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

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	Repositories
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	2019臺灣學術機構典藏研討會
	機構典藏系統RC7版本已發佈

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	機構典藏計畫網站
	ROAR
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	DSPACE
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	臺大學術典藏NTU Scholars

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Institution	Date	Title	Author
臺大學術典藏	2021-12-22T03:54:35Z	Transcranial color-coded sonography helps differentiation between idiopathic Parkinson's disease and vascular parkinsonism	Tsai C.-F.; Wu R.-M.; Huang Y.-W.; Chen L.-L.; Yip P.-K.; JIANN-SHING JENG
臺大學術典藏	2021-12-02T02:26:11Z	Restless legs syndrome in end-stage renal disease: A multicenter study in Taiwan	Lin C.-H.; Wu V.-C.; WEN-YI LI; Sy H.-N.; Wu S.-L.; Chang C.-C.; Chiu P.-F.; Lion H.-H.; Lin C.-Y.; Chang H.-W.; Lin S.-Y.; Wu K.-D.; Chen Y.-M.; Wu R.-M.
臺大學術典藏	2021-12-02T02:26:10Z	Association of candidate genetic variants with restless legs syndrome in end stage renal disease: A multicenter case-control study in Taiwan	Lin C.-H.; Chen M.-L.; Wu V.-C.; WEN-YI LI; Sy H.-N.; Wu S.-L.; Chang C.-C.; Chiu P.-F.; Liou H.-H.; Lin C.-Y.; Chang H.-W.; Lin S.-Y.; Wu K.-D.; Chen Y.-M.; Wu R.-M.
臺大學術典藏	2021-12-02T02:26:10Z	Restless legs syndrome is associated with cardio/cerebrovascular events and mortality in end-stage renal disease	Lin C.-H.; Sy H.-N.; Chang H.-W.; Liou H.-H.; Lin C.-Y.; Wu V.-C.; Wu S.-L.; Chang C.-C.; Chiu P.-F.; WEN-YI LI; Lin S.-Y.; Wu K.-D.; Chen Y.-M.; Wu R.-M.
臺大學術典藏	2021-11-30T04:54:14Z	Restless legs syndrome in end-stage renal disease: A multicenter study in Taiwan	Lin C.-H.; VIN-CENT WU; Li W.-Y.; Sy H.-N.; Wu S.-L.; Chang C.-C.; Chiu P.-F.; Lion H.-H.; Lin C.-Y.; Chang H.-W.; Lin S.-Y.; Wu K.-D.; Chen Y.-M.; Wu R.-M.
臺大學術典藏	2021-11-30T04:54:08Z	Association of candidate genetic variants with restless legs syndrome in end stage renal disease: A multicenter case-control study in Taiwan	Lin C.-H.; Chen M.-L.; VIN-CENT WU; Li W.-Y.; Sy H.-N.; Wu S.-L.; Chang C.-C.; Chiu P.-F.; Liou H.-H.; Lin C.-Y.; Chang H.-W.; Lin S.-Y.; Wu K.-D.; Chen Y.-M.; Wu R.-M.
臺大學術典藏	2021-11-30T04:54:04Z	Restless legs syndrome is associated with cardio/cerebrovascular events and mortality in end-stage renal disease	Lin C.-H.; Sy H.-N.; Chang H.-W.; Liou H.-H.; Lin C.-Y.; VIN-CENT WU; Wu S.-L.; Chang C.-C.; Chiu P.-F.; Li W.-Y.; Lin S.-Y.; Wu K.-D.; Chen Y.-M.; Wu R.-M.
臺大學術典藏	2021-11-30T03:31:03Z	Monitoring of the levodopa concentration-response relationship in Parkinson's disease	Wu R.-M.; CHUN-HWEI TAI; Chen R.-C.
臺大學術典藏	2021-11-30T03:31:02Z	Catechol-O-methyltransferase and Parkinson's disease	CHUN-HWEI TAI; Wu R.-M.
臺大學術典藏	2021-11-30T03:31:01Z	Updates on the genetics of parkinson’s disease: Clinical implications and future treatment	Chu Y.-T.; CHUN-HWEI TAI; Lin C.-H.; Wu R.-M.
臺大學術典藏	2021-11-30T03:31:00Z	A Double-Blind, Randomized, Controlled Trial of Lovastatin in Early-Stage Parkinson's Disease	Lin C.-H.; Chang C.-H.; CHUN-HWEI TAI; Cheng M.-F.; Chen Y.-C.; Chao Y.-T.; Huang T.-L.; Yen R.-F.; Wu R.-M.
