Lin CH - Search Results

1

Genetic analysis of IMPDH2 gene in Taiwanese patients with isolated or combined dystonia.

Chen PS, Wu MC, Tai CH, Chang YY, Lan MY, Chen YF, Lin HI, Lee NC, Lin CH. Chen PS, et al. Among authors: lin ch, lin hi. Parkinsonism Relat Disord. 2023 Feb;107:105294. doi: 10.1016/j.parkreldis.2023.105294. Epub 2023 Jan 17. Parkinsonism Relat Disord. 2023. PMID: 36657279

2

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. 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

3

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. 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

4

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. Among authors: lin ch. 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.

5

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: lin ch. Mov Disord. 2010 Jun 15;25(8):1034-9. doi: 10.1002/mds.23017. Mov Disord. 2010. PMID: 20131392

6

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: lin ch. Phys Ther. 2011 Jan;91(1):114-21. doi: 10.2522/ptj.20090126. Epub 2010 Oct 14. Phys Ther. 2011. PMID: 20947672

7

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. 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

8

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. 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.

9

Advanced Theory of Mind in patients at early stage of Parkinson's disease.

Yu RL, Wu RM, Chiu MJ, Tai CH, Lin CH, Hua MS. Yu RL, et al. Among authors: lin ch. Parkinsonism Relat Disord. 2012 Jan;18(1):21-4. doi: 10.1016/j.parkreldis.2011.08.003. Epub 2011 Aug 24. Parkinsonism Relat Disord. 2012. PMID: 21868278

10

Neuropsychological profile in patients with early stage of Parkinson's disease in Taiwan.

Yu RL, Wu RM, Tai CH, Lin CH, Cheng TW, Hua MS. Yu RL, et al. Among authors: lin ch. Parkinsonism Relat Disord. 2012 Dec;18(10):1067-72. doi: 10.1016/j.parkreldis.2012.06.002. Epub 2012 Jun 30. Parkinsonism Relat Disord. 2012. PMID: 22749792

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