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Showing items 211-220 of 367  (37 Page(s) Totally)
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Institution Date Title Author
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

Showing items 211-220 of 367  (37 Page(s) Totally)
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View [10|25|50] records per page