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Showing items 51-60 of 212  (22 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2021-09-17T05:40:30Z Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry Chen C.-Y.J.; Juang J.-M.J.; Lin L.-Y.; Liu Y.-B.; Ho L.-T.; Yu C.-C.; Huang H.-C.; Lin T.-T.; Liao M.-C.; Chen J.-J.; Hwang J.-J.; Chen W.-J.; Yeh S.-F.S.; Yang D.-H.; Chiang F.-T.; Lin J.-L.; Lai L.-P.; Horie M.; Wu M.-H.; Wu T.-J.; Chen S.-A.; Wang C.-C.; Chang K.-C.; Feng A.-N.; Lin Y.-J.; Ueng K.-C.; Tsao H.-M.; Huang J.-L.; Tsai W.-C.; Tsai C.-F.; Chang S.-L.; Lo L.-W.; Hu Y.-F.; Chung F.-P.; Chang C.-J.; Lo H.-M.; Chiang M.-C.; Hsia C.-P.; Liu J.-F.; SHUENN-NAN CHIU; Lin M.-T.; Chua S.-K.; Hsieh Y.-C.; Li C.-H.; Liao Y.-C.; Lin H.-H.; Liu Z.-Z.; Ye G.-H.; Chiu W.-R.; Chang J.-R.; Feng W.-J.; Chang S.-X.; Lei M.-H.; Ko W.-C.; Kong C.-W.; Kuo C.-T.; Huang B.-X.; Li K.-T.; Chen W.-D.; Luo J.-L.; Lin J.-Y.; Tsai T.-N.; Hsu C.-T.; Lin L.-R.; Chen R.-Y.; Li P.-T.; Stephen Huang S.K.; SADS-TW BrS Registry
臺大學術典藏 2021-09-17T05:40:26Z Impact of genetic tests on survivors of paediatric sudden cardiac arrest SHUENN-NAN CHIU; Juang J.-M.J.; Tseng W.-C.; Chen W.-P.; Lee N.-C.; Wu M.-H.
臺大學術典藏 2021-09-09T07:52:46Z Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations Juang J.-M.J.; Chen C.-Y.; Yeh H.-M.; Chiu W.-Y.; CHIH-CHIEH YU; Liu Y.-B.; Tsai C.-T.; Lo L.-W.; Yeh S.-F.S.; Lai L.-P.
臺大學術典藏 2021-09-09T07:52:45Z 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 2021-09-09T07:52:45Z 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.; Lin L.-Y.; CHIH-CHIEH YU; 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 2021-09-09T07:52:44Z Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan Juang J.M.J.; Tsai C.-T.; Lin L.-Y.; Liu Y.-B.; CHIH-CHIEH YU; 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 2021-09-09T07:52:44Z Spironolactone is associated with reduced risk of new-onset atrial fibrillation in patients receiving renal replacement therapy Chung Y.-W.; Yang Y.-H.; Wu C.-K.; CHIH-CHIEH YU; Juang J.-M.J.; Wang Y.-C.; Tsai C.-T.; Lin L.-Y.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Chen P.-C.; Lin J.-L.
臺大學術典藏 2021-09-09T07:52:42Z 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.; Lin L.-Y.; Hwang J.-J.; Ho L.-T.; CHIH-CHIEH YU; 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 2021-09-09T07:52:41Z Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry Chen C.-Y.J.; Juang J.-M.J.; Lin L.-Y.; Liu Y.-B.; Ho L.-T.; CHIH-CHIEH YU; Huang H.-C.; Lin T.-T.; Liao M.-C.; Chen J.-J.; Hwang J.-J.; Chen W.-J.; Yeh S.-F.S.; Yang D.-H.; Chiang F.-T.; Lin J.-L.; Lai L.-P.; Horie M.; Wu M.-H.; Wu T.-J.; Chen S.-A.; Wang C.-C.; Chang K.-C.; Feng A.-N.; Lin Y.-J.; Ueng K.-C.; Tsao H.-M.; Huang J.-L.; Tsai W.-C.; Tsai C.-F.; Chang S.-L.; Lo L.-W.; Hu Y.-F.; Chung F.-P.; Chang C.-J.; Lo H.-M.; Chiang M.-C.; Hsia C.-P.; Liu J.-F.; Chiu S.-N.; Lin M.-T.; Chua S.-K.; Hsieh Y.-C.; Li C.-H.; Liao Y.-C.; Lin H.-H.; Liu Z.-Z.; Ye G.-H.; Chiu W.-R.; Chang J.-R.; Feng W.-J.; Chang S.-X.; Lei M.-H.; Ko W.-C.; Kong C.-W.; Kuo C.-T.; Huang B.-X.; Li K.-T.; Chen W.-D.; Luo J.-L.; Lin J.-Y.; Tsai T.-N.; Hsu C.-T.; Lin L.-R.; Chen R.-Y.; Li P.-T.; Stephen Huang S.K.; SADS-TW BrS Registry
臺大學術典藏 2021-09-09T07:52:40Z 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.; Lin L.-Y.; CHIH-CHIEH YU; 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.

Showing items 51-60 of 212  (22 Page(s) Totally)
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