Han F - 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. 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. Among authors: han f. 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. Among authors: han f. 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. Mov Disord. 2007 Apr 30;22(6):888-92. doi: 10.1002/mds.21400. Mov Disord. 2007. PMID: 17274032

5

A novel locus for inherited myoclonus-dystonia on 18p11.

Grimes DA, Han F, Lang AE, St George-Hyssop P, Racacho L, Bulman DE. Grimes DA, et al. Among authors: han f. Neurology. 2002 Oct 22;59(8):1183-6. doi: 10.1212/wnl.59.8.1183. Neurology. 2002. PMID: 12391345

6

Mutations in the epsilon-sarcoglycan gene found to be uncommon in seven myoclonus-dystonia families.

Han F, Lang AE, Racacho L, Bulman DE, Grimes DA. Han F, et al. Neurology. 2003 Jul 22;61(2):244-6. doi: 10.1212/01.wnl.0000073142.40185.c1. Neurology. 2003. PMID: 12874409

7

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: han f. Mov Disord. 2002 Nov;17(6):1205-12. doi: 10.1002/mds.10272. Mov Disord. 2002. PMID: 12465058

8

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. Int J Neurosci. 2016;126(5):415-21. doi: 10.3109/00207454.2015.1023436. Epub 2015 Aug 18. Int J Neurosci. 2016. PMID: 26000814

9

LRRK2 screening in a Canadian Parkinson's disease cohort.

Grimes DA, Racacho L, Han F, Panisset M, Bulman DE. Grimes DA, et al. Among authors: han f. Can J Neurol Sci. 2007 Aug;34(3):336-8. doi: 10.1017/s0317167100006788. Can J Neurol Sci. 2007. PMID: 17803033

10

Neurofilament M gene in a French-Canadian population with Parkinson's disease.

Han F, Bulman DE, Panisset M, Grimes DA. Han F, et al. Can J Neurol Sci. 2005 Feb;32(1):68-70. doi: 10.1017/s0317167100016905. Can J Neurol Sci. 2005. PMID: 15825549

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