English  |  正體中文  |  简体中文  |  總筆數 :2851812  
造訪人次 :  44812436    線上人數 :  1379
教育部委託研究計畫      計畫執行:國立臺灣大學圖書館
 
臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
關於TAIR

瀏覽

消息

著作權

相關連結

"wu r m"的相關文件

回到依作者瀏覽
依題名排序 依日期排序

顯示項目 161-185 / 414 (共17頁)
<< < 2 3 4 5 6 7 8 9 10 11 > >>
每頁顯示[10|25|50]項目

機構 日期 題名 作者
臺大學術典藏 2020-03-12T06:42:01Z Acute hydrocephalus upregulates monoamine oxidase mRNA in neonatal rat brain Kuo M.-F.;Wu K.-D.;Wu R.-M.;Yong-Kwang Tu;Wang H.-S.; Kuo M.-F.; Wu K.-D.; Wu R.-M.; YONG-KWANG TU; Wang H.-S.
臺大學術典藏 2020-03-07T06:42:16Z O6-Methylguanine-DNA methyltransferase expression and prognostic value in brain metastases of lung cancers Wu P.-F.;Kuan-Ting Kuo;Kuo L.-T.;Lin Y.-T.;Lee W.-C.;Lu Y.-S.;Yang C.-H.;Wu R.-M.;Tu Y.-K.;Tasi J.-C.;Tseng H.-M.;Tseng S.-H.;Cheng A.-L.;Lin C.-H.; Wu P.-F.; KUAN-TING KUO; Kuo L.-T.; Lin Y.-T.; Lee W.-C.; Lu Y.-S.; Yang C.-H.; Wu R.-M.; Tu Y.-K.; Tasi J.-C.; Tseng H.-M.; Tseng S.-H.; Cheng A.-L.; Lin C.-H.
臺大學術典藏 2020-03-06T01:32:29Z A novel neuropsychiatric phenotype of KCNJ2 mutation in one Taiwanese family with Andersen-Tawil syndrome Chan H.-F.; Chen M.-L.; JEN-JEN SU; Ko L.-C.; Lin C.-H.; Wu R.-M.
臺大學術典藏 2020-03-05T05:37:55Z Neurocysticercosis presenting with epilepsia partialis continua: A clinicopathologic report and literature review Shin-Joe Yeh;Wu R.-M.; SHIN-JOE YEH; Wu R.-M.
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 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 2020-03-05T01:18:08Z 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.
臺大學術典藏 2020-03-05T01:18:08Z Non-synonymous GIGYF2 variants in Parkinson's disease from two Asian populations Tan E.-K.; Lin C.-H.; CHUN-HWEI TAI; Tan L.C.; Chen M.-L.; Li R.; Lim H.-Q.; Pavanni R.; Yuen Y.; Prakash K.M.; Zhao Y.; Wu R.-M.
臺大學術典藏 2020-03-05T01:18:07Z Deep brain stimulation therapy for Parkinson's disease using frameless stereotaxy: Comparison with frame-based surgery CHUN-HWEI TAI; Wu R.-M.; Lin C.-H.; Pan M.-K.; Chen Y.-F.; Liu H.-M.; Lu H.-H.; Tsai C.-W.; Tseng S.-H.
臺大學術典藏 2020-03-05T01:18:07Z Feeling-of-knowing in episodic memory in patients with Parkinson's disease with various motor symptoms Yu R.-L.; Wu R.-M.; CHUN-HWEI TAI; Lin C.-H.; Hua M.-S.
臺大學術典藏 2020-03-05T01:18:06Z Meige syndrome relieved by bilateral pallidal stimulation with cycling mode: Case report CHUN-HWEI TAI; Wu R.-M.; Liu H.-M.; Tsai C.-W.; Tseng S.-H.
臺大學術典藏 2020-03-05T01:18:06Z Lrrk2 S1647T and BDNF V66M interact with environmental factors to increase risk of Parkinson's disease Lin C.-H.; Wu R.-M.; CHUN-HWEI TAI; Chen M.-L.; Hu F.-C.
臺大學術典藏 2020-03-05T01:18:06Z Minimal detectable change of the timed "up & go" test and the dynamic gait index in people with parkinson disease Huang S.-L.; Hsieh C.-L.; Wu R.-M.; CHUN-HWEI TAI; Lin C.-H.; Lu W.-S.
臺大學術典藏 2020-03-05T01:18:05Z Novel variant Pro143Ala in HTRA2 contributes to Parkinson's disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria Lin C.-H.; Chen M.-L.; Chen G.S.; CHUN-HWEI TAI; Wu R.-M.
臺大學術典藏 2020-03-05T01:18:05Z Neuropsychological profile in patients with early stage of Parkinson's disease in Taiwan Yu R.-L.; Wu R.-M.; CHUN-HWEI TAI; Lin C.-H.; Cheng T.-W.; Hua M.-S.
臺大學術典藏 2020-03-05T01:18:05Z Gene therapy for aromatic L-amino acid decarboxylase deficiency Hwu W.-L.; Muramatsu S.-I.; Tseng S.-H.; Tzen K.-Y.; Lee N.-C.; Chien Y.-H.; Snyder R.O.; Byrne B.J.; CHUN-HWEI TAI; Wu R.-M.
臺大學術典藏 2020-03-05T01:18:05Z Advanced Theory of Mind in patients at early stage of Parkinson's disease Yu R.-L.; Wu R.-M.; Chiu M.-J.; CHUN-HWEI TAI; Lin C.-H.; Hua M.-S.
臺大學術典藏 2020-03-05T01:18:04Z Mutational analysis of FBXO7 gene in Parkinson's disease in a Taiwanese population Lin C.-H.; Chen M.-L.; Lai T.-T.; CHUN-HWEI TAI; Wu R.-M.
臺大學術典藏 2020-03-05T01:18:03Z 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; Lin C.-H.; Wu R.-M.
臺大學術典藏 2020-03-05T01:18:03Z Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese population Chen K.-H.; Wu R.-M.; Lin H.-I.; CHUN-HWEI TAI; Lin C.-H.
臺大學術典藏 2020-03-05T01:18:03Z Mutational analysis of Angiogenin gene in Parkinson's disease Chen M.-L.; Wu R.-M.; CHUN-HWEI TAI; Lin C.-H.
臺大學術典藏 2020-03-05T01:18:02Z Clinical heterogeneity of LRRK2 p.I2012T mutation Fan T.-S.; Wu R.-M.; Chen P.-L.; Chen T.-F.; Li H.-Y.; Lin Y.-H.; Chen C.-Y.; Chen M.-L.; CHUN-HWEI TAI; Lin H.-I.; Lin C.-H.
臺大學術典藏 2020-03-05T01:18:02Z Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort Lin H.-H.; Wu R.-M.; Lin H.-I.; Chen M.-L.; CHUN-HWEI TAI; Lin C.-H.

顯示項目 161-185 / 414 (共17頁)
<< < 2 3 4 5 6 7 8 9 10 11 > >>
每頁顯示[10|25|50]項目