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Journal Abstract Search

496 related items for PubMed ID: 25312043

  • 1. 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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  • 3. 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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  • 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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  • 6. Clinical and molecular analysis of Stargardt disease with preserved foveal structure and function.
    Fujinami K, Sergouniotis PI, Davidson AE, Wright G, Chana RK, Tsunoda K, Tsubota K, Egan CA, Robson AG, Moore AT, Holder GE, Michaelides M, Webster AR.
    Am J Ophthalmol; 2013 Sep; 156(3):487-501.e1. PubMed ID: 23953153
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  • 8. The Rapid-Onset Chorioretinopathy Phenotype of ABCA4 Disease.
    Tanaka K, Lee W, Zernant J, Schuerch K, Ciccone L, Tsang SH, Sparrow JR, Allikmets R.
    Ophthalmology; 2018 Jan; 125(1):89-99. PubMed ID: 28947085
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  • 9. Electroretinographic findings in patients with Stargardt disease and fundus flavimaculatus.
    Oh KT, Weleber RG, Stone EM, Oh DM, Rosenow J, Billingslea AM.
    Retina; 2004 Dec; 24(6):920-8. PubMed ID: 15579991
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  • 10. 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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  • 12. 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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  • 15. Foveal sparing in Stargardt disease.
    van Huet RA, Bax NM, Westeneng-Van Haaften SC, Muhamad M, Zonneveld-Vrieling MN, Hoefsloot LH, Cremers FP, Boon CJ, Klevering BJ, Hoyng CB.
    Invest Ophthalmol Vis Sci; 2014 Oct 16; 55(11):7467-78. PubMed ID: 25324290
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  • 16. ULTRAWIDEFIELD AUTOFLUORESENCE IN ABCA4 STARGARDT DISEASE.
    Klufas MA, Tsui I, Sadda SR, Hosseini H, Schwartz SD.
    Retina; 2018 Feb 16; 38(2):403-415. PubMed ID: 28248825
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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 16; 120(11):2324-31. PubMed ID: 23769331
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