BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

242 related articles for article (PubMed ID: 3499417)

  • 1. Characteristic ERG-flicker anomaly in incomplete congenital stationary night blindness.
    Miyake Y; Horiguchi M; Ota I; Shiroyama N
    Invest Ophthalmol Vis Sci; 1987 Nov; 28(11):1816-23. PubMed ID: 3499417
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Electrophysiological findings in patients with Oguchi's disease.
    Miyake Y; Horiguchi M; Suzuki S; Kondo M; Tanikawa A
    Jpn J Ophthalmol; 1996; 40(4):511-9. PubMed ID: 9130055
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 31(1):81-7. PubMed ID: 3498069
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel CACNA1F mutations in Japanese patients with incomplete congenital stationary night blindness.
    Nakamura M; Ito S; Terasaki H; Miyake Y
    Invest Ophthalmol Vis Sci; 2001 Jun; 42(7):1610-6. PubMed ID: 11381068
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Oscillatory potentials and pattern electroretinogram: are they related?
    Litao RE; Miyake Y; Yagasaki K
    Jpn J Ophthalmol; 1986; 30(4):402-8. PubMed ID: 3495681
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bull's-eye maculopathy and negative electroretinogram.
    Miyake Y; Shiroyama N; Horiguchi M; Saito A; Yagasaki K
    Retina; 1989; 9(3):210-5. PubMed ID: 2595114
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 13. Photoreceptor and postreceptor responses in congenital stationary night blindness.
    Raghuram A; Hansen RM; Moskowitz A; Fulton AB
    Invest Ophthalmol Vis Sci; 2013 Jul; 54(7):4648-58. PubMed ID: 23761088
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Rod-cone interactions in night-blinding disease.
    Arden GB
    Jpn J Ophthalmol; 1987; 31(1):6-19. PubMed ID: 3498067
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 10(6):368-75. PubMed ID: 17970998
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.