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Journal Abstract Search

238 related items for PubMed ID: 3499417

  • 1.
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  • 3. The photopic electroretinogram in congenital stationary night blindness with myopia.
    Lachapelle P, Little JM, Polomeno RC.
    Invest Ophthalmol Vis Sci; 1983 Apr; 24(4):442-50. PubMed ID: 6601088
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  • 4. Scotopic threshold response in complete and incomplete types of congenital stationary night blindness.
    Miyake Y, Horiguchi M, Terasaki H, Kondo M.
    Invest Ophthalmol Vis Sci; 1994 Sep; 35(10):3770-5. PubMed ID: 8088964
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  • 5. 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 Sep; 31(1):81-7. PubMed ID: 3498069
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  • 7. [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
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  • 8. Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.
    Zeitz C, van Genderen M, Neidhardt J, Luhmann UF, Hoeben F, Forster U, Wycisk K, Mátyás G, Hoyng CB, Riemslag F, Meire F, Cremers FP, Berger W.
    Invest Ophthalmol Vis Sci; 2005 Nov; 46(11):4328-35. PubMed ID: 16249515
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  • 10. Bull's-eye maculopathy and negative electroretinogram.
    Miyake Y, Shiroyama N, Horiguchi M, Saito A, Yagasaki K.
    Retina; 1989 Nov; 9(3):210-5. PubMed ID: 2595114
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  • 11. A form of congenital stationary night blindness with apparent defect of rod phototransduction.
    Peachey NS, Fishman GA, Kilbride PE, Alexander KR, Keehan KM, Derlacki DJ.
    Invest Ophthalmol Vis Sci; 1990 Feb; 31(2):237-46. PubMed ID: 2303327
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  • 14. 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
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  • 15. Rod-cone interactions in night-blinding disease.
    Arden GB.
    Jpn J Ophthalmol; 1987 Nov; 31(1):6-19. PubMed ID: 3498067
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  • 16. [Establishment of the concept of new clinical entities--complete and incomplete form of congenital stationary night blindness].
    Miyake Y.
    Nippon Ganka Gakkai Zasshi; 2002 Dec; 106(12):737-55; discussion 756. PubMed ID: 12610835
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  • 17. 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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  • 18. 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
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  • 19. Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy.
    Hayashi T, Hosono K, Kurata K, Katagiri S, Mizobuchi K, Ueno S, Kondo M, Nakano T, Hotta Y.
    Doc Ophthalmol; 2020 Apr; 140(2):147-157. PubMed ID: 31583501
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  • 20. 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 Apr; 10(6):368-75. PubMed ID: 17970998
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