| 臺大學術典藏 |
2022-09-20T06:48:41Z |
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
|
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 |
2022-09-20T06:48:31Z |
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, JUEY-JEN; 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 |
2022-09-06T02:41:58Z |
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 |
2022-09-06T02:41:47Z |
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 |
2022-02-23T08:10:45Z |
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 |
2022-02-23T08:10:41Z |
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.; 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 |
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. |
| 臺大學術典藏 |
2021-03-29T06:08:22Z |
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.; 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.; ERIC YAO-YU CHUANG |
| 臺大學術典藏 |
2021-03-08T06:51:49Z |
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.;Yu C.-C.;Ho L.-T.;Huang H.-C.;Chen C.-Y.J.;Lu T.-P.;Liang-Chuan Lai;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Rivolta I.;Antzelevitch C.; 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.; Liang-Chuan Lai; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Antzelevitch C. |
| 臺大學術典藏 |
2021-03-08T06:51:49Z |
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.;Yu C.-C.;Ho L.-T.;Huang H.-C.;Chen C.-Y.J.;Lu T.-P.;Liang-Chuan Lai;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Rivolta I.;Antzelevitch C.; 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.; Liang-Chuan Lai; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Antzelevitch C. |
| 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. |
