Mackey DA - Search Results

1

Autosomal dominant optic atrophy: penetrance and expressivity in patients with OPA1 mutations.

Cohn AC, Toomes C, Potter C, Towns KV, Hewitt AW, Inglehearn CF, Craig JE, Mackey DA. Cohn AC, et al. Among authors: mackey da. Am J Ophthalmol. 2007 Apr;143(4):656-62. doi: 10.1016/j.ajo.2006.12.038. Epub 2007 Feb 15. Am J Ophthalmol. 2007. PMID: 17306754

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

A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology.

Mackey D, Howell N. Mackey D, et al. Am J Hum Genet. 1992 Dec;51(6):1218-28. Am J Hum Genet. 1992. PMID: 1463007 Free PMC article.

4

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.

5

Glaucoma genetics: where are we? Where will we go?

Craig JE, Mackey DA. Craig JE, et al. Among authors: mackey da. Curr Opin Ophthalmol. 1999 Apr;10(2):126-34. doi: 10.1097/00055735-199904000-00009. Curr Opin Ophthalmol. 1999. PMID: 10537763 Review.

6

Accuracy and implications of a reported family history of glaucoma: experience from the Glaucoma Inheritance Study in Tasmania.

McNaught AI, Allen JG, Healey DL, McCartney PJ, Coote MA, Wong TL, Craig JE, Green CM, Rait JL, Mackey DA. McNaught AI, et al. Among authors: mackey da. Arch Ophthalmol. 2000 Jul;118(7):900-4. Arch Ophthalmol. 2000. PMID: 10900101

7

Evaluation of the myocilin (MYOC) glaucoma gene in monkey and human steroid-induced ocular hypertension.

Fingert JH, Clark AF, Craig JE, Alward WL, Snibson GR, McLaughlin M, Tuttle L, Mackey DA, Sheffield VC, Stone EM. Fingert JH, et al. Among authors: mackey da. Invest Ophthalmol Vis Sci. 2001 Jan;42(1):145-52. Invest Ophthalmol Vis Sci. 2001. PMID: 11133859

8

Laboratory methods in ophthalmic genetics: obtaining DNA from patients.

Dickinson JL, Sale MM, Craig JE, Mackey DA. Dickinson JL, et al. Among authors: mackey da. Ophthalmic Genet. 2001 Mar;22(1):49-60. doi: 10.1076/opge.22.1.49.2240. Ophthalmic Genet. 2001. PMID: 11262650 Review.

9

The Taa1 restriction enzyme provides a simple means to identify the Q368STOP mutation of the myocilin gene in primary open angle glaucoma.

Baird PN, Dickinson J, Craig JE, Mackey DA. Baird PN, et al. Among authors: mackey da. Am J Ophthalmol. 2001 Apr;131(4):510-1. doi: 10.1016/s0002-9394(00)00812-6. Am J Ophthalmol. 2001. PMID: 11292420

10

Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy.

Toomes C, Marchbank NJ, Mackey DA, Craig JE, Newbury-Ecob RA, Bennett CP, Vize CJ, Desai SP, Black GC, Patel N, Teimory M, Markham AF, Inglehearn CF, Churchill AJ. Toomes C, et al. Among authors: mackey da. Hum Mol Genet. 2001 Jun 15;10(13):1369-78. doi: 10.1093/hmg/10.13.1369. Hum Mol Genet. 2001. PMID: 11440989

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