| 臺大學術典藏 |
2022-09-20T06:49:30Z |
Genetic variation in the carbonyl reductase 3 gene confers risk of type 2 diabetes and insulin resistance: A potential regulator of adipogenesis
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Chang Y.-C.; Liu P.-H.; Tsai Y.-C.; Chiu Y.-F.; Shih S.-R.; Ho L.-T.; Lee W.-J.; Lu C.-H.; Quertermous T.; Curb J.D.; Lee W.-J.; Lee P.-C.; He Y.-H.; Yeh J.-I.; HWANG, JUEY-JEN; Tsai S.-H.; Chuang L.-M. |
| 臺大學術典藏 |
2022-09-20T06:49:28Z |
erratum: Genetic variation in the carbonyl reductase 3 gene confers risk of type 2 diabetes and insulin resistance: A potential regulator of adipogenesis (Journal of Molecular Medicine DOI: 10.1007/s00109-012-0898-8)
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Chang Y.-C.; Liu P.-H.; Tsai Y.-C.; Chiu Y.-F.; Shih S.-R.; Ho L.-T.; Lee W.-J.; Lu C.-H.; Quertermous T.; Curb J.D.; Lee W.-J.; Lee P.-C.; He Y.-H.; Yeh J.-I.; HWANG, JUEY-JEN; Tsai S.-H.; Chuang L.-M. |
| 臺大學術典藏 |
2022-09-20T06:49:12Z |
Statin therapy lowers the risk of new-onset atrial fibrillation in patients with end-stage renal disease
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Ho L.-T.; Lin L.-Y.; Yang Y.-H.; Wu C.-K.; Juang J.-M.J.; Wang Y.-C.; Tsai C.-T.; Lai L.-P.; HWANG, JUEY-JEN; Chiang F.-T.; Lin J.-L.; Chen P.-C. |
| 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 |
2022-09-20T06:48:39Z |
Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry
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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.; 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.; Chang C.-J.; Lo H.-M.; Chiang M.-C.; Hsia C.-P.; Liu J.-F.; Chiu S.-N.; Lin M.-T.; Chua S.-K.; Hsieh Y.-C.; Li C.-H.; 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.; Li P.-T.; Stephen Huang S.K.; SADS-TW BrS Registry |
| 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
|
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 |
2022-09-16T08:49:05Z |
Factors Associated With Edoxaban Concentration Among Patients With Atrial Fibrillation
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Lin S.-Y.; CHING-HUA KUO; Ho L.-T.; Liu Y.-B.; Huang C.-F.; Tang S.-C.; Jeng J.-S. |
| 臺大學術典藏 |
2022-09-06T02:42:17Z |
Statin therapy lowers the risk of new-onset atrial fibrillation in patients with end-stage renal disease
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Ho L.-T.; LIAN-YU LIN; Yang Y.-H.; Wu C.-K.; Juang J.-M.J.; Wang Y.-C.; Tsai C.-T.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L.; Chen P.-C. |
| 臺大學術典藏 |
2022-09-06T02:42:12Z |
KCNN2 polymorphisms and cardiac tachyarrhythmias
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Yu C.-C.; Chia-Ti T.; Chen P.-L.; Wu C.-K.; Chiu F.-C.; Chiang F.-T.; Chen P.-S.; Chen C.-L.; LIAN-YU LIN; Juang J.-M.; Ho L.-T.; La L.-P.; Yang W.-S.; Lin J.-L. |
| 臺大學術典藏 |
2022-09-06T02:42:03Z |
Comparisons of clinical impacts on individuals with Brugada electrocardiographic patterns defined by ISHNE criteria or EHRA/HRS/APHRS criteria: a nationwide community-based study
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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.; LIAN-YU LIN; Hwang J.-J.; 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. |
| 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 |
2022-09-06T02:41:53Z |
Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry
