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Journal Abstract Search

440 related items for PubMed ID: 22277927

  • 1. The characterization of retinal phenotype in a family with C1QTNF5-related late-onset retinal degeneration.
    Vincent A, Munier FL, Vandenhoven CC, Wright T, Westall CA, Héon E.
    Retina; 2012 Sep; 32(8):1643-51. PubMed ID: 22277927
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  • 5. Long anterior lens zonules in late-onset retinal degeneration (L-ORD).
    Subrayan V, Morris B, Armbrecht AM, Wright AF, Dhillon B.
    Am J Ophthalmol; 2005 Dec; 140(6):1127-9. PubMed ID: 16376663
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  • 6. Retinal fluorescein and indocyanine green angiography and spectral-domain optical coherence tomography findings in acute retinal pigment epitheliitis.
    Baillif S, Wolff B, Paoli V, Gastaud P, Mauget-Faÿsse M.
    Retina; 2011 Jun; 31(6):1156-63. PubMed ID: 21293312
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  • 7. Analysis of retinal flecks in fundus flavimaculatus using high-definition spectral-domain optical coherence tomography.
    Voigt M, Querques G, Atmani K, Leveziel N, Massamba N, Puche N, Bouzitou-Mfoumou R, Souied EH.
    Am J Ophthalmol; 2010 Sep; 150(3):330-7. PubMed ID: 20579629
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  • 8. Phenotypic marker for early disease detection in dominant late-onset retinal degeneration.
    Jacobson SG, Cideciyan AV, Wright E, Wright AF.
    Invest Ophthalmol Vis Sci; 2001 Jul; 42(8):1882-90. PubMed ID: 11431457
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  • 11. Outer retinal circular structures in patients with Bietti crystalline retinopathy.
    Kojima H, Otani A, Ogino K, Nakagawa S, Makiyama Y, Kurimoto M, Guo C, Yoshimura N.
    Br J Ophthalmol; 2012 Mar; 96(3):390-3. PubMed ID: 21803923
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  • 13. Characteristic spectral-domain optical coherence tomography findings of multifocal choroiditis.
    Vance SK, Khan S, Klancnik JM, Freund KB.
    Retina; 2011 Apr; 31(4):717-23. PubMed ID: 21386760
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  • 15. WAGNER syndrome: anatomic, functional and genetic characterization of a Portuguese family.
    Araújo JR, Tavares-Ferreira J, Estrela-Silva S, Rocha P, Brandão E, Faria PA, Falcão-Reis F, Rocha-Sousa A.
    Graefes Arch Clin Exp Ophthalmol; 2018 Jan; 256(1):163-171. PubMed ID: 29071374
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  • 17. Fundus albipunctatus associated with compound heterozygous mutations in RPE65.
    Schatz P, Preising M, Lorenz B, Sander B, Larsen M, Rosenberg T.
    Ophthalmology; 2011 May; 118(5):888-94. PubMed ID: 21211845
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  • 18. CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy.
    Aleman TS, Soumittra N, Cideciyan AV, Sumaroka AM, Ramprasad VL, Herrera W, Windsor EA, Schwartz SB, Russell RC, Roman AJ, Inglehearn CF, Kumaramanickavel G, Stone EM, Fishman GA, Jacobson SG.
    Invest Ophthalmol Vis Sci; 2009 Dec; 50(12):5944-54. PubMed ID: 19578027
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  • 19. Cross-sectional anatomic configurations of peripapillary atrophy evaluated with spectral domain-optical coherence tomography.
    Lee KY, Tomidokoro A, Sakata R, Konno S, Mayama C, Saito H, Hayashi K, Iwase A, Araie M.
    Invest Ophthalmol Vis Sci; 2010 Feb; 51(2):666-71. PubMed ID: 19850838
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