ISCEV extended protocol for derivation and analysis of the strong flash rod-isolated ERG a-wave.
    Brigell M, Jeffrey BG, Mahroo OA, Tzekov R.
    Doc Ophthalmol; 2020 Feb; 140(1):5-12. PubMed ID: 31902035
    [Abstract] [Full Text] [Related]

  • 23. A computational model of the amplitude and implicit time of the b-wave of the human ERG.
    Hood DC, Birch DG.
    Vis Neurosci; 1992 Feb; 8(2):107-26. PubMed ID: 1558823
    [Abstract] [Full Text] [Related]

  • 24. Quantitative electroretinogram measures of phototransduction in cone and rod photoreceptors: normal aging, progression with disease, and test-retest variability.
    Birch DG, Hood DC, Locke KG, Hoffman DR, Tzekov RT.
    Arch Ophthalmol; 2002 Aug; 120(8):1045-51. PubMed ID: 12149058
    [Abstract] [Full Text] [Related]

  • 25. Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic association.
    Marmor MF, Zeitz C.
    Doc Ophthalmol; 2018 Aug; 137(1):57-62. PubMed ID: 30051303
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  • 26. Human retinal dark adaptation tracked in vivo with the electroretinogram: insights into processes underlying recovery of cone- and rod-mediated vision.
    Jiang X, Mahroo OA.
    J Physiol; 2022 Nov; 600(21):4603-4621. PubMed ID: 35612091
    [Abstract] [Full Text] [Related]

  • 27. Novel homozygous in-frame deletion of GNAT1 gene causes golden appearance of fundus and reduced scotopic ERGs similar to that in Oguchi disease in Japanese family.
    Kubota D, Oishi N, Gocho K, Kikuchi S, Yamaki K, Igarashi T, Takahashi H, Ishida N, Iwata T, Mizota A, Kameya S.
    Ophthalmic Genet; 2019 Oct; 40(5):480-487. PubMed ID: 31696758
    [Abstract] [Full Text] [Related]

  • 28. Influence of the rod photoresponse on light adaptation and circadian rhythmicity in the cone ERG.
    Cameron MA, Lucas RJ.
    Mol Vis; 2009 Oct 30; 15():2209-16. PubMed ID: 19898639
    [Abstract] [Full Text] [Related]

  • 29. Photoresponses of human rods in vivo derived from paired-flash electroretinograms.
    Pepperberg DR, Birch DG, Hood DC.
    Vis Neurosci; 1997 Oct 30; 14(1):73-82. PubMed ID: 9057270
    [Abstract] [Full Text] [Related]

  • 30. A comparison of ERG abnormalities in XLRS and XLCSNB.
    Bradshaw K, Allen L, Trump D, Hardcastle A, George N, Moore A.
    Doc Ophthalmol; 2004 Mar 30; 108(2):135-45. PubMed ID: 15455796
    [Abstract] [Full Text] [Related]

  • 31. Rod photoreceptor dysfunction in diabetes: activation, deactivation, and dark adaptation.
    Phipps JA, Yee P, Fletcher EL, Vingrys AJ.
    Invest Ophthalmol Vis Sci; 2006 Jul 30; 47(7):3187-94. PubMed ID: 16799066
    [Abstract] [Full Text] [Related]

  • 32. Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.
    Zeitz C, van Genderen M, Neidhardt J, Luhmann UF, Hoeben F, Forster U, Wycisk K, Mátyás G, Hoyng CB, Riemslag F, Meire F, Cremers FP, Berger W.
    Invest Ophthalmol Vis Sci; 2005 Nov 30; 46(11):4328-35. PubMed ID: 16249515
    [Abstract] [Full Text] [Related]

  • 33. Macular Dysfunction in Oguchi Disease with the Frequent Mutation 1147delA in the SAG Gene.
    Hayashi T, Tsuzuranuki S, Kozaki K, Urashima M, Tsuneoka H.
    Ophthalmic Res; 2011 Oct 30; 46(4):175-80. PubMed ID: 21447990
    [Abstract] [Full Text] [Related]

  • 34. RDH5 gene mutations and electroretinogram in fundus albipunctatus with or without macular dystrophy: RDH5 mutations and ERG in fundus albipunctatus.
    Nakamura M, Skalet J, Miyake Y.
    Doc Ophthalmol; 2003 Jul 30; 107(1):3-11. PubMed ID: 12906118
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  • 35. Full-field electroretinogram in autism spectrum disorder.
    Constable PA, Gaigg SB, Bowler DM, Jägle H, Thompson DA.
    Doc Ophthalmol; 2016 Apr 30; 132(2):83-99. PubMed ID: 26868825
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  • 36. Oguchi disease: phenotypic characteristics of patients with the frequent 1147delA mutation in the arrestin gene.
    Nakazawa M, Wada Y, Fuchs S, Gal A, Tamai M.
    Retina; 1997 Apr 30; 17(1):17-22. PubMed ID: 9051837
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  • 37. Cone phototransduction and growth of the ERG b-wave during light adaptation.
    Alexander KR, Raghuram A, Rajagopalan AS.
    Vision Res; 2006 Oct 30; 46(22):3941-8. PubMed ID: 16750238
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  • 38. The scotopic threshold response of the dark-adapted electroretinogram of the mouse.
    Saszik SM, Robson JG, Frishman LJ.
    J Physiol; 2002 Sep 15; 543(Pt 3):899-916. PubMed ID: 12231647
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  • 39. Subjects with unilateral neovascular AMD have bilateral delays in rod-mediated phototransduction activation kinetics and in dark adaptation recovery.
    Dimopoulos IS, Tennant M, Johnson A, Fisher S, Freund PR, Sauvé Y.
    Invest Ophthalmol Vis Sci; 2013 Aug 05; 54(8):5186-95. PubMed ID: 23821195
    [Abstract] [Full Text] [Related]

  • 40. Using Silent Substitution to Track the Mesopic Transition From Rod- to Cone-Based Vision in Mice.
    Allen AE, Lucas RJ.
    Invest Ophthalmol Vis Sci; 2016 Jan 01; 57(1):276-87. PubMed ID: 26818794
    [Abstract] [Full Text] [Related]

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