Tai CH - Search Results

1

Feeling-of-knowing in episodic memory in patients with Parkinson's disease with various motor symptoms.

Yu RL, Wu RM, Tai CH, Lin CH, Hua MS. Yu RL, et al. Among authors: tai ch. Mov Disord. 2010 Jun 15;25(8):1034-9. doi: 10.1002/mds.23017. Mov Disord. 2010. PMID: 20131392

2

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. Among authors: tai ch. Mov Disord. 2002 Jul;17(4):670-5. doi: 10.1002/mds.10184. Mov Disord. 2002. PMID: 12210855

3

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: tai ch. 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

4

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: tai ch. 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

5

Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation.

Tai CH, Yen RF, Lin CH, Yen KY, Yip PK, Wu RM, Lee MJ. Tai CH, et al. Parkinsonism Relat Disord. 2009 Sep;15(8):614-6. doi: 10.1016/j.parkreldis.2008.11.007. Epub 2009 Mar 3. Parkinsonism Relat Disord. 2009. PMID: 19261534 No abstract available.

6

Non-synonymous GIGYF2 variants in Parkinson's disease from two Asian populations.

Tan EK, Lin CH, Tai CH, Tan LC, Chen ML, Li R, Lim HQ, Pavanni R, Yuen Y, Prakash KM, Zhao Y, Wu RM. Tan EK, et al. Among authors: tai ch. Hum Genet. 2009 Sep;126(3):425-30. doi: 10.1007/s00439-009-0678-x. Epub 2009 May 16. Hum Genet. 2009. PMID: 19449032

7

Minimal detectable change of the timed "up & go" test and the dynamic gait index in people with Parkinson disease.

Huang SL, Hsieh CL, Wu RM, Tai CH, Lin CH, Lu WS. Huang SL, et al. Among authors: tai ch. Phys Ther. 2011 Jan;91(1):114-21. doi: 10.2522/ptj.20090126. Epub 2010 Oct 14. Phys Ther. 2011. PMID: 20947672

8

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: tai ch. 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

9

Novel variant Pro143Ala in HTRA2 contributes to Parkinson's disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria.

Lin CH, Chen ML, Chen GS, Tai CH, Wu RM. Lin CH, et al. Among authors: tai ch. Hum Genet. 2011 Dec;130(6):817-27. doi: 10.1007/s00439-011-1041-6. Epub 2011 Jun 24. Hum Genet. 2011. PMID: 21701785 Free PMC article.

10

Meige syndrome relieved by bilateral pallidal stimulation with cycling mode: case report.

Tai CH, Wu RM, Liu HM, Tsai CW, Tseng SH. Tai CH, et al. Neurosurgery. 2011 Dec;69(6):E1333-7. doi: 10.1227/NEU.0b013e31822a9ad2. Neurosurgery. 2011. PMID: 21712740

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