公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2022 | A case of senile-onset progressive hemiballism and cognitive decline with diffuse brain iron accumulations | Lin I.-T.; NI-CHUNG LEE ; Fan, Sung-Pin; Huang C.-J.; Cheng P.; Chen J.-H.; CHIN-HSIEN LIN | Parkinsonism and Related Disorders | 2 | 1 | |
2018 | Catechol-O-methyltransferase (COMT) genetic variants are associated with cognitive decline in patients with Parkinson's disease | CHIN-HSIEN LIN ; Fan J.-Y.; Lin H.-I.; Chang C.-W.; Wu Y.-R. | Parkinsonism and Related Disorders | 9 | 9 | |
2014 | Cauda equina-conus medullaris syndrome as an isolated presenting symptom of intravascular large B-cell lymphoma: Case report and review of the literature | MENG-CHEN WU ; CHIN-HSIEN LIN | Neurology Asia | | | |
2019 | Circulating long noncoding RNA DKFZP434I0714 predicts adverse cardiovascular outcomes in patients with end-stage renal disease | CHUN-FU LAI ; Chen Y.-T.; Gu J.; Nerbonne J.M.; CHIN-HSIEN LIN ; KAI-CHIEN YANG | International Journal of Cardiology | 19 | 18 | |
2020 | Classifications of neurodegenerative disorders using a multiplex blood biomarkers-based machine learning model | CHIN-HSIEN LIN ; Chiu, S.-I.; TA-FU CHEN ; Jang, J.-S.R.; MING-JANG CHIU ; JYH-SHING JANG | International Journal of Molecular Sciences | 27 | 18 | |
2020 | Clinical and electrophysiological characteristics of a type 1 sialidosis patient with a novel deletion mutation in NEU1 gene | Fan S.-P.; NI-CHUNG LEE ; CHIN-HSIEN LIN | Journal of the Formosan Medical Association | 12 | 7 | |
2021 | Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48) | Chen H.-Y.; Hsu C.-L.; SHU-CHUN TENG ; Huang T.-C.; Tsai S.-F.; Cheng C.-L.; Li Y.-R.; Tsai J.-W.; Teng S.-C.; CHIN-HSIEN LIN ; Yang T.-L. | Journal of Biomedical Science | 7 | 7 | |
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 | |
2022 | A Clinical and Integrated Genetic Study of Isolated and Combined Dystonia in Taiwan | MENG-CHEN WU ; Chang, Yung-Yee; Lan, Min-Yu; Chen, Ying-Fa; Tai, Chun-Hwei; Lin, Yung-Feng; Tsai, Shih-Feng; PEI-LUNG CHEN ; CHIN-HSIEN LIN | Journal of Molecular Diagnostics | 9 | 6 | |
2023 | Clinical Characteristics, Genetic Features, and Long-Term Outcome of Wilson's Disease in a Taiwanese Population: An 11-Year Follow-Up Study | Fan, Sung-Pin; Kuo, Yih-Chih; NI-CHUNG LEE ; YIN-HSIU CHIEN ; WUH-LIANG HWU ; Huang, Yu-Hsuan; Lin, Han-I; TAI-CHUNG TSENG ; TUNG-HUNG SU ; SHIOU-RU TZENG ; Hsu, Chien-Ting; HUEY-LING CHEN ; CHIN-HSIEN LIN ; YEN-HSUAN NI | Journal of Movement Disorders | 2 | | |
2019 | Clinical spectrum of glutamic acid decarboxylase antibodies in a Taiwanese population | Kuo Y.-C.; CHIN-HSIEN LIN | European Journal of Neurology | 6 | 3 | |
2020 | Clinical, radiological, and genetic characteristics in patients with Huntington's disease in a Taiwanese cohort | Chen, Szu-Ju; BO-CHING LEE ; NI-CHUNG LEE ; YIN-HSIU CHIEN ; WUH-LIANG HWU ; CHIN-HSIEN LIN | American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics | 0 | 0 | |
2022 | Colonic Leucine-Rich Repeat Kinase 2 Expression Is Increased and Associated With Disease Severity in Patients With Parkinson’s Disease | Liao, Peng-Hsiang; Chiang, Han-Lin; CHIA-TUNG SHUN ; Hang, Jen-Fan; HAN-MO CHIU ; MING-SHIANG WU ; CHIN-HSIEN LIN | Frontiers in Aging Neuroscience | 5 | 4 | |
2016 | Comparison of the effects of serotonin-norepinephrine reuptake inhibitors versus selective serotonin reuptake inhibitors on cerebrovascular events | Lee Y.-C.; CHIN-HSIEN LIN ; Lin M.-S.; Lu Y.; CHIA-HSUIN CHANG ; JOU-WEI LIN | Journal of Clinical Psychiatry | 15 | 13 | |
2012 | A comparison study of the effects on road crossing behavior between normal and parkinson disease | Ou Y.-K.; CHIN-HSIEN LIN ; Liu Y.-C. | Advances in Usability Evaluation Part I | 0 | | |
2022 | COQ2 and SNCA polymorphisms interact with environmental factors to modulate the risk of multiple system atrophy and subtype disposition | MING-CHE KUO ; Lu Y.-C.; Tai C.-H.; Soong B.-W.; Hu F.-C.; Chen M.-L.; CHIN-HSIEN LIN ; RUEY-MEEI WU | European Journal of Neurology | 1 | 1 | |
2015 | COQ2 gene variants associate with cerebellar subtype of multiple system atrophy in Chinese | CHIN-HSIEN LIN ; Tan E.-K.; Yang C.-C.; Yi Z.; RUEY-MEEI WU | Movement Disorders | 33 | 31 | |
2015 | COQ2 p.V393A variant, rs148156462, is not associated with Parkinson's disease in a Taiwanese population | CHIN-HSIEN LIN ; Lin H.-I.; Chen M.-L.; RUEY-MEEI WU | Neurobiology of Aging | 4 | 3 | |
2019 | Craniocervical dystonia with levodopa-responsive parkinsonism co-segregating with a pathogenic ANO3 mutation in a Taiwanese family | MING-CHE KUO ; Lin H.-I.; CHIN-HSIEN LIN | Parkinsonism and Related Disorders | 9 | 10 | |
2016 | DCTN1 p.K56R in progressive supranuclear palsy | Gustavsson E.K.; Trinh J.; Guella I.; Szu-Tu C.; Khinda J.; CHIN-HSIEN LIN ; RUEY-MEEI WU ; Stoessl J.; Appel-Cresswell S.; McKeown M.; Rajput A.; Rajput A.H.; Petersen M.S.; Jeon B.S.; Aasly J.O.; Farrer M.J. | Parkinsonism and Related Disorders | 26 | 26 | |