Racacho L - 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: racacho l. Mov Disord. 2008 Feb 15;23(3):456-60. doi: 10.1002/mds.21895. Mov Disord. 2008. PMID: 18098280

2

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

3

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: racacho l. Neurology. 2002 Oct 22;59(8):1183-6. doi: 10.1212/wnl.59.8.1183. Neurology. 2002. PMID: 12391345

4

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. Among authors: racacho l. Neurology. 2003 Jul 22;61(2):244-6. doi: 10.1212/01.wnl.0000073142.40185.c1. Neurology. 2003. PMID: 12874409

5

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: racacho l. Mov Disord. 2006 Jul;21(7):906-9. doi: 10.1002/mds.20820. Mov Disord. 2006. PMID: 16532445

6

Refinement of the DYT15 locus in myoclonus dystonia.

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

7

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: racacho l. Can J Neurol Sci. 2007 Aug;34(3):336-8. doi: 10.1017/s0317167100006788. Can J Neurol Sci. 2007. PMID: 17803033

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. Among authors: racacho l. 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

Mutations in GDF5 presenting as semidominant brachydactyly A1.

Byrnes AM, Racacho L, Nikkel SM, Xiao F, MacDonald H, Underhill TM, Bulman DE. Byrnes AM, et al. Among authors: racacho l. Hum Mutat. 2010 Oct;31(10):1155-62. doi: 10.1002/humu.21338. Hum Mutat. 2010. PMID: 20683927

10

Brachydactyly A-1 mutations restricted to the central region of the N-terminal active fragment of Indian Hedgehog.

Byrnes AM, Racacho L, Grimsey A, Hudgins L, Kwan AC, Sangalli M, Kidd A, Yaron Y, Lau YL, Nikkel SM, Bulman DE. Byrnes AM, et al. Among authors: racacho l. Eur J Hum Genet. 2009 Sep;17(9):1112-20. doi: 10.1038/ejhg.2009.18. Epub 2009 Mar 11. Eur J Hum Genet. 2009. PMID: 19277064 Free PMC article.

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