328 related articles for article (PubMed ID: 21436265)
1. 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]
2. 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]
3. 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]
4. 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]
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. 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]
7. Autosomal recessive bestrophinopathy: differential diagnosis and treatment options.
Boon CJ; van den Born LI; Visser L; Keunen JE; Bergen AA; Booij JC; Riemslag FC; Florijn RJ; van Schooneveld MJ
Ophthalmology; 2013 Apr; 120(4):809-20. PubMed ID: 23290749
[TBL] [Abstract][Full Text] [Related]
8. Course of visual decline in relation to the Best1 genotype in vitelliform macular dystrophy.
Booij JC; Boon CJ; van Schooneveld MJ; ten Brink JB; Bakker A; de Jong PT; Hoyng CB; Bergen AA; Klaver CC
Ophthalmology; 2010 Jul; 117(7):1415-22. PubMed ID: 20381869
[TBL] [Abstract][Full Text] [Related]
9. Functional and clinical data of Best vitelliform macular dystrophy patients with mutations in the BEST1 gene.
Querques G; Zerbib J; Santacroce R; Margaglione M; Delphin N; Rozet JM; Kaplan J; Martinelli D; Delle Noci N; Soubrane G; Souied EH
Mol Vis; 2009 Dec; 15():2960-72. PubMed ID: 20057903
[TBL] [Abstract][Full Text] [Related]
10. OCT findings in young asymptomatic subjects carrying familial BEST1 gene mutations.
Chacon-Camacho OF; Camarillo-Blancarte L; Zenteno JC
Ophthalmic Genet; 2011 Mar; 32(1):24-30. PubMed ID: 21077756
[TBL] [Abstract][Full Text] [Related]
11. Detailed analysis of family with autosomal recessive bestrophinopathy associated with new BEST1 mutation.
Kubota D; Gocho K; Akeo K; Kikuchi S; Sugahara M; Matsumoto CS; Shinoda K; Mizota A; Yamaki K; Takahashi H; Kameya S
Doc Ophthalmol; 2016 Jun; 132(3):233-43. PubMed ID: 27071392
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Autosomal dominant Best disease with an unusual electrooculographic light rise and risk of angle-closure glaucoma: a clinical and molecular genetic study.
Low S; Davidson AE; Holder GE; Hogg CR; Bhattacharya SS; Black GC; Foster PJ; Webster AR
Mol Vis; 2011; 17():2272-82. PubMed ID: 21921978
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. High-definition optical coherence tomography features in vitelliform macular dystrophy.
Querques G; Regenbogen M; Quijano C; Delphin N; Soubrane G; Souied EH
Am J Ophthalmol; 2008 Oct; 146(4):501-507. PubMed ID: 18619572
[TBL] [Abstract][Full Text] [Related]
18. Clinical and genetic heterogeneity in Slovenian patients with BEST disease.
Glavač D; Jarc-Vidmar M; Vrabec K; Ravnik-Glavač M; Fakin A; Hawlina M
Acta Ophthalmol; 2016 Dec; 94(8):e786-e794. PubMed ID: 27775230
[TBL] [Abstract][Full Text] [Related]
19. Optical Coherence Tomography Examination of the Retinal Pigment Epithelium in Best Vitelliform Macular Dystrophy.
Qian CX; Charran D; Strong CR; Steffens TJ; Jayasundera T; Heckenlively JR
Ophthalmology; 2017 Apr; 124(4):456-463. PubMed ID: 28187978
[TBL] [Abstract][Full Text] [Related]
20. Novel BEST1 Mutations and Special Clinical Features of Best Vitelliform Macular Dystrophy.
Liu J; Zhang Y; Xuan Y; Liu W; Wang M
Ophthalmic Res; 2016; 56(4):178-185. PubMed ID: 27078032
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
