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Journal Abstract Search

95 related items for PubMed ID: 8198367

  • 1. Photoreceptor dysfunction in central areolar choroidal dystrophy.
    Rothman RJ.
    Ann Ophthalmol; 1994; 26(1):25-30. PubMed ID: 8198367
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Central areolar choroidal and retinal pigment epithelial dystrophy: a family report.
    Chen KJ, Chen SN, Chen TL, Ho CL.
    Chang Gung Med J; 2001 Feb 20; 24(2):120-4. PubMed ID: 11360402
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  • 4. Autosomal dominant macular atrophy at 6q14 excludes CORD7 and MCDR1/PBCRA loci.
    Griesinger IB, Sieving PA, Ayyagari R.
    Invest Ophthalmol Vis Sci; 2000 Jan 20; 41(1):248-55. PubMed ID: 10634627
    [Abstract] [Full Text] [Related]

  • 5. Electrophysiology findings in a large family with central areolar choroidal dystrophy.
    Lotery AJ, Silvestri G, Collins AD.
    Doc Ophthalmol; 2000 Jan 20; 97(2):103-19. PubMed ID: 10765965
    [Abstract] [Full Text] [Related]

  • 6. An inherited central retinal pigment epithelial dystrophy.
    Klein R, Bresnick G.
    Birth Defects Orig Artic Ser; 1982 Jan 20; 18(6):281-96. PubMed ID: 7171762
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  • 9. Early findings in central areolar choroidal dystrophy.
    Hoyng CB, Pinckers AJ, Deutman AF.
    Acta Ophthalmol (Copenh); 1990 Jun 20; 68(3):356-60. PubMed ID: 2392919
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  • 10. Best's vitelliform macular dystrophy.
    Godel V, Chaine G, Regenbogen L, Coscas G.
    Acta Ophthalmol Suppl (1985); 1986 Jun 20; 175():1-31. PubMed ID: 3006423
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  • 11. The development of central areolar choroidal dystrophy.
    Hoyng CB, Deutman AF.
    Graefes Arch Clin Exp Ophthalmol; 1996 Feb 20; 234(2):87-93. PubMed ID: 8720677
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  • 12. Central cone dysfunction in autosomal dominant vitreoretino choroidopathy (ADVIRC).
    Oh KT, Vallar C.
    Am J Ophthalmol; 2006 May 20; 141(5):940-3. PubMed ID: 16678511
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  • 15. [Macular dystrophies--hereditary macular degenerations].
    Walter P, Mazinani B.
    Klin Monbl Augenheilkd; 2010 Jan 20; 227(1):R1-R14. PubMed ID: 20091442
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  • 16. 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 20; 54(10):589-94. PubMed ID: 19696794
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  • 17. 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
    [Abstract] [Full Text] [Related]

  • 18. Multifocal electroretinograms in cases of central areolar choroidal dystrophy.
    Nagasaka K, Horiguchi M, Shimada Y, Yuzawa M.
    Invest Ophthalmol Vis Sci; 2003 Apr 20; 44(4):1673-9. PubMed ID: 12657608
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  • 19. North Carolina macular dystrophy: clinicopathologic correlation.
    Voo I, Glasgow BJ, Flannery J, Udar N, Small KW.
    Am J Ophthalmol; 2001 Dec 20; 132(6):933-5. PubMed ID: 11730667
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