328 related articles for article (PubMed ID: 18235024)
1. Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.
Wissinger B; Dangel S; Jägle H; Hansen L; Baumann B; Rudolph G; Wolf C; Bonin M; Koeppen K; Ladewig T; Kohl S; Zrenner E; Rosenberg T
Invest Ophthalmol Vis Sci; 2008 Feb; 49(2):751-7. PubMed ID: 18235024
[TBL] [Abstract][Full Text] [Related]
2. [Differential diagnosis of cone dystrophies].
Sadowski B; Zrenner E
Ophthalmologe; 1994 Dec; 91(6):719-29. PubMed ID: 7849422
[TBL] [Abstract][Full Text] [Related]
3. Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) gene.
Jacobson SG; Cideciyan AV; Huang Y; Hanna DB; Freund CL; Affatigato LM; Carr RE; Zack DJ; Stone EM; McInnes RR
Invest Ophthalmol Vis Sci; 1998 Nov; 39(12):2417-26. PubMed ID: 9804150
[TBL] [Abstract][Full Text] [Related]
4. Clinical course of two siblings with potassium voltage-gated channel modifier subfamily V member 2 (KCNV2)-associated retinopathy.
Sato T; Kuniyoshi K; Hayashi T; Nishiwaki H; Mizobuchi K; Kusaka S
Doc Ophthalmol; 2024 Jun; 148(3):173-182. PubMed ID: 38630375
[TBL] [Abstract][Full Text] [Related]
5. Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosa.
Jacobson SG; Kemp CM; Cideciyan AV; Macke JP; Sung CH; Nathans J
Invest Ophthalmol Vis Sci; 1994 Apr; 35(5):2521-34. PubMed ID: 8163341
[TBL] [Abstract][Full Text] [Related]
6. Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel.
Kohl S; Marx T; Giddings I; Jägle H; Jacobson SG; Apfelstedt-Sylla E; Zrenner E; Sharpe LT; Wissinger B
Nat Genet; 1998 Jul; 19(3):257-9. PubMed ID: 9662398
[TBL] [Abstract][Full Text] [Related]
7. [Colored light stimuli in ERG for differential diagnosis of cone dystrophies].
Kellner U; Foerster MH
Klin Monbl Augenheilkd; 1992 Aug; 201(2):102-6. PubMed ID: 1434375
[TBL] [Abstract][Full Text] [Related]
8. Cone-rod dystrophy: a case report.
Norden LC; Amos JF; Newcomb RD
Am J Optom Physiol Opt; 1978 Dec; 55(12):824-35. PubMed ID: 313711
[TBL] [Abstract][Full Text] [Related]
9. [Multi-flash ERG in cone dystrophies and cone-rod dystrophies].
Walter P; Widder RA; Brunner R
Klin Monbl Augenheilkd; 1998 Feb; 212(2):88-92. PubMed ID: 9577807
[TBL] [Abstract][Full Text] [Related]
10. Cone dystrophies: clinical and electrophysiological findings.
Kellner U; Kleine-Hartlage P; Foerster MH
Ger J Ophthalmol; 1992; 1(2):105-9. PubMed ID: 1477624
[TBL] [Abstract][Full Text] [Related]
11. Color vision defects in pigmentary retinal dystrophy.
Okajima O; Tanino T; Okamoto M
Jpn J Ophthalmol; 1982; 26(3):292-301. PubMed ID: 6984101
[TBL] [Abstract][Full Text] [Related]
12. Selective cone dystrophy with protan genotype.
Kellner U; Sadowski B; Zrenner E; Foerster MH
Invest Ophthalmol Vis Sci; 1995 Nov; 36(12):2381-7. PubMed ID: 7591627
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Neuro-ophthalmic presentation of cone dysfunction syndromes in the adult.
Zervas JP; Smith JL
J Clin Neuroophthalmol; 1987 Dec; 7(4):202-18. PubMed ID: 2963026
[TBL] [Abstract][Full Text] [Related]
15. Color vision defect as first symptom of progressive cone-rod dystrophy.
Mäntyjärvi MI
J Clin Neuroophthalmol; 1990 Dec; 10(4):266-70. PubMed ID: 2150845
[TBL] [Abstract][Full Text] [Related]
16. [ERG diagnosis and differential diagnosis: results of examination over 6 years].
Stemeyer G; Stähli P
Klin Monbl Augenheilkd; 1996 May; 208(5):306-10. PubMed ID: 8766035
[TBL] [Abstract][Full Text] [Related]
17. Long-term follow-up of Stargardt's disease and fundus flavimaculatus.
Armstrong JD; Meyer D; Xu S; Elfervig JL
Ophthalmology; 1998 Mar; 105(3):448-57; discussion 457-8. PubMed ID: 9499775
[TBL] [Abstract][Full Text] [Related]
18. Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesis.
Seeliger MW; Biesalski HK; Wissinger B; Gollnick H; Gielen S; Frank J; Beck S; Zrenner E
Invest Ophthalmol Vis Sci; 1999 Jan; 40(1):3-11. PubMed ID: 9888420
[TBL] [Abstract][Full Text] [Related]
19. Foveal cone dysfunction syndrome.
ten Hove MW; Siatkowski RM; Smith JL
J Neuroophthalmol; 1998 Mar; 18(1):9-14. PubMed ID: 9532531
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
