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Quantitative fundus autofluorescence in recessive Stargardt disease.
Burke TR, Duncker T, Woods RL, Greenberg JP, Zernant J, Tsang SH, Smith RT, Allikmets R, Sparrow JR, Delori FC. Burke TR, et al. Invest Ophthalmol Vis Sci. 2014 May 1;55(5):2841-52. doi: 10.1167/iovs.13-13624. Invest Ophthalmol Vis Sci. 2014. PMID: 24677105 Free PMC article.
Analysis of the ABCA4 gene by next-generation sequencing.
Zernant J, Schubert C, Im KM, Burke T, Brown CM, Fishman GA, Tsang SH, Gouras P, Dean M, Allikmets R. Zernant J, et al. Invest Ophthalmol Vis Sci. 2011 Oct 31;52(11):8479-87. doi: 10.1167/iovs.11-8182. Invest Ophthalmol Vis Sci. 2011. PMID: 21911583 Free PMC article.
The external limiting membrane in early-onset Stargardt disease.
Lee W, Nõupuu K, Oll M, Duncker T, Burke T, Zernant J, Bearelly S, Tsang SH, Sparrow JR, Allikmets R. Lee W, et al. Invest Ophthalmol Vis Sci. 2014 Aug 19;55(10):6139-49. doi: 10.1167/iovs.14-15126. Invest Ophthalmol Vis Sci. 2014. PMID: 25139735 Free PMC article.
Disruption in Bruch membrane in patients with Stargardt disease.
Park SP, Chang S, Allikmets R, Smith RT, Burke TR, Gregory-Roberts E, Tsang SH. Park SP, et al. Among authors: burke tr. Ophthalmic Genet. 2012 Mar;33(1):49-52. doi: 10.3109/13816810.2011.628358. Epub 2011 Nov 7. Ophthalmic Genet. 2012. PMID: 22060670 Free PMC article.
Familial discordance in Stargardt disease.
Burke TR, Tsang SH, Zernant J, Smith RT, Allikmets R. Burke TR, et al. Mol Vis. 2012;18:227-33. Epub 2012 Jan 28. Mol Vis. 2012. PMID: 22312191 Free PMC article.
Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 gene.
Burke TR, Fishman GA, Zernant J, Schubert C, Tsang SH, Smith RT, Ayyagari R, Koenekoop RK, Umfress A, Ciccarelli ML, Baldi A, Iannaccone A, Cremers FP, Klaver CC, Allikmets R. Burke TR, et al. Invest Ophthalmol Vis Sci. 2012 Jul 3;53(8):4458-67. doi: 10.1167/iovs.11-9166. Invest Ophthalmol Vis Sci. 2012. PMID: 22661473 Free PMC article.
310 results