Elder JE - Search Results

1

Hereditary hyperferritinemia-cataract syndrome: prevalence, lens morphology, spectrum of mutations, and clinical presentations.

Craig JE, Clark JB, McLeod JL, Kirkland MA, Grant G, Elder JE, Toohey MG, Kowal L, Savoia HF, Chen C, Roberts S, Wirth MG, Mackey DA. Craig JE, et al. Among authors: elder je. Arch Ophthalmol. 2003 Dec;121(12):1753-61. doi: 10.1001/archopht.121.12.1753. Arch Ophthalmol. 2003. PMID: 14662596

2

Adjunctive intra-operative local anaesthesia in paediatric strabismus surgery: a randomized controlled trial.

Carden SM, Colville DJ, Davidson AJ, McKenzie IM, Mackey DA, McKenzie J, Elder JE. Carden SM, et al. Among authors: elder je. Aust N Z J Ophthalmol. 1998 Nov;26(4):289-97. doi: 10.1111/j.1442-9071.1998.tb01332.x. Aust N Z J Ophthalmol. 1998. PMID: 9843256 Clinical Trial.

3

Visual improvement despite radiologically stable disease after treatment with carboplatin in children with progressive low-grade optic/thalamic gliomas.

Mitchell AE, Elder JE, Mackey DA, Waters KD, Ashley DM. Mitchell AE, et al. Among authors: elder je. J Pediatr Hematol Oncol. 2001 Dec;23(9):572-7. doi: 10.1097/00043426-200112000-00004. J Pediatr Hematol Oncol. 2001. PMID: 11902299 Review.

4

Aetiology of congenital and paediatric cataract in an Australian population.

Wirth MG, Russell-Eggitt IM, Craig JE, Elder JE, Mackey DA. Wirth MG, et al. Among authors: elder je. Br J Ophthalmol. 2002 Jul;86(7):782-6. doi: 10.1136/bjo.86.7.782. Br J Ophthalmol. 2002. PMID: 12084750 Free PMC article.

5

Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation.

Burdon KP, McKay JD, Sale MM, Russell-Eggitt IM, Mackey DA, Wirth MG, Elder JE, Nicoll A, Clarke MP, FitzGerald LM, Stankovich JM, Shaw MA, Sharma S, Gajovic S, Gruss P, Ross S, Thomas P, Voss AK, Thomas T, Gécz J, Craig JE. Burdon KP, et al. Among authors: elder je. Am J Hum Genet. 2003 Nov;73(5):1120-30. doi: 10.1086/379381. Epub 2003 Oct 16. Am J Hum Genet. 2003. PMID: 14564667 Free PMC article.

6

Investigation of crystallin genes in familial cataract, and report of two disease associated mutations.

Burdon KP, Wirth MG, Mackey DA, Russell-Eggitt IM, Craig JE, Elder JE, Dickinson JL, Sale MM. Burdon KP, et al. Among authors: elder je. Br J Ophthalmol. 2004 Jan;88(1):79-83. doi: 10.1136/bjo.88.1.79. Br J Ophthalmol. 2004. PMID: 14693780 Free PMC article.

7

Primary infantile glaucoma in an Australian population.

MacKinnon JR, Giubilato A, Elder JE, Craig JE, Mackey DA. MacKinnon JR, et al. Among authors: elder je. Clin Exp Ophthalmol. 2004 Feb;32(1):14-8. doi: 10.1046/j.1442-9071.2004.00750.x. Clin Exp Ophthalmol. 2004. PMID: 14746584

8

A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance.

Burdon KP, Wirth MG, Mackey DA, Russell-Eggitt IM, Craig JE, Elder JE, Dickinson JL, Sale MM. Burdon KP, et al. Among authors: elder je. J Med Genet. 2004 Aug;41(8):e106. doi: 10.1136/jmg.2004.018333. J Med Genet. 2004. PMID: 15286166 Free PMC article. No abstract available.

9

Familial transmission risk of infantile glaucoma in Australia.

Hewitt AW, MacKinnon JR, Giubilato A, Elder JE, Craig JE, Mackey DA. Hewitt AW, et al. Among authors: elder je. Ophthalmic Genet. 2006 Sep;27(3):93-7. doi: 10.1080/13816810600870843. Ophthalmic Genet. 2006. PMID: 17050285

10

Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucoma.

Dimasi DP, Hewitt AW, Straga T, Pater J, MacKinnon JR, Elder JE, Casey T, Mackey DA, Craig JE. Dimasi DP, et al. Among authors: elder je. Clin Genet. 2007 Sep;72(3):255-60. doi: 10.1111/j.1399-0004.2007.00864.x. Clin Genet. 2007. PMID: 17718864

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