245 related articles for article (PubMed ID: 25936525)
1. Two novel mutations in the bestrophin-1 gene and associated clinical observations in patients with best vitelliform macular dystrophy.
Lin Y; Gao H; Liu Y; Liang X; Liu X; Wang Z; Zhang W; Chen J; Lin Z; Huang X; Liu Y
Mol Med Rep; 2015 Aug; 12(2):2584-8. PubMed ID: 25936525
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Bestrophin 1 gene analysis and associated clinical findings in a Chinese patient with Best vitelliform macular dystrophy.
Lin Y; Li T; Gao H; Lian Y; Chen C; Zhu Y; Li Y; Liu B; Zhou W; Jiang H; Liu X; Zhao X; Liang X; Jin C; Huang X; Lu L
Mol Med Rep; 2017 Oct; 16(4):4751-4755. PubMed ID: 28791410
[TBL] [Abstract][Full Text] [Related]
5. Anterior segment abnormalities and angle-closure glaucoma in a family with a mutation in the BEST1 gene and Best vitelliform macular dystrophy.
Wittström E; Ponjavic V; Bondeson ML; Andréasson S
Ophthalmic Genet; 2011 Nov; 32(4):217-27. PubMed ID: 21473666
[TBL] [Abstract][Full Text] [Related]
6. Screening for BEST1 gene mutations in Chinese patients with bestrophinopathy.
Tian R; Yang G; Wang J; Chen Y
Mol Vis; 2014; 20():1594-604. PubMed ID: 25489231
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Clinical evaluation of two consanguineous families with homozygous mutations in BEST1.
Piñeiro-Gallego T; Álvarez M; Pereiro I; Campos S; Sharon D; Schatz P; Valverde D
Mol Vis; 2011; 17():1607-17. PubMed ID: 21738390
[TBL] [Abstract][Full Text] [Related]
9. Genetic variations in Bestrophin‑1 and associated clinical findings in two Chinese patients with juvenile‑onset and adult‑onset best vitelliform macular dystrophy.
Lin Y; Li T; Ma C; Gao H; Chen C; Zhu Y; Liu B; Lian Y; Huang Y; Li H; Wu Q; Liang X; Jin C; Huang X; Ye J; Lu L
Mol Med Rep; 2018 Jan; 17(1):225-233. PubMed ID: 29115605
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. 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]
14. Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients.
Sodi A; Menchini F; Manitto MP; Passerini I; Murro V; Torricelli F; Menchini U
Mol Vis; 2011; 17():3078-87. PubMed ID: 22162627
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. Screening of BEST1 Gene in a Chinese Cohort With Best Vitelliform Macular Dystrophy or Autosomal Recessive Bestrophinopathy.
Tian L; Sun T; Xu K; Zhang X; Peng X; Li Y
Invest Ophthalmol Vis Sci; 2017 Jul; 58(9):3366-3375. PubMed ID: 28687848
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Mutation analysis of BEST1 in Japanese patients with Best's vitelliform macular dystrophy.
Katagiri S; Hayashi T; Ohkuma Y; Sekiryu T; Takeuchi T; Gekka T; Kondo M; Iwata T; Tsuneoka H
Br J Ophthalmol; 2015 Nov; 99(11):1577-82. PubMed ID: 26201355
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
