Mellick G - Search Results

1

Lehn A, Boyle R, Brown H, Airey C, Mellick G. Lehn A, et al. Among authors: mellick g. Parkinsonism Relat Disord. 2012 Sep;18(8):909-15. doi: 10.1016/j.parkreldis.2012.06.021. Epub 2012 Jul 17. Parkinsonism Relat Disord. 2012. PMID: 22818529 Review.

2

The parkin gene S/N167 polymorphism in Australian Parkinson's disease patients and controls.

Mellick GD, Buchanan DD, Hattori N, Brookes AJ, Mizuno Y, Le Couteur DG, Silburn PA. Mellick GD, et al. Parkinsonism Relat Disord. 2001 Apr;7(2):89-91. doi: 10.1016/s1353-8020(00)00018-3. Parkinsonism Relat Disord. 2001. PMID: 11248588

3

Late-onset presentation of pyruvate dehydrogenase deficiency.

Mellick G, Price L, Boyle R. Mellick G, et al. Mov Disord. 2004 Jun;19(6):727-9. doi: 10.1002/mds.20063. Mov Disord. 2004. PMID: 15197721

4

Parkinson's disease and family history.

Sellbach AN, Boyle RS, Silburn PA, Mellick GD. Sellbach AN, et al. Parkinsonism Relat Disord. 2006 Oct;12(7):399-409. doi: 10.1016/j.parkreldis.2006.03.002. Epub 2006 Jun 22. Parkinsonism Relat Disord. 2006. PMID: 16797215 Review.

5

Utility of a patient survey in identifying fluctuations in early stage Parkinson's disease.

Silburn PA, Mellick GD, Vieira BI, Danta G, Boyle RS, Herawati L. Silburn PA, et al. Among authors: mellick gd. J Clin Neurosci. 2008 Nov;15(11):1235-9. doi: 10.1016/j.jocn.2007.09.018. Epub 2008 Sep 27. J Clin Neurosci. 2008. PMID: 18824360

6

Haplotype analysis of the PARK 11 gene, GIGYF2, in sporadic Parkinson's disease.

Sutherland GT, Siebert GA, Newman JR, Silburn PA, Boyle RS, O'Sullivan JD, Mellick GD. Sutherland GT, et al. Mov Disord. 2009 Feb 15;24(3):449-52. doi: 10.1002/mds.22427. Mov Disord. 2009. PMID: 19117363

7

Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease?

Sutherland GT, Halliday GM, Silburn PA, Mastaglia FL, Rowe DB, Boyle RS, O'Sullivan JD, Ly T, Wilton SD, Mellick GD. Sutherland GT, et al. Mov Disord. 2009 Apr 30;24(6):833-8. doi: 10.1002/mds.22214. Mov Disord. 2009. PMID: 19224617

8

Teaching NeuroImages: neuroferritinopathy.

Lehn A, Mellick G, Boyle R. Lehn A, et al. Among authors: mellick g. Neurology. 2011 Nov 1;77(18):e107. doi: 10.1212/WNL.0b013e318236492c. Neurology. 2011. PMID: 22042801 No abstract available.

9

Common polymorphisms in dystonia-linked genes and susceptibility to the sporadic primary dystonias.

Newman JR, Sutherland GT, Boyle RS, Limberg N, Blum S, O'Sullivan JD, Silburn PA, Mellick GD. Newman JR, et al. Parkinsonism Relat Disord. 2012 May;18(4):351-7. doi: 10.1016/j.parkreldis.2011.11.024. Epub 2011 Dec 14. Parkinsonism Relat Disord. 2012. PMID: 22172551 Free article.

10

Screening for rare sequence variants in the THAP1 gene in a primary dystonia cohort.

Newman JR, Lehn AC, Boyle RS, Silburn PA, Mellick GD. Newman JR, et al. Mov Disord. 2013 Oct;28(12):1752-3. doi: 10.1002/mds.25479. Epub 2013 May 6. Mov Disord. 2013. PMID: 23649788 No abstract available.

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