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Journal Abstract Search

763 related items for PubMed ID: 19376587

  • 21. Discrete arcs of increased fundus autofluorescence in retinal dystrophies and functional correlate on microperimetry.
    Fleckenstein M, Charbel Issa P, Fuchs HA, Finger RP, Helb HM, Scholl HP, Holz FG.
    Eye (Lond); 2009 Mar; 23(3):567-75. PubMed ID: 18344954
    [Abstract] [Full Text] [Related]

  • 22. Retinal structure, function, and molecular pathologic features in gyrate atrophy.
    Sergouniotis PI, Davidson AE, Lenassi E, Devery SR, Moore AT, Webster AR.
    Ophthalmology; 2012 Mar; 119(3):596-605. PubMed ID: 22182799
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  • 23. Wide-field fundus autofluorescence abnormalities and visual function in patients with cone and cone-rod dystrophies.
    Oishi M, Oishi A, Ogino K, Makiyama Y, Gotoh N, Kurimoto M, Yoshimura N.
    Invest Ophthalmol Vis Sci; 2014 May 20; 55(6):3572-7. PubMed ID: 24845635
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  • 24. Autofluorescence in female carriers with choroideremia: A familial case with a novel mutation in the CHM gene.
    Ortiz-Ramirez GY, Villanueva-Mendoza C, Zenteno Ruiz JC, Reyes M, Cortés-González V.
    Ophthalmic Genet; 2020 Dec 20; 41(6):625-628. PubMed ID: 32835561
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  • 25. High-resolution retinal imaging of cone-rod dystrophy.
    Wolfing JI, Chung M, Carroll J, Roorda A, Williams DR.
    Ophthalmology; 2006 Jun 20; 113(6):1019.e1. PubMed ID: 16650474
    [Abstract] [Full Text] [Related]

  • 26. Fundus autofluorescence in patients with leber congenital amaurosis.
    Scholl HP, Chong NH, Robson AG, Holder GE, Moore AT, Bird AC.
    Invest Ophthalmol Vis Sci; 2004 Aug 20; 45(8):2747-52. PubMed ID: 15277500
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  • 27. X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60.
    Fishman GA, Grover S, Jacobson SG, Alexander KR, Derlacki DJ, Wu W, Buraczynska M, Swaroop A.
    Ophthalmology; 1998 Dec 20; 105(12):2286-96. PubMed ID: 9855162
    [Abstract] [Full Text] [Related]

  • 28. Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophy.
    Robson AG, Michaelides M, Luong VA, Holder GE, Bird AC, Webster AR, Moore AT, Fitzke FW.
    Br J Ophthalmol; 2008 Jan 20; 92(1):95-102. PubMed ID: 17962389
    [Abstract] [Full Text] [Related]

  • 29. Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypes.
    Neidhardt J, Barthelmes D, Farahmand F, Fleischhauer JC, Berger W.
    Invest Ophthalmol Vis Sci; 2006 Apr 20; 47(4):1630-5. PubMed ID: 16565402
    [Abstract] [Full Text] [Related]

  • 30. "Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology.
    Robson AG, Webster AR, Michaelides M, Downes SM, Cowing JA, Hunt DM, Moore AT, Holder GE.
    Retina; 2010 Jan 20; 30(1):51-62. PubMed ID: 19952985
    [Abstract] [Full Text] [Related]

  • 31. Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy.
    Tyni T, Kivelä T, Lappi M, Summanen P, Nikoskelainen E, Pihko H.
    Ophthalmology; 1998 May 20; 105(5):810-24. PubMed ID: 9593380
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  • 32. Retinal pigment epithelial dysfunction in human immunodeficiency virus-infected patients with cytomegalovirus retinitis.
    Harrison JM, van Heuven WA.
    Ophthalmology; 1999 Apr 20; 106(4):790-7. PubMed ID: 10201604
    [Abstract] [Full Text] [Related]

  • 33. 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 20; 47(7):3085-97. PubMed ID: 16799055
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  • 34. Peripheral cone dystrophy: a variant of cone dystrophy with predominant dysfunction in the peripheral cone system.
    Kondo M, Miyake Y, Kondo N, Ueno S, Takakuwa H, Terasaki H.
    Ophthalmology; 2004 Apr 20; 111(4):732-9. PubMed ID: 15051206
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  • 35. Localized retinal electrophysiological and fundus autofluorescence imaging abnormalities in maternal inherited diabetes and deafness.
    Bellmann C, Neveu MM, Scholl HP, Hogg CR, Rath PP, Jenkins S, Bird AC, Holder GE.
    Invest Ophthalmol Vis Sci; 2004 Jul 20; 45(7):2355-60. PubMed ID: 15223817
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  • 36. Long-term follow-up of retinitis pigmentosa patients with multifocal electroretinography.
    Nagy D, Schönfisch B, Zrenner E, Jägle H.
    Invest Ophthalmol Vis Sci; 2008 Oct 20; 49(10):4664-71. PubMed ID: 18566474
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  • 37. Progression of geographic atrophy and impact of fundus autofluorescence patterns in age-related macular degeneration.
    Holz FG, Bindewald-Wittich A, Fleckenstein M, Dreyhaupt J, Scholl HP, Schmitz-Valckenberg S, FAM-Study Group.
    Am J Ophthalmol; 2007 Mar 20; 143(3):463-72. PubMed ID: 17239336
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  • 38. Spectrum of Disease Severity and Phenotype in Choroideremia Carriers.
    Jauregui R, Park KS, Tanaka AJ, Cho A, Paavo M, Zernant J, Francis JH, Allikmets R, Sparrow JR, Tsang SH.
    Am J Ophthalmol; 2019 Nov 20; 207():77-86. PubMed ID: 31181178
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  • 39. [Diagnosis of retinal diseases. Comparison between multifocal ERG and fundus perimetry - a case study].
    Rohrschneider K, Bültmann S, Kiel R, Weimer P, Krastel H, Blankenagel A.
    Ophthalmologe; 2002 Sep 20; 99(9):695-702. PubMed ID: 12219258
    [Abstract] [Full Text] [Related]

  • 40. Novel mutations and electrophysiologic findings in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia).
    Michaelides M, Li Z, Rana NA, Richardson EC, Hykin PG, Moore AT, Holder GE, Webster AR.
    Ophthalmology; 2010 Jan 20; 117(1):120-127.e1. PubMed ID: 19818506
    [Abstract] [Full Text] [Related]

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