157 related articles for article (PubMed ID: 1513061)
1. Japanese family with blue cone monochromatism.
Terasaki H; Miyake Y
Jpn J Ophthalmol; 1992; 36(2):132-41. PubMed ID: 1513061
[TBL] [Abstract][Full Text] [Related]
2. [The properties of visual functions and familial analysis in blue cone monochromatism].
Terasaki H; Miyake Y
Nippon Ganka Gakkai Zasshi; 1992 Apr; 96(4):523-30. PubMed ID: 1621595
[TBL] [Abstract][Full Text] [Related]
3. Association of acquired color vision defects in blue cone monochromatism.
Terasaki H; Miyake Y
Jpn J Ophthalmol; 1995; 39(1):55-9. PubMed ID: 7643484
[TBL] [Abstract][Full Text] [Related]
4. Blue cone monochromatism: a phenotype and genotype assessment with evidence of progressive loss of cone function in older individuals.
Michaelides M; Johnson S; Simunovic MP; Bradshaw K; Holder G; Mollon JD; Moore AT; Hunt DM
Eye (Lond); 2005 Jan; 19(1):2-10. PubMed ID: 15094734
[TBL] [Abstract][Full Text] [Related]
5. [X-linked blue cone monochromatism. A familial case report].
Coco Martín RM
Arch Soc Esp Oftalmol; 2005 Jan; 80(1):35-40. PubMed ID: 15692892
[TBL] [Abstract][Full Text] [Related]
6. [Differential diagnosis of cone dystrophies].
Sadowski B; Zrenner E
Ophthalmologe; 1994 Dec; 91(6):719-29. PubMed ID: 7849422
[TBL] [Abstract][Full Text] [Related]
7. [Electroretinogram and electrooculogram in a family with Stargardt's disease].
Pojda-Wilczek D; Makowiecka-Obidzińska K; Herba E
Klin Oczna; 2004; 106(3 Suppl):540-1. PubMed ID: 15636262
[TBL] [Abstract][Full Text] [Related]
8. Eye movement abnormalities in carriers of blue-cone monochromatism.
Gottlob I
Invest Ophthalmol Vis Sci; 1994 Aug; 35(9):3556-60. PubMed ID: 8056533
[TBL] [Abstract][Full Text] [Related]
9. Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced S-cone syndrome demonstrate compound heterozygosity.
Hayashi T; Gekka T; Goto-Omoto S; Takeuchi T; Kubo A; Kitahara K
Ophthalmology; 2005 Dec; 112(12):2115. PubMed ID: 16225923
[TBL] [Abstract][Full Text] [Related]
10. Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the family.
Van Ghelue M; Eriksen HL; Ponjavic V; Fagerheim T; Andréasson S; Forsman-Semb K; Sandgren O; Holmgren G; Tranebjaerg L
Ophthalmic Genet; 2000 Dec; 21(4):197-209. PubMed ID: 11135490
[TBL] [Abstract][Full Text] [Related]
11. Bilateral macular atrophy in blue cone monochromacy (BCM) with loss of the locus control region (LCR) and part of the red pigment gene.
Ayyagari R; Kakuk LE; Coats CL; Bingham EL; Toda Y; Felius J; Sieving PA
Mol Vis; 1999 Jul; 5():13. PubMed ID: 10427103
[TBL] [Abstract][Full Text] [Related]
12. X-linked incomplete achromatopsia with more than one class of functional cones.
Smith VC; Pokorny J; Delleman JW; Cozijnsen M; Houtman WA; Went LN
Invest Ophthalmol Vis Sci; 1983 Apr; 24(4):451-7. PubMed ID: 6601089
[TBL] [Abstract][Full Text] [Related]
13. Colour vision, ophthalmological and linkage studies in a pedigree with a tritan defect.
Went LN; Völker-Dieben H; de Vries-de Mol EC
Mod Probl Ophthalmol; 1974; 13(0):272-6. PubMed ID: 4548144
[No Abstract] [Full Text] [Related]
14. Blue cone monochromatism in a female due to skewed X-inactivation.
Frederiksen AL; Duno M; Welinder LG
Ophthalmic Genet; 2013; 34(1-2):101-4. PubMed ID: 22998501
[TBL] [Abstract][Full Text] [Related]
15. Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.
Jacobson SG; Buraczynska M; Milam AH; Chen C; Järvaläinen M; Fujita R; Wu W; Huang Y; Cideciyan AV; Swaroop A
Invest Ophthalmol Vis Sci; 1997 Sep; 38(10):1983-97. PubMed ID: 9331262
[TBL] [Abstract][Full Text] [Related]
16. Mutation in the gene GUCA1A, encoding guanylate cyclase-activating protein 1, causes cone, cone-rod, and macular dystrophy.
Michaelides M; Wilkie SE; Jenkins S; Holder GE; Hunt DM; Moore AT; Webster AR
Ophthalmology; 2005 Aug; 112(8):1442-7. PubMed ID: 15953638
[TBL] [Abstract][Full Text] [Related]
17. H244R VSX1 is associated with selective cone ON bipolar cell dysfunction and macular degeneration in a PPCD family.
Valleix S; Nedelec B; Rigaudiere F; Dighiero P; Pouliquen Y; Renard G; Le Gargasson JF; Delpech M
Invest Ophthalmol Vis Sci; 2006 Jan; 47(1):48-54. PubMed ID: 16384943
[TBL] [Abstract][Full Text] [Related]
18. Electroretinogram in cone dystrophy.
Iijima H; Yamaguchi S; Kogure S; Hosaka O; Shibutani T
Jpn J Ophthalmol; 1991; 35(4):453-66. PubMed ID: 1821435
[TBL] [Abstract][Full Text] [Related]
19. [Blue cone monochromasia: diagnosis, genetic counseling and optical aids].
Zrenner E; Magnussen S; Lorenz B
Klin Monbl Augenheilkd; 1988 Nov; 193(5):510-7. PubMed ID: 3264866
[TBL] [Abstract][Full Text] [Related]
20. X-linked cone dysfunction syndrome with myopia and protanopia.
Michaelides M; Johnson S; Bradshaw K; Holder GE; Simunovic MP; Mollon JD; Moore AT; Hunt DM
Ophthalmology; 2005 Aug; 112(8):1448-54. PubMed ID: 15953640
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
