Tsang SH - Search Results

1

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: tsang sh. 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.

2

Lentiviral transduction of green fluorescent protein in retinal epithelium: evidence of rejection.

Doi K, Hargitai J, Kong J, Tsang SH, Wheatley M, Chang S, Goff S, Gouras P. Doi K, et al. Among authors: tsang sh. Vision Res. 2002 Feb;42(4):551-8. doi: 10.1016/s0042-6989(01)00237-1. Vision Res. 2002. PMID: 11853772 Free article.

3

Non-vascular vision loss in pseudoxanthoma elasticum.

Tsui I, Fuchs BS, Chou CL, Chang S, Tsang SH. Tsui I, et al. Among authors: tsang sh. Doc Ophthalmol. 2008 Jul;117(1):65-7. doi: 10.1007/s10633-007-9100-y. Epub 2007 Nov 22. Doc Ophthalmol. 2008. PMID: 18034271 Free PMC article.

4

Preferred retinal locus in macular disease: characteristics and clinical implications.

Greenstein VC, Santos RA, Tsang SH, Smith RT, Barile GR, Seiple W. Greenstein VC, et al. Among authors: tsang sh. Retina. 2008 Oct;28(9):1234-40. doi: 10.1097/IAE.0b013e31817c1b47. Retina. 2008. PMID: 18628727 Free PMC article.

5

A novel mutation and phenotypes in phosphodiesterase 6 deficiency.

Tsang SH, Tsui I, Chou CL, Zernant J, Haamer E, Iranmanesh R, Tosi J, Allikmets R. Tsang SH, et al. Am J Ophthalmol. 2008 Nov;146(5):780-8. doi: 10.1016/j.ajo.2008.06.017. Epub 2008 Aug 23. Am J Ophthalmol. 2008. PMID: 18723146 Free PMC article.

6

G1961E mutant allele in the Stargardt disease gene ABCA4 causes bull's eye maculopathy.

Cella W, Greenstein VC, Zernant-Rajang J, Smith TR, Barile G, Allikmets R, Tsang SH. Cella W, et al. Among authors: tsang sh. Exp Eye Res. 2009 Jun 15;89(1):16-24. doi: 10.1016/j.exer.2009.02.001. Epub 2009 Feb 13. Exp Eye Res. 2009. PMID: 19217903 Free PMC article.

7

A comparison of fundus autofluorescence and retinal structure in patients with Stargardt disease.

Gomes NL, Greenstein VC, Carlson JN, Tsang SH, Smith RT, Carr RE, Hood DC, Chang S. Gomes NL, et al. Among authors: tsang sh. Invest Ophthalmol Vis Sci. 2009 Aug;50(8):3953-9. doi: 10.1167/iovs.08-2657. Epub 2009 Mar 25. Invest Ophthalmol Vis Sci. 2009. PMID: 19324865 Free PMC article.

8

Case report: autofluorescence imaging and phenotypic variance in a sibling pair with early-onset retinal dystrophy due to defective CRB1 function.

Tosi J, Tsui I, Lima LH, Wang NK, Tsang SH. Tosi J, et al. Among authors: tsang sh. Curr Eye Res. 2009 May;34(5):395-400. doi: 10.1080/02713680902859639. Curr Eye Res. 2009. PMID: 19401883 Free PMC article.

9

Cellular and molecular origin of circumpapillary dysgenesis of the pigment epithelium.

Tosi J, Janisch KM, Wang NK, Kasanuki JM, Flynn JT, Lin CS, Tsang SH. Tosi J, et al. Among authors: tsang sh. Ophthalmology. 2009 May;116(5):971-80. doi: 10.1016/j.ophtha.2008.10.032. Ophthalmology. 2009. PMID: 19410955 Free PMC article.

10

Cellular origin of fundus autofluorescence in patients and mice with a defective NR2E3 gene.

Wang NK, Fine HF, Chang S, Chou CL, Cella W, Tosi J, Lin CS, Nagasaki T, Tsang SH. Wang NK, et al. Among authors: tsang sh. Br J Ophthalmol. 2009 Sep;93(9):1234-40. doi: 10.1136/bjo.2008.153577. Epub 2009 May 7. Br J Ophthalmol. 2009. PMID: 19429590 Free PMC article.

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