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机构 日期 题名 作者
臺大學術典藏 2020-12-04T07:45:01Z Prevalence of atrial fibrillation in patients with brugada syndrome in Taiwan Juang J.-M.J.; Chen C.-Y.; Liu Y.B.; LIAN-YU LIN; Chen W.-J.; Lai L.-P.; Tsai C.-T.; Lin J.-L.
臺大學術典藏 2020-12-04T07:44:59Z A new method to estimate the amplitude spectrum analysis of ventricular fibrillation during cardiopulmonary resuscitation Lo M.-T.; LIAN-YU LIN; Hsieh W.-H.; Ko P.C.I.; Liu Y.-B.; Lin C.; Chang Y.-C.; Wang C.-Y.; Young V.H.W.; Chiang W.-C.; Lin J.-L.; Chen W.-J.; Ma M.H.M.
臺大學術典藏 2020-12-04T07:44:55Z 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.; LIAN-YU LIN; 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.
臺大學術典藏 2020-12-04T07:44:54Z Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan Juang J.M.J.; Tsai C.-T.; LIAN-YU LIN; 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 2020-12-04T07:44:54Z 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.; LIAN-YU LIN; 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 2020-12-04T07:44:45Z 2016 Guidelines of the Taiwan Heart Rhythm Society and the Taiwan Society of Cardiology for the management of atrial fibrillation 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.; Tsai C.-T.; Liu Y.-B.; Lee K.-T.; Lin L.-J.; LIAN-YU LIN; Wang K.-L.; Chen Y.-J.; Chen M.-C.; Cheng C.-C.; Wen M.-S.; 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 2020-12-04T07:44:36Z 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.; LIAN-YU LIN; 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 2020-12-04T07:44:31Z Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry Yang D.-H.; Lin J.-L.; Lu T.-P.; Chuang E.Y.; Ackerman M.J.; Jyh-Ming J.-J.; Liu Y.-B.; Julius Chen C.-Y.; Yu Q.-Y.; Chattopadhyay A.; LIAN-YU LIN; 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.
臺大學術典藏 2020-12-04T07:44:29Z Increases in repolarization heterogeneity predict left ventricular systolic dysfunction and response to cardiac resynchronization therapy in patients with left bundle branch block Huang H.-C.; Chien K.-L.; Chang Y.-C.; LIAN-YU LIN; Wang J.; Liu Y.-B.
臺大學術典藏 2020-12-04T07:44:29Z 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.; LIAN-YU LIN; 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.

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