Wu Chou YH - Search Results

1

The parkinsonian phenotype of spinocerebellar ataxia type 2.

Lu CS, Wu Chou YH, Kuo PC, Chang HC, Weng YH. Lu CS, et al. Among authors: wu chou yh. Arch Neurol. 2004 Jan;61(1):35-8. doi: 10.1001/archneur.61.1.35. Arch Neurol. 2004. PMID: 14732617

2

Dopa-responsive parkinsonism phenotype of spinocerebellar ataxia type 2.

Lu CS, Wu Chou YH, Yen TC, Tsai CH, Chen RS, Chang HC. Lu CS, et al. Among authors: wu chou yh. Mov Disord. 2002 Sep;17(5):1046-51. doi: 10.1002/mds.10243. Mov Disord. 2002. PMID: 12360557

3

Screening for C9orf72 repeat expansions in parkinsonian syndromes.

Yeh TH, Lai SC, Weng YH, Kuo HC, Wu-Chou YH, Huang CL, Chen RS, Chang HC, Traynor B, Lu CS. Yeh TH, et al. Among authors: wu chou yh. Neurobiol Aging. 2013 Apr;34(4):1311.e3-4. doi: 10.1016/j.neurobiolaging.2012.09.002. Epub 2012 Oct 11. Neurobiol Aging. 2013. PMID: 23063644 Free PMC article.

4

Analysis of the LRRK2 Gly2385Arg variant in primary dystonia and multiple system atrophy in Taiwan.

Lu CS, Chang HC, Weng YH, Chen RS, Bonifati V, Wu-Chou YH. Lu CS, et al. Among authors: wu chou yh. Parkinsonism Relat Disord. 2008;14(5):393-6. doi: 10.1016/j.parkreldis.2008.03.004. Epub 2008 May 2. Parkinsonism Relat Disord. 2008. PMID: 18450497

5

The LRRK2 Arg1628Pro variant is a risk factor for Parkinson's disease in the Chinese population.

Lu CS, Wu-Chou YH, van Doeselaar M, Simons EJ, Chang HC, Breedveld GJ, Di Fonzo A, Chen RS, Weng YH, Lai SC, Oostra BA, Bonifati V. Lu CS, et al. Among authors: wu chou yh. Neurogenetics. 2008 Oct;9(4):271-6. doi: 10.1007/s10048-008-0140-6. Epub 2008 Aug 21. Neurogenetics. 2008. PMID: 18716801

6

High frequency of multiexonic deletion of the GCH1 gene in a Taiwanese cohort of dopa-response dystonia.

Wu-Chou YH, Yeh TH, Wang CY, Lin JJ, Huang CC, Chang HC, Lai SC, Chen RS, Weng YH, Huang CL, Lu CS. Wu-Chou YH, et al. Am J Med Genet B Neuropsychiatr Genet. 2010 Jun 5;153B(4):903-8. doi: 10.1002/ajmg.b.31058. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20082337

7

Oculopharyngeal muscular dystrophy--a genetically verified taiwanese family.

Huang CL, Wu SL, Lai SC, Lu CS, Wu-Chou YH. Huang CL, et al. Among authors: wu chou yh, wu sl. Chang Gung Med J. 2010 Jan-Feb;33(1):44-50. Chang Gung Med J. 2010. PMID: 20184794 Free article.

8

Large SGCE deletion contributes to Taiwanese myoclonus-dystonia syndrome.

Huang CL, Lan MY, Chang YY, Hsu CY, Lai SC, Chen RS, Chang HC, Lu CS, Wu-Chou YH. Huang CL, et al. Among authors: wu chou yh. Parkinsonism Relat Disord. 2010 Nov;16(9):585-9. doi: 10.1016/j.parkreldis.2010.06.016. Epub 2010 Aug 30. Parkinsonism Relat Disord. 2010. PMID: 20800530

9

PLA2G6 mutations in PARK14-linked young-onset parkinsonism and sporadic Parkinson's disease.

Lu CS, Lai SC, Wu RM, Weng YH, Huang CL, Chen RS, Chang HC, Wu-Chou YH, Yeh TH. Lu CS, et al. Among authors: wu chou yh, wu rm. Am J Med Genet B Neuropsychiatr Genet. 2012 Mar;159B(2):183-91. doi: 10.1002/ajmg.b.32012. Epub 2011 Dec 27. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22213678

10

Genetic variants of SNCA and LRRK2 genes are associated with sporadic PD susceptibility: a replication study in a Taiwanese cohort.

Wu-Chou YH, Chen YT, Yeh TH, Chang HC, Weng YH, Lai SC, Huang CL, Chen RS, Huang YZ, Chen CC, Hung J, Chuang WL, Lin WY, Chen CH, Lu CS. Wu-Chou YH, et al. Parkinsonism Relat Disord. 2013 Feb;19(2):251-5. doi: 10.1016/j.parkreldis.2012.10.019. Epub 2012 Nov 20. Parkinsonism Relat Disord. 2013. PMID: 23182315

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