Chen PL - Search Results

1

Identification of VPS35 p.D620N mutation-related Parkinson's disease in a Taiwanese family with successful bilateral subthalamic nucleus deep brain stimulation: a case report and literature review.

Chen YF, Chang YY, Lan MY, Chen PL, Lin CH. Chen YF, et al. Among authors: chen pl. BMC Neurol. 2017 Oct 6;17(1):191. doi: 10.1186/s12883-017-0972-5. BMC Neurol. 2017. PMID: 28985717 Free PMC article. Review.

2

Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing.

Lin YH, Wu CC, Hsu TY, Chiu WY, Hsu CJ, Chen PL. Lin YH, et al. Among authors: chen pl. Mutat Res. 2015 Jan;771:1-5. doi: 10.1016/j.mrfmmm.2014.11.001. Epub 2014 Nov 13. Mutat Res. 2015. PMID: 25771973

3

Clinical heterogeneity of LRRK2 p.I2012T mutation.

Fan TS, Wu RM, Chen PL, Chen TF, Li HY, Lin YH, Chen CY, Chen ML, Tai CH, Lin HI, Lin CH. Fan TS, et al. Among authors: chen ml, chen tf, chen cy, chen pl. Parkinsonism Relat Disord. 2016 Dec;33:36-43. doi: 10.1016/j.parkreldis.2016.09.008. Epub 2016 Sep 7. Parkinsonism Relat Disord. 2016. PMID: 27628070

4

Intrafamilial phenotypic heterogeneity in a Taiwanese family with a MAPT p.R5H mutation: a case report and literature review.

Lin HC, Lin CH, Chen PL, Cheng SJ, Chen PH. Lin HC, et al. Among authors: chen ph, chen pl. BMC Neurol. 2017 Sep 18;17(1):186. doi: 10.1186/s12883-017-0966-3. BMC Neurol. 2017. PMID: 28923025 Free PMC article. Review.

5

A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing.

Lin CH, Chen PL, Tai CH, Lin HI, Chen CS, Chen ML, Wu RM. Lin CH, et al. Among authors: chen cs, chen ml, chen pl. Mov Disord. 2019 Apr;34(4):506-515. doi: 10.1002/mds.27633. Epub 2019 Feb 20. Mov Disord. 2019. PMID: 30788857 Free PMC article.

6

Distinctive genetic variation of long-segment Hirschsprung's disease in Taiwan.

Yang W, Chen SC, Lai JY, Ming YC, Chen JC, Chen PL. Yang W, et al. Among authors: chen sc, chen jc, chen pl. Neurogastroenterol Motil. 2019 Nov;31(11):e13665. doi: 10.1111/nmo.13665. Epub 2019 Jun 25. Neurogastroenterol Motil. 2019. PMID: 31240788

7

Genetic Epidemiology and Clinical Features of Hereditary Hearing Impairment in the Taiwanese Population.

Wu CC, Tsai CY, Lin YH, Chen PY, Lin PH, Cheng YF, Wu CM, Lin YH, Lee CY, Erdenechuluun J, Liu TC, Chen PL, Hsu CJ. Wu CC, et al. Among authors: chen py, chen pl. Genes (Basel). 2019 Oct 1;10(10):772. doi: 10.3390/genes10100772. Genes (Basel). 2019. PMID: 31581539 Free PMC article.

8

Genotype-phenotype correlations of adult-onset PLA2G6-associated Neurodegeneration: case series and literature review.

Chu YT, Lin HY, Chen PL, Lin CH. Chu YT, et al. Among authors: chen pl. BMC Neurol. 2020 Mar 17;20(1):101. doi: 10.1186/s12883-020-01684-6. BMC Neurol. 2020. PMID: 32183746 Free PMC article. Review.

9

Genetic study of young-onset dementia using targeted gene panel sequencing in Taiwan.

Hsu JL, Lin CH, Chen PL, Lin KJ, Chen TF. Hsu JL, et al. Among authors: chen tf, chen pl. Am J Med Genet B Neuropsychiatr Genet. 2021 Mar;186(2):67-76. doi: 10.1002/ajmg.b.32836. Epub 2021 Feb 13. Am J Med Genet B Neuropsychiatr Genet. 2021. PMID: 33580635

10

Investigating DYT1 in a Taiwanese dystonia cohort.

Wu MC, Chang YY, Chen YF, Lan MY, Chen PL, Tai CH, Lin CH. Wu MC, et al. Among authors: chen pl, chen yf. J Formos Med Assoc. 2022 Jan;121(1 Pt 2):375-380. doi: 10.1016/j.jfma.2021.05.017. Epub 2021 Jun 4. J Formos Med Assoc. 2022. PMID: 34092466 Free article.

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