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

關於TAIR
	計畫說明

瀏覽
	典藏機構
	作者
	題名
	日期
	統計圖表
	機構即時統計
	學術趨勢

消息
	2019臺灣學術機構典藏研討會
	機構典藏系統RC7版本已發佈

著作權
	出版社及期刊政策查詢
	TAIR著作權會議記錄

相關連結
	機構典藏計畫網站
	ROAR
	OpenDOAR
	SHERPA
	OAIster
	JAIRO
	Ira
	DSPACE
	RWWR
	臺大學術典藏NTU Scholars

"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 61-85 / 414 (共17頁)
<< < 1 2 3 4 5 6 7 8 9 10 > >>
每頁顯示[10|25|50]項目

機構	日期	題名	作者
臺大學術典藏	2020-11-03T12:21:54Z	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	2020-11-03T12:21:53Z	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.; Yu R.-L.;Wu R.-M.;Chun-Hwei Tai;Lin C.-H.;Hua M.-S.
臺大學術典藏	2020-11-03T12:21:52Z	Meige syndrome relieved by bilateral pallidal stimulation with cycling mode: Case report	Wu R.-M.; Liu H.-M.; Tsai C.-W.; Tseng S.-H.; Chun-Hwei Tai;Wu R.-M.;Liu H.-M.;Tsai C.-W.;Tseng S.-H.; CHUN-HWEI TAI
臺大學術典藏	2020-11-03T12:21:52Z	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.; Lin C.-H.;Wu R.-M.;Chun-Hwei Tai;Chen M.-L.;Hu F.-C.
臺大學術典藏	2020-11-03T12:21:51Z	Neuropsychological profile in patients with early stage of Parkinson's disease in Taiwan	Hua M.-S.; Cheng T.-W.; Lin C.-H.; CHUN-HWEI TAI; Wu R.-M.; Yu R.-L.
臺大學術典藏	2020-11-03T12:21:51Z	Gene therapy for aromatic L-amino acid decarboxylase deficiency	Wu R.-M.; CHUN-HWEI TAI; Byrne B.J.; Snyder R.O.; Chien Y.-H.; Hwu W.-L.; Muramatsu S.-I.; Tseng S.-H.; Tzen K.-Y.; Lee N.-C.
臺大學術典藏	2020-11-03T12:21:51Z	Advanced Theory of Mind in patients at early stage of Parkinson's disease	Hua M.-S.; Yu R.-L.; Wu R.-M.; Chiu M.-J.; CHUN-HWEI TAI; Lin C.-H.
臺大學術典藏	2020-11-03T12:21:50Z	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	2020-11-03T12:21:50Z	Mutational analysis of Angiogenin gene in Parkinson's disease	Lin C.-H.; CHUN-HWEI TAI; Wu R.-M.; Chen M.-L.
臺大學術典藏	2020-11-03T12:21:49Z	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.; Lin H.-H.; Wu R.-M.; Lin H.-I.; Chen M.-L.; CHUN-HWEI TAI; Lin C.-H.
臺大學術典藏	2020-11-03T12:21:47Z	Modified frameless stereotactic system for intracerebral delivery of viral vector in young children	Chun-Hwei Tai;Hwu W.-L.;Wu R.-M.;Tseng S.-H.; CHUN-HWEI TAI; Hwu W.-L.; Wu R.-M.; Tseng S.-H.
臺大學術典藏	2020-11-03T12:12:59Z	Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism	Farrer M.J.; Wu R.-M.; CHIN-HSIEN LIN; Lincoln S.; Kachergus J.; Hulihan M.; Bounds R.; Lockhart P.J.; Lockhart P.J.;Bounds R.;Hulihan M.;Kachergus J.;Lincoln S.;Chin-Hsien Lin;Wu R.-M.;Farrer M.J.
臺大學術典藏	2020-11-03T12:12:58Z	LRRK2 mutation in familial Parkinson's disease in a Taiwanese population: Clinical, PET, and functional studies	Yu C.-Y.; Tai C.-H.; Farrer M.J.; Wu R.-M.; Tzen K.-Y.; CHIN-HSIEN LIN
臺大學術典藏	2020-11-03T12:12:58Z	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; Hwu W.-L.; Chiang S.-C.; Tai C.-H.; Wu R.-M.
臺大學術典藏	2020-11-03T12:12:58Z	Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia	Farrer M.J.; Stone J.T.; CHIN-HSIEN LIN; D?chsel J.C.; Hulihan M.M.; Haugarvoll K.; Ross O.A.; Wu R.-M.
