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Showing items 401-410 of 727  (73 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2020-12-28T12:03:20Z The effect and molecular mechanism of statins on the expression of human anti-coagulation genes HWANG, JUEY-JEN; Tsai C.-T.; Chang S.-N.; Wu C.-K.; Lai L.-P.; Chiang F.-T.
臺大學術典藏 2020-12-28T12:03:19Z Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry Lin J.-L.; Yang D.-H.; Chuang J.-Y.; Sherri Yeh S.-F.; Chen J.-J.; Liao M.-T.; 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, JUEY-JEN; Lin T.-T.; Lu T.-P.; Chuang E.Y.; Ackerman M.J.
臺大學術典藏 2020-12-28T12:03:16Z GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death Antzelevitch C.; Rivolta I.; Chuang E.Y.; Lai L.-P.; Yeh S.-F.S.; Lai L.-C.; Lu T.-P.; Huang H.-C.; Chen C.-Y.J.; Ho L.-T.; Yu C.-C.; Lin L.-Y.; Liu Y.-B.; Juang J.-M.J.; Binda A.; Lee S.-J.; HWANG, JUEY-JEN; Chen W.-J.
臺大學術典藏 2020-12-28T10:52:56Z 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.; HUI-CHUN HUANG; 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 2020-12-28T10:52:55Z Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry Liu Y.-B.; Jyh-Ming J.-J.; Julius Chen C.-Y.; Yu Q.-Y.; Chattopadhyay A.; Lin L.-Y.; Chen W.-J.; Yu C.-C.; HUI-CHUN HUANG; 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.
臺大學術典藏 2020-12-28T10:52:54Z GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death Binda A.; Juang J.-M.J.; Lee S.-J.; Hwang J.-J.; Chen W.-J.; Liu Y.-B.; Lin L.-Y.; Yu C.-C.; Ho L.-T.; HUI-CHUN HUANG; 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 2020-12-28T10:02:50Z Proximal common pathway in the circuit of atrioventricular nodal reentrant tachycardia. CHIH-CHIEH YU; Lai L.P.; Lin J.L.
臺大學術典藏 2020-12-28T10:02:49Z Arrhythmogenic right ventricular dysplasia: Clinical characteristics and identification of novel desmosome gene mutations Yang C.-T.; Juang J.-M.; Hwang J.-J.; Lin J.-L.; Lai L.-P.; CHIH-CHIEH YU; Yu C.-H.; Hsueh C.-H.
臺大學術典藏 2020-12-28T10:02:49Z Successful radiofrequency catheter ablation of idiopathic ventricular fibrillation presented as recurrent syncope and diagnosed by an implanted loop recorder CHIH-CHIEH YU; Tsai C.-T.; Lai L.-P.; Lin J.-L.
臺大學術典藏 2020-12-28T10:02:49Z Provocation of Masked Left Ventricular Mechanical Dyssynchrony by Treadmill Exercise in Patients With Systolic Heart Failure and Narrow QRS Complex Lin J.-L.; Katra R.; Lin L.-C.; Tsai C.-T.; Wang Y.-C.; Hwang J.-J.; CHIH-CHIEH YU; Lai L.-P.

Showing items 401-410 of 727  (73 Page(s) Totally)
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