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Journal Abstract Search

125 related items for PubMed ID: 1475092

  • 1. Long-term follow-up of dominant macular dystrophy with flecks (Stargardt).
    Mansour AM.
    Ophthalmologica; 1992; 205(3):138-43. PubMed ID: 1475092
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  • 2. Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14.
    Edwards AO, Miedziak A, Vrabec T, Verhoeven J, Acott TS, Weleber RG, Donoso LA.
    Am J Ophthalmol; 1999 Apr; 127(4):426-35. PubMed ID: 10218695
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  • 3. Dominant slowly progressive macular dystrophy.
    Singerman LJ, Berkow JW, Patz A.
    Am J Ophthalmol; 1977 May; 83(5):680-93. PubMed ID: 868967
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  • 9. RETINAL FLECKS IN STARGARDT DISEASE REVEAL CHARACTERISTIC FLUORESCENCE LIFETIME TRANSITION OVER TIME.
    Solberg Y, Dysli C, Escher P, Berger L, Wolf S, Zinkernagel MS.
    Retina; 2019 May; 39(5):879-888. PubMed ID: 30985551
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  • 14. 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
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  • 15. Photoreceptor dysfunction in central areolar choroidal dystrophy.
    Rothman RJ.
    Ann Ophthalmol; 1994 Sep 01; 26(1):25-30. PubMed ID: 8198367
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  • 18. Atypical vitelliform macular dystrophy in a 5-generation family.
    Hittner HM, Ferrell RE, Borda RP, Justice J.
    Br J Ophthalmol; 1984 Mar 01; 68(3):199-207. PubMed ID: 6607743
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  • 19. A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1.
    Michaelides M, Holder GE, Hunt DM, Fitzke FW, Bird AC, Moore AT.
    Br J Ophthalmol; 2005 Feb 01; 89(2):198-206. PubMed ID: 15665353
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