Kotschet KE - Search Results

1

A blinded, controlled trial of objective measurement in Parkinson's disease.

Woodrow H, Horne MK, Fernando CV, Kotschet KE; Treat to Target Study Group. Woodrow H, et al. Among authors: kotschet ke. NPJ Parkinsons Dis. 2020 Nov 20;6(1):35. doi: 10.1038/s41531-020-00136-9. NPJ Parkinsons Dis. 2020. PMID: 33298955 Free PMC article.

2

Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease.

Huang Y, Halliday GM, Vandebona H, Mellick GD, Mastaglia F, Stevens J, Kwok J, Garlepp M, Silburn PA, Horne MK, Kotschet K, Venn A, Rowe DB, Rubio JP, Sue CM. Huang Y, et al. Mov Disord. 2007 May 15;22(7):982-9. doi: 10.1002/mds.21477. Mov Disord. 2007. PMID: 17427941

3

Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism.

Loesch DZ, Khaniani MS, Slater HR, Rubio JP, Bui QM, Kotschet K, D'Souza W, Venn A, Kalitsis P, Choo AK, Burgess T, Johnson L, Evans A, Horne M. Loesch DZ, et al. Clin Genet. 2009 Nov;76(5):471-6. doi: 10.1111/j.1399-0004.2009.01275.x. Epub 2009 Sep 30. Clin Genet. 2009. PMID: 19796183 Free PMC article.

4

Sensitive and specific detection of α-synuclein in human plasma.

Tinsley RB, Kotschet K, Modesto D, Ng H, Wang Y, Nagley P, Shaw G, Horne MK. Tinsley RB, et al. J Neurosci Res. 2010 Sep;88(12):2693-700. doi: 10.1002/jnr.22417. J Neurosci Res. 2010. PMID: 20648655

5

Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism.

Loesch DZ, Godler DE, Evans A, Bui QM, Gehling F, Kotschet KE, Trost N, Storey E, Stimpson P, Kinsella G, Francis D, Thorburn DR, Venn A, Slater HR, Horne M. Loesch DZ, et al. Among authors: kotschet ke. Genet Med. 2011 May;13(5):392-9. doi: 10.1097/GIM.0b013e3182064362. Genet Med. 2011. PMID: 21270637 Free PMC article.

6

White matter changes in basis pontis in small expansion FMR1 allele carriers with parkinsonism.

Loesch DZ, Kotschet K, Trost N, Greco CM, Kinsella G, Slater HR, Venn A, Horne M. Loesch DZ, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Jun;156B(4):502-6. doi: 10.1002/ajmg.b.31189. Epub 2011 Mar 28. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21445959 Free PMC article.

7

A DNA resequencing array for genes involved in Parkinson's disease.

Wilkins EJ, Rubio JP, Kotschet KE, Cowie TF, Boon WC, O'Hely M, Burfoot R, Wang W, Sue CM, Speed TP, Stankovitch J, Horne MK. Wilkins EJ, et al. Among authors: kotschet ke. Parkinsonism Relat Disord. 2012 May;18(4):386-90. doi: 10.1016/j.parkreldis.2011.12.012. Epub 2012 Jan 12. Parkinsonism Relat Disord. 2012. PMID: 22243833

8

Automated assessment of bradykinesia and dyskinesia in Parkinson's disease.

Griffiths RI, Kotschet K, Arfon S, Xu ZM, Johnson W, Drago J, Evans A, Kempster P, Raghav S, Horne MK. Griffiths RI, et al. J Parkinsons Dis. 2012;2(1):47-55. doi: 10.3233/JPD-2012-11071. J Parkinsons Dis. 2012. PMID: 23939408

9

A conditioned response as a measure of impulsive-compulsive behaviours in Parkinson's disease.

Evans AH, Kettlewell J, McGregor S, Kotschet K, Griffiths RI, Horne M. Evans AH, et al. PLoS One. 2014 Feb 24;9(2):e89319. doi: 10.1371/journal.pone.0089319. eCollection 2014. PLoS One. 2014. PMID: 24586685 Free PMC article.

10

Daytime sleep in Parkinson's disease measured by episodes of immobility.

Kotschet K, Johnson W, McGregor S, Kettlewell J, Kyoong A, O'Driscoll DM, Turton AR, Griffiths RI, Horne MK. Kotschet K, et al. Parkinsonism Relat Disord. 2014 Jun;20(6):578-83. doi: 10.1016/j.parkreldis.2014.02.011. Epub 2014 Feb 24. Parkinsonism Relat Disord. 2014. PMID: 24674770

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