BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

384 related articles for article (PubMed ID: 21473666)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. A novel homozygous BEST1 mutation correlates with complex ocular phenotypes.
    Sheng X; Chen X; Zhao K; Liu Y; Vollrath D; Zhao C
    Ophthalmology; 2013 Jul; 120(7):1511-2.e2. PubMed ID: 23823511
    [No Abstract]   [Full Text] [Related]  

  • 5. The Clinical Features and Genetic Spectrum of a Large Cohort of Chinese Patients With Vitelliform Macular Dystrophies.
    Xuan Y; Zhang Y; Zong Y; Wang M; Li L; Ye X; Liu W; Chen J; Sun X; Zhang Y; Chen Y
    Am J Ophthalmol; 2020 Aug; 216():69-79. PubMed ID: 32278767
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Biallelic Mutations in the BEST1 Gene: Additional Families with Autosomal Recessive Bestrophinopathy.
    Wivestad Jansson R; Berland S; Bredrup C; Austeng D; Andréasson S; Wittström E
    Ophthalmic Genet; 2016 Jun; 37(2):183-93. PubMed ID: 26333019
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Autosomal recessive bestrophinopathy associated with angle-closure glaucoma.
    Crowley C; Paterson R; Lamey T; McLaren T; De Roach J; Chelva E; Khan J
    Doc Ophthalmol; 2014 Aug; 129(1):57-63. PubMed ID: 24859690
    [TBL] [Abstract][Full Text] [Related]  

  • 10. BESTROPHINOPATHY: A Spectrum of Ocular Abnormalities Caused by the c.614T>C Mutation in the BEST1 Gene.
    Toto L; Boon CJ; Di Antonio L; Battaglia Parodi M; Mastropasqua R; Antonucci I; Stuppia L; Mastropasqua L
    Retina; 2016 Aug; 36(8):1586-95. PubMed ID: 26716959
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series.
    Zhong Y; Guo X; Xiao H; Luo J; Zuo C; Huang X; Huang J; Mi L; Zhang Q; Liu X
    PLoS One; 2017; 12(1):e0169395. PubMed ID: 28056057
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Morphological and functional changes in multifocal vitelliform retinopathy and biallelic mutations in BEST1.
    Wittström E; Ekvall S; Schatz P; Bondeson ML; Ponjavic V; Andréasson S
    Ophthalmic Genet; 2011 Jun; 32(2):83-96. PubMed ID: 21192766
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 20.