第 1 到 24 筆結果,共 24 筆。
公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 | |
---|---|---|---|---|---|---|---|
1 | 2023 | Blood neurofilament light chain as a surrogate marker for dystonia | MENG-CHEN WU ; Chang, Yung-Yee; Lan, Min-Yu; Chen, Ying-Fa; CHUN-HWEI TAI ; Chen, Szu-Ju; CHIN-HSIEN LIN | European journal of neurology | 0 | 0 | |
2 | 2023 | Genetic analysis of IMPDH2 gene in Taiwanese patients with isolated or combined dystonia | Chen, Pin-Shiuan; MENG-CHEN WU ; CHUN-HWEI TAI ; Chang, Yung-Yee; Lan, Min-Yu; Chen, Ying-Fa; Lin, Han-I; NI-CHUNG LEE ; CHIN-HSIEN LIN | Parkinsonism & related disorders | 1 | 1 | |
3 | 2022 | Long-Term Outcomes of Idiopathic and Acquired Dystonia After Pallidal Deep Brain Stimulation: A Case Series | CHUN-HWEI TAI ; SHENG-CHE CHOU ; CHIN-HSIEN LIN ; WANG-TSO LEE ; RUEY-MEEI WU ; SHENG-HONG TSENG | World neurosurgery | 0 | 0 | |
4 | 2022 | Amantadine treatment and delayed onset of levodopa-induced dyskinesia in patients with early Parkinson's disease | CHI-CHUAN WANG ; Wu, Tsai-Ling; FANG-JU LIN ; CHUN-HWEI TAI ; CHIN-HSIEN LIN ; RUEY-MEEI WU | European Journal of Neurology | 8 | 8 | |
5 | 2022 | Investigating DYT1 in a Taiwanese dystonia cohort | MENG-CHEN WU ; Chang, Yung-Yee; Chen, Ying-Fa; Lan, Min-Yu; PEI-LUNG CHEN ; CHUN-HWEI TAI ; CHIN-HSIEN LIN | Journal of the Formosan Medical Association | 2 | 2 | |
6 | 2021 | A Double-Blind, Randomized, Controlled Trial of Lovastatin in Early-Stage Parkinson's Disease | CHIN-HSIEN LIN ; Chang, Chin-Hao; CHUN-HWEI TAI ; MEI-FANG CHENG ; Chen, Yi-Chieh; Chao, Ying-Ting; Huang, Tse-Le; RUOH-FANG YEN ; RUEY-MEEI WU | Movement disorders : official journal of the Movement Disorder Society | 23 | 22 | |
7 | 2021 | Updates on the genetics of parkinson’s disease: Clinical implications and future treatment | Chu, Yung-Tsai; CHUN-HWEI TAI ; CHIN-HSIEN LIN ; RUEY-MEEI WU | Acta Neurologica Taiwanica | 9 | 0 | |
8 | 2021 | Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-070-02) from a patient with neurodegeneration with brain iron accumulation (NBIA) having compound heterozygous mutations in PANK2 gene | Ou-Yang C.-H.; CHUN-HWEI TAI ; Lin H.-Y.; Huang C.-Y.; CHIN-HSIEN LIN | Stem Cell Research | 1 | 1 | |
9 | 2019 | A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing | CHIN-HSIEN LIN ; PEI-LUNG CHEN ; CHUN-HWEI TAI ; Lin H.-I.; Chen C.-S.; Chen M.-L.; RUEY-MEEI WU | Movement Disorders | 64 | 58 | |
10 | 2017 | Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort | Lin H.-H.; RUEY-MEEI WU ; Lin H.-I.; Chen M.-L.; CHUN-HWEI TAI ; CHIN-HSIEN LIN | Neurobiology of Aging | 9 | 8 | |
11 | 2015 | The impact of nonmotor symptoms on quality of life in patients with parkinson's disease in Taiwan | Liu W.-M.; Lin R.-J.; Yu R.-L.; CHUN-HWEI TAI ; CHIN-HSIEN LIN ; RUEY-MEEI WU | Neuropsychiatric Disease and Treatment | 31 | 26 | |
