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PUBMED FOR HANDHELDS

Journal Abstract Search

148 related items for PubMed ID: 12003605

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  • 4. 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; 89(2):198-206. PubMed ID: 15665353
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  • 8. Reversible bull's-eye maculopathy associated with intravitreal fomivirsen therapy for cytomegalovirus retinitis.
    Stone TW, Jaffe GJ.
    Am J Ophthalmol; 2000 Aug; 130(2):242-3. PubMed ID: 11004306
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  • 10. [Chance discovery of a unilateral bull's eye maculopathy].
    Suárez Baraza J, López Tizón E, Suárez Parra S.
    Arch Soc Esp Oftalmol; 2004 Sep; 79(9):461-4. PubMed ID: 15389369
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  • 16. Main types of bull's eye maculopathy. Functional classification.
    Pinckers A, Cruysberg JR, aan de Kerk AL.
    Doc Ophthalmol; 1984 Nov 15; 58(3):257-67. PubMed ID: 6518979
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  • 17. Whole Exome Sequencing Identifies an Adult-Onset Case of Methylmalonic Aciduria and Homocystinuria Type C (cblC) with Non-Syndromic Bull's Eye Maculopathy.
    Collison FT, Xie YA, Gambin T, Jhangiani S, Muzny D, Gibbs R, Lupski JR, Fishman GA, Allikmets R.
    Ophthalmic Genet; 2015 Nov 15; 36(3):270-5. PubMed ID: 25687216
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  • 18. Juvenile neuronal ceroid lipofuscinosis (Batten disease) CLN3 mutation (Chrom 16p11.2) with different phenotypes in a sibling pair and low intensity in vivo autofluorescence.
    Mantel I, Brantley MA, Bellmann C, Robson AG, Holder GE, Taylor A, Anderson G, Moore AT.
    Klin Monbl Augenheilkd; 2004 May 15; 221(5):427-30. PubMed ID: 15162299
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  • 19. Bull's eye and pigment maculopathy are further retinal manifestations of an abnormal Bruch's membrane in Alport syndrome.
    Savige J, Wang Y, Crawford A, Smith J, Symons A, Mack H, Nicholls K, Wilson D, Colville D.
    Ophthalmic Genet; 2017 May 15; 38(3):238-244. PubMed ID: 27485810
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