Yeh TH - Search Results

1

EIF2AK2 Missense Variants Associated with Early Onset Generalized Dystonia.

Kuipers DJS, Mandemakers W, Lu CS, Olgiati S, Breedveld GJ, Fevga C, Tadic V, Carecchio M, Osterman B, Sagi-Dain L, Wu-Chou YH, Chen CC, Chang HC, Wu SL, Yeh TH, Weng YH, Elia AE, Panteghini C, Marotta N, Pauly MG, Kühn AA, Volkmann J, Lace B, Meijer IA, Kandaswamy K, Quadri M, Garavaglia B, Lohmann K, Bauer P, Mencacci NE, Lubbe SJ, Klein C, Bertoli-Avella AM, Bonifati V. Kuipers DJS, et al. Among authors: yeh th. Ann Neurol. 2021 Mar;89(3):485-497. doi: 10.1002/ana.25973. Epub 2020 Dec 15. Ann Neurol. 2021. PMID: 33236446 Free PMC article.

2

Focal hand myoclonus caused by a small hematoma underneath the cerebral motor cortex.

Tsai PC, Chang FC, Tsai CH, Jang FR, Shen AN, Huang YT, Lai SC, Yeh TH, Lu MK, Lu CS. Tsai PC, et al. Among authors: yeh th. Eur Neurol. 2003;50(2):114-7. doi: 10.1159/000072512. Eur Neurol. 2003. PMID: 12944720 No abstract available.

3

Autonomic dysfunction in Machado-Joseph disease.

Yeh TH, Lu CS, Chou YH, Chong CC, Wu T, Han NH, Chen RS. Yeh TH, et al. Arch Neurol. 2005 Apr;62(4):630-6. doi: 10.1001/archneur.62.4.630. Arch Neurol. 2005. PMID: 15824264

4

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. Among authors: yeh th. 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

5

HDAC inhibitor sodium butyrate reverses transcriptional downregulation and ameliorates ataxic symptoms in a transgenic mouse model of SCA3.

Chou AH, Chen SY, Yeh TH, Weng YH, Wang HL. Chou AH, et al. Among authors: yeh th. Neurobiol Dis. 2011 Feb;41(2):481-8. doi: 10.1016/j.nbd.2010.10.019. Epub 2010 Nov 1. Neurobiol Dis. 2011. PMID: 21047555

6

PARK6 PINK1 mutants are defective in maintaining mitochondrial membrane potential and inhibiting ROS formation of substantia nigra dopaminergic neurons.

Wang HL, Chou AH, Wu AS, Chen SY, Weng YH, Kao YC, Yeh TH, Chu PJ, Lu CS. Wang HL, et al. Among authors: yeh th. Biochim Biophys Acta. 2011 Jun;1812(6):674-84. doi: 10.1016/j.bbadis.2011.03.007. Epub 2011 Mar 21. Biochim Biophys Acta. 2011. PMID: 21421046 Free article.

7

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: yeh th. 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

8

Familial paroxysmal nonkinesigenic dyskinesia: clinical and genetic analysis of a Taiwanese family.

Yeh TH, Lin JJ, Lai SC, Wu-Chou YH, Chen AC, Yueh KC, Chen RS, Lu CS. Yeh TH, et al. J Neurol Sci. 2012 Dec 15;323(1-2):80-4. doi: 10.1016/j.jns.2012.08.015. Epub 2012 Sep 8. J Neurol Sci. 2012. PMID: 22967746 Review.

9

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. 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.

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. Among authors: yeh th. 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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