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Journal Abstract Search

183 related items for PubMed ID: 3498069

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  • 2. Characteristic ERG-flicker anomaly in incomplete congenital stationary night blindness.
    Miyake Y, Horiguchi M, Ota I, Shiroyama N.
    Invest Ophthalmol Vis Sci; 1987 Nov; 28(11):1816-23. PubMed ID: 3499417
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  • 3. Scotopic threshold response in complete and incomplete types of congenital stationary night blindness.
    Miyake Y, Horiguchi M, Terasaki H, Kondo M.
    Invest Ophthalmol Vis Sci; 1994 Sep; 35(10):3770-5. PubMed ID: 8088964
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  • 4. Electrophysiological findings in patients with Oguchi's disease.
    Miyake Y, Horiguchi M, Suzuki S, Kondo M, Tanikawa A.
    Jpn J Ophthalmol; 1996 Sep; 40(4):511-9. PubMed ID: 9130055
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  • 5. Primate Retinal Signaling Pathways: Suppressing ON-Pathway Activity in Monkey With Glutamate Analogues Mimics Human CSNB1-NYX Genetic Night Blindness.
    Khan NW, Kondo M, Hiriyanna KT, Jamison JA, Bush RA, Sieving PA.
    J Neurophysiol; 2005 Jan; 93(1):481-92. PubMed ID: 15331616
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  • 16. Clinical findings in patients with congenital stationary night blindness of the Schubert-Bornschein type.
    Ruether K, Apfelstedt-Sylla E, Zrenner E.
    Ger J Ophthalmol; 1993 Nov; 2(6):429-35. PubMed ID: 8312830
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  • 17. Paradoxic pupillary constriction in a patient with congenital stationary night blindness.
    Myers GA, Barricks ME, Stark L.
    Invest Ophthalmol Vis Sci; 1985 May; 26(5):736-40. PubMed ID: 3873442
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  • 18. Congenital stationary night blindness with negative electroretinogram. A new classification.
    Miyake Y, Yagasaki K, Horiguchi M, Kawase Y, Kanda T.
    Arch Ophthalmol; 1986 Jul; 104(7):1013-20. PubMed ID: 3488053
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  • 20. A rod-cone dysfunction syndrome with separate clinical entity: incomplete-type congenital stationary night blindness (Miyake).
    Miyake Y, Yagasaki K, Horiguchi M.
    Prog Clin Biol Res; 1987 Jul; 247():137-45. PubMed ID: 3500478
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