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

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机构	日期	题名	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.

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