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Journal Abstract Search

146 related items for PubMed ID: 14700671

  • 1. Detection of localized retinal dysfunction in a choroideremia carrier.
    Cheung MC, Nune GC, Wang M, McTaggart KE, MacDonald IM, Duncan JL.
    Am J Ophthalmol; 2004 Jan; 137(1):189-91. PubMed ID: 14700671
    [Abstract] [Full Text] [Related]

  • 2. Detection of mosaic retinal dysfunction in choroideremia carriers electroretinographic and psychophysical testing.
    Vajaranant TS, Fishman GA, Szlyk JP, Grant-Jordan P, Lindeman M, Seiple W.
    Ophthalmology; 2008 Apr; 115(4):723-9. PubMed ID: 18201765
    [Abstract] [Full Text] [Related]

  • 3. Fundus autofluorescence in carriers of choroideremia and correlation with electrophysiologic and psychophysical data.
    Preising MN, Wegscheider E, Friedburg C, Poloschek CM, Wabbels BK, Lorenz B.
    Ophthalmology; 2009 Jun; 116(6):1201-9.e1-2. PubMed ID: 19376587
    [Abstract] [Full Text] [Related]

  • 4. Choroideremia: variability of clinical and electrophysiological characteristics and first report of a negative electroretinogram.
    Renner AB, Kellner U, Cropp E, Preising MN, MacDonald IM, van den Hurk JA, Cremers FP, Foerster MH.
    Ophthalmology; 2006 Nov; 113(11):2066.e1-10. PubMed ID: 16935340
    [Abstract] [Full Text] [Related]

  • 5. Progression of retinal pigment epithelial alterations during long-term follow-up in female carriers of choroideremia and report of a novel CHM mutation.
    Renner AB, Fiebig BS, Cropp E, Weber BH, Kellner U.
    Arch Ophthalmol; 2009 Jul; 127(7):907-12. PubMed ID: 19597113
    [Abstract] [Full Text] [Related]

  • 6. Detection using the multifocal electroretinogram of mosaic retinal dysfunction in carriers of X-linked retinitis pigmentosa.
    Vajaranant TS, Seiple W, Szlyk JP, Fishman GA.
    Ophthalmology; 2002 Mar; 109(3):560-8. PubMed ID: 11874762
    [Abstract] [Full Text] [Related]

  • 7. Comparison of intraocular light scatter in carriers of choroideremia and X-linked retinitis pigmentosa.
    Grover S, Alexander KR, Fishman GA, Ryan J.
    Ophthalmology; 2002 Jan; 109(1):159-63. PubMed ID: 11772598
    [Abstract] [Full Text] [Related]

  • 8. Clinical findings in a carrier of a new mutation in the choroideremia gene.
    Potter MJ, Wong E, Szabo SM, McTaggart KE.
    Ophthalmology; 2004 Oct; 111(10):1905-9. PubMed ID: 15465555
    [Abstract] [Full Text] [Related]

  • 9. Visual Function at the Atrophic Border in Choroideremia Assessed with Adaptive Optics Microperimetry.
    Tuten WS, Vergilio GK, Young GJ, Bennett J, Maguire AM, Aleman TS, Brainard DH, Morgan JIW.
    Ophthalmol Retina; 2019 Oct; 3(10):888-899. PubMed ID: 31235310
    [Abstract] [Full Text] [Related]

  • 10. Clinical and functional findings in choroideremia due to complete deletion of the CHM gene.
    Mura M, Sereda C, Jablonski MM, MacDonald IM, Iannaccone A.
    Arch Ophthalmol; 2007 Aug; 125(8):1107-13. PubMed ID: 17698759
    [Abstract] [Full Text] [Related]

  • 11. Phenotypic variability in three carriers from a family with choroideremia and a frameshift mutation 1388delCCinsG in the REP-1 gene.
    Rudolph G, Preising M, Kalpadakis P, Haritoglou C, Lang GE, Lorenz B.
    Ophthalmic Genet; 2003 Dec; 24(4):203-14. PubMed ID: 14566650
    [Abstract] [Full Text] [Related]

  • 12. Retinal dysfunction in a presymptomatic patient with Huntington's disease.
    Knapp J, VanNasdale DA, Ramsey K, Racine J.
    Doc Ophthalmol; 2018 Jun; 136(3):213-221. PubMed ID: 29691705
    [Abstract] [Full Text] [Related]

  • 13. Multifocal ERG in chloroquine retinopathy: regional variance of retinal dysfunction.
    Kellner U, Kraus H, Foerster MH.
    Graefes Arch Clin Exp Ophthalmol; 2000 Jan; 238(1):94-7. PubMed ID: 10664060
    [Abstract] [Full Text] [Related]

  • 14. Cobalt-Chromium Metallosis With Normal Electroretinogram.
    Grillo LM, Nguyen HV, Tsang SH, Hood DC, Odel JG.
    J Neuroophthalmol; 2016 Dec; 36(4):383-388. PubMed ID: 27295601
    [Abstract] [Full Text] [Related]

  • 15. Retinal dystrophy and subretinal drusenoid deposits in female choroideremia carriers.
    Murro V, Mucciolo DP, Passerini I, Palchetti S, Sodi A, Virgili G, Rizzo S.
    Graefes Arch Clin Exp Ophthalmol; 2017 Nov; 255(11):2099-2111. PubMed ID: 28752371
    [Abstract] [Full Text] [Related]

  • 16. Multifocal electroretinogram and central visual field testing in central areolar choroidal dystrophy.
    Gundogan FC, Dinç UA, Erdem U, Ozge G, Sobaci G.
    Eur J Ophthalmol; 2010 Nov; 20(5):919-24. PubMed ID: 20306439
    [Abstract] [Full Text] [Related]

  • 17. Detailed retinal phenotype of Boucher-Neuhäuser syndrome associated with mutations in PNPLA6 mimicking choroideremia.
    O'Neil E, Serrano L, Scoles D, Cunningham KE, Han G, Chiang J, Bennett J, Aleman TS.
    Ophthalmic Genet; 2019 Jun; 40(3):267-275. PubMed ID: 31135245
    [Abstract] [Full Text] [Related]

  • 18. Lines of Blaschko and choroideremia.
    MacDonald IM, Sui R, Zein W.
    Ophthalmology; 2009 May; 116(5):1017-8; author reply 1018. PubMed ID: 19410966
    [No Abstract] [Full Text] [Related]

  • 19. Macular Dysfunction in Oguchi Disease with the Frequent Mutation 1147delA in the SAG Gene.
    Hayashi T, Tsuzuranuki S, Kozaki K, Urashima M, Tsuneoka H.
    Ophthalmic Res; 2011 Oct; 46(4):175-80. PubMed ID: 21447990
    [Abstract] [Full Text] [Related]

  • 20. Abnormal multifocal electroretinogram (mfERG) in ethambutol toxicity.
    Kardon RH, Morrisey MC, Lee AG.
    Semin Ophthalmol; 2006 Oct; 21(4):215-22. PubMed ID: 17182409
    [Abstract] [Full Text] [Related]

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