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Journal Abstract Search

199 related items for PubMed ID: 31900741

  • 21. "Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology.
    Robson AG, Webster AR, Michaelides M, Downes SM, Cowing JA, Hunt DM, Moore AT, Holder GE.
    Retina; 2010 Jan; 30(1):51-62. PubMed ID: 19952985
    [Abstract] [Full Text] [Related]

  • 22. 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
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  • 23. Two cases of unilateral cone-rod dysfunction with negative electroretinograms.
    Ozawa K, Takahashi S, Mochizuki K, Miyake Y.
    Doc Ophthalmol; 2019 Dec; 139(3):247-256. PubMed ID: 31375969
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  • 24. Acute unilateral inner retinal dysfunction with photophobia: importance of electrodiagnosis.
    Hirakata T, Fujinami K, Saito W, Kanda A, Hirakata A, Ishida S, Murakami A, Tsunoda K, Miyake Y.
    Jpn J Ophthalmol; 2021 Jan; 65(1):42-53. PubMed ID: 33180210
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  • 25. Novel biallelic TRPM1 variants in an elderly patient with complete congenital stationary night blindness.
    Hayashi T, Mizobuchi K, Kikuchi S, Nakano T.
    Doc Ophthalmol; 2021 Apr; 142(2):265-273. PubMed ID: 33068213
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  • 28. Cone dystrophy with "supernormal" rod ERG: psychophysical testing shows comparable rod and cone temporal sensitivity losses with no gain in rod function.
    Stockman A, Henning GB, Michaelides M, Moore AT, Webster AR, Cammack J, Ripamonti C.
    Invest Ophthalmol Vis Sci; 2014 Feb 10; 55(2):832-40. PubMed ID: 24370833
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  • 33. Electroretinographic (ERG) responses in pediatric patients using vigabatrin.
    Moskowitz A, Hansen RM, Eklund SE, Fulton AB.
    Doc Ophthalmol; 2012 Jun 10; 124(3):197-209. PubMed ID: 22426576
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  • 34. Autosomal dominant congenital stationary night blindness and normal fundus with an electronegative electroretinogram.
    Noble KG, Carr RE, Siegel IM.
    Am J Ophthalmol; 1990 Jan 15; 109(1):44-8. PubMed ID: 2297031
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  • 35. Verifying complaints of difficulties in night vision using electroretinography and dark adaptation tests.
    Allon G, Friedrich Y, Mezer E, Itzhaki A, Leibu R, Perlman I.
    Doc Ophthalmol; 2020 Apr 15; 140(2):169-180. PubMed ID: 31621038
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  • 36. Clinical course of two siblings with potassium voltage-gated channel modifier subfamily V member 2 (KCNV2)-associated retinopathy.
    Sato T, Kuniyoshi K, Hayashi T, Nishiwaki H, Mizobuchi K, Kusaka S.
    Doc Ophthalmol; 2024 Jun 15; 148(3):173-182. PubMed ID: 38630375
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  • 37. A Japanese pedigree of autosomal dominant congenital stationary night blindness with variable expressivity.
    Hayakawa M, Imai Y, Wakita M, Kato K, Yanashima K, Miyake Y, Kanai A.
    Ophthalmic Paediatr Genet; 1992 Dec 15; 13(4):211-7. PubMed ID: 1488221
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  • 38. RP cone-rod degeneration.
    Heckenlively JR.
    Trans Am Ophthalmol Soc; 1987 Dec 15; 85():438-70. PubMed ID: 3447340
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  • 39. Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.
    Lines MA, Hébert M, McTaggart KE, Flynn SJ, Tennant MT, MacDonald IM.
    Ophthalmology; 2002 Oct 15; 109(10):1862-70. PubMed ID: 12359607
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  • 40. A circadian clock regulates the process of ERG b- and d-wave dominance transition in dark-adapted zebrafish.
    Ren JQ, Li L.
    Vision Res; 2004 Oct 15; 44(18):2147-52. PubMed ID: 15183681
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