Staffieri SE - Search Results

1

Pathogenic genetic variants identified in Australian families with paediatric cataract.

Jones JL, McComish BJ, Staffieri SE, Souzeau E, Kearns LS, Elder JE, Charlesworth JC, Mackey DA, Ruddle JB, Taranath D, Pater J, Casey T, Craig JE, Burdon KP. Jones JL, et al. Among authors: staffieri se. BMJ Open Ophthalmol. 2022 Aug;7(1):e001064. doi: 10.1136/bmjophth-2022-001064. BMJ Open Ophthalmol. 2022. PMID: 36161833 Free PMC article.

2

Retinoblastoma in Victoria, 1976-2000: changing management trends and outcomes.

Dondey JC, Staffieri S, McKenzie J, Davie G, Elder J. Dondey JC, et al. Clin Exp Ophthalmol. 2004 Aug;32(4):354-9. doi: 10.1111/j.1442-9071.2004.00836.x. Clin Exp Ophthalmol. 2004. PMID: 15281966

3

Rock, paper and scissors? Traumatic paediatric cataract in Victoria 1992-2006.

Staffieri SE, Ruddle JB, Mackey DA. Staffieri SE, et al. Clin Exp Ophthalmol. 2010 Apr;38(3):237-41. doi: 10.1111/j.1442-9071.2010.02236.x. Clin Exp Ophthalmol. 2010. PMID: 20447118

4

Best's macular dystrophy in Australia: phenotypic profile and identification of novel BEST1 mutations.

Cohn AC, Turnbull C, Ruddle JB, Guymer RH, Kearns LS, Staffieri S, Daggett HT, Hewitt AW, Mackey DA. Cohn AC, et al. Eye (Lond). 2011 Feb;25(2):208-17. doi: 10.1038/eye.2010.180. Epub 2010 Nov 26. Eye (Lond). 2011. PMID: 21109774 Free PMC article.

5

Mitochondrial oxidative phosphorylation compensation may preserve vision in patients with OPA1-linked autosomal dominant optic atrophy.

Van Bergen NJ, Crowston JG, Kearns LS, Staffieri SE, Hewitt AW, Cohn AC, Mackey DA, Trounce IA. Van Bergen NJ, et al. Among authors: staffieri se. PLoS One. 2011;6(6):e21347. doi: 10.1371/journal.pone.0021347. Epub 2011 Jun 22. PLoS One. 2011. PMID: 21731710 Free PMC article.

6

Telemedicine model to prevent blindness from familial glaucoma.

Staffieri SE, Ruddle JB, Kearns LS, Barbour JM, Edwards TL, Paul P, Mackey DA. Staffieri SE, et al. Clin Exp Ophthalmol. 2011 Nov;39(8):760-5. doi: 10.1111/j.1442-9071.2011.02556.x. Epub 2011 Apr 27. Clin Exp Ophthalmol. 2011. PMID: 21749595

7

Familial retinal detachment associated with COL2A1 exon 2 and FZD4 mutations.

Edwards TL, Burt BO, Black GC, Perveen R, Kearns LS, Staffieri SE, Toomes C, Buttery RG, Mackey DA. Edwards TL, et al. Among authors: staffieri se. Clin Exp Ophthalmol. 2012 Jul;40(5):476-83. doi: 10.1111/j.1442-9071.2012.02804.x. Epub 2012 Jun 19. Clin Exp Ophthalmol. 2012. PMID: 22574936

8

Heritability of strabismus: genetic influence is specific to eso-deviation and independent of refractive error.

Sanfilippo PG, Hammond CJ, Staffieri SE, Kearns LS, Melissa Liew SH, Barbour JM, Hewitt AW, Ge D, Snieder H, Mackinnon JR, Brown SA, Lorenz B, Spector TD, Martin NG, Wilmer JB, Mackey DA. Sanfilippo PG, et al. Among authors: staffieri se. Twin Res Hum Genet. 2012 Oct;15(5):624-30. doi: 10.1017/thg.2012.22. Epub 2012 Jun 13. Twin Res Hum Genet. 2012. PMID: 22877876

9

Incidence and predictors of glaucoma following surgery for congenital cataract in the first year of life in Victoria, Australia.

Ruddle JB, Staffieri SE, Crowston JG, Sherwin JC, Mackey DA. Ruddle JB, et al. Among authors: staffieri se. Clin Exp Ophthalmol. 2013 Sep-Oct;41(7):653-61. doi: 10.1111/ceo.12067. Epub 2013 Mar 12. Clin Exp Ophthalmol. 2013. PMID: 23332011

10

Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern Australia.

Dave A, Laurie K, Staffieri SE, Taranath D, Mackey DA, Mitchell P, Wang JJ, Craig JE, Burdon KP, Sharma S. Dave A, et al. Among authors: staffieri se. PLoS One. 2013 Aug 27;8(8):e72518. doi: 10.1371/journal.pone.0072518. eCollection 2013. PLoS One. 2013. PMID: 24014202 Free PMC article. Clinical Trial.

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