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機構 日期 題名 作者
臺大學術典藏 2020-12-28T12:03:36Z 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 Y.-H.; Wu I.-C.; Hsu C.-C.; Wu R.-C.; Chen K.-C.; Liaw W.-J.; Tsai T.-L.; Lin L.-Y.; HWANG, JUEY-JEN; 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.; Chen C.-Y.J.; Juang J.-M.J.
臺大學術典藏 2020-12-28T12:03:29Z 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.; Huang H.-C.; Lai L.-P.; HWANG, JUEY-JEN; Yeh S.-F.S.; Wu C.-K.; Juang J.-M.J.; Antzelevitch C.
臺大學術典藏 2020-12-28T12:03:27Z Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry Li C.-H.; Hsieh Y.-C.; Chua S.-K.; Lin M.-T.; Chiu S.-N.; Liu J.-F.; Hsia C.-P.; Chiang M.-C.; Lo H.-M.; Chang C.-J.; 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.; 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, JUEY-JEN; 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.; Li P.-T.; Stephen Huang S.K.; SADS-TW BrS Registry; 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.
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 2020-12-28T10:52:54Z 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 2020-12-28T10:02:42Z Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome 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.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.
臺大學術典藏 2020-12-28T10:02:42Z Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations Yeh S.-F.S.; Lai L.-P.; 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.
臺大學術典藏 2020-12-28T10:02:41Z 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 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.

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