These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


208 related items for PubMed ID: 8768469

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26. A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder.
    Littink KW, van Genderen MM, Collin RW, Roosing S, de Brouwer AP, Riemslag FC, Venselaar H, Thiadens AA, Hoyng CB, Rohrschneider K, den Hollander AI, Cremers FP, van den Born LI.
    Invest Ophthalmol Vis Sci; 2009 May; 50(5):2344-50. PubMed ID: 19074807
    [Abstract] [Full Text] [Related]

  • 27. [Congenital stationary night blindness].
    Kocyła-Karczmarewicz B, Grałek M, Juszko J, Trzebicka A, Sarti G.
    Klin Oczna; 2004 May; 106(3 Suppl):509-11. PubMed ID: 15636252
    [Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. Autosomal dominant congenital stationary night blindness and normal fundus with an electronegative electroretinogram.
    Noble KG, Carr RE, Siegel IM.
    Am J Ophthalmol; 1990 Jan 15; 109(1):44-8. PubMed ID: 2297031
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33. A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness.
    al-Jandal N, Farrar GJ, Kiang AS, Humphries MM, Bannon N, Findlay JB, Humphries P, Kenna PF.
    Hum Mutat; 1999 Jan 15; 13(1):75-81. PubMed ID: 9888392
    [Abstract] [Full Text] [Related]

  • 34. A Japanese pedigree of autosomal dominant congenital stationary night blindness with variable expressivity.
    Hayakawa M, Imai Y, Wakita M, Kato K, Yanashima K, Miyake Y, Kanai A.
    Ophthalmic Paediatr Genet; 1992 Dec 15; 13(4):211-7. PubMed ID: 1488221
    [Abstract] [Full Text] [Related]

  • 35. Clinical and electroretinographic characteristics of congenital stationary night blindness in the Appaloosa and the association with the leopard complex.
    Sandmeyer LS, Breaux CB, Archer S, Grahn BH.
    Vet Ophthalmol; 2007 Dec 15; 10(6):368-75. PubMed ID: 17970998
    [Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. Nystagmus characteristics in congenital stationary night blindness (CSNB).
    Pieh C, Simonsz-Toth B, Gottlob I.
    Br J Ophthalmol; 2008 Feb 15; 92(2):236-40. PubMed ID: 18227204
    [Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. 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 15; 42(11):2728-36. PubMed ID: 11581222
    [Abstract] [Full Text] [Related]

  • 40. Congenital stationary night blindness: an animal model.
    Witzel DA, Smith EL, Wilson RD, Aguirre GD.
    Invest Ophthalmol Vis Sci; 1978 Aug 15; 17(8):788-95. PubMed ID: 308060
    [Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 11.