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2. [Congenital stationary night blindness]. Sui RF; Zhao JL Zhonghua Yan Ke Za Zhi; 2006 May; 42(5):472-5. PubMed ID: 16762251 [TBL] [Abstract][Full Text] [Related]
3. [Congenital stationary night blindness]. Kocyła-Karczmarewicz B; Grałek M; Juszko J; Trzebicka A; Sarti G Klin Oczna; 2004; 106(3 Suppl):509-11. PubMed ID: 15636252 [TBL] [Abstract][Full Text] [Related]
4. Oguchi's disease and night blindness. Rao BM Indian J Ophthalmol; 1977 Jul; 25(2):5. PubMed ID: 307531 [No Abstract] [Full Text] [Related]
5. 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]
6. Congenital stationary night blindness in a Thoroughbred and a Paso Fino. Nunnery C; Pickett JP; Zimmerman KL Vet Ophthalmol; 2005; 8(6):415-9. PubMed ID: 16359365 [TBL] [Abstract][Full Text] [Related]
7. Comparison of focal macular cone ERGs in complete-type congenital stationary night blindness and APB-treated monkeys. Kondo M; Ueno S; Piao CH; Miyake Y; Terasaki H Vision Res; 2008 Jan; 48(2):273-80. PubMed ID: 18158169 [TBL] [Abstract][Full Text] [Related]
10. Altered G-protein coupling in an mGluR6 point mutant associated with congenital stationary night blindness. Beqollari D; Betzenhauser MJ; Kammermeier PJ Mol Pharmacol; 2009 Nov; 76(5):992-7. PubMed ID: 19666700 [TBL] [Abstract][Full Text] [Related]
11. [On a special form of congenital hemeralopia]. Slezak H; Hommer K Albrecht Von Graefes Arch Klin Exp Ophthalmol; 1965 Dec; 168(6):614-9. PubMed ID: 5296190 [No Abstract] [Full Text] [Related]
12. Congenital stationary nightblindness in a patient with osteopetrosis. Matsui Y; Okinami S; Oono S; Matsui M Br J Ophthalmol; 1995 Dec; 79(12):1142-3. PubMed ID: 8562556 [No Abstract] [Full Text] [Related]
13. Multifocal oscillatory potentials in CSNB1 and CSNB2 type congenital stationary night blindness. Schuster A; Pusch CM; Gamer D; Apfelstedt-Sylla E; Zrenner E; Kurtenbach A Int J Mol Med; 2005 Jan; 15(1):159-67. PubMed ID: 15583843 [TBL] [Abstract][Full Text] [Related]
14. Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness. Zeitz C; Minotti R; Feil S; Mátyás G; Cremers FP; Hoyng CB; Berger W Mol Vis; 2005 Mar; 11():179-83. PubMed ID: 15761389 [TBL] [Abstract][Full Text] [Related]
15. Nystagmus characteristics in congenital stationary night blindness (CSNB). Pieh C; Simonsz-Toth B; Gottlob I Br J Ophthalmol; 2008 Feb; 92(2):236-40. PubMed ID: 18227204 [TBL] [Abstract][Full Text] [Related]
16. 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]
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18. Mutations in NYX of individuals with high myopia, but without night blindness. Zhang Q; Xiao X; Li S; Jia X; Yang Z; Huang S; Caruso RC; Guan T; Sergeev Y; Guo X; Hejtmancik JF Mol Vis; 2007 Mar; 13():330-6. PubMed ID: 17392683 [TBL] [Abstract][Full Text] [Related]
19. p.Gln200Glu, a putative constitutively active mutant of rod alpha-transducin (GNAT1) in autosomal dominant congenital stationary night blindness. Szabo V; Kreienkamp HJ; Rosenberg T; Gal A Hum Mutat; 2007 Jul; 28(7):741-2. PubMed ID: 17584859 [TBL] [Abstract][Full Text] [Related]
20. [Case of congenital night blindness with visual modifications of pigmentation in the fundus oculi (so-called Oguchi's disease)]. KRAWCZYK Z; SZOSLAND M Klin Oczna; 1954; 24(2):139-41. PubMed ID: 13184639 [No Abstract] [Full Text] [Related] [Next] [New Search]