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Journal Abstract Search

120 related items for PubMed ID: 8720677

  • 21. Central areolar choroidal dystrophy associated with dominantly inherited drusen.
    Klevering BJ, van Driel M, van Hogerwou AJ, van De Pol DJ, Deutman AF, Pinckers AJ, Cremers FP, Hoyng CB.
    Br J Ophthalmol; 2002 Jan; 86(1):91-6. PubMed ID: 11801511
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  • 24. Annular fundus autofluorescence abnormality in a case of macular dystrophy.
    Poloschek CM, Hansen LL, Bach M.
    Doc Ophthalmol; 2008 Mar; 116(2):91-5. PubMed ID: 18008096
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  • 26. 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
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  • 27. 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
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  • 28. Evolution of benign concentric annular macular dystrophy.
    van den Biesen PR, Deutman AF, Pinckers AJ.
    Am J Ophthalmol; 1985 Jul 15; 100(1):73-8. PubMed ID: 4014382
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  • 33. Central areolar choroidal dystrophy associated with inherited drusen in a multigeneration Tunisian family: exclusion of the PRPH2 gene and the 17p13 locus.
    Ouechtati F, Belhadj Tahar O, Mhenni A, Chakroun S, Chouchene I, Oueslati S, Rebai A, Abdelhak S, Jeddi-Blouza A.
    J Hum Genet; 2009 Oct 15; 54(10):589-94. PubMed ID: 19696794
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  • 35. 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
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  • 36. 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 29; 92(3):238-42. PubMed ID: 23617333
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  • 38. Central areolar choroidal dystrophy.
    Noble KG.
    Am J Ophthalmol; 1977 Sep 29; 84(3):310-8. PubMed ID: 900227
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  • 40. Ocular phenotype of CORD5, an autosomal dominant retinal dystrophy associated with PITPNM3 p.Q626H mutation.
    Reinis A, Golovleva I, Köhn L, Sandgren O.
    Acta Ophthalmol; 2013 May 29; 91(3):259-66. PubMed ID: 22405330
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