212 related articles for article (PubMed ID: 8312830)
1. 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]
2. Genotype and phenotype of 101 dutch patients with congenital stationary night blindness.
Bijveld MM; Florijn RJ; Bergen AA; van den Born LI; Kamermans M; Prick L; Riemslag FC; van Schooneveld MJ; Kappers AM; van Genderen MM
Ophthalmology; 2013 Oct; 120(10):2072-81. PubMed ID: 23714322
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 gene.
Sergouniotis PI; Robson AG; Li Z; Devery S; Holder GE; Moore AT; Webster AR
Acta Ophthalmol; 2012 May; 90(3):e192-7. PubMed ID: 22008250
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. 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]
7. [The hereditary factor as a criterion for the classification of stationary congenital night blindness (author's transl)].
Thaler A; Heilig P; Hommer K; Hofbauer R
Klin Monbl Augenheilkd; 1981 Oct; 179(4):285-7. PubMed ID: 6975855
[TBL] [Abstract][Full Text] [Related]
8. Unique characteristics of two types of retinitis pigmentosa patients with different rod sensitivities.
Takahashi H; Miyake Y; Horiguchi M; Tomida N; Takakuwa H
Jpn J Ophthalmol; 2005; 49(2):114-20. PubMed ID: 15838727
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic association.
Marmor MF; Zeitz C
Doc Ophthalmol; 2018 Aug; 137(1):57-62. PubMed ID: 30051303
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. 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]
14. 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]
15. 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]
16. Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type.
Langrová H; Gamer D; Friedburg C; Besch D; Zrenner E; Apfelstedt-Sylla E
Vision Res; 2002 May; 42(11):1475-83. PubMed ID: 12044753
[TBL] [Abstract][Full Text] [Related]
17. The negative ERG is not synonymous with nightblindness.
Cibis GW; Fitzgerald KM
Trans Am Ophthalmol Soc; 2001; 99():171-5; discussion 175-6. PubMed ID: 11797304
[TBL] [Abstract][Full Text] [Related]
18. Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
Bech-Hansen NT; Naylor MJ; Maybaum TA; Pearce WG; Koop B; Fishman GA; Mets M; Musarella MA; Boycott KM
Nat Genet; 1998 Jul; 19(3):264-7. PubMed ID: 9662400
[TBL] [Abstract][Full Text] [Related]
19. A rod-cone dysfunction syndrome with separate clinical entity: incomplete-type congenital stationary night blindness (Miyake).
Miyake Y; Yagasaki K; Horiguchi M
Prog Clin Biol Res; 1987; 247():137-45. PubMed ID: 3500478
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]