| 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 |
2020-12-02T11:04:29Z |
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.; Yu C.-C.; Lee J.-K.; CHO-KAI WU; 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 |
2020-12-02T09:15:17Z |
Genome-wide methylation profiles in coronary artery ectasia
|
Lu T.-P.; Chuang N.-C.; Cheng C.-Y.; Hsu C.-A.; YI-CHIH WANG; Lin Y.-H.; Lee J.-K.; Wu C.-K.; Hwang J.-J.; Lin L.-Y.; Yeh S.-F.S.; Chien K.-L.; Juang J.-M.J. |
| 臺大學術典藏 |
2020-11-25T07:22:53Z |
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 |
| 臺大學術典藏 |
2020-11-17T02:45:33Z |
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
|
Chuang E.Y.; Lin J.-L.; Juang J.-M.J.;Tzu-Pin Lu;Lai L.-C.;Ho C.-C.;Liu Y.-B.;Tsai C.-T.;Lin L.-Y.;Yu C.-C.;Chen W.-J.;Chiang F.-T.;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Lin J.-L.; Juang J.-M.J.; TZU-PIN LU; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Chen W.-J.; Chiang F.-T.; Yeh S.-F.S.; Lai L.-P. |
| 臺大學術典藏 |
2020-11-17T02:45:26Z |
Genome-wide methylation profiles in coronary artery ectasia
|
Chuang N.-C.; Cheng C.-Y.; Hsu C.-A.; Wang Y.-C.; Lin Y.-H.; Lee J.-K.; Wu C.-K.; Hwang J.-J.; Lin L.-Y.; Yeh S.-F.S.; Chien K.-L.; Juang J.-M.J.; Tzu-Pin Lu;Chuang N.-C.;Cheng C.-Y.;Hsu C.-A.;Wang Y.-C.;Lin Y.-H.;Lee J.-K.;Wu C.-K.;Hwang J.-J.;Lin L.-Y.;Yeh S.-F.S.;Chien K.-L.;Juang J.-M.J.; TZU-PIN LU |
| 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 |
2020-10-26T11:34:43Z |
Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations
|
Yeh S.-F.S.; Lai L.-P.; Lo L.-W.; Tsai C.-T.; Liu Y.-B.; Yu C.-C.; Chiu W.-Y.; Chen C.-Y.; Yeh H.-M.; JYH-MING JIMMY JUANG |
| 臺大學術典藏 |
2020-10-26T11:34:42Z |
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
|
Ho C.-C.; Lu T.-P.; Lai L.-C.; JYH-MING JIMMY JUANG; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; 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 |
2020-10-26T11:34:36Z |
Genome-wide methylation profiles in coronary artery ectasia
|
JYH-MING JIMMY JUANG; Chien K.-L.; Yeh S.-F.S.; Lin L.-Y.; Lu T.-P.; Chuang N.-C.; Cheng C.-Y.; Hsu C.-A.; Wang Y.-C.; Lin Y.-H.; Lee J.-K.; Wu C.-K.; Hwang J.-J. |
