247 related articles for article (PubMed ID: 26261413)
1. Reduced macular function in ABCA4 carriers.
Kjellström U
Mol Vis; 2015; 21():767-82. PubMed ID: 26261413
[TBL] [Abstract][Full Text] [Related]
2. Full-field ERG as a predictor of the natural course of
Schroeder M; Kjellström U
Mol Vis; 2018; 24():1-16. PubMed ID: 29386879
[TBL] [Abstract][Full Text] [Related]
3. A five-year follow-up of
Kjellström U; Andréasson S
Mol Vis; 2022; 28():300-316. PubMed ID: 36338671
[TBL] [Abstract][Full Text] [Related]
4. Association between genotype and phenotype in families with mutations in the ABCA4 gene.
Kjellström U
Mol Vis; 2014; 20():89-104. PubMed ID: 24453473
[TBL] [Abstract][Full Text] [Related]
5. Modification of the
Lee W; Paavo M; Zernant J; Stong N; Laurente Z; Bearelly S; Nagasaki T; Tsang SH; Goldstein DB; Allikmets R
Ophthalmic Genet; 2019 Aug; 40(4):369-375. PubMed ID: 31576780
[No Abstract] [Full Text] [Related]
6. Quantitative Fundus Autofluorescence and Optical Coherence Tomography in ABCA4 Carriers.
Duncker T; Stein GE; Lee W; Tsang SH; Zernant J; Bearelly S; Hood DC; Greenstein VC; Delori FC; Allikmets R; Sparrow JR
Invest Ophthalmol Vis Sci; 2015 Nov; 56(12):7274-85. PubMed ID: 26551331
[TBL] [Abstract][Full Text] [Related]
7. Early-onset stargardt disease: phenotypic and genotypic characteristics.
Lambertus S; van Huet RA; Bax NM; Hoefsloot LH; Cremers FP; Boon CJ; Klevering BJ; Hoyng CB
Ophthalmology; 2015 Feb; 122(2):335-44. PubMed ID: 25444351
[TBL] [Abstract][Full Text] [Related]
8. Fundus albipunctatus associated with compound heterozygous mutations in RPE65.
Schatz P; Preising M; Lorenz B; Sander B; Larsen M; Rosenberg T
Ophthalmology; 2011 May; 118(5):888-94. PubMed ID: 21211845
[TBL] [Abstract][Full Text] [Related]
9. Phenotypes of 16 Stargardt macular dystrophy/fundus flavimaculatus patients with known ABCA4 mutations and evaluation of genotype-phenotype correlation.
Gerth C; Andrassi-Darida M; Bock M; Preising MN; Weber BH; Lorenz B
Graefes Arch Clin Exp Ophthalmol; 2002 Aug; 240(8):628-38. PubMed ID: 12192456
[TBL] [Abstract][Full Text] [Related]
10. Evaluation of macular structure and function by OCT and electrophysiology in patients with vitelliform macular dystrophy due to mutations in BEST1.
Schatz P; Bitner H; Sander B; Holfort S; Andreasson S; Larsen M; Sharon D
Invest Ophthalmol Vis Sci; 2010 Sep; 51(9):4754-65. PubMed ID: 20375334
[TBL] [Abstract][Full Text] [Related]
11. Different clinical expressions in two families with Stargardt's macular dystrophy (STGD1).
Eksandh L; Ekström U; Abrahamson M; Bauer B; Andréasson S
Acta Ophthalmol Scand; 2001 Oct; 79(5):524-30. PubMed ID: 11594993
[TBL] [Abstract][Full Text] [Related]
12. Retinal phenotypic characterization of patients with
López-Rubio S; Chacon-Camacho OF; Matsui R; Guadarrama-Vallejo D; Astiazarán MC; Zenteno JC
Mol Vis; 2018; 24():105-114. PubMed ID: 29422768
[TBL] [Abstract][Full Text] [Related]
13. The Effect on Retinal Structure and Function of 15 Specific ABCA4 Mutations: A Detailed Examination of 82 Hemizygous Patients.
Fakin A; Robson AG; Chiang JP; Fujinami K; Moore AT; Michaelides M; Holder GE; Webster AR
Invest Ophthalmol Vis Sci; 2016 Nov; 57(14):5963-5973. PubMed ID: 27820952
[TBL] [Abstract][Full Text] [Related]
14. Clinical and genetic characteristics of late-onset Stargardt's disease.
Westeneng-van Haaften SC; Boon CJ; Cremers FP; Hoefsloot LH; den Hollander AI; Hoyng CB
Ophthalmology; 2012 Jun; 119(6):1199-210. PubMed ID: 22449572
[TBL] [Abstract][Full Text] [Related]
15. The Rapid-Onset Chorioretinopathy Phenotype of ABCA4 Disease.
Tanaka K; Lee W; Zernant J; Schuerch K; Ciccone L; Tsang SH; Sparrow JR; Allikmets R
Ophthalmology; 2018 Jan; 125(1):89-99. PubMed ID: 28947085
[TBL] [Abstract][Full Text] [Related]
16. Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy.
Khan KN; Kasilian M; Mahroo OAR; Tanna P; Kalitzeos A; Robson AG; Tsunoda K; Iwata T; Moore AT; Fujinami K; Michaelides M
Ophthalmology; 2018 May; 125(5):735-746. PubMed ID: 29310964
[TBL] [Abstract][Full Text] [Related]
17. Expanding the Mutation Spectrum in
Nassisi M; Mohand-Saïd S; Dhaenens CM; Boyard F; Démontant V; Andrieu C; Antonio A; Condroyer C; Foussard M; Méjécase C; Eandi CM; Sahel JA; Zeitz C; Audo I
Int J Mol Sci; 2018 Jul; 19(8):. PubMed ID: 30060493
[TBL] [Abstract][Full Text] [Related]
18. G1961E mutant allele in the Stargardt disease gene ABCA4 causes bull's eye maculopathy.
Cella W; Greenstein VC; Zernant-Rajang J; Smith TR; Barile G; Allikmets R; Tsang SH
Exp Eye Res; 2009 Jun; 89(1):16-24. PubMed ID: 19217903
[TBL] [Abstract][Full Text] [Related]
19. The spectrum of retinal phenotypes caused by mutations in the ABCA4 gene.
Klevering BJ; Deutman AF; Maugeri A; Cremers FP; Hoyng CB
Graefes Arch Clin Exp Ophthalmol; 2005 Feb; 243(2):90-100. PubMed ID: 15614537
[TBL] [Abstract][Full Text] [Related]
20. Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 gene.
Burke TR; Fishman GA; Zernant J; Schubert C; Tsang SH; Smith RT; Ayyagari R; Koenekoop RK; Umfress A; Ciccarelli ML; Baldi A; Iannaccone A; Cremers FP; Klaver CC; Allikmets R
Invest Ophthalmol Vis Sci; 2012 Jul; 53(8):4458-67. PubMed ID: 22661473
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]