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Journal Abstract Search

309 related items for PubMed ID: 32646556

  • 21. Cone photoreceptor abnormalities correlate with vision loss in patients with Stargardt disease.
    Chen Y, Ratnam K, Sundquist SM, Lujan B, Ayyagari R, Gudiseva VH, Roorda A, Duncan JL.
    Invest Ophthalmol Vis Sci; 2011 May 17; 52(6):3281-92. PubMed ID: 21296825
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  • 23. Mutations in GPR143/OA1 and ABCA4 Inform Interpretations of Short-Wavelength and Near-Infrared Fundus Autofluorescence.
    Paavo M, Zhao J, Kim HJ, Lee W, Zernant J, Cai C, Allikmets R, Tsang SH, Sparrow JR.
    Invest Ophthalmol Vis Sci; 2018 May 01; 59(6):2459-2469. PubMed ID: 29847651
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  • 25. Repeatability and reliability of quantitative fundus autofluorescence imaging in patients with early and intermediate age-related macular degeneration.
    Reiter GS, Told R, Baratsits M, Hecht A, Schlanitz FG, Sacu S, Schmidt-Erfurth U.
    Acta Ophthalmol; 2019 Jun 01; 97(4):e526-e532. PubMed ID: 30549203
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  • 26. Case Report: Multimodal Imaging Features of an ABCA4 Cone Dystrophy.
    Monferrer-Adsuara C, Montero-Hernández J, Castro-Navarro V, Remolí-Sargues L, Cervera-Taulet E.
    Optom Vis Sci; 2022 Feb 01; 99(2):195-201. PubMed ID: 34897229
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  • 27. Identification of novel PROM1 mutations responsible for autosomal recessive maculopathy with rod-cone dystrophy.
    Liang J, She X, Chen J, Zhai Y, Liu Y, Zheng K, Gong Y, Zhu H, Luo X, Sun X.
    Graefes Arch Clin Exp Ophthalmol; 2019 Mar 01; 257(3):619-628. PubMed ID: 30588538
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  • 28. A ROD-CONE DYSTROPHY IS SYSTEMATICALLY ASSOCIATED TO THE RTN4IP1 RECESSIVE OPTIC ATROPHY.
    Meunier I, Bocquet B, Charif M, Dhaenens CM, Manes G, Amati-Bonneau P, Roubertie A, Zanlonghi X, Lenaers G.
    Retina; 2021 Aug 01; 41(8):1771-1779. PubMed ID: 33315831
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  • 30. Monoallelic ABCA4 Mutations Appear Insufficient to Cause Retinopathy: A Quantitative Autofluorescence Study.
    Müller PL, Gliem M, Mangold E, Bolz HJ, Finger RP, McGuinness M, Betz C, Jiang Z, Weber BH, MacLaren RE, Holz FG, Radu RA, Charbel Issa P.
    Invest Ophthalmol Vis Sci; 2015 Dec 01; 56(13):8179-86. PubMed ID: 26720470
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  • 31. Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunction.
    Roosing S, van den Born LI, Hoyng CB, Thiadens AA, de Baere E, Collin RW, Koenekoop RK, Leroy BP, van Moll-Ramirez N, Venselaar H, Riemslag FC, Cremers FP, Klaver CC, den Hollander AI.
    Ophthalmology; 2013 Jun 01; 120(6):1239-46. PubMed ID: 23499059
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  • 32. Cone abnormalities in fundus albipunctatus associated with RDH5 mutations assessed using adaptive optics scanning laser ophthalmoscopy.
    Makiyama Y, Ooto S, Hangai M, Ogino K, Gotoh N, Oishi A, Yoshimura N.
    Am J Ophthalmol; 2014 Mar 01; 157(3):558-70.e1-4. PubMed ID: 24246574
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  • 33. Quantitative Fundus Autofluorescence in Best Vitelliform Macular Dystrophy: RPE Lipofuscin is not Increased in Non-Lesion Areas of Retina.
    Sparrow JR, Duncker T, Woods R, Delori FC.
    Adv Exp Med Biol; 2016 Mar 01; 854():285-90. PubMed ID: 26427423
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  • 35. QUANTITATIVE AUTOFLUORESCENCE IN CENTRAL SEROUS CHORIORETINOPATHY.
    Weber C, Schaetzle LS, Stasik I, von der Emde L, Holz FG, Liegl R.
    Retina; 2024 May 01; 44(5):844-851. PubMed ID: 38147686
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  • 36. A rare case of RGR/CDHR1 haplotype identified in Bulgarian patient with cone-rod dystrophy.
    Mermeklieva E, Kamenarova K, Mihova K, Shakola F, Kaneva R.
    Ophthalmic Genet; 2021 Dec 01; 42(6):747-752. PubMed ID: 34229535
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  • 40. Quantitative fundus autofluorescence in healthy eyes.
    Greenberg JP, Duncker T, Woods RL, Smith RT, Sparrow JR, Delori FC.
    Invest Ophthalmol Vis Sci; 2013 Aug 21; 54(8):5684-93. PubMed ID: 23860757
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