207 related articles for article (PubMed ID: 2328435)
1. 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
[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. Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F.
Boycott KM; Pearce WG; Bech-Hansen NT
Can J Ophthalmol; 2000 Jun; 35(4):204-13. PubMed ID: 10900517
[TBL] [Abstract][Full Text] [Related]
4. Aland eye disease (Forsius-Eriksson-Miyake syndrome) with probability established in a Danish family.
Rosenberg T; Schwartz M; Simonsen SE
Acta Ophthalmol (Copenh); 1990 Jun; 68(3):281-91. PubMed ID: 2392903
[TBL] [Abstract][Full Text] [Related]
5. X-linked congenital stationary night blindness with myopia and nystagmus without clinical complaints of nyctalopia.
Price MJ; Judisch GF; Thompson HS
J Pediatr Ophthalmol Strabismus; 1988; 25(1):33-6. PubMed ID: 3257795
[TBL] [Abstract][Full Text] [Related]
6. Affected females in X-linked congenital stationary night blindness.
Ruttum MS; Lewandowski MF; Bateman JB
Ophthalmology; 1992 May; 99(5):747-52. PubMed ID: 1594221
[TBL] [Abstract][Full Text] [Related]
7. Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23.
Bech-Hansen NT; Boycott KM; Gratton KJ; Ross DA; Field LL; Pearce WG
Hum Genet; 1998 Aug; 103(2):124-30. PubMed ID: 9760193
[TBL] [Abstract][Full Text] [Related]
8. [Incomplete congenital stationary night blindness (CSNB). An important differential diagnosis of congenital nystagmus].
Lorenz B; Andrassi M; Miliczek KD
Klin Monbl Augenheilkd; 1996 Jan; 208(1):48-55. PubMed ID: 8839345
[TBL] [Abstract][Full Text] [Related]
9. X-linked recessive congenital stationary night blindness, myopia, and tilted discs.
Hittner HM; Borda RP; Justice J
J Pediatr Ophthalmol Strabismus; 1981; 18(1):15-20. PubMed ID: 6972443
[TBL] [Abstract][Full Text] [Related]
10. Autosomal dominant congenital stationary night blindness and normal fundus with an electronegative electroretinogram.
Noble KG; Carr RE; Siegel IM
Am J Ophthalmol; 1990 Jan; 109(1):44-8. PubMed ID: 2297031
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Manifestations of X-linked congenital stationary night blindness in three daughters of an affected male: demonstration of homozygosity.
Bech-Hansen NT; Pearce WG
Am J Hum Genet; 1993 Jan; 52(1):71-7. PubMed ID: 8434607
[TBL] [Abstract][Full Text] [Related]
13. 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
[TBL] [Abstract][Full Text] [Related]
14. [Electrophysiologic tests for diagnosis of congenital night blindness].
LubiĆski W; Palacz A; Penkala K; Palacz O
Klin Oczna; 1996 Jan; 98(1):9-12. PubMed ID: 9019583
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. Paradoxical pupillary responses in congenital stationary night blindness.
Barricks ME; Flynn JT; Kushner BJ
Arch Ophthalmol; 1977 Oct; 95(10):1800-4. PubMed ID: 303092
[TBL] [Abstract][Full Text] [Related]
19. Reduced amplitude of oscillatory potentials in female carriers of X-linked recessive congenital stationary night blindness.
Miyake Y; Kawase Y
Am J Ophthalmol; 1984 Aug; 98(2):208-15. PubMed ID: 6332537
[TBL] [Abstract][Full Text] [Related]
20. [Clinical features of congenital stationary night blindness].
Li H; Liu LY; Xu HY; Xu F; Jiang RX; Sui RF
Zhonghua Yi Xue Za Zhi; 2012 Oct; 92(39):2756-9. PubMed ID: 23290162
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]