Wu RM - Search Results

1

Lrrk2 S1647T and BDNF V66M interact with environmental factors to increase risk of Parkinson's disease.

Lin CH, Wu RM, Tai CH, Chen ML, Hu FC. Lin CH, et al. Among authors: wu rm. Parkinsonism Relat Disord. 2011 Feb;17(2):84-8. doi: 10.1016/j.parkreldis.2010.11.011. Epub 2010 Dec 16. Parkinsonism Relat Disord. 2011. PMID: 21167764

2

Catechol-O-methyltransferase and Parkinson's disease.

Tai CH, Wu RM. Tai CH, et al. Among authors: wu rm. Acta Med Okayama. 2002 Feb;56(1):1-6. doi: 10.18926/AMO/31725. Acta Med Okayama. 2002. PMID: 11873938 Free article. Review.

3

Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and parkin gene mutations.

Wu RM, Shan DE, Sun CM, Liu RS, Hwu WL, Tai CH, Hussey J, West A, Gwinn-Hardy K, Hardy J, Chen J, Farrer M, Lincoln S. Wu RM, et al. Mov Disord. 2002 Jul;17(4):670-5. doi: 10.1002/mds.10184. Mov Disord. 2002. PMID: 12210855

4

Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism.

Lockhart PJ, Bounds R, Hulihan M, Kachergus J, Lincoln S, Lin CH, Wu RM, Farrer MJ. Lockhart PJ, et al. Among authors: wu rm. Mov Disord. 2004 Sep;19(9):1065-9. doi: 10.1002/mds.20082. Mov Disord. 2004. PMID: 15372597

5

Parkin mutations and early-onset parkinsonism in a Taiwanese cohort.

Wu RM, Bounds R, Lincoln S, Hulihan M, Lin CH, Hwu WL, Chen J, Gwinn-Hardy K, Farrer M. Wu RM, et al. Arch Neurol. 2005 Jan;62(1):82-7. doi: 10.1001/archneur.62.1.82. Arch Neurol. 2005. PMID: 15642853

6

Lrrk2 pathogenic substitutions in Parkinson's disease.

Mata IF, Kachergus JM, Taylor JP, Lincoln S, Aasly J, Lynch T, Hulihan MM, Cobb SA, Wu RM, Lu CS, Lahoz C, Wszolek ZK, Farrer MJ. Mata IF, et al. Among authors: wu rm. Neurogenetics. 2005 Dec;6(4):171-7. doi: 10.1007/s10048-005-0005-1. Epub 2005 Sep 17. Neurogenetics. 2005. PMID: 16172858

7

The SCA17 phenotype can include features of MSA-C, PSP and cognitive impairment.

Lin IS, Wu RM, Lee-Chen GJ, Shan DE, Gwinn-Hardy K. Lin IS, et al. Among authors: wu rm. Parkinsonism Relat Disord. 2007 May;13(4):246-9. doi: 10.1016/j.parkreldis.2006.04.009. Epub 2006 Jun 21. Parkinsonism Relat Disord. 2007. PMID: 16793320

8

Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia.

Farrer MJ, Stone JT, Lin CH, Dächsel JC, Hulihan MM, Haugarvoll K, Ross OA, Wu RM. Farrer MJ, et al. Among authors: wu rm. Parkinsonism Relat Disord. 2007 Mar;13(2):89-92. doi: 10.1016/j.parkreldis.2006.12.001. Epub 2007 Jan 10. Parkinsonism Relat Disord. 2007. PMID: 17222580

9

Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (ethnic Chinese) cohort of familial and early-onset parkinsonism.

Lin CH, Hwu WL, Chiang SC, Tai CH, Wu RM. Lin CH, et al. Among authors: wu rm. Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):434-8. doi: 10.1002/ajmg.b.30427. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17440947

10

Lack of evidence for association of a parkin promoter polymorphism with early-onset Parkinson's disease in a Chinese population.

Taylor JM, Wu RM, Lin CH, Delatycki MB, Lockhart PJ. Taylor JM, et al. Among authors: wu rm. Parkinsonism Relat Disord. 2009 Feb;15(2):149-52. doi: 10.1016/j.parkreldis.2008.02.010. Epub 2008 Apr 2. Parkinsonism Relat Disord. 2009. PMID: 18387843

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