309 related articles for article (PubMed ID: 26099059)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Systematic screening of BEST1 and PRPH2 in juvenile and adult vitelliform macular dystrophies: a rationale for molecular analysis.
Meunier I; Sénéchal A; Dhaenens CM; Arndt C; Puech B; Defoort-Dhellemmes S; Manes G; Chazalette D; Mazoir E; Bocquet B; Hamel CP
Ophthalmology; 2011 Jun; 118(6):1130-6. PubMed ID: 21269699
[TBL] [Abstract][Full Text] [Related]
8. A novel mutation of BEST1 gene in Best disease.
Campa C; Parmeggiani F; Spena R; Ognibene D; Passerini I; Gualandi F
Eur J Ophthalmol; 2021 May; 31(3):NP93-NP95. PubMed ID: 32321300
[TBL] [Abstract][Full Text] [Related]
9. Unilateral vitelliform maculopathy: a comprehensive phenotype study with molecular screening of BEST1 and PRPH2.
Subash M; Rotsos T; Wright GA; Devery S; Holder GE; Robson AG; Pal B; Tufail A; Webster AR; Moore AT; Michaelides M
Br J Ophthalmol; 2012 May; 96(5):719-22. PubMed ID: 22174098
[TBL] [Abstract][Full Text] [Related]
10. NOVEL BEST1 MUTATIONS DETECTED BY NEXT-GENERATION SEQUENCING IN A CHINESE POPULATION WITH VITELLIFORM MACULAR DYSTROPHY.
Guo J; Gao F; Tang W; Qi Y; Xuan Y; Liu W; Li L; Ye X; Xu G; Wu J; Zhang Y
Retina; 2019 Aug; 39(8):1613-1622. PubMed ID: 29781975
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Unilateral BEST1-Associated Retinopathy.
Arora R; Khan K; Kasilian ML; Strauss RW; Holder GE; Robson AG; Thompson DA; Moore AT; Michaelides M
Am J Ophthalmol; 2016 Sep; 169():24-32. PubMed ID: 27287821
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Dome-shaped macula associated with Best vitelliform macular dystrophy.
Battaglia Parodi M; Zucchiatti I; Fasce F; Cascavilla ML; Cicinelli MV; Bandello F
Eur J Ophthalmol; 2015; 25(2):180-1. PubMed ID: 25384969
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Novel mutation in BEST1 associated with retinoschisis.
Silva RA; Berrocal AM; Lam BL; Albini TA
JAMA Ophthalmol; 2013 Jun; 131(6):794-8. PubMed ID: 23572118
[No Abstract] [Full Text] [Related]
18. 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]
19. 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]
20. 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]
[Next] [New Search]