臺大學術典藏	2020-11-03T12:12:58Z	Acute disseminated encephalomyelitis: A follow-up study in Taiwan	Wu R.-M.; Yip P.-K.; Hsieh S.-T.; Jeng J.-S.; CHIN-HSIEN LIN
臺大學術典藏	2020-11-03T12:12:57Z	Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore	CHIN-HSIEN LIN; Wu R.M.; Chen G.S.; Tan E.K.; Chen M.L.; Tan L.C.; Lim H.Q.
臺大學術典藏	2020-11-03T12:12:56Z	Multiple LRRK2 variants modulate risk of Parkinson disease: A Chinese multicenter study	Tan E.-K.;Peng R.;Teo Y.-Y.;Tan L.C.;Angeles D.;Ho P.;Chen M.-L.;Chin-Hsien Lin;Mao X.-Y.;Chang X.-L.;Prakash K.M.;Liu J.-J.;Au W.-L.;Le W.-D.;Jankovic J.;Burgunder J.-M.;Zhao Y.;Wu R.-M.; Wu R.-M.; Zhao Y.; Burgunder J.-M.; Jankovic J.; Le W.-D.; Tan E.-K.; Peng R.; Teo Y.-Y.; Tan L.C.; Angeles D.; Ho P.; Chen M.-L.; CHIN-HSIEN LIN; Mao X.-Y.; Chang X.-L.; Prakash K.M.; Liu J.-J.; Au W.-L.
臺大學術典藏	2020-11-03T12:12:56Z	A novel neuropsychiatric phenotype of KCNJ2 mutation in one Taiwanese family with Andersen-Tawil syndrome	Chan H.-F.;Chen M.-L.;Su J.-J.;Ko L.-C.;Chin-Hsien Lin;Wu R.-M.; Chan H.-F.; Chen M.-L.; Su J.-J.; Ko L.-C.; CHIN-HSIEN LIN; Wu R.-M.
臺大學術典藏	2020-11-03T12:12:56Z	Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism	Ross O.A.;Spanaki C.;Griffith A.;Chin-Hsien Lin;Kachergus J.;Haugarvoll K.;Latsoudis H.;Plaitakis A.;Ferreira J.J.;Sampaio C.;Bonifati V.;Wu R.-M.;Zabetian C.P.;Farrer M.J.; Ross O.A.; Spanaki C.; Griffith A.; CHIN-HSIEN LIN; Kachergus J.; Haugarvoll K.; Latsoudis H.; Plaitakis A.; Ferreira J.J.; Farrer M.J.; Zabetian C.P.; Sampaio C.; Bonifati V.; Wu R.-M.
臺大學術典藏	2020-11-03T12:12:55Z	LRRK2 G2019S mutation induces dendrite degeneration through mislocalization and phosphorylation of tau by recruiting autoactivated GSK3β	CHIN-HSIEN LIN; Tsai P.-I.; Wu R.-M.; Chien C.-T.; Chin-Hsien Lin;Tsai P.-I.;Wu R.-M.;Chien C.-T.
臺大學術典藏	2020-11-03T12:12:55Z	Feeling-of-knowing in episodic memory in patients with Parkinson's disease with various motor symptoms	Tai C.-H.; CHIN-HSIEN LIN; Hua M.-S.; Wu R.-M.; Yu R.-L.;Wu R.-M.;Tai C.-H.;Chin-Hsien Lin;Hua M.-S.; Yu R.-L.
臺大學術典藏	2020-11-03T12:12:54Z	Lrrk2 S1647T and BDNF V66M interact with environmental factors to increase risk of Parkinson's disease	CHIN-HSIEN LIN; Wu R.-M.; Tai C.-H.; Chen M.-L.; Hu F.-C.; Chin-Hsien Lin;Wu R.-M.;Tai C.-H.;Chen M.-L.;Hu F.-C.
臺大學術典藏	2020-11-03T12:12:53Z	Early-onset autosomal-recessive parkinsonian-pyramidal syndrome	Wu R.-M.; CHIN-HSIEN LIN; Lai H.-J.
臺大學術典藏	2020-11-03T12:12:53Z	Unusual association of diseases/symptoms: Psychotic-affective symptoms and multiple system atrophy expand phenotypes of spinocerebellar ataxia type 2	Chen K.-H.; CHIN-HSIEN LIN; Wu R.-M.

顯示項目 61-85 / 414 (共17頁)
<< < 1 2 3 4 5 6 7 8 9 10 > >>
每頁顯示[10|25|50]項目

	English \| 正體中文 \| 简体中文 \| 總筆數 :2831195
	造訪人次 : 33220607 線上人數 : 640 教育部委託研究計畫計畫執行:國立臺灣大學圖書館