BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

342 related articles for article (PubMed ID: 25267528)

  • 1. Dominant cystoid macular dystrophy.
    Saksens NT; van Huet RA; van Lith-Verhoeven JJ; den Hollander AI; Hoyng CB; Boon CJ
    Ophthalmology; 2015 Jan; 122(1):180-91. PubMed ID: 25267528
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Mitochondrial retinal dystrophy associated with the m.3243A>G mutation.
    de Laat P; Smeitink JAM; Janssen MCH; Keunen JEE; Boon CJF
    Ophthalmology; 2013 Dec; 120(12):2684-2696. PubMed ID: 23806424
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Long-term follow-up of Stargardt's disease and fundus flavimaculatus.
    Armstrong JD; Meyer D; Xu S; Elfervig JL
    Ophthalmology; 1998 Mar; 105(3):448-57; discussion 457-8. PubMed ID: 9499775
    [TBL] [Abstract][Full Text] [Related]  

  • 5. IMPG2-associated retinitis pigmentosa displays relatively early macular involvement.
    van Huet RA; Collin RW; Siemiatkowska AM; Klaver CC; Hoyng CB; Simonelli F; Khan MI; Qamar R; Banin E; Cremers FP; Theelen T; den Hollander AI; van den Born LI; Klevering BJ
    Invest Ophthalmol Vis Sci; 2014 May; 55(6):3939-53. PubMed ID: 24876279
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A reappraisal of the clinical spectrum of North Carolina macular dystrophy.
    Khurana RN; Sun X; Pearson E; Yang Z; Harmon J; Goldberg MF; Zhang K
    Ophthalmology; 2009 Oct; 116(10):1976-83. PubMed ID: 19616854
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Characterization of CDH3-Related Congenital Hypotrichosis With Juvenile Macular Dystrophy.
    Hull S; Arno G; Robson AG; Broadgate S; Plagnol V; McKibbin M; Halford S; Michaelides M; Holder GE; Moore AT; Khan KN; Webster AR
    JAMA Ophthalmol; 2016 Sep; 134(9):992-1000. PubMed ID: 27386845
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Retinal functions in dominant cystoid macular dystrophy (DCMD).
    Pinckers A; Deutman AF; Notting JG
    Acta Ophthalmol (Copenh); 1976 Oct; 54(5):579-90. PubMed ID: 990013
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Correlation of fundus autofluorescence with spectral-domain optical coherence tomography and vision in diabetic macular edema.
    Chung H; Park B; Shin HJ; Kim HC
    Ophthalmology; 2012 May; 119(5):1056-65. PubMed ID: 22342014
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Fundus Autofluorescence and SD-OCT Document Rapid Progression in Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Associated with a c.256G > A Mutation in BEST1.
    Kellner S; Stöhr H; Fiebig B; Weinitz S; Farmand G; Kellner U; Weber BH
    Ophthalmic Genet; 2016 Jun; 37(2):201-8. PubMed ID: 26771239
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Early-onset stargardt disease: phenotypic and genotypic characteristics.
    Lambertus S; van Huet RA; Bax NM; Hoefsloot LH; Cremers FP; Boon CJ; Klevering BJ; Hoyng CB
    Ophthalmology; 2015 Feb; 122(2):335-44. PubMed ID: 25444351
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Central areolar choroidal dystrophy.
    Boon CJ; Klevering BJ; Cremers FP; Zonneveld-Vrieling MN; Theelen T; Den Hollander AI; Hoyng CB
    Ophthalmology; 2009 Apr; 116(4):771-82, 782.e1. PubMed ID: 19243827
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Octreotide acetate in dominant cystoid macular dystrophy.
    Hogewind BF; Pieters G; Hoyng CB
    Eur J Ophthalmol; 2008; 18(1):99-103. PubMed ID: 18203093
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunction.
    Roosing S; van den Born LI; Hoyng CB; Thiadens AA; de Baere E; Collin RW; Koenekoop RK; Leroy BP; van Moll-Ramirez N; Venselaar H; Riemslag FC; Cremers FP; Klaver CC; den Hollander AI
    Ophthalmology; 2013 Jun; 120(6):1239-46. PubMed ID: 23499059
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Best vitelliform macular dystrophy in a Swedish family: genetic analysis and a seven-year follow-up of photodynamic treatment of a young boy with choroidal neovascularization.
    Frennesson CI; Wadelius C; Nilsson SE
    Acta Ophthalmol; 2014 May; 92(3):238-42. PubMed ID: 23617333
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Ophthalmic Manifestations of ROSAH (Retinal Dystrophy, Optic Nerve Edema, Splenomegaly, Anhidrosis, and Headache) Syndrome, an Inherited NF κB-Mediated Autoinflammatory Disease with Retinal Dystrophy.
    Huryn LA; Kozycki CT; Serpen JY; Zein WM; Ullah E; Iannaccone A; Williams LB; Sobrin L; Brooks BP; Sen HN; Hufnagel RB; Kastner DL; Kodati S
    Ophthalmology; 2023 Apr; 130(4):423-432. PubMed ID: 36332842
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Late onset is common in best macular dystrophy associated with VMD2 gene mutations.
    Renner AB; Tillack H; Kraus H; Krämer F; Mohr N; Weber BH; Foerster MH; Kellner U
    Ophthalmology; 2005 Apr; 112(4):586-92. PubMed ID: 15808248
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Patterns of macular edema in patients with uveitis: qualitative and quantitative assessment using optical coherence tomography.
    Markomichelakis NN; Halkiadakis I; Pantelia E; Peponis V; Patelis A; Theodossiadis P; Theodossiadis G
    Ophthalmology; 2004 May; 111(5):946-53. PubMed ID: 15121373
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.