臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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Institution	Date	Title	Author
臺大學術典藏	2020-12-04T07:44:49Z	Spironolactone is associated with reduced risk of new-onset atrial fibrillation in patients receiving renal replacement therapy	Chen P.-C.; Chung Y.-W.; Yang Y.-H.; Wu C.-K.; Yu C.-C.; Juang J.-M.J.; Wang Y.-C.; Tsai C.-T.; LIAN-YU LIN; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L.
臺大學術典藏	2020-12-04T07:44:48Z	Myocardial Regional Interstitial Fibrosis is Associated with Left Intra-Ventricular Dyssynchrony in Patients with Heart Failure: A Cardiovascular Magnetic Resonance Study	LIAN-YU LIN; Wu C.-K.; Juang J.-M.J.; Wang Y.-C.; Su M.-Y.M.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Tseng W.-Y.I.; Lin J.-L.
臺大學術典藏	2020-12-04T07:44:40Z	Comparisons of clinical impacts on individuals with Brugada electrocardiographic patterns defined by ISHNE criteria or EHRA/HRS/APHRS criteria: a nationwide community-based study	Chen C.-Y.J.; Juang J.-M.J.; Chen Y.-H.; Wu I.-C.; Hsu C.-C.; Wu R.-C.; Chen K.-C.; Liaw W.-J.; Tsai T.-L.; LIAN-YU LIN; Hwang J.-J.; Ho L.-T.; Yu C.-C.; Lee J.-K.; Wu C.-K.; Yeh S.-F.S.; Yang D.-H.; Chang I.-S.; Lai L.-P.; Chiang F.-T.; Lin J.-L.; Hsiung C.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	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.
臺大學術典藏	2020-12-04T04:19:11Z	Predictors of therapeutic response to beta-blockers in patients with heart failure in Taiwan	Hu H.; Jui H.-Y.; Hu F.-C.; Chen Y.-H.; Lai L.-P.; CHII-MING LEE
臺大學術典藏	2020-12-02T11:04:49Z	Renin-angiotensin system gene polymorphisms and diastolic heart failure	CHO-KAI WU; Tsai C.-T.; Hwang J.-J.; Luo J.-L.; Juang J.J.-M.; Hsu K.-L.; Lai L.-P.; Lin J.-L.; Tseng C.-D.; Chiang F.-T.
臺大學術典藏	2020-12-02T11:04:47Z	Increased Expression of Mineralocorticoid Receptor in Human Atrial Fibrillation and a Cellular Model of Atrial Fibrillation	Tsai C.-T.; Chiang F.-T.; Tseng C.-D.; Hwang J.-J.; Kuo K.-T.; CHO-KAI WU; Yu C.-C.; Wang Y.-C.; Lai L.-P.; Lin J.-L.
臺大學術典藏	2020-12-02T11:04:45Z	Significant Association of rs13376333 in KCNN3 on Chromosome 1q21 with Atrial Fibrillation in a Taiwanese Population	Chang S.-H.; Hwang J.-J.; Chiang F.-T.; Tseng C.-D.; Lai L.-P.; Lin J.-L.; CHO-KAI WU; Tsai C.-T.

Showing items 496-505 of 727 (73 Page(s) Totally)
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