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機構 日期 題名 作者
臺大學術典藏 2020-12-28T10:02:41Z 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.; CHIH-CHIEH YU; 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 2020-12-28T09:31:24Z Neurocognitive improvement after carotid artery stenting in patients with chronic internal carotid artery occlusion and cerebral ischemia Huang C.-C.; Wu Y.-W.; Chiu M.-J.; Lin M.-S.; Chao C.-C.; YING-HSIEN CHEN; 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 2020-12-28T07:56:58Z 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) JYH-MING JIMMY JUANG; Chiang F.-T.; Hsieh F.-J.; Su Y.-N.; Lai L.-P.; Lin J.-L.; Huang S.K.S.; Lo H.-M.; Wu M.-H.; Lin T.-K.; 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.
臺大學術典藏 2020-12-28T07:56:52Z Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations Lo L.-W.; Tsai C.-T.; Liu Y.-B.; Yu C.-C.; Chiu W.-Y.; Yeh H.-M.; Chen C.-Y.; JYH-MING JIMMY JUANG; Yeh S.-F.S.; Lai L.-P.
臺大學術典藏 2020-12-28T07:56:52Z Prevalence of atrial fibrillation in patients with brugada syndrome in Taiwan Chen W.-J.; Lin L.-Y.; Liu Y.B.; Chen C.-Y.; JYH-MING JIMMY JUANG; Lai L.-P.; Tsai C.-T.; Lin J.-L.
臺大學術典藏 2020-12-28T07:56:41Z 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 Liu Y.-B.; Lin L.-Y.; Lu T.-P.; Chen C.-Y.J.; 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 2020-12-28T07:56:37Z GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death Huang H.-C.; Yu C.-C.; Ho L.-T.; Liu Y.-B.; Lin L.-Y.; Chen W.-J.; Hwang J.-J.; JYH-MING JIMMY JUANG; Binda A.; Lee S.-J.; Chen C.-Y.J.; Lu T.-P.; Lai L.-C.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Antzelevitch C.
臺大學術典藏 2020-12-28T07:15:35Z An eight-week, multicenter, randomized, double-blind study to evaluate the efficacy and tolerability of fixed-dose amlodipine/benazepril combination in comparison with amlodipine as first-line therapy in Chinese patients with mild to moderate hypertension Lin T.-H.; PO-YUAN CHANG; Su H.-M.; Liu Y.-B.; Lin M.-C.; Voon W.-C.; Lin L.-C.; Ueng K.-C.; Chen W.-L.; Wu C.-C.; Lai W.-T.; Lin C.-S.
臺大學術典藏 2020-12-28T06:26:05Z Alterations in ultrasonic backscatter during intra-aortic balloon counterpulsation support in patients with acute myocardial infarction HSIEN-LI KAO; Ho Y.-L.; Lin L.-C.; Wu C.-C.; Liu Y.-B.; Lee Y.-T.
臺大學術典藏 2020-12-28T06:25:53Z Neurocognitive improvement after carotid artery stenting in patients with chronic internal carotid artery occlusion and cerebral ischemia Tseng W.-Y.I.; Chao C.-L.; Liu Y.-B.; Lin L.-C.; Chen Y.-F.; Lin M.-S.; Chiu M.-J.; Wu Y.-W.; Huang C.-C.; Chao C.-C.; Chen Y.-H.; Lin H.-J.; Li H.-Y.; Chen M.-F.; HSIEN-LI KAO

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