Jamieson RV - Search Results

1

A case of neurofibromatosis type 1 and unilateral glaucoma with ectropion uveae.

Thananjeyan AL, Karaconji T, Flaherty M, Zagora S, Jamieson RV, Grigg JRB. Thananjeyan AL, et al. Among authors: jamieson rv. Ophthalmic Genet. 2022 Oct;43(5):709-712. doi: 10.1080/13816810.2022.2089362. Epub 2022 Jun 20. Ophthalmic Genet. 2022. PMID: 35722677 No abstract available.

2

Congenital fibrosis of the extraocular muscles associated with cortical dysplasia and maldevelopment of the basal ganglia.

Flaherty MP, Grattan-Smith P, Steinberg A, Jamieson R, Engle EC. Flaherty MP, et al. Ophthalmology. 2001 Jul;108(7):1313-22. doi: 10.1016/s0161-6420(01)00582-6. Ophthalmology. 2001. PMID: 11425694

3

Congenital iris ectropion as an indicator of variant aniridia.

Willcock C, Grigg J, Wilson M, Tam P, Billson F, Jamieson R. Willcock C, et al. Br J Ophthalmol. 2006 May;90(5):658-569. doi: 10.1136/bjo.2005.089698. Br J Ophthalmol. 2006. PMID: 16622108 Free PMC article. Review. No abstract available.

4

Deletion at 14q22-23 indicates a contiguous gene syndrome comprising anophthalmia, pituitary hypoplasia, and ear anomalies.

Nolen LD, Amor D, Haywood A, St Heaps L, Willcock C, Mihelec M, Tam P, Billson F, Grigg J, Peters G, Jamieson RV. Nolen LD, et al. Among authors: jamieson rv. Am J Med Genet A. 2006 Aug 15;140(16):1711-8. doi: 10.1002/ajmg.a.31335. Am J Med Genet A. 2006. PMID: 16835935

5

Secondary glaucoma after paediatric cataract surgery.

Swamy BN, Billson F, Martin F, Donaldson C, Hing S, Jamieson R, Grigg J, Smith JE. Swamy BN, et al. Br J Ophthalmol. 2007 Dec;91(12):1627-30. doi: 10.1136/bjo.2007.117887. Epub 2007 May 2. Br J Ophthalmol. 2007. PMID: 17475699 Free PMC article.

6

Chromosomal rearrangements and novel genes in disorders of eye development, cataract and glaucoma.

Mihelec M, St Heaps L, Flaherty M, Billson F, Rudduck C, Tam PP, Grigg JR, Peters GB, Jamieson RV. Mihelec M, et al. Among authors: jamieson rv. Twin Res Hum Genet. 2008 Aug;11(4):412-21. doi: 10.1375/twin.11.4.412. Twin Res Hum Genet. 2008. PMID: 18637741 Review.

7

Congenital fibrosis of the extraocular muscles type 1, distinctive conjunctival changes and intrapapillary disc colobomata.

Flaherty MP, Balachandran C, Jamieson R, Engle EC. Flaherty MP, et al. Ophthalmic Genet. 2009 Jun;30(2):91-5. doi: 10.1080/13816810802697473. Ophthalmic Genet. 2009. PMID: 19373680 Free PMC article.

8

Novel SOX2 partner-factor domain mutation in a four-generation family.

Mihelec M, Abraham P, Gibson K, Krowka R, Susman R, Storen R, Chen Y, Donald J, Tam PP, Grigg JR, Flaherty M, Gole GA, Jamieson RV. Mihelec M, et al. Among authors: jamieson rv. Eur J Hum Genet. 2009 Nov;17(11):1417-22. doi: 10.1038/ejhg.2009.79. Epub 2009 May 27. Eur J Hum Genet. 2009. PMID: 19471311 Free PMC article.

9

Port-wine vascular malformations and glaucoma risk in Sturge-Weber syndrome.

Sharan S, Swamy B, Taranath DA, Jamieson R, Yu T, Wargon O, Grigg JR. Sharan S, et al. J AAPOS. 2009 Aug;13(4):374-8. doi: 10.1016/j.jaapos.2009.04.007. J AAPOS. 2009. PMID: 19683189

10

Twist2: role in corneal stromal keratocyte proliferation and corneal thickness.

Weaving L, Mihelec M, Storen R, Sosic D, Grigg JR, Tam PP, Jamieson RV. Weaving L, et al. Among authors: jamieson rv. Invest Ophthalmol Vis Sci. 2010 Nov;51(11):5561-70. doi: 10.1167/iovs.09-5123. Epub 2010 Jun 23. Invest Ophthalmol Vis Sci. 2010. PMID: 20574024

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