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Journal Abstract Search

125 related items for PubMed ID: 1475092

  • 21. Segregation of ophthalmoscopic characteristics according to choroidal thickness in patients with early age-related macular degeneration.
    Switzer DW, Mendonça LS, Saito M, Zweifel SA, Spaide RF.
    Retina; 2012 Jul; 32(7):1265-71. PubMed ID: 22222760
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  • 25. Autosomal dominant Stargardt-like macular dystrophy.
    Donoso LA, Edwards AO, Frost A, Vrabec T, Stone EM, Hageman GS, Perski T.
    Surv Ophthalmol; 2001 Jul; 46(2):149-63. PubMed ID: 11578648
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  • 28. A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13.
    Gerber S, Rozet JM, Bonneau D, Souied E, Camuzat A, Dufier JL, Amalric P, Weissenbach J, Munnich A, Kaplan J.
    Am J Hum Genet; 1995 Feb; 56(2):396-9. PubMed ID: 7847373
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  • 29. Iris pigment epithelial translocation in the treatment of exudative macular degeneration: a 3-year follow-up.
    Aisenbrey S, Lafaut BA, Szurman P, Hilgers RD, Esser P, Walter P, Bartz-Schmidt KU, Thumann G.
    Arch Ophthalmol; 2006 Feb; 124(2):183-8. PubMed ID: 16476887
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  • 33. Fenestrated sheen macular dystrophy. A new autosomal dominant maculopathy.
    O'Donnell FE, Welch RB.
    Arch Ophthalmol; 1979 Jul; 97(7):1292-6. PubMed ID: 454265
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  • 37. Fenestrated sheen macular dystrophy. A new autosomal dominant maculopathy.
    Slagsvold JE.
    Acta Ophthalmol (Copenh); 1981 Oct; 59(5):683-8. PubMed ID: 7315222
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  • 38. Patterned dystrophy of the retinal pigment epithelium.
    Pinckers A, Cruysberg JR.
    Ophthalmic Paediatr Genet; 1986 Mar; 7(1):35-43. PubMed ID: 3703489
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  • 40. 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; 92(3):238-42. PubMed ID: 23617333
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