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機構 日期 題名 作者
臺大學術典藏 2021-05-31T06:18:13Z Dietary cholesterol affects sympathetic nerve function in rabbit hearts Luo T.-Y.; Wu C.-C.; Liu Y.-B.; Fu Y.-K.; MING-JAI SU
臺大學術典藏 2021-05-31T06:18:12Z Effect of hypercholesterolemia on myocardial function in New Zealand white rabbits Luo T.-Y.; MING-JAI SU; Yang Y.-F.; Liu Y.-B.; Liang H.-C.; Wu C.-C.; Lee Y.-T.
臺大學術典藏 2021-05-31T06:18:10Z Optical mapping of myocardial reactive oxygen species production throughout the reperfusion of global ischemia Lu L.-S.; Liu Y.-B.; Sun C.-W.; Lin L.-C.; MING-JAI SU; Wu C.-C.
臺大學術典藏 2021-05-31T06:18:06Z Functional studies on three novel HCNH2 mutations in Taiwan: Identification of distinct mechanisms of channel defect and dissociation between glycosylation defect and assembly defect Hsueh C.-H.; Chen W.-P.; Lin J.-L.; Liu Y.-B.; MING-JAI SU; Lai L.-P.
臺大學術典藏 2021-05-31T06:18:05Z Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations Hsueh C.-H.; Chen W.-P.; Lin J.-L.; Tsai C.-T.; Liu Y.-B.; Juang J.-M.; Tsao H.-M.; MING-JAI SU; Lai L.-P.
臺大學術典藏 2021-04-15T07:52:48Z Functional studies on three novel HCNH2 mutations in Taiwan: Identification of distinct mechanisms of channel defect and dissociation between glycosylation defect and assembly defect Hsueh C.-H.; WEN-PIN CHEN; Lin J.-L.; Liu Y.-B.; Su M.-J.; Lai L.-P.
臺大學術典藏 2021-04-15T07:52:45Z Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations Hsueh C.-H.; WEN-PIN CHEN; Lin J.-L.; Tsai C.-T.; Liu Y.-B.; Juang J.-M.; Tsao H.-M.; Su M.-J.; Lai L.-P.
臺大學術典藏 2021-04-15T07:52:33Z 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 J.-J.; Chiang F.-T.; Yeh S.S.-F.; WEN-PIN CHEN; Chuang E.Y.; Lai L.-P.; Lin J.-L.
臺大學術典藏 2021-03-29T06:08:22Z GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death Juang, J.-M.J.; Binda, A.; Lee, S.-J.; Hwang, J.-J.; Chen, W.-J.; Liu, Y.-B.; Lin, L.-Y.; Yu, C.-C.; Ho, L.-T.; Huang, H.-C.; Chen, C.-Y.J.; Lu, T.-P.; Lai, L.-C.; Yeh, S.-F.S.; Lai, L.-P.; Chuang, E.Y.; Rivolta, I.; Antzelevitch, C.; ERIC YAO-YU CHUANG
臺大學術典藏 2021-03-29T06:08:19Z Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry 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, J.-J.; Lin, T.-T.; Liao, M.-T.; Chen, J.-J.; Sherri Yeh, S.-F.; Chuang, J.-Y.; Yang, D.-H.; Lin, J.-L.; Lu, T.-P.; Chuang, E.Y.; Ackerman, M.J.; ERIC YAO-YU CHUANG
臺大學術典藏 2021-03-18T08:54:52Z Extensive scar myocardium in hypertrophic cardiomyopathy with severe myocardial bridge Cheng M.-F.; YEN-WEN WU; Liu Y.-B.; Huang P.-J.; Tzen K.-Y.; Yen R.-F.
臺大學術典藏 2021-03-18T08:54:38Z Neurocognitive improvement after carotid artery stenting in patients with chronic internal carotid artery occlusion and cerebral ischemia Lin M.-S.; Chiu M.-J.; YEN-WEN WU; Huang C.-C.; 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 2021-03-18T08:54:33Z Usefulness of magnetocardiography to detect coronary artery disease and cardiac allograft vasculopathy YEN-WEN WU; Lee C.-M.; Liu Y.-B.; Wang S.-S.; Huang H.-C.; Tseng W.-K.; Jui H.-Y.; Wang S.-Y.; Horng H.-E.; Yang H.-C.; Wu C.-C.
臺大學術典藏 2021-03-18T08:54:32Z QTcheterogeneity in rest magnetocardiography is sensitive to detect coronary artery disease: In comparison with stress myocardial perfusion imaging YEN-WEN WU; Lin L.-C.; Tseng W.-K.; Liu Y.-B.; Kao H.-L.; Lin M.-S.; Huang H.-C.; Wang S.-Y.; Horng H.-E.; Yang H.-C.; Wu C.-C.
