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机构 日期 题名 作者
臺大學術典藏 2020-12-30T07:47:47Z 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.; YEN BIN LIU; 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 2020-12-30T07:47:44Z 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.; YEN BIN LIU; Lin L.-Y.; 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 2020-12-28T12:03:29Z 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 2020-12-28T12:03:16Z 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 2020-12-28T07:57:02Z Coexistence of atrioventricular accessory pathways and drug-induced type 1 Brugada pattern Kocabas U.; Kose S.; JYH-MING JIMMY JUANG; Hasdemir C.; Orman M.N.; Payzin S.; Sahin H.; Celen C.; Ozcan E.E.; Chen C.-Y.J.; Gunduz R.; Turan O.E.; Senol O.; Burashnikov E.; Antzelevitch C.
臺大學術典藏 2020-12-28T07:56:41Z 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 Liu Y.-B.; Lin L.-Y.; Lu T.-P.; Chen C.-Y.J.; Ho L.-T.; Huang H.-C.; Lai L.-P.; Hwang J.-J.; Yeh S.-F.S.; Wu C.-K.; JYH-MING JIMMY JUANG; Antzelevitch C.
臺大學術典藏 2020-12-28T07:56:37Z GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death Huang H.-C.; Yu C.-C.; Ho L.-T.; Liu Y.-B.; Lin L.-Y.; Chen W.-J.; Hwang J.-J.; JYH-MING JIMMY JUANG; Binda A.; Lee S.-J.; 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 2020-12-04T07:44:36Z 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 2020-12-04T07:44:29Z 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 2020-12-02T11:04:29Z 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 J.-J.; Yeh S.-F.S.; CHO-KAI WU; Juang J.-M.J.; Antzelevitch C.
臺大學術典藏 2020-11-17T02:45:22Z 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.;Tzu-Pin Lu;Lin L.-Y.;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.; Chen C.-Y.J.; TZU-PIN LU; Lin L.-Y.; 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 2020-11-17T02:45:22Z 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.;Tzu-Pin Lu;Lin L.-Y.;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.; Chen C.-Y.J.; TZU-PIN LU; Lin L.-Y.; 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 2020-10-26T11:34:31Z Coexistence of atrioventricular accessory pathways and drug-induced type 1 Brugada pattern Hasdemir C.; JYH-MING JIMMY JUANG; Kose S.; Kocabas U.; Orman M.N.; Payzin S.; Sahin H.; Celen C.; Ozcan E.E.; Chen C.-Y.J.; Gunduz R.; Turan O.E.; Senol O.; Burashnikov E.; Antzelevitch C.
臺大學術典藏 2020-10-26T11:34:30Z 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 J.-J.; Yeh S.-F.S.; Wu C.-K.; JYH-MING JIMMY JUANG; Antzelevitch C.
臺大學術典藏 2020-10-26T11:34:25Z GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death JYH-MING JIMMY JUANG; Binda A.; Lee S.-J.; Hwang J.-J.; Chen W.-J.; Liu Y.-B.; Lin L.-Y.; 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 GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death Juang J.-M.J.; TZU-PIN LU; Chen C.-Y.J.; Huang H.-C.; Ho L.-T.; Yu C.-C.; Lin L.-Y.; Binda A.; Lee S.-J.; Hwang J.-J.; Chen W.-J.; Liu Y.-B.; Antzelevitch C.; Lai L.-C.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Juang J.-M.J.;Binda A.;Lee S.-J.;Hwang J.-J.;Chen W.-J.;Liu Y.-B.;Lin L.-Y.;Yu C.-C.;Ho L.-T.;Huang H.-C.;Chen C.-Y.J.;Tzu-Pin Lu;Lai L.-C.;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Rivolta I.;Antzelevitch C.
臺大學術典藏 2020 GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death Juang J.-M.J.; TZU-PIN LU; Chen C.-Y.J.; Huang H.-C.; Ho L.-T.; Yu C.-C.; Lin L.-Y.; Binda A.; Lee S.-J.; Hwang J.-J.; Chen W.-J.; Liu Y.-B.; Antzelevitch C.; Lai L.-C.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Juang J.-M.J.;Binda A.;Lee S.-J.;Hwang J.-J.;Chen W.-J.;Liu Y.-B.;Lin L.-Y.;Yu C.-C.;Ho L.-T.;Huang H.-C.;Chen C.-Y.J.;Tzu-Pin Lu;Lai L.-C.;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Rivolta I.;Antzelevitch C.
臺大學術典藏 2020 GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death Binda A.; Juang J.-M.J.; Antzelevitch C.; Chuang E.Y.; Rivolta I.; Lee S.-J.; Hwang J.-J.; WEN-JONE CHEN; Liu Y.-B.; Lin L.-Y.; 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.
臺大學術典藏 2020 GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death Chen, W.-J.; Lee, S.-J.; Hwang, J.-J.; Binda, A.; Juang, J.-M.J.; Juang, J.-M.J.;Binda, A.;Lee, S.-J.;Hwang, J.-J.;Chen, W.-J.;Liu, Y.-B.;Lin, L.-Y.;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.; SHYH-JYE LEE; Liu, Y.-B.; Lin, L.-Y.; 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 GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death Chen, W.-J.; Lee, S.-J.; Hwang, J.-J.; Binda, A.; Juang, J.-M.J.; Juang, J.-M.J.;Binda, A.;Lee, S.-J.;Hwang, J.-J.;Chen, W.-J.;Liu, Y.-B.;Lin, L.-Y.;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.; SHYH-JYE LEE; Liu, Y.-B.; Lin, L.-Y.; 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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