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Journal Abstract Search

330 related items for PubMed ID: 15579991

  • 21. Peripheral Visual Fields in ABCA4 Stargardt Disease and Correlation With Disease Extent on Ultra-widefield Fundus Autofluorescence.
    Abalem MF, Otte B, Andrews C, Joltikov KA, Branham K, Fahim AT, Schlegel D, Qian CX, Heckenlively JR, Jayasundera T.
    Am J Ophthalmol; 2017 Dec; 184():181-188. PubMed ID: 29038010
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  • 22. Homozygous null mutations in the ABCA4 gene in two families with autosomal recessive retinal dystrophy.
    Singh HP, Jalali S, Hejtmancik JF, Kannabiran C.
    Am J Ophthalmol; 2006 May; 141(5):906-13. PubMed ID: 16546111
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  • 23. Three families displaying the combination of Stargardt's disease with cone-rod dystrophy or retinitis pigmentosa.
    Klevering BJ, Maugeri A, Wagner A, Go SL, Vink C, Cremers FP, Hoyng CB.
    Ophthalmology; 2004 Mar; 111(3):546-53. PubMed ID: 15019334
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  • 24. Clinical and Genetic Characteristics Analysis of Korean Patients with Stargardt Disease Using Targeted Exome Sequencing.
    Sung Y, Choi SW, Shim SH, Song WK.
    Ophthalmologica; 2019 Mar; 241(1):38-48. PubMed ID: 29975949
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  • 25. Prognostication in Stargardt Disease Using Fundus Autofluorescence: Improving Patient Care.
    Daich Varela M, Laich Y, Hashem SA, Mahroo OA, Webster AR, Michaelides M.
    Ophthalmology; 2023 Nov; 130(11):1182-1190. PubMed ID: 37331482
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  • 29. Screening of ABCA4 Gene in a Chinese Cohort With Stargardt Disease or Cone-Rod Dystrophy With a Report on 85 Novel Mutations.
    Jiang F, Pan Z, Xu K, Tian L, Xie Y, Zhang X, Chen J, Dong B, Li Y.
    Invest Ophthalmol Vis Sci; 2016 Jan 01; 57(1):145-52. PubMed ID: 26780318
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  • 30. 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 01; 125(1):89-99. PubMed ID: 28947085
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  • 31. 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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  • 34. Evaluation of the common variants of the ABCA4 gene in families with Stargardt disease and autosomal recessive retinitis pigmentosa.
    Shastry BS.
    Int J Mol Med; 2008 Jun 16; 21(6):715-20. PubMed ID: 18506364
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  • 37. Phenotype/genotype correlation in a case series of Stargardt's patients identifies novel mutations in the ABCA4 gene.
    Gemenetzi M, Lotery AJ.
    Eye (Lond); 2013 Nov 16; 27(11):1316-9. PubMed ID: 23949494
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  • 39. The natural history of stargardt disease with specific sequence mutation in the ABCA4 gene.
    Genead MA, Fishman GA, Stone EM, Allikmets R.
    Invest Ophthalmol Vis Sci; 2009 Dec 16; 50(12):5867-71. PubMed ID: 19578016
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