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343 related items for PubMed ID: 22182799

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Gyrate atrophy: clinical and genetic findings in a female without arginine-restricted diet during her first 39 years of life and report of a new OAT gene mutation.
    Renner AB, Walter A, Fiebig BS, Jägle H.
    Doc Ophthalmol; 2012 Aug; 125(1):81-9. PubMed ID: 22674428
    [Abstract] [Full Text] [Related]

  • 3. OAT mutations and clinical features in two Japanese brothers with gyrate atrophy of the choroid and retina.
    Katagiri S, Gekka T, Hayashi T, Ida H, Ohashi T, Eto Y, Tsuneoka H.
    Doc Ophthalmol; 2014 Apr; 128(2):137-48. PubMed ID: 24429551
    [Abstract] [Full Text] [Related]

  • 4. Microperimetric correlations of autofluorescence and optical coherence tomography imaging in dry age-related macular degeneration.
    Querques L, Querques G, Forte R, Souied EH.
    Am J Ophthalmol; 2012 Jun; 153(6):1110-5. PubMed ID: 22321805
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Cystoid macular edema in gyrate atrophy of the choroid and retina: a fluorescein angiography and optical coherence tomography evaluation.
    Oliveira TL, Andrade RE, Muccioli C, Sallum J, Belfort R.
    Am J Ophthalmol; 2005 Jul; 140(1):147-9. PubMed ID: 16038665
    [Abstract] [Full Text] [Related]

  • 7. A 15-bp deletion in exon 5 of the ornithine aminotransferase (OAT) locus associated with gyrate atrophy.
    Park JK, O'Donnell JJ, Shih VE, Gusella JF, Ramesh V.
    Hum Mutat; 1992 Jul; 1(4):293-7. PubMed ID: 1301936
    [Abstract] [Full Text] [Related]

  • 8. Gyrate atrophy of the choroid and retina diagnosed by ornithine-δ-aminotransferase gene analysis: a case report.
    Kim SJ, Lim DH, Kim JH, Kang SW.
    Korean J Ophthalmol; 2013 Oct; 27(5):388-91. PubMed ID: 24082780
    [Abstract] [Full Text] [Related]

  • 9. A systematic comparison of spectral-domain optical coherence tomography and fundus autofluorescence in patients with geographic atrophy.
    Sayegh RG, Simader C, Scheschy U, Montuoro A, Kiss C, Sacu S, Kreil DP, Prünte C, Schmidt-Erfurth U.
    Ophthalmology; 2011 Sep; 118(9):1844-51. PubMed ID: 21496928
    [Abstract] [Full Text] [Related]

  • 10. Microperimetry and fundus autofluorescence in diabetic macular edema: subthreshold micropulse diode laser versus modified early treatment diabetic retinopathy study laser photocoagulation.
    Vujosevic S, Bottega E, Casciano M, Pilotto E, Convento E, Midena E.
    Retina; 2010 Jun; 30(6):908-16. PubMed ID: 20168272
    [Abstract] [Full Text] [Related]

  • 11. Autosomal recessive bestrophinopathy: differential diagnosis and treatment options.
    Boon CJ, van den Born LI, Visser L, Keunen JE, Bergen AA, Booij JC, Riemslag FC, Florijn RJ, van Schooneveld MJ.
    Ophthalmology; 2013 Apr; 120(4):809-20. PubMed ID: 23290749
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Natural history and retinal structure in patients with Usher syndrome type 1 owing to MYO7A mutation.
    Lenassi E, Saihan Z, Cipriani V, Le Quesne Stabej P, Moore AT, Luxon LM, Bitner-Glindzicz M, Webster AR.
    Ophthalmology; 2014 Feb; 121(2):580-7. PubMed ID: 24199935
    [Abstract] [Full Text] [Related]

  • 14. Gyrate atrophy-like phenotype with normal plasma ornithine.
    Kellner U, Weleber RG, Kennaway NG, Fishman GA, Foerster MH.
    Retina; 1997 Feb; 17(5):403-13. PubMed ID: 9355188
    [Abstract] [Full Text] [Related]

  • 15. A homozygous frameshift mutation in LRAT causes retinitis punctata albescens.
    Littink KW, van Genderen MM, van Schooneveld MJ, Visser L, Riemslag FC, Keunen JE, Bakker B, Zonneveld MN, den Hollander AI, Cremers FP, van den Born LI.
    Ophthalmology; 2012 Sep; 119(9):1899-906. PubMed ID: 22559933
    [Abstract] [Full Text] [Related]

  • 16. Molecular pathology of gyrate atrophy of the choroid and retina due to ornithine aminotransferase deficiency.
    Ramesh V, Gusella JF, Shih VE.
    Mol Biol Med; 1991 Feb; 8(1):81-93. PubMed ID: 1682785
    [Abstract] [Full Text] [Related]

  • 17. Gyrate atrophy of the choroid and retina: lymphocyte ornithine-delta-aminotransferase activity in different mutations and carriers.
    Heinänen K, Näntö-Salonen K, Leino L, Pulkki K, Heinonen O, Valle D, Simell O.
    Pediatr Res; 1998 Sep; 44(3):381-5. PubMed ID: 9727717
    [Abstract] [Full Text] [Related]

  • 18. Correlation of fundus autofluorescence with photoreceptor morphology and functional changes in eyes with retinitis pigmentosa.
    Wakabayashi T, Sawa M, Gomi F, Tsujikawa M.
    Acta Ophthalmol; 2010 Aug; 88(5):e177-83. PubMed ID: 20491687
    [Abstract] [Full Text] [Related]

  • 19. Correlation between macular morphology and sensitivity in patients with retinitis pigmentosa and hyperautofluorescent ring.
    Lenassi E, Troeger E, Wilke R, Hawlina M.
    Invest Ophthalmol Vis Sci; 2012 Jan 03; 53(1):47-52. PubMed ID: 22110079
    [Abstract] [Full Text] [Related]

  • 20. Reversal of cystoid macular edema in gyrate atrophy patients.
    Heller D, Weiner C, Nasie I, Anikster Y, Landau Y, Koren T, Pokroy R, Abulafia A, Pras E.
    Ophthalmic Genet; 2017 Dec 03; 38(6):549-554. PubMed ID: 28388263
    [Abstract] [Full Text] [Related]

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