臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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Showing items 46-55 of 138 (14 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2020-11-03T12:21:46Z	Correction to: Feasibility of Smartphone-Based Gait Assessment for Parkinson's Disease (Journal of Medical and Biological Engineering, (2020), 40, 4, (582-591), 10.1007/s40846-020-00551-6)	Tang S.T.;Chun-Hwei Tai;Yang C.Y.;Lin J.H.; Tang S.T.; CHUN-HWEI TAI; Yang C.Y.; Lin J.H.
臺大學術典藏	2020-11-03T12:21:46Z	Hyperpolarization of the subthalamic nucleus alleviates hyperkinetic movement disorders	Chun-Hwei Tai;Pan M.-K.;Tseng S.-H.;Wang T.-R.;Kuo C.-C.; CHUN-HWEI TAI; Pan M.-K.; Tseng S.-H.; Wang T.-R.; Kuo C.-C.
臺大學術典藏	2020-03-05T01:18:09Z	Bilateral deep brain stimulation of subthalamic nucleus alleviates tardive dystonia	CHUN-HWEI TAI; Tseng S.-H.; Liu H.-M.; Wu R.-M.
臺大學術典藏	2020-03-05T01:18:09Z	High-frequency stimulation of both zona incerta and subthalamic nucleus induces a similar normalization of basal ganglia metabolic activity in experimental parkinsonism.	Benazzouz A.; CHUN-HWEI TAI; Meissner W.; Bioulac B.; Bezard E.; Gross C.
臺大學術典藏	2020-03-05T01:18:09Z	Electrophysiological and metabolic evidence that high-frequency stimulation of the subthalamic nucleus bridles neuronal activity in the subthalamic nucleus and the substantia nigra reticulata	CHUN-HWEI TAI; Boraud T.; Bezard E.; Bioulac B.; Gross C.; Benazzouz A.
臺大學術典藏	2020-03-05T01:18:09Z	Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and Parkin gene mutations	Wu R.-M.; Shan D.-E.; Sun C.-M.; Liu R.-S.; Hwu W.-L.; CHUN-HWEI TAI; Hussey J.; West A.; Gwinn-Hardy K.; Hardy J.; Chen J.; Farrer M.; Lincoln S.
臺大學術典藏	2020-03-05T01:18:09Z	Electrophysiology of subthalamic nucleus in normal and Parkinson's disease	CHUN-HWEI TAI; Kuo C.-C.
臺大學術典藏	2020-03-05T01:18:08Z	Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation	CHUN-HWEI TAI; Yen R.-F.; Lin C.-H.; Yen K.-Y.; Yip P.-K.; Wu R.-M.; Lee M.-J.
臺大學術典藏	2020-03-05T01:18:08Z	LRRK2 mutation in familial Parkinson's disease in a Taiwanese population: Clinical, PET, and functional studies	Lin C.-H.; Tzen K.-Y.; Yu C.-Y.; CHUN-HWEI TAI; Farrer M.J.; Wu R.-M.
臺大學術典藏	2020-03-05T01:18:08Z	Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (Ethnic Chinese) cohort of familial and early-onset parkinsonism	Lin C.-H.; Hwu W.-L.; Chiang S.-C.; CHUN-HWEI TAI; Wu R.-M.

Showing items 46-55 of 138 (14 Page(s) Totally)
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