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Journal Abstract Search

223 related items for PubMed ID: 27409480

  • 1. Outer Retinal Changes Including the Ellipsoid Zone Band in Usher Syndrome 1B due to MYO7A Mutations.
    Sumaroka A, Matsui R, Cideciyan AV, McGuigan DB, Sheplock R, Schwartz SB, Jacobson SG.
    Invest Ophthalmol Vis Sci; 2016 Jul 01; 57(9):OCT253-61. PubMed ID: 27409480
    [Abstract] [Full Text] [Related]

  • 2. Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutations.
    Jacobson SG, Aleman TS, Sumaroka A, Cideciyan AV, Roman AJ, Windsor EA, Schwartz SB, Rehm HL, Kimberling WJ.
    Invest Ophthalmol Vis Sci; 2009 Apr 01; 50(4):1886-94. PubMed ID: 19074810
    [Abstract] [Full Text] [Related]

  • 3. Retinal disease course in Usher syndrome 1B due to MYO7A mutations.
    Jacobson SG, Cideciyan AV, Gibbs D, Sumaroka A, Roman AJ, Aleman TS, Schwartz SB, Olivares MB, Russell RC, Steinberg JD, Kenna MA, Kimberling WJ, Rehm HL, Williams DS.
    Invest Ophthalmol Vis Sci; 2011 Oct 07; 52(11):7924-36. PubMed ID: 21873662
    [Abstract] [Full Text] [Related]

  • 4. CLINICAL PRESENTATION AND DISEASE COURSE OF USHER SYNDROME BECAUSE OF MUTATIONS IN MYO7A OR USH2A.
    Testa F, Melillo P, Bonnet C, Marcelli V, de Benedictis A, Colucci R, Gallo B, Kurtenbach A, Rossi S, Marciano E, Auricchio A, Petit C, Zrenner E, Simonelli F.
    Retina; 2017 Aug 07; 37(8):1581-1590. PubMed ID: 27828912
    [Abstract] [Full Text] [Related]

  • 5. Multicentric Longitudinal Prospective Study in a European Cohort of MYO7A Patients: Disease Course and Implications for Gene Therapy.
    Testa F, Carreño E, van den Born LI, Melillo P, Perea-Romero I, Di Iorio V, Risca G, Iodice CM, Pennings RJE, Karali M, Banfi S, Auricchio A, Galimberti S, Ayuso C, Simonelli F.
    Invest Ophthalmol Vis Sci; 2024 Jun 03; 65(6):25. PubMed ID: 38884554
    [Abstract] [Full Text] [Related]

  • 6. 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 03; 121(2):580-7. PubMed ID: 24199935
    [Abstract] [Full Text] [Related]

  • 7. ACUTE ZONAL OCCULT OUTER RETINOPATHY: Structural and Functional Analysis Across the Transition Zone Between Healthy and Diseased Retina.
    Duncker T, Lee W, Jiang F, Ramachandran R, Hood DC, Tsang SH, Sparrow JR, Greenstein VC.
    Retina; 2018 Jan 03; 38(1):118-127. PubMed ID: 28590963
    [Abstract] [Full Text] [Related]

  • 8. PHENOTYPIC CHARACTERISTICS OF ROD-CONE DYSTROPHY ASSOCIATED WITH MYO7A MUTATIONS IN A LARGE FRENCH COHORT.
    Khateb S, Mohand-Saïd S, Nassisi M, Bonnet C, Roux AF, Andrieu C, Antonio A, Condroyer C, Zeitz C, Devisme C, Loundon N, Marlin S, Petit C, Bodaghi B, Sahel JA, Audo I.
    Retina; 2020 Aug 03; 40(8):1603-1615. PubMed ID: 31479088
    [Abstract] [Full Text] [Related]

