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

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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
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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	2021-03-04T08:55:10Z	Reinforcement of patient education improved physicians’ adherence to guideline-recommended medical therapy after acute coronary syndrome	CHIH-KUO LEE; Lai C.-L.; Lee M.-H.; Su F.-Y.; Yeh T.-S.; Cheng L.-Y.; Hsieh M.-Y.; Wu Y.-W.; Liu Y.-B.; Wu C.-C.
臺大學術典藏	2021-01-15T02:46:27Z	Cardiac involvement of natural killer/T-cell lymphoma presenting with electrical storm after cardioverter-defibrillator implantation	Huang S.-H.; SONG-CHOU HSIEH; Ko B.-S.; Liu Y.-B.
臺大學術典藏	2021-01-06T06:51:38Z	Spatial repolarization heterogeneity detected by magnetocardiography correlates with cardiac iron overload and adverse cardiac events in beta-thalassemia major	Jou S.-T.; Yang Y.-L.; Chang H.-H.; Lin K.-H.; Peng S.-F.; Lu M.-Y.; CHUN-AN CHEN; Chun-An Chen;Lu M.-Y.;Peng S.-F.;Lin K.-H.;Chang H.-H.;Yang Y.-L.;Jou S.-T.;Lin D.-T.;Liu Y.-B.;Horng H.-E.;Yang H.-C.;Wang J.-K.;Wu M.-H.;Wu C.-C.; Lin D.-T.; Liu Y.-B.; Horng H.-E.; Yang H.-C.; Wang J.-K.; Wu M.-H.; Wu C.-C.
臺大學術典藏	2021-01-06T05:46:22Z	Spatial repolarization heterogeneity detected by magnetocardiography correlates with cardiac iron overload and adverse cardiac events in beta-thalassemia major	Chen C.-A.; Lu M.-Y.; Peng S.-F.; Lin K.-H.; Chang H.-H.; Yang Y.-L.; Jou S.-T.; Lin D.-T.; Liu Y.-B.; Horng H.-E.; Yang H.-C.; JOU-KOU WANG; Wu M.-H.; Wu C.-C.
臺大學術典藏	2021-01-06T03:39:03Z	Spatial repolarization heterogeneity detected by magnetocardiography correlates with cardiac iron overload and adverse cardiac events in beta-thalassemia major	Chen C.-A.; Lu M.-Y.; Peng S.-F.; Lin K.-H.; Chang H.-H.; YUNG-LI YANG; Jou S.-T.; Lin D.-T.; Liu Y.-B.; Horng H.-E.; Yang H.-C.; Wang J.-K.; Wu M.-H.; Wu C.-C.
臺大學術典藏	2021-01-05T08:07:44Z	Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms	Lo H.-M.; Huang S.K.S.; Lin J.-L.; Lai L.-P.;Su Y.-N.;Chiang F.-T.;Juang J.-M.;Liu Y.-B.;Ho Y.-L.;Chen W.-J.;Yeh S.-J.;Wang C.-C.;Ko Y.-L.;Wu T.-J.;Ueng K.-C.;Lei M.-H.;Tsao H.-M.;Chen S.-A.;Lin T.-K.;Mei-Hwan Wu;Lo H.-M.;Huang S.K.S.;Lin J.-L.; Lai L.-P.; Su Y.-N.; Chiang F.-T.; Juang J.-M.; Liu Y.-B.; Ho Y.-L.; Chen W.-J.; Yeh S.-J.; Wang C.-C.; Ko Y.-L.; Wu T.-J.; Ueng K.-C.; Lei M.-H.; Tsao H.-M.; Chen S.-A.; Lin T.-K.; MEI-HWAN WU
臺大學術典藏	2021-01-05T08:07:36Z	Erratum: Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms (Journal of Human Genetics (2005) 50 (490-496) DOI: 10.1007/s10038-005-0283-3)	Huang S.K.S.; Lo H.-M.; MEI-HWAN WU; Lin T.-K.; Chen S.-A.; Tsao H.-M.; Lei M.-H.; Lai L.-P.; Su Y.-N.; Hsieh F.-J.; Chiang F.-T.; Juang J.-M.; Liu Y.-B.; Ho Y.-L.; Chen W.-J.; Yeh S.-J.; Wang C.-C.; Ko Y.-L.; Wu T.-J.; Ueng K.-C.; Lin J.-L.
