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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
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Showing items 201-225 of 367  (15 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2020-12-01T07:10:36Z Traumatic tricuspid regurgitation complicating endocarditis and right-to-left intracardiac shunt. A case report of successful operation Liu Y.-B.; YI-LWUN HO; Lin F.-Y.; Lee Y.-T.
臺大學術典藏 2020-12-01T07:10:35Z Alterations in ultrasonic backscatter during intra-aortic balloon counterpulsation support in patients with acute myocardial infarction Liu Y.-B.;Wu C.-C.;Lin L.-C.;Yi-Lwun Ho;Kao H.-L.;Lee Y.-T.; Liu Y.-B.; Wu C.-C.; Lin L.-C.; YI-LWUN HO; Kao H.-L.; Lee Y.-T.
臺大學術典藏 2020-12-01T07:10:34Z Derangement of heart rate variability during a catastrophic earthquake: A possible mechanism for increased heart attacks Lin L.-Y.;Wu C.-C.;Liu Y.-B.;Yi-Lwun Ho;Liau C.-S.;Lee Y.-T.; Lin L.-Y.; Wu C.-C.; Liu Y.-B.; YI-LWUN HO; Liau C.-S.; Lee Y.-T.
臺大學術典藏 2020-12-01T07:10:34Z Ultrasonic tissue characterization with integrated backscatter during inotropic stimulation Wu C.-C.;Liu Y.-B.;Lin L.-C.;Yi-Lwun Ho;Liau C.-S.;Lee Y.-T.; Wu C.-C.; Liu Y.-B.; Lin L.-C.; YI-LWUN HO; Liau C.-S.; Lee Y.-T.
臺大學術典藏 2020-12-01T07:10:31Z 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.;Chiang F.-T.;Juang J.-M.;Liu Y.-B.;Yi-Lwun Ho;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.; Chiang F.-T.; Juang J.-M.; Liu Y.-B.; YI-LWUN HO; 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 2020-12-01T07:10:28Z 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.;Chiang F.-T.;Juang J.-M.;Liu Y.-B.;Yi-Lwun Ho;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.; Hsieh F.-J.; Chiang F.-T.; Juang J.-M.; Liu Y.-B.; YI-LWUN HO; 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 2020-12-01T07:10:26Z Management of patients with implantable cardioverter defibrillators at emergency departments Liu C.-P.; YI-LWUN HO; Lin Y.-H.; Liu Y.-B.; Chang W.-T.; Huang C.-H.; Chen W.-J.
臺大學術典藏 2020-12-01T07:10:20Z The immediate effects of pacemaker-related electric remodelling on left ventricular function in patients with sick sinus syndrome Wang Y.-C.; Lin Y.-H.; Liu Y.-B.; Lee J.-K.; Chen Y.-S.; Lee H.-H.; Lin L.-C.; YI-LWUN HO; Chen W.-J.
臺大學術典藏 2020-11-25T07:22:53Z 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; Chiang, F-T; Lin, J-L; Lai, L-P; Horie, M
臺大學術典藏 2020-11-17T02:45:34Z Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome Lin J.-L.; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Hwang J.-J.; Juang J.-M.J.;Tzu-Pin Lu;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.;Chen W.-P.;Chuang E.Y.;Lai L.-P.;Lin J.-L.; Juang J.-M.J.; TZU-PIN LU; Lai L.-C.; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.
臺大學術典藏 2020-11-17T02:45:33Z Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome Chuang E.Y.; Lin J.-L.; Juang J.-M.J.;Tzu-Pin Lu;Lai L.-C.;Ho C.-C.;Liu Y.-B.;Tsai C.-T.;Lin L.-Y.;Yu C.-C.;Chen W.-J.;Chiang F.-T.;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Lin J.-L.; Juang J.-M.J.; TZU-PIN LU; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Chen W.-J.; Chiang F.-T.; Yeh S.-F.S.; Lai L.-P.
臺大學術典藏 2020-11-17T02:45:22Z 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.;Tzu-Pin Lu;Lin L.-Y.;Liu Y.-B.;Ho L.-T.;Huang H.-C.;Lai L.-P.;Hwang J.-J.;Yeh S.-F.S.;Wu C.-K.;Juang J.-M.J.;Antzelevitch C.; Chen C.-Y.J.; TZU-PIN LU; Lin L.-Y.; Liu Y.-B.; Ho L.-T.; Huang H.-C.; Lai L.-P.; Hwang J.-J.; Yeh S.-F.S.; Wu C.-K.; Juang J.-M.J.; Antzelevitch C.
