Wu RM - Search Results

1

RIT2 variant is not associated with Parkinson's disease in a Taiwanese population.

Lin CH, Chen ML, Yu CY, Wu RM. Lin CH, et al. Among authors: wu rm. Neurobiol Aging. 2013 Sep;34(9):2236.e1-3. doi: 10.1016/j.neurobiolaging.2013.04.005. Epub 2013 Apr 28. Neurobiol Aging. 2013. PMID: 23635658

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

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

4

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

5

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

6

Transcranial imaging of substantia nigra hyperechogenicity in a Taiwanese cohort of Parkinson's disease.

Huang YW, Jeng JS, Tsai CF, Chen LL, Wu RM. Huang YW, et al. Among authors: wu rm. Mov Disord. 2007 Mar 15;22(4):550-5. doi: 10.1002/mds.21372. Mov Disord. 2007. PMID: 17260344

7

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

8

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

9

Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease.

Ross OA, Wu YR, Lee MC, Funayama M, Chen ML, Soto AI, Mata IF, Lee-Chen GJ, Chen CM, Tang M, Zhao Y, Hattori N, Farrer MJ, Tan EK, Wu RM. Ross OA, et al. Among authors: wu yr, wu rm. Ann Neurol. 2008 Jul;64(1):88-92. doi: 10.1002/ana.21405. Ann Neurol. 2008. PMID: 18412265

10

LRRK2 mutation in familial Parkinson's disease in a Taiwanese population: clinical, PET, and functional studies.

Lin CH, Tzen KY, Yu CY, Tai CH, Farrer MJ, Wu RM. Lin CH, et al. Among authors: wu rm. J Biomed Sci. 2008 Sep;15(5):661-7. doi: 10.1007/s11373-008-9260-0. Epub 2008 Jun 4. J Biomed Sci. 2008. PMID: 18523869

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