臺大學術典藏	2021-01-05T08:07:02Z	Spatial repolarization heterogeneity detected by magnetocardiography correlates with cardiac iron overload and adverse cardiac events in beta-thalassemia major	Chen C.-A.;Lu M.-Y.;Peng S.-F.;Lin K.-H.;Chang H.-H.;Yang Y.-L.;Jou S.-T.;Lin D.-T.;Liu Y.-B.;Horng H.-E.;Yang H.-C.;Wang J.-K.;Mei-Hwan Wu;Wu C.-C.; Chang H.-H.; Lin K.-H.; Peng S.-F.; Lu M.-Y.; Chen C.-A.; Yang Y.-L.; Jou S.-T.; Lin D.-T.; Liu Y.-B.; Horng H.-E.; Yang H.-C.; Wang J.-K.; MEI-HWAN WU; Wu C.-C.
臺大學術典藏	2021-01-05T02:28:53Z	Spatial repolarization heterogeneity detected by magnetocardiography correlates with cardiac iron overload and adverse cardiac events in beta-thalassemia major	Lu M.-Y.; Chen C.-A.; Wu C.-C.; Wu M.-H.; Wang J.-K.; Yang H.-C.; Horng H.-E.; Peng S.-F.; Lin K.-H.; Chang H.-H.; Yang Y.-L.; SHIANN-TANG JOU; Lin D.-T.; Liu Y.-B.
臺大學術典藏	2020-12-31T02:57:32Z	Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms	LING-PING LAI; Su Y.-N.; Chiang F.-T.; Juang J.-M.; Liu Y.-B.; Ho Y.-L.; Chen W.-J.; Yeh S.-J.; Wang C.-C.; Ko Y.-L.; Wu T.-J.; Ueng K.-C.; Lei M.-H.; Tsao H.-M.; Chen S.-A.; Lin T.-K.; Wu M.-H.; Lo H.-M.; Huang S.K.S.; Lin J.-L.
臺大學術典藏	2020-12-31T02:57:06Z	Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan	Juang J.M.J.; Tsai C.-T.; Lin L.-Y.; Liu Y.-B.; Yu C.-C.; Hwang J.-J.; Chen J.-J.; Chiu F.-C.; Chen W.-J.; Tseng C.-D.; Chiang F.-T.; Yeh H.-M.; Sherri Yeh S.-F.; LING-PING LAI; Lin J.-L.
臺大學術典藏	2020-12-30T08:47:47Z	Prevalence of atrial fibrillation in patients with brugada syndrome in Taiwan	Lin L.-Y.; Chen W.-J.; Lai L.-P.; CHIA-TI TSAI; Lin J.-L.; Juang J.-M.J.; Chen C.-Y.; Liu Y.B.
臺大學術典藏	2020-12-30T08:47:45Z	Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations	Juang J.-M.J.; Chen C.-Y.; Yeh H.-M.; Chiu W.-Y.; Yu C.-C.; Liu Y.-B.; CHIA-TI TSAI; Lo L.-W.; Yeh S.-F.S.; Lai L.-P.
臺大學術典藏	2020-12-30T08:47:44Z	Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome	Chiang F.-T.; Hwang J.-J.; Lin L.-Y.; Yu C.-C.; CHIA-TI TSAI; Liu Y.-B.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L.
臺大學術典藏	2020-12-30T08:47:43Z	Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome	Lin J.-L.; Chuang E.Y.; Lai L.-P.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Ho C.-C.; Liu Y.-B.; CHIA-TI TSAI; Lin L.-Y.; Yu C.-C.; Chen W.-J.; Chiang F.-T.; Yeh S.-F.S.
臺大學術典藏	2020-12-30T08:47:42Z	Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan	Juang J.M.J.; CHIA-TI TSAI; Lin L.-Y.; Liu Y.-B.; Yu C.-C.; Hwang J.-J.; Chen J.-J.; Chiu F.-C.; Chen W.-J.; Tseng C.-D.; Chiang F.-T.; Yeh H.-M.; Sherri Yeh S.-F.; Lai L.-P.; Lin J.-L.
臺大學術典藏	2020-12-30T08:47:37Z	2016 Guidelines of the Taiwan Heart Rhythm Society and the Taiwan Society of Cardiology for the management of atrial fibrillation	Wen M.-S.; Cheng C.-C.; Chen Y.-J.; Chen M.-C.; Wang K.-L.; Lin L.-Y.; Chiang C.-E.; Wu T.-J.; Ueng K.-C.; Chao T.-F.; Chang K.-C.; Wang C.-C.; Lin Y.-J.; Yin W.-H.; Kuo J.-Y.; Lin W.-S.; CHIA-TI TSAI; Liu Y.-B.; Lee K.-T.; Lin L.-J.; Chen W.-J.; Chen J.-H.; Lai W.-T.; Chiou C.-W.; Lin J.-L.; Yeh S.-J.; Chen S.-A.
