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Journal Abstract Search

193 related items for PubMed ID: 3498070

  • 1. Possible pathogenesis of congenital stationary night blindness.
    Kato M, Aonuma H, Kawamura H, Miura Y, Watanabe I.
    Jpn J Ophthalmol; 1987; 31(1):88-101. PubMed ID: 3498070
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  • 4. Oscillatory potentials and pattern electroretinogram: are they related?
    Litao RE, Miyake Y, Yagasaki K.
    Jpn J Ophthalmol; 1986; 30(4):402-8. PubMed ID: 3495681
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  • 5. [Congenital stationary night blindness].
    Svĕrák J, Jebavá R, Peregrin J, Zizka J, Hartmann M.
    Cesk Slov Oftalmol; 1996 Jul; 52(3):135-42. PubMed ID: 8768469
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  • 6. 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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  • 7. The negative ERG is not synonymous with nightblindness.
    Cibis GW, Fitzgerald KM.
    Trans Am Ophthalmol Soc; 2001 Nov; 99():171-5; discussion 175-6. PubMed ID: 11797304
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  • 8. The photopic electroretinogram in congenital stationary night blindness with myopia.
    Lachapelle P, Little JM, Polomeno RC.
    Invest Ophthalmol Vis Sci; 1983 Apr; 24(4):442-50. PubMed ID: 6601088
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  • 9. [ERG characteristics of congenital stationary night blindness].
    Wu DZ.
    Zhonghua Yan Ke Za Zhi; 1989 Jul; 25(4):203-5. PubMed ID: 2620613
    [Abstract] [Full Text] [Related]

  • 10. Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness.
    Vincent A, Audo I, Tavares E, Maynes JT, Tumber A, Wright T, Li S, Michiels C, GNB3 Consortium, Condroyer C, MacDonald H, Verdet R, Sahel JA, Hamel CP, Zeitz C, Héon E.
    Am J Hum Genet; 2016 May 05; 98(5):1011-1019. PubMed ID: 27063057
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  • 11. [Histological examination of the human retina with congenital stationary night blindness].
    Yamaguchi K, Yamada T, Tamai M.
    Nippon Ganka Gakkai Zasshi; 1995 Apr 05; 99(4):440-4. PubMed ID: 7741056
    [Abstract] [Full Text] [Related]

  • 12. Novel CACNA1F mutations in Japanese patients with incomplete congenital stationary night blindness.
    Nakamura M, Ito S, Terasaki H, Miyake Y.
    Invest Ophthalmol Vis Sci; 2001 Jun 05; 42(7):1610-6. PubMed ID: 11381068
    [Abstract] [Full Text] [Related]

  • 13. 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 05; 137(1):57-62. PubMed ID: 30051303
    [Abstract] [Full Text] [Related]

  • 14. Anesthetically blocked optic nerve conduction in congenital stationary night blindness.
    Miyake Y.
    Jpn J Ophthalmol; 1992 Aug 05; 36(3):239-41. PubMed ID: 1464964
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  • 15. On- and off-responses in photopic electroretinogram in complete and incomplete types of congenital stationary night blindness.
    Miyake Y, Yagasaki K, Horiguchi M, Kawase Y.
    Jpn J Ophthalmol; 1987 Aug 05; 31(1):81-7. PubMed ID: 3498069
    [Abstract] [Full Text] [Related]

  • 16. Congenital stationary night blindness: an animal model.
    Witzel DA, Smith EL, Wilson RD, Aguirre GD.
    Invest Ophthalmol Vis Sci; 1978 Aug 05; 17(8):788-95. PubMed ID: 308060
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  • 17. [Establishment of the concept of new clinical entities--complete and incomplete form of congenital stationary night blindness].
    Miyake Y.
    Nippon Ganka Gakkai Zasshi; 2002 Dec 05; 106(12):737-55; discussion 756. PubMed ID: 12610835
    [Abstract] [Full Text] [Related]

  • 18. 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 05; 35(10):3770-5. PubMed ID: 8088964
    [Abstract] [Full Text] [Related]

  • 19. Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type.
    Langrová H, Gamer D, Friedburg C, Besch D, Zrenner E, Apfelstedt-Sylla E.
    Vision Res; 2002 May 05; 42(11):1475-83. PubMed ID: 12044753
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  • 20. Congenital stationary night blindness and a "Schubert-Bornschein" type electrophysiology in a family with dominant inheritance.
    Kabanarou SA, Holder GE, Fitzke FW, Bird AC, Webster AR.
    Br J Ophthalmol; 2004 Aug 05; 88(8):1018-22. PubMed ID: 15258017
    [Abstract] [Full Text] [Related]

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