12 | 2015 | Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese population | KAI-HSIANG CHEN ; RUEY-MEEI WU ; Lin H.-I.; CHUN-HWEI TAI ; CHIN-HSIEN LIN | Neurobiology of Aging | 14 | 12 | |
13 | 2014 | Mutational analysis of Angiogenin gene in Parkinson's disease | Chen M.-L.; RUEY-MEEI WU ; CHUN-HWEI TAI ; CHIN-HSIEN LIN | PLoS ONE | 5 | 5 | |
14 | 2013 | Mutational analysis of FBXO7 gene in Parkinson's disease in a Taiwanese population | CHIN-HSIEN LIN ; Chen M.-L.; Lai T.-T.; CHUN-HWEI TAI ; RUEY-MEEI WU | Neurobiology of Aging | 18 | 14 | |
15 | 2012 | Neuropsychological profile in patients with early stage of Parkinson's disease in Taiwan | Yu R.-L.; RUEY-MEEI WU ; CHUN-HWEI TAI ; CHIN-HSIEN LIN ; Cheng T.-W.; Hua M.-S. | Parkinsonism and Related Disorders | 41 | 35 | |
16 | 2012 | Advanced Theory of Mind in patients at early stage of Parkinson's disease | Yu R.-L.; RUEY-MEEI WU ; MING-JANG CHIU ; CHUN-HWEI TAI ; CHIN-HSIEN LIN ; Hua M.-S. | Parkinsonism and Related Disorders | 43 | 40 | |
17 | 2011 | Minimal detectable change of the timed "up & go" test and the dynamic gait index in people with parkinson disease | SHEAU-LING HUANG ; CHING-LIN HSIEH ; RUEY-MEEI WU ; CHUN-HWEI TAI ; CHIN-HSIEN LIN ; Lu W.-S. | Physical Therapy | 250 | 233 | |
18 | 2011 | Lrrk2 S1647T and BDNF V66M interact with environmental factors to increase risk of Parkinson's disease | CHIN-HSIEN LIN ; RUEY-MEEI WU ; CHUN-HWEI TAI ; Chen M.-L.; Hu F.-C. | Parkinsonism and Related Disorders | 31 | 28 | |
19 | 2011 | Novel variant Pro143Ala in HTRA2 contributes to Parkinson's disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria | CHIN-HSIEN LIN ; Chen M.-L.; Chen G.S.; CHUN-HWEI TAI ; RUEY-MEEI WU | Human Genetics | 48 | 26 | |
20 | 2010 | Feeling-of-knowing in episodic memory in patients with Parkinson's disease with various motor symptoms | Yu R.-L.; RUEY-MEEI WU ; CHUN-HWEI TAI ; CHIN-HSIEN LIN ; Hua M.-S. | Movement Disorders | 17 | 17 | |
21 | 2010 | Deep brain stimulation therapy for Parkinson's disease using frameless stereotaxy: Comparison with frame-based surgery | CHUN-HWEI TAI ; RUEY-MEEI WU ; CHIN-HSIEN LIN ; MING-KAI PAN ; YA-FANG CHEN ; HON-MAN LIU ; Lu H.-H.; Tsai C.-W.; SHENG-HONG TSENG | European Journal of Neurology | 28 | 23 | |
22 | 2009 | Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation | CHUN-HWEI TAI ; RUOH-FANG YEN ; CHIN-HSIEN LIN ; Yen K.-Y.; Yip P.-K.; RUEY-MEEI WU ; MING-JEN LEE | Parkinsonism and Related Disorders | 3 | 2 | |
23 | 2008 | LRRK2 mutation in familial Parkinson's disease in a Taiwanese population: Clinical, PET, and functional studies | CHIN-HSIEN LIN ; KAI-YUAN TZEN ; Yu C.-Y.; CHUN-HWEI TAI ; Farrer M.J.; RUEY-MEEI WU | Journal of Biomedical Science | 50 | 46 | |
24 | 2007 | Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (Ethnic Chinese) cohort of familial and early-onset parkinsonism | CHIN-HSIEN LIN ; WUH-LIANG HWU ; Chiang S.-C.; CHUN-HWEI TAI ; RUEY-MEEI WU | American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics | 8 | 7 |