Frazer DG - Search Results

1

Tuft SJ, Hassan H, George S, Frazer DG, Willoughby CE, Liskova P. Tuft SJ, et al. Among authors: frazer dg. Acta Ophthalmol. 2012 Sep;90(6):e482-6. doi: 10.1111/j.1755-3768.2012.02448.x. Epub 2012 Jun 8. Acta Ophthalmol. 2012. PMID: 22682160 Free article.

2

Mutational screening of VSX1 in keratoconus patients from the European population.

Dash DP, George S, O'Prey D, Burns D, Nabili S, Donnelly U, Hughes AE, Silvestri G, Jackson J, Frazer D, Héon E, Willoughby CE. Dash DP, et al. Eye (Lond). 2010 Jun;24(6):1085-92. doi: 10.1038/eye.2009.217. Epub 2009 Sep 18. Eye (Lond). 2010. PMID: 19763142

3

Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation.

Lechner J, Dash DP, Muszynska D, Hosseini M, Segev F, George S, Frazer DG, Moore JE, Kaye SB, Young T, Simpson DA, Churchill AJ, Héon E, Willoughby CE. Lechner J, et al. Among authors: frazer dg. Invest Ophthalmol Vis Sci. 2013 May 3;54(5):3215-23. doi: 10.1167/iovs.13-11781. Invest Ophthalmol Vis Sci. 2013. PMID: 23599324 Free article.

4

Keratoconus: an analysis of corneal asymmetry.

Burns DM, Johnston FM, Frazer DG, Patterson C, Jackson AJ. Burns DM, et al. Among authors: frazer dg. Br J Ophthalmol. 2004 Oct;88(10):1252-5. doi: 10.1136/bjo.2003.033670. Br J Ophthalmol. 2004. PMID: 15377544 Free PMC article.

5

Familial keratoconus with cataract: linkage to the long arm of chromosome 15 and exclusion of candidate genes.

Hughes AE, Dash DP, Jackson AJ, Frazer DG, Silvestri G. Hughes AE, et al. Among authors: frazer dg. Invest Ophthalmol Vis Sci. 2003 Dec;44(12):5063-6. doi: 10.1167/iovs.03-0399. Invest Ophthalmol Vis Sci. 2003. PMID: 14638698

6

Effect of tear hyperosmolarity and signs of clinical ocular surface pathology upon conjunctival goblet cell function in the human ocular surface.

Moore JE, Vasey GT, Dartt DA, McGilligan VE, Atkinson SD, Grills C, Lamey PJ, Leccisotti A, Frazer DG, Moore TC. Moore JE, et al. Among authors: frazer dg. Invest Ophthalmol Vis Sci. 2011 Aug 3;52(9):6174-80. doi: 10.1167/iovs.10-7022. Invest Ophthalmol Vis Sci. 2011. PMID: 21519030

7

Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy.

Irvine AD, Corden LD, Swensson O, Swensson B, Moore JE, Frazer DG, Smith FJ, Knowlton RG, Christophers E, Rochels R, Uitto J, McLean WH. Irvine AD, et al. Among authors: frazer dg. Nat Genet. 1997 Jun;16(2):184-7. doi: 10.1038/ng0697-184. Nat Genet. 1997. PMID: 9171831

8

Corneal guttata: a comparative clinical and specular micrographic study.

Jackson AJ, Robinson FO, Frazer DG, Archer DB. Jackson AJ, et al. Among authors: frazer dg. Eye (Lond). 1999 Dec;13 ( Pt 6):737-43. doi: 10.1038/eye.1999.219. Eye (Lond). 1999. PMID: 10707136

9

Keratoconus, myopia, and personality.

Cooke CA, Cooper C, Dowds E, Frazer DG, Jackson AJ. Cooke CA, et al. Among authors: frazer dg. Cornea. 2003 Apr;22(3):239-42. doi: 10.1097/00003226-200304000-00011. Cornea. 2003. PMID: 12658090

10

Acute rigid gas permeable contact lens intolerance.

Jackson AJ, Wolsley C, Briggs JL, Frazer DG. Jackson AJ, et al. Among authors: frazer dg. Cont Lens Anterior Eye. 2001;24(4):161-7. doi: 10.1016/s1367-0484(01)80035-7. Cont Lens Anterior Eye. 2001. PMID: 16303471

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