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Journal Abstract Search

249 related items for PubMed ID: 17970998

  • 21. [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
    [Abstract] [Full Text] [Related]

  • 22. Nystagmus characteristics in congenital stationary night blindness (CSNB).
    Pieh C, Simonsz-Toth B, Gottlob I.
    Br J Ophthalmol; 2008 Feb; 92(2):236-40. PubMed ID: 18227204
    [Abstract] [Full Text] [Related]

  • 23. 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]

  • 24. Twenty-five thousand years of fluctuating selection on leopard complex spotting and congenital night blindness in horses.
    Ludwig A, Reissmann M, Benecke N, Bellone R, Sandoval-Castellanos E, Cieslak M, Fortes GG, Morales-Muñiz A, Hofreiter M, Pruvost M.
    Philos Trans R Soc Lond B Biol Sci; 2015 Jan 19; 370(1660):20130386. PubMed ID: 25487337
    [Abstract] [Full Text] [Related]

  • 25. [Family investigation and clinical genetic analysis of a large pedigree with congenital stationary night blindness].
    Fei YJ.
    Zhonghua Yan Ke Za Zhi; 1992 May 19; 28(3):162-5. PubMed ID: 1286605
    [Abstract] [Full Text] [Related]

  • 26. Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse.
    Bellone RR, Holl H, Setaluri V, Devi S, Maddodi N, Archer S, Sandmeyer L, Ludwig A, Foerster D, Pruvost M, Reissmann M, Bortfeldt R, Adelson DL, Lim SL, Nelson J, Haase B, Engensteiner M, Leeb T, Forsyth G, Mienaltowski MJ, Mahadevan P, Hofreiter M, Paijmans JL, Gonzalez-Fortes G, Grahn B, Brooks SA.
    PLoS One; 2013 May 19; 8(10):e78280. PubMed ID: 24167615
    [Abstract] [Full Text] [Related]

  • 27. Electroretinographic abnormalities in a rat glaucoma model with chronic elevated intraocular pressure.
    Bayer AU, Danias J, Brodie S, Maag KP, Chen B, Shen F, Podos SM, Mittag TW.
    Exp Eye Res; 2001 Jun 19; 72(6):667-77. PubMed ID: 11384155
    [Abstract] [Full Text] [Related]

  • 28. 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 19; 42(11):1475-83. PubMed ID: 12044753
    [Abstract] [Full Text] [Related]

  • 29. The negative ERG is not synonymous with nightblindness.
    Cibis GW, Fitzgerald KM.
    Trans Am Ophthalmol Soc; 2001 May 19; 99():171-5; discussion 175-6. PubMed ID: 11797304
    [Abstract] [Full Text] [Related]

  • 30. 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 19; 69(Pt 3):315-21. PubMed ID: 15845035
    [Abstract] [Full Text] [Related]

  • 31. 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 19; 15(1):159-67. PubMed ID: 15583843
    [Abstract] [Full Text] [Related]

  • 32. Oscillatory potentials of X-linked carriers of congenital stationary night blindness.
    Young RS, Chaparro A, Price J, Walters J.
    Invest Ophthalmol Vis Sci; 1989 May 19; 30(5):806-12. PubMed ID: 2785978
    [Abstract] [Full Text] [Related]

  • 33. Genotyping microarray for CSNB-associated genes.
    Zeitz C, Labs S, Lorenz B, Forster U, Uksti J, Kroes HY, De Baere E, Leroy BP, Cremers FP, Wittmer M, van Genderen MM, Sahel JA, Audo I, Poloschek CM, Mohand-Saïd S, Fleischhauer JC, Hüffmeier U, Moskova-Doumanova V, Levin AV, Hamel CP, Leifert D, Munier FL, Schorderet DF, Zrenner E, Friedburg C, Wissinger B, Kohl S, Berger W.
    Invest Ophthalmol Vis Sci; 2009 Dec 19; 50(12):5919-26. PubMed ID: 19578023
    [Abstract] [Full Text] [Related]

  • 34. A common NYX mutation in Flemish patients with X linked CSNB.
    Leroy BP, Budde BS, Wittmer M, De Baere E, Berger W, Zeitz C.
    Br J Ophthalmol; 2009 May 19; 93(5):692-6. PubMed ID: 18617546
    [Abstract] [Full Text] [Related]

  • 35. Whole-genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse.
    Hack YL, Crabtree EE, Avila F, Sutton RB, Grahn R, Oh A, Gilger B, Bellone RR.
    Equine Vet J; 2021 Mar 19; 53(2):316-323. PubMed ID: 32654228
    [Abstract] [Full Text] [Related]

  • 36. Possible pathogenesis of congenital stationary night blindness.
    Kato M, Aonuma H, Kawamura H, Miura Y, Watanabe I.
    Jpn J Ophthalmol; 1987 Mar 19; 31(1):88-101. PubMed ID: 3498070
    [Abstract] [Full Text] [Related]

  • 37. Retinal on-pathway deficit in congenital disorder of glycosylation due to phosphomannomutase deficiency.
    Thompson DA, Lyons RJ, Liasis A, Russell-Eggitt I, Jägle H, Grünewald S.
    Arch Ophthalmol; 2012 Jun 19; 130(6):712-9. PubMed ID: 22801829
    [Abstract] [Full Text] [Related]

  • 38. [Flash full-field electroretinography in diseases with night blindness].
    Pojda-Wilczek D, Herba E, Pojda SM.
    Klin Oczna; 2005 Jun 19; 107(1-3):28-30. PubMed ID: 16052794
    [Abstract] [Full Text] [Related]

  • 39. Electroretinographic characteristics in children with infantile nystagmus syndrome and early-onset retinal dystrophies.
    Kurent A, Stirn-Kranjc B, Brecelj J.
    Eur J Ophthalmol; 2015 Jun 19; 25(1):33-42. PubMed ID: 25096283
    [Abstract] [Full Text] [Related]

  • 40. Behavioral phenotypic properties of a natural occurring rat model of congenital stationary night blindness with Cacna1f mutation.
    An J, Wang L, Guo Q, Li L, Xia F, Zhang Z.
    J Neurogenet; 2012 Sep 19; 26(3-4):363-73. PubMed ID: 22800190
    [Abstract] [Full Text] [Related]

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