Singleton AB - Search Results

1

The Birth of the Modern Era of Parkinson's Disease Genetics.

Singleton AB, Hardy JA, Gasser T. Singleton AB, et al. J Parkinsons Dis. 2017;7(s1):S87-S93. doi: 10.3233/JPD-179009. J Parkinsons Dis. 2017. PMID: 28282818 Free PMC article. Review.

2

Case-control study of dopamine transporter-1, monoamine oxidase-B, and catechol-O-methyl transferase polymorphisms in Parkinson's disease.

Goudreau JL, Maraganore DM, Farrer MJ, Lesnick TG, Singleton AB, Bower JH, Hardy JA, Rocca WA. Goudreau JL, et al. Among authors: singleton ab. Mov Disord. 2002 Nov;17(6):1305-11. doi: 10.1002/mds.10268. Mov Disord. 2002. PMID: 12465073

3

SCA2 may present as levodopa-responsive parkinsonism.

Payami H, Nutt J, Gancher S, Bird T, McNeal MG, Seltzer WK, Hussey J, Lockhart P, Gwinn-Hardy K, Singleton AA, Singleton AB, Hardy J, Farrer M. Payami H, et al. Among authors: singleton ab, singleton aa. Mov Disord. 2003 Apr;18(4):425-9. doi: 10.1002/mds.10375. Mov Disord. 2003. PMID: 12671950

4

Unaltered alpha-synuclein blood levels in juvenile Parkinsonism with a parkin exon 4 deletion.

Miller DW, Crawley A, Gwinn-Hardy K, Lopez G, Nussbaum R, Cookson MR, Singleton AB, Hardy J, Dogu O. Miller DW, et al. Among authors: singleton ab. Neurosci Lett. 2005 Feb 21;374(3):189-91. doi: 10.1016/j.neulet.2004.10.053. Epub 2004 Nov 19. Neurosci Lett. 2005. PMID: 15663960

5

Mutation analysis of patients with neuronal intermediate filament inclusion disease (NIFID).

Momeni P, Cairns NJ, Perry RH, Bigio EH, Gearing M, Singleton AB, Hardy J. Momeni P, et al. Among authors: singleton ab. Neurobiol Aging. 2006 May;27(5):778.e1-778.e6. doi: 10.1016/j.neurobiolaging.2005.03.030. Epub 2005 Jul 7. Neurobiol Aging. 2006. PMID: 16005115

6

Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosis.

Garcia ML, Singleton AB, Hernandez D, Ward CM, Evey C, Sapp PA, Hardy J, Brown RH Jr, Cleveland DW. Garcia ML, et al. Among authors: singleton ab. Neurobiol Dis. 2006 Jan;21(1):102-9. doi: 10.1016/j.nbd.2005.06.016. Epub 2005 Aug 3. Neurobiol Dis. 2006. PMID: 16084104

7

Analysis of the PINK1 gene in a cohort of patients with sporadic early-onset parkinsonism in Taiwan.

Fung HC, Chen CM, Hardy J, Singleton AB, Lee-Chen GJ, Wu YR. Fung HC, et al. Among authors: singleton ab. Neurosci Lett. 2006 Feb 6;394(1):33-6. doi: 10.1016/j.neulet.2005.10.005. Epub 2005 Oct 27. Neurosci Lett. 2006. PMID: 16257123

8

Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23.

Shatunov A, Sambuughin N, Jankovic J, Elble R, Lee HS, Singleton AB, Dagvadorj A, Ji J, Zhang Y, Kimonis VE, Hardy J, Hallett M, Goldfarb LG. Shatunov A, et al. Among authors: singleton ab. Brain. 2006 Sep;129(Pt 9):2318-31. doi: 10.1093/brain/awl120. Epub 2006 May 15. Brain. 2006. PMID: 16702189 Free article.

9

A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan.

Fung HC, Chen CM, Hardy J, Singleton AB, Wu YR. Fung HC, et al. Among authors: singleton ab. BMC Neurol. 2006 Dec 22;6:47. doi: 10.1186/1471-2377-6-47. BMC Neurol. 2006. PMID: 17187665 Free PMC article.

10

IL1RN VNTR polymorphism in ischemic stroke: analysis in 3 populations.

Worrall BB, Brott TG, Brown RD Jr, Brown WM, Rich SS, Arepalli S, Wavrant-De Vrièze F, Duckworth J, Singleton AB, Hardy J, Meschia JF; SWISS, ISGS, and MSGD Investigators. Worrall BB, et al. Among authors: singleton ab. Stroke. 2007 Apr;38(4):1189-96. doi: 10.1161/01.STR.0000260099.42744.b0. Epub 2007 Mar 1. Stroke. 2007. PMID: 17332449 Free PMC article.

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