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Journal Abstract Search

99 related items for PubMed ID: 7887150

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  • 9. A variant of central areolar choroidal dystrophy.
    Chopdar A.
    Ophthalmic Paediatr Genet; 1993 Dec; 14(4):151-64. PubMed ID: 8015786
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  • 10. Familial macular cone dystrophy: diagnostic value of multifocal ERG and two-color threshold perimetry.
    Kretschmann U, Stilling R, Rüther K, Zrenner E.
    Graefes Arch Clin Exp Ophthalmol; 1999 May; 237(5):429-32. PubMed ID: 10333111
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  • 13. The development of central areolar choroidal dystrophy.
    Hoyng CB, Deutman AF.
    Graefes Arch Clin Exp Ophthalmol; 1996 Feb; 234(2):87-93. PubMed ID: 8720677
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  • 14. Foveal cone dysfunction syndrome.
    ten Hove MW, Siatkowski RM, Smith JL.
    J Neuroophthalmol; 1998 Mar; 18(1):9-14. PubMed ID: 9532531
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  • 17. CNGB3 achromatopsia with progressive loss of residual cone function and impaired rod-mediated function.
    Khan NW, Wissinger B, Kohl S, Sieving PA.
    Invest Ophthalmol Vis Sci; 2007 Aug; 48(8):3864-71. PubMed ID: 17652762
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  • 18. High-Resolution Adaptive Optics Retinal Image Analysis at Early Stage Central Areolar Choroidal Dystrophy With PRPH2 Mutation.
    Gocho K, Akeo K, Itoh N, Kameya S, Hayashi T, Katagiri S, Gekka T, Ohkuma Y, Tsuneoka H, Takahashi H.
    Ophthalmic Surg Lasers Imaging Retina; 2016 Dec 01; 47(12):1115-1126. PubMed ID: 27977834
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  • 19. 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 01; 42(6):1380-9. PubMed ID: 11328755
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