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183 related items for PubMed ID: 3498069

  • 21. Multifocal oscillatory potentials in CSNB1 and CSNB2 type congenital stationary night blindness.
    Schuster A, Pusch CM, Gamer D, Apfelstedt-Sylla E, Zrenner E, Kurtenbach A.
    Int J Mol Med; 2005 Jan; 15(1):159-67. PubMed ID: 15583843
    [Abstract] [Full Text] [Related]

  • 22. Possible pathogenesis of congenital stationary night blindness.
    Kato M, Aonuma H, Kawamura H, Miura Y, Watanabe I.
    Jpn J Ophthalmol; 1987 Jan; 31(1):88-101. PubMed ID: 3498070
    [Abstract] [Full Text] [Related]

  • 23. Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene.
    Scholl HP, Langrová H, Pusch CM, Wissinger B, Zrenner E, Apfelstedt-Sylla E.
    Invest Ophthalmol Vis Sci; 2001 Oct; 42(11):2728-36. PubMed ID: 11581222
    [Abstract] [Full Text] [Related]

  • 24. [Flash full-field electroretinography in diseases with night blindness].
    Pojda-Wilczek D, Herba E, Pojda SM.
    Klin Oczna; 2005 Oct; 107(1-3):28-30. PubMed ID: 16052794
    [Abstract] [Full Text] [Related]

  • 25. The negative ERG is not synonymous with nightblindness.
    Cibis GW, Fitzgerald KM.
    Trans Am Ophthalmol Soc; 2001 Oct; 99():171-5; discussion 175-6. PubMed ID: 11797304
    [Abstract] [Full Text] [Related]

  • 26. Blue-on-yellow perimetry in the complete type of congenital stationary night blindness.
    Terasaki H, Miyake Y, Nomura R, Horiguchi M, Suzuki S, Kondo M.
    Invest Ophthalmol Vis Sci; 1999 Oct; 40(11):2761-4. PubMed ID: 10509678
    [Abstract] [Full Text] [Related]

  • 27. Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX gene.
    Jacobi FK, Andréasson S, Langrova H, Meindl A, Zrenner E, Apfelstedt-Sylla E, Pusch CM.
    Graefes Arch Clin Exp Ophthalmol; 2002 Oct; 240(10):822-8. PubMed ID: 12397430
    [Abstract] [Full Text] [Related]

  • 28. Visual evoked potentials with crossed asymmetry in incomplete congenital stationary night blindness.
    Tremblay F, De Becker I, Cheung C, LaRoche GR.
    Invest Ophthalmol Vis Sci; 1996 Aug; 37(9):1783-92. PubMed ID: 8759345
    [Abstract] [Full Text] [Related]

  • 29. Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.
    Zeitz C, van Genderen M, Neidhardt J, Luhmann UF, Hoeben F, Forster U, Wycisk K, Mátyás G, Hoyng CB, Riemslag F, Meire F, Cremers FP, Berger W.
    Invest Ophthalmol Vis Sci; 2005 Nov; 46(11):4328-35. PubMed ID: 16249515
    [Abstract] [Full Text] [Related]

  • 30. Rapid off-response and retinal receptor diseases.
    Iijima H.
    Jpn J Ophthalmol; 1984 Nov; 28(2):147-58. PubMed ID: 6471606
    [Abstract] [Full Text] [Related]

  • 31. 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
    [Abstract] [Full Text] [Related]

  • 32. 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; 88(8):1018-22. PubMed ID: 15258017
    [Abstract] [Full Text] [Related]

  • 33. Undetectable S cone electroretinogram b-wave in complete congenital stationary night blindness.
    Kamiyama M, Yamamoto S, Nitta K, Hayasaka S.
    Br J Ophthalmol; 1996 Jul; 80(7):637-9. PubMed ID: 8795377
    [Abstract] [Full Text] [Related]

  • 34. Anesthetically blocked optic nerve conduction in congenital stationary night blindness.
    Miyake Y.
    Jpn J Ophthalmol; 1992 Jul; 36(3):239-41. PubMed ID: 1464964
    [Abstract] [Full Text] [Related]

  • 35. A dominant form of congenital stationary night blindness (adCSNB) in a large Chinese family.
    Liu X, Zhuang S, Hu S, Zhang F, Lin B, Li X, Xu D, Chen SH.
    Ann Hum Genet; 2005 May; 69(Pt 3):315-21. PubMed ID: 15845035
    [Abstract] [Full Text] [Related]

  • 36. A naturally occurring mouse model of X-linked congenital stationary night blindness.
    Pardue MT, McCall MA, LaVail MM, Gregg RG, Peachey NS.
    Invest Ophthalmol Vis Sci; 1998 Nov; 39(12):2443-9. PubMed ID: 9804152
    [Abstract] [Full Text] [Related]

  • 37. Photopic ON- and OFF-responses in complete type of congenital stationary night blindness in relation to stimulus intensity.
    Sustar M, Stirn-Kranjc B, Hawlina M, Brecelj J.
    Doc Ophthalmol; 2008 Jul; 117(1):37-46. PubMed ID: 18026866
    [Abstract] [Full Text] [Related]

  • 38. Congenital stationary night blindness: an animal model.
    Witzel DA, Smith EL, Wilson RD, Aguirre GD.
    Invest Ophthalmol Vis Sci; 1978 Aug; 17(8):788-95. PubMed ID: 308060
    [Abstract] [Full Text] [Related]

  • 39. 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; 42(11):1475-83. PubMed ID: 12044753
    [Abstract] [Full Text] [Related]

  • 40. Extracting the ON and OFF contributions to the full-field photopic flash electroretinogram using summed growth curves.
    Akula JD, Ambrosio L, Howard FI, Hansen RM, Fulton AB.
    Exp Eye Res; 2019 Dec; 189():107827. PubMed ID: 31600486
    [Abstract] [Full Text] [Related]

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