Grimes DA - Search Results

1

Large deletions account for an increasing number of mutations in SGCE.

Han F, Racacho L, Yang H, Read T, Suchowersky O, Lang AE, Grimes DA, Bulman DE. Han F, et al. Among authors: grimes da. Mov Disord. 2008 Feb 15;23(3):456-60. doi: 10.1002/mds.21895. Mov Disord. 2008. PMID: 18098280

2

Hereditary chin trembling: a new family with exclusion of the chromosome 9q13-q21 Locus.

Grimes DA, Han F, Bulman D, Nicolson ML, Suchowersky O. Grimes DA, et al. Mov Disord. 2002 Nov;17(6):1390-2. doi: 10.1002/mds.10275. Mov Disord. 2002. PMID: 12465093

3

Translated mutation in the Nurr1 gene as a cause for Parkinson's disease.

Grimes DA, Han F, Panisset M, Racacho L, Xiao F, Zou R, Westaff K, Bulman DE. Grimes DA, et al. Mov Disord. 2006 Jul;21(7):906-9. doi: 10.1002/mds.20820. Mov Disord. 2006. PMID: 16532445

4

Refinement of the DYT15 locus in myoclonus dystonia.

Han F, Racacho L, Lang AE, Bulman DE, Grimes DA. Han F, et al. Among authors: grimes da. Mov Disord. 2007 Apr 30;22(6):888-92. doi: 10.1002/mds.21400. Mov Disord. 2007. PMID: 17274032

5

Large French-Canadian family with Lewy body parkinsonism: exclusion of known loci.

Grimes DA, Grimes JD, Racacho L, Scoggan KA, Han F, Schwarz BA, Woulfe J, Bulman D. Grimes DA, et al. Among authors: grimes jd. Mov Disord. 2002 Nov;17(6):1205-12. doi: 10.1002/mds.10272. Mov Disord. 2002. PMID: 12465058

6

Is there seasonal variation in risk of Parkinson's disease?

Postuma RB, Wolfson C, Rajput A, Stoessl AJ, Martin WR, Suchowersky O, Chouinard S, Panisset M, Jog MS, Grimes DA, Marras C, Lang AE. Postuma RB, et al. Among authors: grimes da. Mov Disord. 2007 Jun 15;22(8):1097-101. doi: 10.1002/mds.21272. Mov Disord. 2007. PMID: 17486603

7

Mutations in the glucocerebrosidase gene are common in patients with Parkinson's disease from Eastern Canada.

Han F, Grimes DA, Li F, Wang T, Yu Z, Song N, Wu S, Racacho L, Bulman DE. Han F, et al. Among authors: grimes da. Int J Neurosci. 2016;126(5):415-21. doi: 10.3109/00207454.2015.1023436. Epub 2015 Aug 18. Int J Neurosci. 2016. PMID: 26000814

8

A Nurr1 point mutant, implicated in Parkinson's disease, uncouples ERK1/2-dependent regulation of tyrosine hydroxylase transcription.

Jacobsen KX, MacDonald H, Lemonde S, Daigle M, Grimes DA, Bulman DE, Albert PR. Jacobsen KX, et al. Among authors: grimes da. Neurobiol Dis. 2008 Jan;29(1):117-22. doi: 10.1016/j.nbd.2007.08.003. Epub 2007 Aug 21. Neurobiol Dis. 2008. PMID: 17890097

9

Functional alteration of PARL contributes to mitochondrial dysregulation in Parkinson's disease.

Shi G, Lee JR, Grimes DA, Racacho L, Ye D, Yang H, Ross OA, Farrer M, McQuibban GA, Bulman DE. Shi G, et al. Among authors: grimes da. Hum Mol Genet. 2011 May 15;20(10):1966-74. doi: 10.1093/hmg/ddr077. Epub 2011 Feb 25. Hum Mol Genet. 2011. PMID: 21355049

10

Motor Phenotype in Neurodegenerative Disorders: Gait and Balance Platform Study Design Protocol for the Ontario Neurodegenerative Research Initiative (ONDRI).

Montero-Odasso M, Pieruccini-Faria F, Bartha R, Black SE, Finger E, Freedman M, Greenberg B, Grimes DA, Hegele RA, Hudson C, Kleinstiver PW, Lang AE, Masellis M, McLaughlin PM, Munoz DP, Strother S, Swartz RH, Symons S, Tartaglia MC, Zinman L, Strong MJ; ONDRI Investigators; McIlroy W. Montero-Odasso M, et al. Among authors: grimes da. J Alzheimers Dis. 2017;59(2):707-721. doi: 10.3233/JAD-170149. J Alzheimers Dis. 2017. PMID: 28671116 Free PMC article.

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