  • 9. Assessing Photoreceptor Structure in Retinitis Pigmentosa and Usher Syndrome.
    Sun LW, Johnson RD, Langlo CS, Cooper RF, Razeen MM, Russillo MC, Dubra A, Connor TB, Han DP, Pennesi ME, Kay CN, Weinberg DV, Stepien KE, Carroll J.
    Invest Ophthalmol Vis Sci; 2016 May 01; 57(6):2428-42. PubMed ID: 27145477
    [Abstract] [Full Text] [Related]

  • 10. Restoration of foveal thickness and architecture after macula-off retinal detachment repair.
    dell'Omo R, Viggiano D, Giorgio D, Filippelli M, Di Iorio R, Calo' R, Cardone M, Rinaldi M, dell'Omo E, Costagliola C.
    Invest Ophthalmol Vis Sci; 2015 Jan 22; 56(2):1040-50. PubMed ID: 25613940
    [Abstract] [Full Text] [Related]

  • 11. Outer retina analysis by optical coherence tomography in cone-rod dystrophy patients.
    Lima LH, Sallum JM, Spaide RF.
    Retina; 2013 Oct 22; 33(9):1877-80. PubMed ID: 23648999
    [Abstract] [Full Text] [Related]

  • 12. Cone structure in patients with usher syndrome type III and mutations in the Clarin 1 gene.
    Ratnam K, Västinsalo H, Roorda A, Sankila EM, Duncan JL.
    JAMA Ophthalmol; 2013 Jan 22; 131(1):67-74. PubMed ID: 22964989
    [Abstract] [Full Text] [Related]

  • 13. ELLIPSOID ZONE MAPPING AND OUTER RETINAL ASSESSMENT IN STARGARDT DISEASE.
    Arepalli S, Traboulsi EI, Ehlers JP.
    Retina; 2018 Jul 22; 38(7):1427-1431. PubMed ID: 28613213
    [Abstract] [Full Text] [Related]

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  • 16. CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural History.
    de Guimaraes TAC, Robson AG, de Guimaraes IMC, Laich Y, Aychoua N, Wright G, Kalitzeos A, Mahroo OA, Webster AR, Michaelides M.
    Invest Ophthalmol Vis Sci; 2024 Jul 01; 65(8):27. PubMed ID: 39017633
    [Abstract] [Full Text] [Related]

  • 17. STARGARDT DISEASE: Beyond Flecks and Atrophy.
    Light JG, Fard MA, Yaseri M, Aiyetan P, Handa JT, Ebrahimi KB.
    Retina; 2017 Dec 01; 37(12):2352-2361. PubMed ID: 28099317
    [Abstract] [Full Text] [Related]

  • 18. Quantitative analysis of external limiting membrane, ellipsoid zone and interdigitation zone defects in patients with macular holes.
    Houly JR, Veloso CE, Passos E, Nehemy MB.
    Graefes Arch Clin Exp Ophthalmol; 2017 Jul 01; 255(7):1297-1306. PubMed ID: 28412772
    [Abstract] [Full Text] [Related]

  • 19. Efficacy Outcome Measures for Clinical Trials of USH2A Caused by the Common c.2299delG Mutation.
    Calzetti G, Levy RA, Cideciyan AV, Garafalo AV, Roman AJ, Sumaroka A, Charng J, Heon E, Jacobson SG.
    Am J Ophthalmol; 2018 Sep 01; 193():114-129. PubMed ID: 29953849
    [Abstract] [Full Text] [Related]

  • 20. REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA.
    Langlo CS, Erker LR, Parker M, Patterson EJ, Higgins BP, Summerfelt P, Razeen MM, Collison FT, Fishman GA, Kay CN, Zhang J, Weleber RG, Yang P, Pennesi ME, Lam BL, Chulay JD, Dubra A, Hauswirth WW, Wilson DJ, Carroll J, ACHM-001 study group.
    Retina; 2017 Oct 01; 37(10):1956-1966. PubMed ID: 28145975
    [Abstract] [Full Text] [Related]

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