Mastaglia FL - Search Results

1

Antisense oligonucleotide induction of progerin in human myogenic cells.

Luo YB, Mitrpant C, Adams AM, Johnsen RD, Fletcher S, Mastaglia FL, Wilton SD. Luo YB, et al. Among authors: mastaglia fl. PLoS One. 2014 Jun 3;9(6):e98306. doi: 10.1371/journal.pone.0098306. eCollection 2014. PLoS One. 2014. PMID: 24892300 Free PMC article.

2

Autosomal dominant distal myopathy: linkage to chromosome 14.

Laing NG, Laing BA, Meredith C, Wilton SD, Robbins P, Honeyman K, Dorosz S, Kozman H, Mastaglia FL, Kakulas BA. Laing NG, et al. Among authors: mastaglia fl. Am J Hum Genet. 1995 Feb;56(2):422-7. Am J Hum Genet. 1995. PMID: 7847377 Free PMC article.

3

Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy.

Mastaglia FL, Nowak KJ, Stell R, Phillips BA, Edmondston JE, Dorosz SM, Wilton SD, Hallmayer J, Kakulas BA, Laing NG. Mastaglia FL, et al. J Neurol Neurosurg Psychiatry. 1999 Aug;67(2):174-9. doi: 10.1136/jnnp.67.2.174. J Neurol Neurosurg Psychiatry. 1999. PMID: 10406984 Free PMC article.

4

Prevalence of stroke in Parkinson's disease: a postmortem study.

Mastaglia FL, Johnsen RD, Kakulas BA. Mastaglia FL, et al. Mov Disord. 2002 Jul;17(4):772-4. doi: 10.1002/mds.10199. Mov Disord. 2002. PMID: 12210874

5

Prevalence of amyloid-beta deposition in the cerebral cortex in Parkinson's disease.

Mastaglia FL, Johnsen RD, Byrnes ML, Kakulas BA. Mastaglia FL, et al. Mov Disord. 2003 Jan;18(1):81-6. doi: 10.1002/mds.10295. Mov Disord. 2003. PMID: 12518303

6

Prevalence of cerebral vascular amyloid-beta deposition and stroke in an aging Australian population: a postmortem study.

Mastaglia FL, Byrnes ML, Johnsen RD, Kakulas BA. Mastaglia FL, et al. J Clin Neurosci. 2003 Mar;10(2):186-9. doi: 10.1016/s0967-5868(02)00317-x. J Clin Neurosci. 2003. PMID: 12637046

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. Among authors: mastaglia fl. Mov Disord. 2009 Apr 30;24(6):833-8. doi: 10.1002/mds.22214. Mov Disord. 2009. PMID: 19224617

8

The association of sporadic inclusion body myositis and Sjögren's syndrome in carriers of HLA-DR3 and the 8.1 MHC ancestral haplotype.

Rojana-udomsart A, Needham M, Luo YB, Fabian V, Walters S, Zilko PJ, Mastaglia FL. Rojana-udomsart A, et al. Among authors: mastaglia fl. Clin Neurol Neurosurg. 2011 Sep;113(7):559-63. doi: 10.1016/j.clineuro.2011.03.016. Epub 2011 Apr 20. Clin Neurol Neurosurg. 2011. PMID: 21507567

9

Co-regulation of survival of motor neuron and Bcl-xL expression: implications for neuroprotection in spinal muscular atrophy.

Anderton RS, Price LL, Turner BJ, Meloni BP, Mitrpant C, Mastaglia FL, Goh C, Wilton SD, Boulos S. Anderton RS, et al. Among authors: mastaglia fl. Neuroscience. 2012 Sep 18;220:228-36. doi: 10.1016/j.neuroscience.2012.06.042. Epub 2012 Jun 23. Neuroscience. 2012. PMID: 22732506

10

Analysis of HLA-DRB3 alleles and supertypical genotypes in the MHC Class II region in sporadic inclusion body myositis.

Rojana-udomsart A, Mitrpant C, James I, Witt C, Needham M, Day T, Kiers L, Corbett A, Martinez P, Wilton SD, Mastaglia FL. Rojana-udomsart A, et al. Among authors: mastaglia fl. J Neuroimmunol. 2013 Jan 15;254(1-2):174-7. doi: 10.1016/j.jneuroim.2012.09.003. Epub 2012 Sep 23. J Neuroimmunol. 2013. PMID: 23010279

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