臺大學術典藏 2020-11-17T02:45:19Z 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.; TZU-PIN LU; Chuang E.Y.; Ackerman M.J.
臺大學術典藏 2020-11-03T12:37:38Z Real-World Rivaroxaban and Apixaban Levels in Asian Patients With Atrial Fibrillation Jeng J.-S.; Tang S.-C.; Huang C.-F.; Liu Y.-B.; LI-KAI TSAI; Yeh S.-J.; Kuo C.-H.; Lin S.-Y.; Lin S.-Y.;Kuo C.-H.;Yeh S.-J.;Li-Kai Tsai;Liu Y.-B.;Huang C.-F.;Tang S.-C.;Jeng J.-S.
臺大學術典藏 2020-11-03T11:57:12Z Neurocognitive improvement after carotid artery stenting in patients with chronic internal carotid artery occlusion and cerebral ischemia Lin M.-S. ;Ming-Jang Chiu ;Wu Y.-W. ;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.; Lin M.-S.; MING-JANG CHIU; Wu Y.-W.; 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 2020-11-03T11:07:55Z Real-World Rivaroxaban and Apixaban Levels in Asian Patients With Atrial Fibrillation Lin S.-Y.;Kuo C.-H.;Yeh S.-J.;Tsai L.-K.;Liu Y.-B.;Huang C.-F.;Sung-Chun Tang;Jeng J.-S.; Lin S.-Y.; Kuo C.-H.; Yeh S.-J.; Tsai L.-K.; Liu Y.-B.; Huang C.-F.; SUNG-CHUN TANG; Jeng J.-S.
臺大學術典藏 2020-10-26T11:34:49Z 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.; Wu M.-H.; Lin T.-K.; Chen S.-A.; Lei M.-H.; Tsao H.-M.; Wu T.-J.; Ueng K.-C.; JYH-MING JIMMY JUANG; Su Y.-N.; Chiang F.-T.; Lai L.-P.; Ko Y.-L.; Wang C.-C.; Chen W.-J.; Yeh S.-J.; Ho Y.-L.; Liu Y.-B.
臺大學術典藏 2020-10-26T11:34:47Z Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations Chen W.-P.; Hsueh C.-H.; Lin J.-L.; Tsai C.-T.; Liu Y.-B.; JYH-MING JIMMY JUANG; Tsao H.-M.; Su M.-J.; Lai L.-P.
臺大學術典藏 2020-10-26T11:34:44Z Prevalence of atrial fibrillation in patients with brugada syndrome in Taiwan Chen C.-Y.; JYH-MING JIMMY JUANG; Liu Y.B.; Lin L.-Y.; Chen W.-J.; Lai L.-P.; Tsai C.-T.; Lin J.-L.
臺大學術典藏 2020-10-26T11:34:43Z Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations Yeh S.-F.S.; Lai L.-P.; Lo L.-W.; Tsai C.-T.; Liu Y.-B.; Yu C.-C.; Chiu W.-Y.; Chen C.-Y.; Yeh H.-M.; JYH-MING JIMMY JUANG
臺大學術典藏 2020-10-26T11:34:42Z Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome Ho C.-C.; Lu T.-P.; Lai L.-C.; JYH-MING JIMMY JUANG; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Chen W.-J.; Chiang F.-T.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Lin J.-L.
臺大學術典藏 2020-10-26T11:34:41Z Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan Lai L.-P.; Lin J.-L.; Sherri Yeh S.-F.; Yeh H.-M.; Chiang F.-T.; Tseng C.-D.; Chen W.-J.; Chiu F.-C.; Chen J.-J.; JYH-MING JIMMY JUANG; Tsai C.-T.; Lin L.-Y.; Liu Y.-B.; Yu C.-C.; Hwang J.-J.
臺大學術典藏 2020-10-26T11:34:30Z 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 J.-J.; Yeh S.-F.S.; Wu C.-K.; JYH-MING JIMMY JUANG; Antzelevitch C.
臺大學術典藏 2020-10-26T11:34:27Z Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry SADS-TW BrS Registry; Stephen Huang S.K.; Hsu C.-T.; Lin L.-R.; Chen R.-Y.; Li P.-T.; Lin J.-Y.; Tsai T.-N.; Chen W.-D.; Luo J.-L.; Chen C.-Y.J.; JYH-MING JIMMY JUANG; Lin L.-Y.; Liu Y.-B.; LI-TING HO; 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.; Chiang F.-T.; 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.
臺大學術典藏 2020-10-26T11:34:25Z GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death JYH-MING JIMMY JUANG; 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.

Showing items 201-225 of 367  (15 Page(s) Totally)
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