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Journal Abstract Search


126 related items for PubMed ID: 9381682

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  • 43. 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
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  • 44. The contribution of human cone photoreceptors to the photopic flicker electroretinogram.
    Verma R, Pianta MJ.
    J Vis; 2009 Mar 13; 9(3):9.1-12. PubMed ID: 19757948
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  • 45. Electrophysiological findings in patients with Oguchi's disease.
    Miyake Y, Horiguchi M, Suzuki S, Kondo M, Tanikawa A.
    Jpn J Ophthalmol; 1996 Mar 13; 40(4):511-9. PubMed ID: 9130055
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  • 46. 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 13; 42(11):2728-36. PubMed ID: 11581222
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  • 51. 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 Oct 13; 31(1):81-7. PubMed ID: 3498069
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  • 52. Temporal frequency deficits in the electroretinogram of the cone system in X-linked retinoschisis.
    Alexander KR, Fishman GA, Grover S.
    Vision Res; 2000 Oct 13; 40(20):2861-8. PubMed ID: 10960656
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  • 57. [Congenital stationary night blindness (CSNB)--a case report].
    Liláková D, Svĕrák J, Hejcmanová D.
    Cesk Slov Oftalmol; 2005 May 13; 61(3):218-23. PubMed ID: 15981496
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