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Journal Abstract Search

112 related items for PubMed ID: 8015786

  • 1. A variant of central areolar choroidal dystrophy.
    Chopdar A.
    Ophthalmic Paediatr Genet; 1993 Dec; 14(4):151-64. PubMed ID: 8015786
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  • 2. Early findings in central areolar choroidal dystrophy.
    Hoyng CB, Pinckers AJ, Deutman AF.
    Acta Ophthalmol (Copenh); 1990 Jun; 68(3):356-60. PubMed ID: 2392919
    [Abstract] [Full Text] [Related]

  • 3. Clinical features of progressive bifocal chorioretinal atrophy: a retinal dystrophy linked to chromosome 6q.
    Godley BF, Tiffin PA, Evans K, Kelsell RE, Hunt DM, Bird AC.
    Ophthalmology; 1996 Jun; 103(6):893-8. PubMed ID: 8643244
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  • 4. Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS gene.
    Hoyng CB, Heutink P, Testers L, Pinckers A, Deutman AF, Oostra BA.
    Am J Ophthalmol; 1996 Jun; 121(6):623-9. PubMed ID: 8644804
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  • 5. The development of central areolar choroidal dystrophy.
    Hoyng CB, Deutman AF.
    Graefes Arch Clin Exp Ophthalmol; 1996 Feb; 234(2):87-93. PubMed ID: 8720677
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  • 6. Clinical findings in a multigeneration family with autosomal dominant central areolar choroidal dystrophy associated with an Arg195Leu mutation in the peripherin/RDS gene.
    Keilhauer CN, Meigen T, Weber BH.
    Arch Ophthalmol; 2006 Jul; 124(7):1020-7. PubMed ID: 16832026
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  • 8. Clinical features and linkage analysis for a Chinese family with autosomal dominant central areolar choroidal dystrophy.
    Ma K, Yang XF, Han C, Zhang N, Xu J, Liu SB, Lu H, Snellingen T, Wang NL, Liu NP.
    Chin Med J (Engl); 2009 Nov 20; 122(22):2686-90. PubMed ID: 19951596
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  • 11. Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy.
    Tyni T, Kivelä T, Lappi M, Summanen P, Nikoskelainen E, Pihko H.
    Ophthalmology; 1998 May 20; 105(5):810-24. PubMed ID: 9593380
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  • 12. Electrophysiology findings in a large family with central areolar choroidal dystrophy.
    Lotery AJ, Silvestri G, Collins AD.
    Doc Ophthalmol; 1998 May 20; 97(2):103-19. PubMed ID: 10765965
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  • 13. Photoreceptor dysfunction in central areolar choroidal dystrophy.
    Rothman RJ.
    Ann Ophthalmol; 1994 May 20; 26(1):25-30. PubMed ID: 8198367
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  • 14. Juvenile atrophy of pigment epithelium and choriocapillaris.
    Hoyng C, Pinckers A, Deutman A.
    Graefes Arch Clin Exp Ophthalmol; 1992 May 20; 230(3):230-2. PubMed ID: 1597287
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  • 15. Clinical course of newly developed or progressive patchy chorioretinal atrophy in pathological myopia.
    Ito-Ohara M, Seko Y, Morita H, Imagawa N, Tokoro T.
    Ophthalmologica; 1998 May 20; 212(1):23-9. PubMed ID: 9438580
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  • 17. [The ocular features in a father and a son with central areolar choroidal dystrophy].
    Okuno T, Oku H, Sugasawa J, Hamamura HW, Nakamura K, Ikeda T.
    Nippon Ganka Gakkai Zasshi; 2008 Aug 20; 112(8):688-94. PubMed ID: 18767495
    [Abstract] [Full Text] [Related]

  • 18. The variable expressivity of a family with central areolar pigment epithelial dystrophy.
    Keithahn MA, Huang M, Keltner JL, Small KW, Morse LS.
    Ophthalmology; 1996 Mar 20; 103(3):406-15. PubMed ID: 8600416
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  • 19. 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 20; 86(1):91-6. PubMed ID: 11801511
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  • 20. Sorsby's fundus dystrophy.
    Hamilton WK, Ewing CC, Ives EJ, Carruthers JD.
    Ophthalmology; 1989 Dec 20; 96(12):1755-62. PubMed ID: 2695876
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