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Journal Abstract Search


62 related items for PubMed ID: 2785978

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

  • 22. 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]

  • 23. Study of rod- and cone-driven oscillatory potentials in mice.
    Lei B, Yao G, Zhang K, Hofeldt KJ, Chang B.
    Invest Ophthalmol Vis Sci; 2006 Jun; 47(6):2732-8. PubMed ID: 16723493
    [Abstract] [Full Text] [Related]

  • 24. Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
    Bech-Hansen NT, Naylor MJ, Maybaum TA, Pearce WG, Koop B, Fishman GA, Mets M, Musarella MA, Boycott KM.
    Nat Genet; 1998 Jul; 19(3):264-7. PubMed ID: 9662400
    [Abstract] [Full Text] [Related]

  • 25. 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
    [Abstract] [Full Text] [Related]

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

  • 27. 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
    [Abstract] [Full Text] [Related]

  • 28. 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
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  • 32. LED-generated multifocal ERG on- and off-responses in complete congenital stationary night blindness -- a case report.
    Leifert D, Todorova MG, Prünte C, Palmowski-Wolfe AM.
    Doc Ophthalmol; 2005 Jul; 111(1):1-6. PubMed ID: 16502301
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  • 33. On- and off-responses in the photopic electroretinogram in complete-type congenital stationary night blindness.
    Quigley M, Roy MS, Barsoum-Homsy M, Chevrette L, Jacob JL, Milot J.
    Doc Ophthalmol; 2005 Jul; 92(3):159-65. PubMed ID: 9181343
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  • 34. Retinal dysfunction in carriers of bardet-biedl syndrome.
    Kim LS, Fishman GA, Seiple WH, Szlyk JP, Stone EM.
    Ophthalmic Genet; 2007 Sep; 28(3):163-8. PubMed ID: 17896315
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  • 35. Abnormalities of the scotopic threshold response correlated with gene mutation in X-linked retinoschisis and congenital stationary night blindness.
    Bradshaw K, Newman D, Allen L, Moore A.
    Doc Ophthalmol; 2003 Sep; 107(2):155-64. PubMed ID: 14661905
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  • 36. Congenital stationary night blindness.
    Haim M.
    Acta Ophthalmol (Copenh); 1986 Apr; 64(2):192-8. PubMed ID: 3487908
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  • 37. Increased phase lag of the fundamental harmonic component of the 30 Hz flicker ERG in Schubert-Bornschein complete type CSNB.
    Kim SH, Bush RA, Sieving PA.
    Vision Res; 1997 Sep; 37(17):2471-5. PubMed ID: 9381682
    [Abstract] [Full Text] [Related]

  • 38. The Briard dog: a new animal model of congenital stationary night blindness.
    Narfström K, Wrigstad A, Nilsson SE.
    Br J Ophthalmol; 1989 Sep; 73(9):750-6. PubMed ID: 2804031
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  • 39. Incomplete congenital stationary night blindness: electroretinogram c-wave and electrooculogram light rise.
    Takahashi Y, Onoe S, Asamizu N, Mori T, Yoshimura Y, Tazawa Y.
    Doc Ophthalmol; 1988 Sep; 70(1):67-75. PubMed ID: 3265910
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