臺大學術典藏	2020-12-30T07:20:34Z	Neurocognitive improvement after carotid artery stenting in patients with chronic internal carotid artery occlusion and cerebral ischemia	Lin M.-S.; Chiu M.-J.; Wu Y.-W.; CHING-CHANG HUANG; Chao C.-C.; Chen Y.-H.; Lin H.-J.; Li H.-Y.; Chen Y.-F.; Lin L.-C.; Liu Y.-B.; Chao C.-L.; Tseng W.-Y.I.; Chen M.-F.; Kao H.-L.
臺大學術典藏	2020-12-28T12:04:03Z	Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome	Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; HWANG, JUEY-JEN; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L.
臺大學術典藏	2020-12-28T12:04:00Z	Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan	Juang J.M.J.; Tsai C.-T.; Lin L.-Y.; Liu Y.-B.; Yu C.-C.; HWANG, JUEY-JEN; Chen J.-J.; Chiu F.-C.; Chen W.-J.; Tseng C.-D.; Chiang F.-T.; Yeh H.-M.; Sherri Yeh S.-F.; Lai L.-P.; Lin J.-L.
臺大學術典藏	2020-12-28T12:03:29Z	Impact of ancestral differences and reassessment of the classification of previously reported pathogenic variants in patients with brugada syndrome in the genomic era: A SADS-TW BrS registry	Chen C.-Y.J.; Lu T.-P.; Lin L.-Y.; Liu Y.-B.; Ho L.-T.; Huang H.-C.; Lai L.-P.; HWANG, JUEY-JEN; Yeh S.-F.S.; Wu C.-K.; Juang J.-M.J.; Antzelevitch C.
臺大學術典藏	2020-12-28T12:03:27Z	Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry	Li C.-H.; Hsieh Y.-C.; Chua S.-K.; Lin M.-T.; Chiu S.-N.; Liu J.-F.; Hsia C.-P.; Chiang M.-C.; Lo H.-M.; Chang C.-J.; Chang K.-C.; Feng A.-N.; Lin Y.-J.; Ueng K.-C.; Tsao H.-M.; Huang J.-L.; Tsai W.-C.; Tsai C.-F.; Chang S.-L.; Lo L.-W.; Hu Y.-F.; Chung F.-P.; Chen C.-Y.J.; Juang J.-M.J.; Lin L.-Y.; Liu Y.-B.; Ho L.-T.; Yu C.-C.; Huang H.-C.; Lin T.-T.; Liao M.-C.; Chen J.-J.; HWANG, JUEY-JEN; Chen W.-J.; Yeh S.-F.S.; Yang D.-H.; Chiang F.-T.; Lin J.-L.; Lai L.-P.; Horie M.; Wu M.-H.; Wu T.-J.; Chen S.-A.; Wang C.-C.; Li P.-T.; Stephen Huang S.K.; SADS-TW BrS Registry; Liao Y.-C.; Lin H.-H.; Liu Z.-Z.; Ye G.-H.; Chiu W.-R.; Chang J.-R.; Feng W.-J.; Chang S.-X.; Lei M.-H.; Ko W.-C.; Kong C.-W.; Kuo C.-T.; Huang B.-X.; Li K.-T.; Chen W.-D.; Luo J.-L.; Lin J.-Y.; Tsai T.-N.; Hsu C.-T.; Lin L.-R.; Chen R.-Y.
臺大學術典藏	2020-12-28T12:03:19Z	Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry	Lin J.-L.; Yang D.-H.; Chuang J.-Y.; Sherri Yeh S.-F.; Chen J.-J.; Liao M.-T.; Jyh-Ming J.-J.; Liu Y.-B.; Julius Chen C.-Y.; Yu Q.-Y.; Chattopadhyay A.; Lin L.-Y.; Chen W.-J.; Yu C.-C.; Huang H.-C.; Ho L.-T.; Lai L.-P.; HWANG, JUEY-JEN; Lin T.-T.; Lu T.-P.; Chuang E.Y.; Ackerman M.J.
臺大學術典藏	2020-12-28T12:03:16Z	GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death	Antzelevitch C.; Rivolta I.; Chuang E.Y.; Lai L.-P.; Yeh S.-F.S.; Lai L.-C.; Lu T.-P.; Huang H.-C.; Chen C.-Y.J.; Ho L.-T.; Yu C.-C.; Lin L.-Y.; Liu Y.-B.; Juang J.-M.J.; Binda A.; Lee S.-J.; HWANG, JUEY-JEN; Chen W.-J.
臺大學術典藏	2020-12-28T10:52:58Z	Two-dimensional propagation of magnetocardiac T wave signals for characterizing myocardial ischemia	Lee Y.H.; Pan Y.F.; Wu C.C.; HUI-CHUN HUANG; Liu Y.B.; Lin L.C.; Lin L.Y.; Chen M.F.; Tsai M.C.; Gao Y.L.; Yang S.Y.; Horng H.E.; Yang H.C.; Tseng W.K.; Lee T.L.; Hsuan C.F.

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