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Chen C.-Y.J.; Juang J.-M.J.; LIAN-YU LIN; 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.; Wu M.-H.; Wu T.-J.; Chen S.-A.; Wang C.-C.; 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.; Chang C.-J.; Lo H.-M.; Chiang M.-C.; Hsia C.-P.; Liu J.-F.; Chiu S.-N.; Lin M.-T.; Chua S.-K.; Hsieh Y.-C.; Li C.-H.; 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.; Li P.-T.; Stephen Huang S.K.; SADS-TW BrS Registry |
| 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 |
2022-09-06T02:41:46Z |
Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated With Brugada Syndrome: SADS-TW BrS Registry
|
Jimmy Juang J.-M.; Liu Y.-B.; Julius Chen C.-Y.; Yu Q.-Y.; Chattopadhyay A.; LIAN-YU LIN; Chen W.-J.; Yu C.-C.; Huang H.-C.; Ho L.-T.; Lai L.-P.; Hwang J.-J.; 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 |
2022-09-06T02:41:36Z |
First Asian population study of stereotactic body radiation therapy for ventricular arrhythmias
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Ho L.-T.; Chen J.L.-Y.; Chan H.-M.; Huang Y.-C.; Su M.-Y.; Kuo S.-H.; Chang Y.-C.; Lin J.-L.; Chen W.-J.; Lee W.-J.; LIAN-YU LIN |
| 臺大學術典藏 |
2022-05-10T08:09:23Z |
Efficacy and Safety of Proprotein Convertase Subtilisin/Kexin Type 9 Inhibitors as Adjuvant Treatments for Patients with Hypercholesterolemia Treated with Statin: A Systematic Review and Network Meta-analysis
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Huang Y.-T.; Ho L.-T.; Hsu H.-Y.; YU-KANG TU; Chien K.-L. |
| 臺大學術典藏 |
2022-04-28T12:31:07Z |
Efficacy and Safety of Proprotein Convertase Subtilisin/Kexin Type 9 Inhibitors as Adjuvant Treatments for Patients with Hypercholesterolemia Treated with Statin: A Systematic Review and Network Meta-analysis
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Huang Y.-T.; Ho L.-T.; Hsu H.-Y.; Tu Y.-K.; KUO-LIONG CHIEN |
| 臺大學術典藏 |
2022-03-31T02:38:58Z |
Statin therapy lowers the risk of new-onset atrial fibrillation in patients with end-stage renal disease
|
Ho L.-T.; Lin L.-Y.; Yang Y.-H.; Wu C.-K.; Juang J.-M.J.; Wang Y.-C.; Tsai C.-T.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L.; PAU-CHUNG CHEN |
| 臺大學術典藏 |
2022-03-10T05:59:42Z |
Genetic variation in the carbonyl reductase 3 gene confers risk of type 2 diabetes and insulin resistance: A potential regulator of adipogenesis
|
YI-CHENG CHANG; Liu P.-H.; Tsai Y.-C.; Chiu Y.-F.; Shih S.-R.; Ho L.-T.; Lee W.-J.; Lu C.-H.; Quertermous T.; Curb J.D.; Lee W.-J.; Lee P.-C.; He Y.-H.; Yeh J.-I.; Hwang J.-J.; Tsai S.-H.; Chuang L.-M. |
| 臺大學術典藏 |
2022-03-10T05:59:41Z |
Erratum: Genetic variation in the carbonyl reductase 3 gene confers risk of type 2 diabetes and insulin resistance: A potential regulator of adipogenesis (Journal of Molecular Medicine DOI: 10.1007/s00109-012-0898-8)
|
YI-CHENG CHANG; Liu P.-H.; Tsai Y.-C.; Chiu Y.-F.; Shih S.-R.; Ho L.-T.; Lee W.-J.; Lu C.-H.; Quertermous T.; Curb J.D.; Lee W.-J.; Lee P.-C.; He Y.-H.; Yeh J.-I.; Hwang J.-J.; Tsai S.-H.; Chuang L.-M. |
| 臺大學術典藏 |
2022-03-10T05:59:40Z |
Common ALDH2 genetic variants predict development of hypertension in the SAPPHIRe prospective cohort: Gene-environmental interaction with alcohol consumption
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YI-CHENG CHANG; Chiu Y.-F.; Lee I.-T.; Ho L.-T.; Hung Y.-J.; Hsiung C.A.; Quertermous T.; Donlon T.; Lee W.-J.; Lee P.-C.; Chen C.-H.; Mochly-Rosen D.; Chuang L.-M. |
| 臺大學術典藏 |
2022-03-07T07:05:35Z |
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.; JEN-KUANG LEE; 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. |
| 臺大學術典藏 |
2022-02-27T03:27:17Z |
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; HUI-CHUN HUANG; 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 |
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. |