臺大學術典藏 2021-03-18T08:54:07Z Reinforcement of patient education improved physicians’ adherence to guideline-recommended medical therapy after acute coronary syndrome Lee C.-K.; Lai C.-L.; Lee M.-H.; Su F.-Y.; Yeh T.-S.; Cheng L.-Y.; Hsieh M.-Y.; YEN-WEN WU; Liu Y.-B.; Wu C.-C.
臺大學術典藏 2021-03-18T08:54:04Z Outcomes associated with amiodarone and lidocaine for the treatment of adult in-hospital cardiac arrest with shock-refractory pulseless ventricular tachyarrhythmia Wang C.-H.; Chang W.-T.; Huang C.-H.; Tsai M.-S.; Yu P.-H.; YEN-WEN WU; Liu Y.-B.; Chen W.-J.
臺大學術典藏 2021-03-18T05:59:16Z Extensive scar myocardium in hypertrophic cardiomyopathy with severe myocardial bridge Cheng M.-F.; Wu Y.-W.; Liu Y.-B.; Huang P.-J.; KAI-YUAN TZEN; Yen R.-F.
臺大學術典藏 2021-03-11T04:30:27Z 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 Lai L.-P.;Su Y.-N.;Fu-Tien Chiang;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.; Lai L.-P.; Su Y.-N.; FU-TIEN CHIANG; 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 2021-03-11T04:30:27Z The effect of iron stores on corrected QT dispersion in patients undergoing peritoneal dialysis Wu V.-C.;Huang J.-W.;Wu M.-S.;Chin C.-Y.;Fu-Tien Chiang;Liu Y.-B.;Wu K.-D.; Wu V.-C.; Huang J.-W.; Wu M.-S.; Chin C.-Y.; FU-TIEN CHIANG; Liu Y.-B.; Wu K.-D.
臺大學術典藏 2021-03-11T04:30:23Z 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) Lai L.-P.; Su Y.-N.; Hsieh F.-J.; FU-TIEN CHIANG; 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 2021-03-11T04:29:40Z 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 J.-J.;Fu-Tien Chiang;Yeh S.S.-F.;Chen W.-P.;Chuang E.Y.;Lai L.-P.;Lin J.-L.; 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 J.-J.; FU-TIEN CHIANG; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L.
臺大學術典藏 2021-03-11T04:29:38Z Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome Juang J.-M.J.;Lu T.-P.;Lai L.-C.;Ho C.-C.;Liu Y.-B.;Tsai C.-T.;Lin L.-Y.;Yu C.-C.;Chen W.-J.;Fu-Tien Chiang;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Lin J.-L.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Chen W.-J.; FU-TIEN CHIANG; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Lin J.-L.
臺大學術典藏 2021-03-11T04:29:37Z 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.;Fu-Tien Chiang;Yeh H.-M.;Sherri Yeh S.-F.;Lai L.-P.;Lin J.-L.; 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.; FU-TIEN CHIANG; Yeh H.-M.; Sherri Yeh S.-F.; Lai L.-P.; Lin J.-L.
臺大學術典藏 2021-03-11T04:29:15Z Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry 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 J.-J.;Chen W.-J.;Yeh S.-F.S.;Yang D.-H.;Fu-Tien Chiang;Lin J.-L.;Lai L.-P.;Horie M.;Wu M.-H.;Wu T.-J.;Chen S.-A.;Wang C.-C.;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.;Chang C.-J.;Lo H.-M.;Chiang M.-C.;Hsia C.-P.;Liu J.-F.;Chiu S.-N.;Lin M.-T.;Chua S.-K.;Hsieh Y.-C.;Li C.-H.;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.;Li P.-T.;Stephen Huang S.K.;Sads-Tw Brs Registry; 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 J.-J.; Chen W.-J.; Yeh S.-F.S.; Yang D.-H.; FU-TIEN CHIANG; Lin J.-L.; Lai L.-P.; Horie M.; Wu M.-H.; Wu T.-J.; Chen S.-A.; Wang C.-C.; 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.; Chang C.-J.; Lo H.-M.; Chiang M.-C.; Hsia C.-P.; Liu J.-F.; Chiu S.-N.; Lin M.-T.; Chua S.-K.; Hsieh Y.-C.; Li C.-H.; 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.; Li P.-T.; Stephen Huang S.K.; SADS-TW BrS Registry
臺大學術典藏 2021-03-08T06:51:49Z GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death Juang J.-M.J.;Binda A.;Lee S.-J.;Hwang J.-J.;Chen W.-J.;Liu Y.-B.;Lin L.-Y.;Yu C.-C.;Ho L.-T.;Huang H.-C.;Chen C.-Y.J.;Lu T.-P.;Liang-Chuan Lai;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Rivolta I.;Antzelevitch C.; Juang J.-M.J.; Binda A.; Lee S.-J.; Hwang J.-J.; Chen W.-J.; Liu Y.-B.; Lin L.-Y.; Yu C.-C.; Ho L.-T.; Huang H.-C.; Chen C.-Y.J.; Lu T.-P.; Liang-Chuan Lai; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Antzelevitch C.

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