| 國立成功大學 |
2023 |
Radiotherapy versus low-dose tamoxifen following breast-conserving surgery for low-risk and estrogen receptor-positive breast ductal carcinoma in situ: an international open-label randomized non-inferiority trial (TBCC-ARO DCIS Trial)
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Kuo, S.-H.;Tseng, L.-M.;Chen, S.-T.;Sagara, Y.;Chang, Y.-C.;Yeh, H.-T.;Kuo, Y.-L.;Hung, C.-C.;Lu, T.-P.;Lee, Y.-H.;Toi, M.;Huang, C.-S. |
| 國立成功大學 |
2023 |
Klotho Overexpression Is Frequently Associated With Upstream Rearrangements in Fusion-Negative Phosphaturic Mesenchymal Tumors of Bone and Sinonasal Tract
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Lee, J.-C.;Hsieh, T.-H.;Kao, Y.-C.;Tsai, C.-F.;Huang, Huang H.-Y.;Shih, C.-Y.;Song, H.-L.;Oda, Y.;Chih-Hsueh, Chen P.;Pan, C.-C.;Sittampalam, K.;Petersson, F.;Konishi, E.;Chiu, W.-Y.;Chen, Chen C.-F.;Carpenter, T.O.;Lu, T.-P.;Chang, Chang C.-D.;Huang, S.-C.;Folpe, A.L. |
| 臺大學術典藏 |
2022-09-20T06:49:21Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
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Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; HWANG, JUEY-JEN; 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 |
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
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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
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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 |
2022-09-20T06:48:30Z |
Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated With Brugada Syndrome: SADS-TW BrS Registry
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Jimmy Juang J.-M.; Liu Y.-B.; Julius Chen C.-Y.; Yu Q.-Y.; Chattopadhyay A.; Lin L.-Y.; Chen W.-J.; Yu C.-C.; Huang H.-C.; Ho L.-T.; Lai L.-P.; HWANG, JUEY-JEN; Lin T.-T.; Liao M.-T.; Chen J.-J.; Sherri Yeh S.-F.; Chuang J.-Y.; Yang D.-H.; Lin J.-L.; Lu T.-P.; Chuang E.Y.; Ackerman M.J. |
| 臺大學術典藏 |
2022-09-20T06:48:27Z |
Long-term outcomes and left ventricular diastolic function of sarcomere mutation-positive and mutation-negative patients with hypertrophic cardiomyopathy: a prospective cohort study
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Chen C.-Y.J.; Su M.-Y.M.; Liao Y.-C.; Chang F.-L.; Wu C.-K.; Lin L.-Y.; Chen Y.-S.; Lin Y.-H.; HWANG, JUEY-JEN; Yu S.-L.; Kao H.-L.; Chen W.-J.; Lu T.-P.; Shih C.-Y.; Yeh S.-F.S.; Yang D.-H.; Lai L.-P.; Juang J.-M.J. |
| 臺大學術典藏 |
2022-09-06T02:42:26Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
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Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; LIAN-YU LIN; Yu C.-C.; 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 |
2022-09-06T02:42:23Z |
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
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Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; LIAN-YU LIN; 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 |
2022-09-06T02:42:05Z |
Genome-wide methylation profiles in coronary artery ectasia
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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.; LIAN-YU LIN; Yeh S.-F.S.; Chien K.-L.; Juang J.-M.J. |
