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341 related items for 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
    [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
    [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
    [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
    [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 29; 55(6):3939-53. PubMed ID: 24876279
    [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 29; 116(10):1976-83. PubMed ID: 19616854
    [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 01; 134(9):992-1000. PubMed ID: 27386845
    [Abstract] [Full Text] [Related]

  • 8. Retinal functions in dominant cystoid macular dystrophy (DCMD).
    Pinckers A, Deutman AF, Notting JG.
    Acta Ophthalmol (Copenh); 1976 Oct 01; 54(5):579-90. PubMed ID: 990013
    [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 01; 119(5):1056-65. PubMed ID: 22342014
    [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 01; 158(6):1247-1252.e2. PubMed ID: 25174897
    [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 01; 37(2):201-8. PubMed ID: 26771239
    [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 01; 122(2):335-44. PubMed ID: 25444351
    [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 01; 116(4):771-82, 782.e1. PubMed ID: 19243827
    [Abstract] [Full Text] [Related]

  • 14. Octreotide acetate in dominant cystoid macular dystrophy.
    Hogewind BF, Pieters G, Hoyng CB.
    Eur J Ophthalmol; 2008 Apr 01; 18(1):99-103. PubMed ID: 18203093
    [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 01; 120(6):1239-46. PubMed ID: 23499059
    [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 01; 92(3):238-42. PubMed ID: 23617333
    [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 01; 36(8):1586-95. PubMed ID: 26716959
    [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 01; 130(4):423-432. PubMed ID: 36332842
    [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 01; 112(4):586-92. PubMed ID: 15808248
    [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 01; 111(5):946-53. PubMed ID: 15121373
    [Abstract] [Full Text] [Related]

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