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Journal Abstract Search

156 related items for PubMed ID: 14661912

  • 61. Congenital stationary night blindness with hypoplastic discs, negative electroretinogram and thinning of the inner nuclear layer.
    Al Oreany AA, Al Hadlaq A, Schatz P.
    Graefes Arch Clin Exp Ophthalmol; 2016 Oct; 254(10):1951-1956. PubMed ID: 27084085
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  • 62. Congenital stationary night blindness.
    Haim M.
    Acta Ophthalmol (Copenh); 1986 Apr; 64(2):192-8. PubMed ID: 3487908
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  • 63. Visual Function in Carriers of X-Linked Retinitis Pigmentosa.
    Comander J, Weigel-DiFranco C, Sandberg MA, Berson EL.
    Ophthalmology; 2015 Sep; 122(9):1899-906. PubMed ID: 26143542
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  • 64. Negative electroretinograms in the pediatric and adult population.
    Kim JM, Payne JF, Yan J, Barnes CS.
    Doc Ophthalmol; 2012 Feb; 124(1):41-8. PubMed ID: 22246197
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  • 67. Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness.
    Zeitz C, Kloeckener-Gruissem B, Forster U, Kohl S, Magyar I, Wissinger B, Mátyás G, Borruat FX, Schorderet DF, Zrenner E, Munier FL, Berger W.
    Am J Hum Genet; 2006 Oct; 79(4):657-67. PubMed ID: 16960802
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  • 68. A potential spontaneous rat model of X-linked congenital stationary night blindness.
    Zhang Z, Gu Y, Li L, Long T, Guo Q, Shi L.
    Doc Ophthalmol; 2003 Jul; 107(1):53-7. PubMed ID: 12906122
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  • 69. 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
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  • 71. A comparison of ERG abnormalities in XLRS and XLCSNB.
    Bradshaw K, Allen L, Trump D, Hardcastle A, George N, Moore A.
    Doc Ophthalmol; 2004 Mar; 108(2):135-45. PubMed ID: 15455796
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  • 73. Variable expressivity in X-linked congenital stationary night blindness.
    Pearce WG, Reedyk M, Coupland SG.
    Can J Ophthalmol; 1990 Feb; 25(1):3-10. PubMed ID: 2328435
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  • 74. 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 Feb; 31(1):81-7. PubMed ID: 3498069
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  • 75. 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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  • 80. Clinical and electroretinographic findings of female carriers and affected males in a progressive X-linked cone-rod dystrophy (COD-1) pedigree.
    Brown J, Kimura AE, Gorin MB.
    Ophthalmology; 2000 Jun; 107(6):1104-10. PubMed ID: 10857830
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