Grigg J - Search Results

1

Perspectives of people with inherited retinal diseases on ocular gene therapy in Australia: protocol for a national survey.

Mack HG, Chen FK, Grigg J, Jamieson R, De Roach J, O'Hare F, Britten-Jones AC, McGuinness M, Tindill N, Ayton L; Australian Ocular Gene Therapy Group. Mack HG, et al. Among authors: grigg j. BMJ Open. 2021 Jun 22;11(6):e048361. doi: 10.1136/bmjopen-2020-048361. BMJ Open. 2021. PMID: 34158306 Free PMC article.

2

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. Among authors: grigg j. 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.

3

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. 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.

4

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: grigg jr. 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.

5

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

6

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. 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

7

Australian and New Zealand Registry of Advanced Glaucoma: methodology and recruitment.

Souzeau E, Goldberg I, Healey PR, Mills RA, Landers J, Graham SL, Grigg JR, Usher B, Straga T, Crawford A, Casson RJ, Morgan WH, Ruddle JB, Coote MA, White A, Stewart J, Hewitt AW, Mackey DA, Burdon KP, Craig JE. Souzeau E, et al. Among authors: grigg jr. Clin Exp Ophthalmol. 2012 Aug;40(6):569-75. doi: 10.1111/j.1442-9071.2011.02742.x. Clin Exp Ophthalmol. 2012. PMID: 22171965

8

A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same family.

Ng WY, Pasutto F, Bardakjian TM, Wilson MJ, Watson G, Schneider A, Mackey DA, Grigg JR, Zenker M, Jamieson RV. Ng WY, et al. Among authors: grigg jr. Clin Genet. 2013 Feb;83(2):162-8. doi: 10.1111/j.1399-0004.2012.01851.x. Epub 2012 Feb 20. Clin Genet. 2013. PMID: 22283518

9

Microphthalmia, anophthalmia, and coloboma and associated ocular and systemic features: understanding the spectrum.

Skalicky SE, White AJ, Grigg JR, Martin F, Smith J, Jones M, Donaldson C, Smith JE, Flaherty M, Jamieson RV. Skalicky SE, et al. Among authors: grigg jr. JAMA Ophthalmol. 2013 Dec;131(12):1517-24. doi: 10.1001/jamaophthalmol.2013.5305. JAMA Ophthalmol. 2013. PMID: 24177921

10

The importance of electrophysiology in revealing a complete homozygous deletion of KCNV2.

Grigg JR, Holder GE, Billson FA, Korsakova M, Jamieson RV. Grigg JR, et al. J AAPOS. 2013 Dec;17(6):641-3. doi: 10.1016/j.jaapos.2013.08.006. Epub 2013 Nov 7. J AAPOS. 2013. PMID: 24210337

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