BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

274 related articles for article (PubMed ID: 21269699)

  • 1. 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]  

  • 2. 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]  

  • 3. Clinical and genetic heterogeneity in multifocal vitelliform dystrophy.
    Boon CJ; Klevering BJ; den Hollander AI; Zonneveld MN; Theelen T; Cremers FP; Hoyng CB
    Arch Ophthalmol; 2007 Aug; 125(8):1100-6. PubMed ID: 17698758
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Peripherin/RDS and VMD2 mutations in macular dystrophies with adult-onset vitelliform lesion.
    Zhuk SA; Edwards AO
    Mol Vis; 2006 Jul; 12():811-5. PubMed ID: 16885924
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Investigating the role of BEST1 and PRPH2 variants in the molecular aetiology of adult-onset vitelliform macular dystrophies.
    Çavdarli C; Çavdarlı B; Alp MN
    Ophthalmic Genet; 2020 Dec; 41(6):585-590. PubMed ID: 32942919
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. [Gene mutations and clinical features of adult vitelliform macular dystrophy in 5 patients].
    Xue Y; Zhang Y; Wang M; Liu W; Xu G
    Zhonghua Yan Ke Za Zhi; 2014 Jul; 50(7):523-8. PubMed ID: 25312462
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 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. 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]  

  • 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 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]  

  • 15. 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]  

  • 16. Morphology and functional characteristics in adult vitelliform macular dystrophy.
    Renner AB; Tillack H; Kraus H; Kohl S; Wissinger B; Mohr N; Weber BH; Kellner U; Foerster MH
    Retina; 2004 Dec; 24(6):929-39. PubMed ID: 15579992
    [TBL] [Abstract][Full Text] [Related]  

  • 17. PRPH2 (Peripherin/RDS) mutations associated with different macular dystrophies in a Spanish population: a new mutation.
    Coco RM; Tellería JJ; Sanabria MR; Rodríguez-Rúa E; García MT
    Eur J Ophthalmol; 2010; 20(4):724-32. PubMed ID: 20213611
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Best's vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene.
    Eksandh L; Bakall B; Bauer B; Wadelius C; Andréasson S
    Ophthalmic Genet; 2001 Jun; 22(2):107-15. PubMed ID: 11449320
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Association of pattern dystrophy with an HTRA1 single-nucleotide polymorphism.
    Jaouni T; Averbukh E; Burstyn-Cohen T; Grunin M; Banin E; Sharon D; Chowers I
    Arch Ophthalmol; 2012 Aug; 130(8):987-91. PubMed ID: 22893068
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.