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Journal Abstract Search

246 related items for PubMed ID: 10189180

  • 1. Evidence supportive of a functional discrimination between photopic oscillatory potentials as revealed with cone and rod mediated retinopathies.
    Lachapelle P, Rousseau S, McKerral M, Benoit J, Polomeno RC, Koenekoop RK, Little JM.
    Doc Ophthalmol; 1998; 95(1):35-54. PubMed ID: 10189180
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  • 2. A distinctive form of congenital stationary night blindness with cone ON-pathway dysfunction.
    Barnes CS, Alexander KR, Fishman GA.
    Ophthalmology; 2002 Mar; 109(3):575-83. PubMed ID: 11874764
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  • 3. The electroretinographic diagnosis of the incomplete form of congenital stationary night blindness.
    Tremblay F, Laroche RG, De Becker I.
    Vision Res; 1995 Aug; 35(16):2383-93. PubMed ID: 7571473
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  • 4. Photoreceptor and postreceptor responses in congenital stationary night blindness.
    Raghuram A, Hansen RM, Moskowitz A, Fulton AB.
    Invest Ophthalmol Vis Sci; 2013 Jul 10; 54(7):4648-58. PubMed ID: 23761088
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  • 5. The photopic electroretinogram in congenital stationary night blindness with myopia.
    Lachapelle P, Little JM, Polomeno RC.
    Invest Ophthalmol Vis Sci; 1983 Apr 10; 24(4):442-50. PubMed ID: 6601088
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  • 6. 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 10; 137(1):57-62. PubMed ID: 30051303
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  • 7. Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy.
    Hayashi T, Hosono K, Kurata K, Katagiri S, Mizobuchi K, Ueno S, Kondo M, Nakano T, Hotta Y.
    Doc Ophthalmol; 2020 Apr 10; 140(2):147-157. PubMed ID: 31583501
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  • 10. "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 10; 30(1):51-62. PubMed ID: 19952985
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  • 11. 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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  • 12. Longitudinal assessment of retinal structure and function reveals a rod-cone degeneration in a guinea pig model initially presented as night blind.
    Racine J, Joly S, Lachapelle P.
    Doc Ophthalmol; 2011 Aug 15; 123(1):1-19. PubMed ID: 21656001
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  • 15. Dysfunction of transmission in the inner retina: incidence and clinical causes of negative electroretinogram.
    Renner AB, Kellner U, Cropp E, Foerster MH.
    Graefes Arch Clin Exp Ophthalmol; 2006 Nov 15; 244(11):1467-73. PubMed ID: 16612636
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