Mackey DA - Search Results

1

Genotypic and phenotypic spectrum of X-linked retinoschisis in Australia.

Hewitt AW, FitzGerald LM, Scotter LW, Mulhall LE, McKay JD, Mackey DA. Hewitt AW, et al. Among authors: mackey da. Clin Exp Ophthalmol. 2005 Jun;33(3):233-9. doi: 10.1111/j.1442-9071.2005.01018.x. Clin Exp Ophthalmol. 2005. PMID: 15932525

2

Leber hereditary optic neuropathy in Australia.

Mackey DA, Buttery RG. Mackey DA, et al. Aust N Z J Ophthalmol. 1992 Aug;20(3):177-84. doi: 10.1111/j.1442-9071.1992.tb00937.x. Aust N Z J Ophthalmol. 1992. PMID: 1449769

3

Finger prick blood testing in Leber hereditary optic neuropathy.

Mackey D, Nasioulas S, Forrest S. Mackey D, et al. Br J Ophthalmol. 1993 May;77(5):311-2. doi: 10.1136/bjo.77.5.311. Br J Ophthalmol. 1993. PMID: 8318469 Free PMC article.

4

Visual field assessment and the Austroads driving standard.

McLean IM, Mueller E, Buttery RG, Mackey DA. McLean IM, et al. Among authors: mackey da. Clin Exp Ophthalmol. 2002 Feb;30(1):3-7. doi: 10.1046/j.1442-9071.2002.00487.x. Clin Exp Ophthalmol. 2002. PMID: 11885792

5

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: mackey da. 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.

6

Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 gene.

Sale MM, Craig JE, Charlesworth JC, FitzGerald LM, Hanson IM, Dickinson JL, Matthews SJ, Heyningen Vv Vv, Fingert JH, Mackey DA. Sale MM, et al. Among authors: mackey da. Hum Mutat. 2002 Oct;20(4):322. doi: 10.1002/humu.9066. Hum Mutat. 2002. PMID: 12325030

7

Pigmentary retinopathy, macular oedema, and abnormal ERG with mitotane treatment.

Ng WT, Toohey MG, Mulhall L, Mackey DA. Ng WT, et al. Among authors: mackey da. Br J Ophthalmol. 2003 Apr;87(4):500-1. doi: 10.1136/bjo.87.4.500-a. Br J Ophthalmol. 2003. PMID: 12642318 Free PMC article. No abstract available.

8

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: mackey da. 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.

9

Primary infantile glaucoma in an Australian population.

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

10

The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes.

McKay JD, Patterson B, Craig JE, Russell-Eggitt IM, Wirth MG, Burdon KP, Hewitt AW, Cohn AC, Kerdraon Y, Mackey DA. McKay JD, et al. Among authors: mackey da. Br J Ophthalmol. 2005 Jul;89(7):831-4. doi: 10.1136/bjo.2004.058495. Br J Ophthalmol. 2005. PMID: 15965161 Free PMC article.

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