416 related articles for article (PubMed ID: 25174897)
1. Near-infrared fundus autofluorescence in subclinical best vitelliform macular dystrophy.
Parodi MB; Iacono P; Del Turco C; Bandello F
Am J Ophthalmol; 2014 Dec; 158(6):1247-1252.e2. PubMed ID: 25174897
[TBL] [Abstract][Full Text] [Related]
2. Fundus autofluorescence patterns in Best vitelliform macular dystrophy.
Parodi MB; Iacono P; Campa C; Del Turco C; Bandello F
Am J Ophthalmol; 2014 Nov; 158(5):1086-92. PubMed ID: 25068640
[TBL] [Abstract][Full Text] [Related]
3. The spectrum of subclinical Best vitelliform macular dystrophy in subjects with mutations in BEST1 gene.
Querques G; Zerbib J; Santacroce R; Margaglione M; Delphin N; Querques L; Rozet JM; Kaplan J; Souied EH
Invest Ophthalmol Vis Sci; 2011 Jun; 52(7):4678-84. PubMed ID: 21436265
[TBL] [Abstract][Full Text] [Related]
4. Functional assessment of the fundus autofluorescence pattern in Best vitelliform macular dystrophy.
Parodi MB; Iacono P; Del Turco C; Triolo G; Bandello F
Graefes Arch Clin Exp Ophthalmol; 2016 Jul; 254(7):1297-302. PubMed ID: 26490373
[TBL] [Abstract][Full Text] [Related]
5. Preferential hyperacuity perimeter in best vitelliform macular dystrophy.
Querques G; Atmani K; Bouzitou-Mfoumou R; Leveziel N; Massamba N; Souied EH
Retina; 2011 May; 31(5):959-66. PubMed ID: 21242858
[TBL] [Abstract][Full Text] [Related]
6. Microperimetric correlations of autofluorescence and optical coherence tomography imaging in dry age-related macular degeneration.
Querques L; Querques G; Forte R; Souied EH
Am J Ophthalmol; 2012 Jun; 153(6):1110-5. PubMed ID: 22321805
[TBL] [Abstract][Full Text] [Related]
7. Frequency and clinical pattern of vitelliform macular dystrophy caused by mutations of interphotoreceptor matrix IMPG1 and IMPG2 genes.
Meunier I; Manes G; Bocquet B; Marquette V; Baudoin C; Puech B; Defoort-Dhellemmes S; Audo I; Verdet R; Arndt C; Zanlonghi X; Le Meur G; Dhaenens CM; Hamel CP
Ophthalmology; 2014 Dec; 121(12):2406-14. PubMed ID: 25085631
[TBL] [Abstract][Full Text] [Related]
8. Autosomal recessive best vitelliform macular dystrophy: report of a family and management of early-onset neovascular complications.
Iannaccone A; Kerr NC; Kinnick TR; Calzada JI; Stone EM
Arch Ophthalmol; 2011 Feb; 129(2):211-7. PubMed ID: 21320969
[TBL] [Abstract][Full Text] [Related]
9. A NOVEL P.ASP304GLY MUTATION IN BEST1 GENE ASSOCIATED WITH ATYPICAL BEST VITELLIFORM MACULAR DYSTROPHY PHENOTYPE AND HIGH INTRAFAMILIAL VARIABILITY.
Peiretti E; Caminiti G; Forma G; Carboni G; Dhaenens CM; Querques L; Souied E; Querques G
Retina; 2016 Sep; 36(9):1733-40. PubMed ID: 26807628
[TBL] [Abstract][Full Text] [Related]
10. Frequency, genotype, and clinical spectrum of best vitelliform macular dystrophy: data from a national center in Denmark.
Bitner H; Schatz P; Mizrahi-Meissonnier L; Sharon D; Rosenberg T
Am J Ophthalmol; 2012 Aug; 154(2):403-412.e4. PubMed ID: 22633354
[TBL] [Abstract][Full Text] [Related]
11. Clinical and molecular genetic analysis of best vitelliform macular dystrophy.
Boon CJ; Theelen T; Hoefsloot EH; van Schooneveld MJ; Keunen JE; Cremers FP; Klevering BJ; Hoyng CB
Retina; 2009 Jun; 29(6):835-47. PubMed ID: 19357557
[TBL] [Abstract][Full Text] [Related]
12. Novel Mutation in BEST1 Associated with Atypical Best Vitelliform Dystrophy.
Matson ME; Ly SV; Monarrez JL
Optom Vis Sci; 2015 Aug; 92(8):e180-9. PubMed ID: 26099059
[TBL] [Abstract][Full Text] [Related]
13. Unilateral vitelliform phenotype in autosomal recessive bestrophinopathy.
Cascavilla ML; Querques G; Stenirri S; Battaglia Parodi M; Querques L; Bandello F
Ophthalmic Res; 2012; 48(3):146-50. PubMed ID: 22584882
[TBL] [Abstract][Full Text] [Related]
14. Microperimetry and fundus autofluorescence in diabetic macular edema: subthreshold micropulse diode laser versus modified early treatment diabetic retinopathy study laser photocoagulation.
Vujosevic S; Bottega E; Casciano M; Pilotto E; Convento E; Midena E
Retina; 2010 Jun; 30(6):908-16. PubMed ID: 20168272
[TBL] [Abstract][Full Text] [Related]
15. BEST1 sequence variants in Italian patients with vitelliform macular dystrophy.
Sodi A; Passerini I; Murro V; Caputo R; Bacci GM; Bodoj M; Torricelli F; Menchini U
Mol Vis; 2012; 18():2736-48. PubMed ID: 23213274
[TBL] [Abstract][Full Text] [Related]
16. A homozygous frameshift mutation in BEST1 causes the classical form of Best disease in an autosomal recessive mode.
Bitner H; Mizrahi-Meissonnier L; Griefner G; Erdinest I; Sharon D; Banin E
Invest Ophthalmol Vis Sci; 2011 Jul; 52(8):5332-8. PubMed ID: 21467170
[TBL] [Abstract][Full Text] [Related]
17. Microperimetric assessment of the two optical coherence tomography subtypes of acute macular neuroretinopathy.
Battaglia Parodi M; Iacono P; Panico D; Cascavilla M; Bandello F
Clin Exp Ophthalmol; 2015; 43(7):637-42. PubMed ID: 25752249
[TBL] [Abstract][Full Text] [Related]
18. Phenotypic variability in a French family with a novel mutation in the BEST1 gene causing multifocal best vitelliform macular dystrophy.
Lacassagne E; Dhuez A; Rigaudière F; Dansault A; Vêtu C; Bigot K; Vieira V; Puech B; Defoort-Dhellemmes S; Abitbol M
Mol Vis; 2011 Jan; 17():309-22. PubMed ID: 21293734
[TBL] [Abstract][Full Text] [Related]
19. Diabetic macular edema: fundus autofluorescence and functional correlations.
Vujosevic S; Casciano M; Pilotto E; Boccassini B; Varano M; Midena E
Invest Ophthalmol Vis Sci; 2011 Jan; 52(1):442-8. PubMed ID: 20720226
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
