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Journal Abstract Search

79 related items for PubMed ID: 18161617

  • 1. Pseudo-vitelliform macular detachment and cuticular drusen: exclusion of 6 candidate genes.
    Barbazetto IA, Yannuzzi NA, Klais CM, Merriam JE, Zernant J, Peiretti E, Yannuzzi LA, Allikmets R.
    Ophthalmic Genet; 2007 Dec; 28(4):192-7. PubMed ID: 18161617
    [Abstract] [Full Text] [Related]

  • 2. Maculopathy due to the R345W substitution in fibulin-3: distinct clinical features, disease variability, and extent of retinal dysfunction.
    Michaelides M, Jenkins SA, Brantley MA, Andrews RM, Waseem N, Luong V, Gregory-Evans K, Bhattacharya SS, Fitzke FW, Webster AR.
    Invest Ophthalmol Vis Sci; 2006 Jul; 47(7):3085-97. PubMed ID: 16799055
    [Abstract] [Full Text] [Related]

  • 3. Peripherin/RDS and VMD2 mutations in macular dystrophies with adult-onset vitelliform lesion.
    Zhuk SA, Edwards AO.
    Mol Vis; 2006 Jul 24; 12():811-5. PubMed ID: 16885924
    [Abstract] [Full Text] [Related]

  • 4. Spectral domain optical coherence tomography in adult-onset vitelliform macular dystrophy with cuticular drusen.
    Finger RP, Charbel Issa P, Kellner U, Schmitz-Valckenberg S, Fleckenstein M, Scholl HP, Holz FG.
    Retina; 2010 Oct 24; 30(9):1455-64. PubMed ID: 20683378
    [Abstract] [Full Text] [Related]

  • 5. Genotype-phenotype correlation of age-related macular degeneration: influence of complement factor H polymorphism.
    Droz I, Mantel I, Ambresin A, Faouzi M, Schorderet DF, Munier FL.
    Br J Ophthalmol; 2008 Apr 24; 92(4):513-7. PubMed ID: 18211923
    [Abstract] [Full Text] [Related]

  • 6. CHOROIDAL THICKENING IN PATIENTS WITH CUTICULAR DRUSEN COMBINED WITH VITELLIFORM MACULAR DETACHMENT.
    Mrejen-Uretsky S, Ayrault S, Nghiem-Buffet S, Quentel G, Cohen SY.
    Retina; 2016 Jun 24; 36(6):1111-8. PubMed ID: 26536099
    [Abstract] [Full Text] [Related]

  • 7. Analysis of the EFEMP1 gene in individuals and families with early onset drusen.
    Narendran N, Guymer RH, Cain M, Baird PN.
    Eye (Lond); 2005 Jan 24; 19(1):11-5. PubMed ID: 15218514
    [Abstract] [Full Text] [Related]

  • 8. Early-onset macular degeneration with drusen in a cynomolgus monkey (Macaca fascicularis) pedigree: exclusion of 13 candidate genes and loci.
    Umeda S, Ayyagari R, Allikmets R, Suzuki MT, Karoukis AJ, Ambasudhan R, Zernant J, Okamoto H, Ono F, Terao K, Mizota A, Yoshikawa Y, Tanaka Y, Iwata T.
    Invest Ophthalmol Vis Sci; 2005 Feb 24; 46(2):683-91. PubMed ID: 15671300
    [Abstract] [Full Text] [Related]

  • 9. The dot-and-fleck retinopathy of X linked Alport syndrome is independent of complement factor H (CFH) gene polymorphisms.
    Liu J, Colville D, Wang YY, Baird PN, Guymer RH, Savige J.
    Br J Ophthalmol; 2009 Mar 24; 93(3):379-82. PubMed ID: 19019939
    [Abstract] [Full Text] [Related]

  • 10. Spectral domain optical coherence tomography characteristics of cuticular drusen.
    Leng T, Rosenfeld PJ, Gregori G, Puliafito CA, Punjabi OS.
    Retina; 2009 Mar 24; 29(7):988-93. PubMed ID: 19584657
    [Abstract] [Full Text] [Related]

  • 11. Mapping of a macular drusen susceptibility locus in rhesus macaques to the homologue of human chromosome 6q14-15.
    Singh KK, Ristau S, Dawson WW, Krawczak M, Schmidtke J.
    Exp Eye Res; 2005 Oct 24; 81(4):401-6. PubMed ID: 16185951
    [Abstract] [Full Text] [Related]

  • 12. Functional aspects of drusen regression in age-related macular degeneration.
    Sallo FB, Rechtman E, Peto T, Stanescu-Segall D, Vogt G, Bird AC, Fitzke FW.
    Br J Ophthalmol; 2009 Oct 24; 93(10):1345-50. PubMed ID: 19535356
    [Abstract] [Full Text] [Related]

  • 13. Acquired vitelliform detachment in patients with subretinal drusenoid deposits (reticular pseudodrusen).
    Zweifel SA, Spaide RF, Yannuzzi LA.
    Retina; 2011 Feb 24; 31(2):229-34. PubMed ID: 20966822
    [Abstract] [Full Text] [Related]

  • 14. Issues in quantifying atrophic macular disease using retinal autofluorescence.
    Sunness JS, Ziegler MD, Applegate CA.
    Retina; 2006 Feb 24; 26(6):666-72. PubMed ID: 16829810
    [Abstract] [Full Text] [Related]

  • 15. The spectrum of phenotypes caused by variants in the CFH gene.
    Boon CJ, van de Kar NC, Klevering BJ, Keunen JE, Cremers FP, Klaver CC, Hoyng CB, Daha MR, den Hollander AI.
    Mol Immunol; 2009 May 24; 46(8-9):1573-94. PubMed ID: 19297022
    [Abstract] [Full Text] [Related]

  • 16. Fundus autofluorescence in Pseudoxanthoma elasticum.
    Finger RP, Charbel Issa P, Ladewig M, Götting C, Holz FG, Scholl HP.
    Retina; 2009 May 24; 29(10):1496-505. PubMed ID: 19823106
    [Abstract] [Full Text] [Related]

  • 17. Clinical and molecular genetic analysis of best vitelliform macular dystrophy.
    Boon CJ, Theelen T, Hoefsloot EH, van Schooneveld MJ, Keunen JE, Cremers FP, Klevering BJ, Hoyng CB.
    Retina; 2009 Jun 24; 29(6):835-47. PubMed ID: 19357557
    [Abstract] [Full Text] [Related]

  • 18. Association of HTRA1 and ARMS2 gene variation with drusen formation in rhesus macaques.
    Singh KK, Krawczak M, Dawson WW, Schmidtke J.
    Exp Eye Res; 2009 Mar 24; 88(3):479-82. PubMed ID: 19028492
    [Abstract] [Full Text] [Related]

  • 19. Extensive macular atrophy with pseudodrusen-like appearance: a new clinical entity.
    Hamel CP, Meunier I, Arndt C, Ben Salah S, Lopez S, Bazalgette C, Bazalgette C, Zanlonghi X, Arnaud B, Defoort-Dellhemmes S, Puech B.
    Am J Ophthalmol; 2009 Apr 24; 147(4):609-20. PubMed ID: 19181301
    [Abstract] [Full Text] [Related]

  • 20. Drusen-like macular deposits in partial trisomy 10q.
    Tabandeh H, Carothers T, Levine L, Monshizadeh R.
    Retina; 2000 Apr 24; 20(6):678-9. PubMed ID: 11131428
    [No Abstract] [Full Text] [Related]

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