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Journal Abstract Search

397 related items for PubMed ID: 29310964

  • 1. Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy.
    Khan KN, Kasilian M, Mahroo OAR, Tanna P, Kalitzeos A, Robson AG, Tsunoda K, Iwata T, Moore AT, Fujinami K, Michaelides M.
    Ophthalmology; 2018 May; 125(5):735-746. PubMed ID: 29310964
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  • 2. Early-onset stargardt disease: phenotypic and genotypic characteristics.
    Lambertus S, van Huet RA, Bax NM, Hoefsloot LH, Cremers FP, Boon CJ, Klevering BJ, Hoyng CB.
    Ophthalmology; 2015 Feb; 122(2):335-44. PubMed ID: 25444351
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  • 3. Clinical and molecular characteristics of childhood-onset Stargardt disease.
    Fujinami K, Zernant J, Chana RK, Wright GA, Tsunoda K, Ozawa Y, Tsubota K, Robson AG, Holder GE, Allikmets R, Michaelides M, Moore AT.
    Ophthalmology; 2015 Feb; 122(2):326-34. PubMed ID: 25312043
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  • 4. Clinical and genetic characteristics of late-onset Stargardt's disease.
    Westeneng-van Haaften SC, Boon CJ, Cremers FP, Hoefsloot LH, den Hollander AI, Hoyng CB.
    Ophthalmology; 2012 Jun; 119(6):1199-210. PubMed ID: 22449572
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  • 5. Multimodal imaging and multifocal electroretinography demonstrate autosomal recessive Stargardt disease may present like occult macular dystrophy.
    Sisk RA, Leng T.
    Retina; 2014 Aug; 34(8):1567-75. PubMed ID: 24743636
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  • 9. Benign Yellow Dot Maculopathy: A New Macular Phenotype.
    Dev Borman A, Rachitskaya A, Suzani M, Sisk RA, Ahmed ZM, Holder GE, Cipriani V, Arno G, Webster AR, Hufnagel RB, Berrocal A, Moore AT.
    Ophthalmology; 2017 Jul; 124(7):1004-1013. PubMed ID: 28366503
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  • 12. The absence of fundus abnormalities in Stargardt disease.
    Bax NM, Lambertus S, Cremers FPM, Klevering BJ, Hoyng CB.
    Graefes Arch Clin Exp Ophthalmol; 2019 Jun; 257(6):1147-1157. PubMed ID: 30903310
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  • 17. Clinical, Genotypic, and Imaging Characterization of the Spectrum of ABCA4 Retinopathies.
    Romano F, Lamanna F, Boon CJF, Siligato A, Kalra G, Agarwal A, Medori C, Bertelli M, Pellegrini M, Invernizzi A, Staurenghi G, Salvetti AP.
    Ophthalmol Retina; 2024 May; 8(5):509-519. PubMed ID: 37924945
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  • 18. The clinical effect of homozygous ABCA4 alleles in 18 patients.
    Fujinami K, Sergouniotis PI, Davidson AE, Mackay DS, Tsunoda K, Tsubota K, Robson AG, Holder GE, Moore AT, Michaelides M, Webster AR.
    Ophthalmology; 2013 Nov; 120(11):2324-31. PubMed ID: 23769331
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  • 19. Stargardt-like Clinical Characteristics and Disease Course Associated with Variants in the WDR19 Gene.
    Sajovic J, Meglič A, Volk M, Maver A, Jarc-Vidmar M, Hawlina M, Fakin A.
    Genes (Basel); 2023 Jan 22; 14(2):. PubMed ID: 36833218
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  • 20. Deep Scleral Exposure: A Degenerative Outcome of End-Stage Stargardt Disease.
    Lee W, Zernant J, Nagasaki T, Tsang SH, Allikmets R.
    Am J Ophthalmol; 2018 Nov 22; 195():16-25. PubMed ID: 30055151
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