臺大學術典藏	2021-11-16T02:44:01Z	Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy	CHIN-HSIEN LIN; Tsai P.-.; Lin H.-Y.; Hattori N.; Funayama M.; Jeon B.; Sato K.; Abe K.; Mukai Y.; Takahashi Y.; Li Y.; Nishioka K.; Yoshino H.; Daida K.; Chen M.-L.; Cheng J.; Huang C.-Y.; Tzeng S.-R.; Wu Y.-S.; Lai H.-J.; Tsai H.-H.; Yen R.-F.; Lee N.-C.; Lo W.-C.; Hung Y.-C.; Chan C.-C.; Ke Y.-C.; Chao C.-C.; Hsieh S.-T.; Farrer M.; Wu R.-M.
臺大學術典藏	2021-11-16T02:43:58Z	Lack of PTRHD1 mutation in patients with young-onset and familial Parkinson's disease in a Taiwanese population	Chen S.-J.; Ho C.-H.; Lin H.-Y.; CHIN-HSIEN LIN; Wu R.-M.
臺大學術典藏	2021-11-16T02:43:57Z	Reply: UQCRC1 variants in Parkinson's disease: a large cohort study in Chinese mainland population	CHIN-HSIEN LIN; Farrer M.J.; Wu R.-M.
臺大學術典藏	2021-11-16T02:43:57Z	A Double-Blind, Randomized, Controlled Trial of Lovastatin in Early-Stage Parkinson's Disease	CHIN-HSIEN LIN; Chang C.-H.; Tai C.-H.; Cheng M.-F.; Chen Y.-C.; Chao Y.-T.; Huang T.-L.; Yen R.-F.; Wu R.-M.
臺大學術典藏	2021-09-23T03:48:58Z	Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy	Lin C.-H.; Tsai P.-.; Lin H.-Y.; Hattori N.; Funayama M.; Jeon B.; Sato K.; Abe K.; Mukai Y.; Takahashi Y.; Li Y.; Nishioka K.; Yoshino H.; Daida K.; Chen M.-L.; Cheng J.; Huang C.-Y.; Tzeng S.-R.; Wu Y.-S.; Lai H.-J.; Tsai H.-H.; Yen R.-F.; Lee N.-C.; Lo W.-C.; Hung Y.-C.; Chan C.-C.; Ke Y.-C.; CHI-CHAO CHAO; Hsieh S.-T.; Farrer M.; Wu R.-M.
臺大學術典藏	2021-09-01T01:54:14Z	O6-Methylguanine-DNA methyltransferase expression and prognostic value in brain metastases of lung cancers	Wu P.-F.; Kuo K.-T.; 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.; ANN-LII CHENG; Lin C.-H.
臺大學術典藏	2021-07-06T02:04:04Z	Clinical heterogeneity of LRRK2 p.I2012T mutation	Fan T.-S.;Wu R.-M.;Pei-Lung Chen;Chen T.-F.;Li H.-Y.;Lin Y.-H.;Chen C.-Y.;Chen M.-L.;Tai C.-H.;Lin H.-I.;Lin C.-H.; Fan T.-S.; Wu R.-M.; PEI-LUNG CHEN; Chen T.-F.; Li H.-Y.; Lin Y.-H.; Chen C.-Y.; Chen M.-L.; Tai C.-H.; Lin H.-I.; Lin C.-H.
臺大學術典藏	2021-07-06T02:03:54Z	A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing	Lin C.-H.;Pei-Lung Chen;Tai C.-H.;Lin H.-I.;Chen C.-S.;Chen M.-L.;Wu R.-M.; Lin C.-H.; PEI-LUNG CHEN; Tai C.-H.; Lin H.-I.; Chen C.-S.; Chen M.-L.; Wu R.-M.
臺大學術典藏	2021-06-01T07:03:25Z	Overexpression of heme oxygenase-1 protects dopaminergic neurons against 1-methyl-4-phenylpyridinium-induced neurotoxicity	Hung S.-Y.; Liou H.-C.; Kang K.-H.; Wu R.-M.; Wen C.-C.; WEN-MEI FU
臺大學術典藏	2021-06-01T07:03:19Z	Increase of oxidative stress by a novel PINK1 mutation, P209A	Chien W.-L.; Lee T.-R.; Hung S.-Y.; Kang K.-H.; Wu R.-M.; Lee M.-J.; WEN-MEI FU
臺大學術典藏	2021-05-26T03:35:59Z	Current role of surgery in the management of pleuropulmonary tuberculosis.	Lee Y.C.; Luh S.P.; Wu R.M.; Lin T.P.; KWEN-TAY LUH
臺大學術典藏	2021-04-29T02:21:10Z	Mystery Case: Hemiballism in a patient with parietal lobe infarction	MENG-CHEN WU; Yen R.-F.; Lin C.-H.; Wu R.-M.; Nita D.A.
臺大學術典藏	2021-03-18T05:59:14Z	Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism	Lee M.-J.; Mata I.F.; Lin C.-H.; KAI-YUAN TZEN; Lincoln S.J.; Bounds R.; Lockhart P.J.; Hulihan M.M.; Farrer M.J.; Wu R.-M.
臺大學術典藏	2021-03-18T05:59:14Z	LRRK2 mutation in familial Parkinson's disease in a Taiwanese population: Clinical, PET, and functional studies	Lin C.-H.; KAI-YUAN TZEN; Yu C.-Y.; Tai C.-H.; Farrer M.J.; Wu R.-M.

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