Storey E - Search Results

1

Influence of single nucleotide polymorphisms in COMT, MAO-A and BDNF genes on dyskinesias and levodopa use in Parkinson's disease.

Cheshire P, Bertram K, Ling H, O'Sullivan SS, Halliday G, McLean C, Bras J, Foltynie T, Storey E, Williams DR. Cheshire P, et al. Among authors: storey e. Neurodegener Dis. 2014;13(1):24-8. doi: 10.1159/000351097. Epub 2013 Sep 5. Neurodegener Dis. 2014. PMID: 24008922 Free PMC article.

2

The D178N (cis-129M) "fatal familial insomnia" mutation associated with diverse clinicopathologic phenotypes in an Australian kindred.

McLean CA, Storey E, Gardner RJ, Tannenberg AE, Cervenáková L, Brown P. McLean CA, et al. Among authors: storey e. Neurology. 1997 Aug;49(2):552-8. doi: 10.1212/wnl.49.2.552. Neurology. 1997. PMID: 9270595

3

Early-onset Alzheimer's disease caused by a novel mutation at codon 219 of the presenilin-1 gene.

Smith MJ, Gardner RJ, Knight MA, Forrest SM, Beyreuther K, Storey E, McLean CA, Cotton RG, Cappal R, Masters CL. Smith MJ, et al. Among authors: storey e. Neuroreport. 1999 Feb 25;10(3):503-7. doi: 10.1097/00001756-199902250-00011. Neuroreport. 1999. PMID: 10208579

4

Sensory neuropathy as part of the cerebellar ataxia neuropathy vestibular areflexia syndrome.

Szmulewicz DJ, Waterston JA, Halmagyi GM, Mossman S, Chancellor AM, McLean CA, Storey E. Szmulewicz DJ, et al. Among authors: storey e. Neurology. 2011 May 31;76(22):1903-10. doi: 10.1212/WNL.0b013e31821d746e. Neurology. 2011. PMID: 21624989 Free PMC article.

5

Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS): a review of the clinical features and video-oculographic diagnosis.

Szmulewicz DJ, Waterston JA, MacDougall HG, Mossman S, Chancellor AM, McLean CA, Merchant S, Patrikios P, Halmagyi GM, Storey E. Szmulewicz DJ, et al. Among authors: storey e. Ann N Y Acad Sci. 2011 Sep;1233:139-47. doi: 10.1111/j.1749-6632.2011.06158.x. Ann N Y Acad Sci. 2011. PMID: 21950986 Review.

6

Cognitive testing in the diagnosis of parkinsonian disorders: a critical appraisal of the literature.

Lee W, Williams DR, Storey E. Lee W, et al. Among authors: storey e. Mov Disord. 2012 Sep 1;27(10):1243-54. doi: 10.1002/mds.25113. Epub 2012 Aug 13. Mov Disord. 2012. PMID: 22890580

7

White matter changes in patients with Parkinson's disease carrying small CGG expansion FMR1 alleles: a pilot study.

Trost N, Cook M, Hammersley E, Bui MQ, Brotchie P, Burgess T, Slater H, Storey E, Loesch DZ. Trost N, et al. Among authors: storey e. Neurodegener Dis. 2014;14(2):67-76. doi: 10.1159/000356190. Epub 2013 Dec 24. Neurodegener Dis. 2014. PMID: 24401315

8

Dorsal root ganglionopathy is responsible for the sensory impairment in CANVAS.

Szmulewicz DJ, McLean CA, Rodriguez ML, Chancellor AM, Mossman S, Lamont D, Roberts L, Storey E, Halmagyi GM. Szmulewicz DJ, et al. Among authors: storey e. Neurology. 2014 Apr 22;82(16):1410-5. doi: 10.1212/WNL.0000000000000352. Epub 2014 Mar 28. Neurology. 2014. PMID: 24682971 Free PMC article.

9

CANVAS an update: clinical presentation, investigation and management.

Szmulewicz DJ, McLean CA, MacDougall HG, Roberts L, Storey E, Halmagyi GM. Szmulewicz DJ, et al. Among authors: storey e. J Vestib Res. 2014;24(5-6):465-74. doi: 10.3233/VES-140536. J Vestib Res. 2014. PMID: 25564090 Review.

10

Serotonergic markers in Parkinson's disease and levodopa-induced dyskinesias.

Cheshire P, Ayton S, Bertram KL, Ling H, Li A, McLean C, Halliday GM, O'Sullivan SS, Revesz T, Finkelstein DI, Storey E, Williams DR. Cheshire P, et al. Among authors: storey e. Mov Disord. 2015 May;30(6):796-804. doi: 10.1002/mds.26144. Epub 2015 Feb 4. Mov Disord. 2015. PMID: 25649148

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