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Journal Abstract Search

330 related items for PubMed ID: 15579991

  • 1. 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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  • 2. 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. Photoreceptor Progenitor mRNA Analysis Reveals Exon Skipping Resulting from the ABCA4 c.5461-10T→C Mutation in Stargardt Disease.
    Sangermano R, Bax NM, Bauwens M, van den Born LI, De Baere E, Garanto A, Collin RW, Goercharn-Ramlal AS, den Engelsman-van Dijk AH, Rohrschneider K, Hoyng CB, Cremers FP, Albert S.
    Ophthalmology; 2016 Jun; 123(6):1375-85. PubMed ID: 26976702
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  • 7. Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family.
    Simonelli F, Testa F, Zernant J, Nesti A, Rossi S, Rinaldi E, Allikmets R.
    Ophthalmic Res; 2004 Jun; 36(2):82-8. PubMed ID: 15017103
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  • 9. The spectrum of retinal phenotypes caused by mutations in the ABCA4 gene.
    Klevering BJ, Deutman AF, Maugeri A, Cremers FP, Hoyng CB.
    Graefes Arch Clin Exp Ophthalmol; 2005 Feb; 243(2):90-100. PubMed ID: 15614537
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  • 10. L- and M-cone-driven electroretinograms in Stargardt's macular dystrophy-fundus flavimaculatus.
    Scholl HP, Kremers J, Vonthein R, White K, Weber BH.
    Invest Ophthalmol Vis Sci; 2001 May; 42(6):1380-9. PubMed ID: 11328755
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  • 11. 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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  • 13. 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 17; 120(11):2324-31. PubMed ID: 23769331
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  • 14. ABCA4 gene mutations in Japanese patients with Stargardt disease and retinitis pigmentosa.
    Fukui T, Yamamoto S, Nakano K, Tsujikawa M, Morimura H, Nishida K, Ohguro N, Fujikado T, Irifune M, Kuniyoshi K, Okada AA, Hirakata A, Miyake Y, Tano Y.
    Invest Ophthalmol Vis Sci; 2002 Sep 17; 43(9):2819-24. PubMed ID: 12202497
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  • 16. Full-field ERG as a predictor of the natural course of ABCA4-associated retinal degenerations.
    Schroeder M, Kjellström U.
    Mol Vis; 2018 Sep 17; 24():1-16. PubMed ID: 29386879
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  • 17. Electrophysiological findings in two young patients with Bothnia dystrophy and a mutation in the RLBP1 gene.
    Gränse L, Abrahamson M, Ponjavic V, Andréasson S.
    Ophthalmic Genet; 2001 Jun 17; 22(2):97-105. PubMed ID: 11449319
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  • 19. Novel ABCA4 compound heterozygous mutations cause severe progressive autosomal recessive cone-rod dystrophy presenting as Stargardt disease.
    Xi Q, Li L, Traboulsi EI, Wang QK.
    Mol Vis; 2009 Jun 17; 15():638-45. PubMed ID: 19352439
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