| 臺大學術典藏 |
2020-12-02T09:15:20Z |
Additive effect of the metabolic syndrome score to the conventional CHADS2 score for the thromboembolic risk stratification of patients with atrial fibrillation
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Tsai C.-T.; Chang S.-H.; Chang S.-N.; Hwang J.-J.; Wu C.-K.; YI-CHIH WANG; Tseng C.-D.; Yeh H.-M.; Lai L.-P.; Chiang F.-T.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-02T09:15:20Z |
Acute effects of biventricular pacing in heart failure patients with a normal ejection fraction and mechanical dyssynchrony
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YI-CHIH WANG; Yu C.-C.; Chiu F.-C.; Splett V.; Klepfer R.; Hilpisch K.; Tsai C.-T.; Lai L.-P.; Hwang J.-J.; Lin J.-L.; Dr. |
| 臺大學術典藏 |
2020-12-02T09:15:19Z |
Spironolactone is associated with reduced risk of new-onset atrial fibrillation in patients receiving renal replacement therapy
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Lin L.-Y.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Chen P.-C.; Lin J.-L.; Chung Y.-W.; Yang Y.-H.; Wu C.-K.; Yu C.-C.; Juang J.-M.J.; YI-CHIH WANG; Tsai C.-T. |
| 臺大學術典藏 |
2020-12-02T09:15:18Z |
Myocardial Regional Interstitial Fibrosis is Associated with Left Intra-Ventricular Dyssynchrony in Patients with Heart Failure: A Cardiovascular Magnetic Resonance Study
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Lin J.-L.; Lin L.-Y.; Wu C.-K.; Juang J.-M.J.; YI-CHIH WANG; Su M.-Y.M.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Tseng W.-Y.I. |
| 臺大學術典藏 |
2020-12-02T09:15:18Z |
Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation
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Lin T.-H.; Tsai C.-F.; Ueng K.-C.; Chuang E.Y.; Chang S.-N.; Hsieh C.-S.; Tsai C.-T.; Wu C.-K.; Lee J.-K.; Lin L.-Y.; YI-CHIH WANG; Yu C.-C.; Lai L.-P.; Tseng C.-D.; Hwang J.-J.; Chiang F.-T.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-01T07:10:40Z |
New electrocardiographic criteria for the differentiation between counterclockwise and clockwise atrial flutter: Correlation with electrophysiological study and radiofrequency catheter ablation
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Lai L.P.; Lin J.L.; Lin L.J.; Chen W.J.; YI-LWUN HO; Tseng Y.Z.; Chen C.H.; Lee Y.T.; Lien W.P.; Huang S.K.S. |
| 臺大學術典藏 |
2020-12-01T07:10:31Z |
Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms
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Lai L.-P.;Su Y.-N.;Chiang F.-T.;Juang J.-M.;Liu Y.-B.;Yi-Lwun Ho;Chen W.-J.;Yeh S.-J.;Wang C.-C.;Ko Y.-L.;Wu T.-J.;Ueng K.-C.;Lei M.-H.;Tsao H.-M.;Chen S.-A.;Lin T.-K.;Wu M.-H.;Lo H.-M.;Huang S.K.S.;Lin J.-L.; Lai L.-P.; Su Y.-N.; Chiang F.-T.; Juang J.-M.; Liu Y.-B.; YI-LWUN HO; Chen W.-J.; Yeh S.-J.; Wang C.-C.; Ko Y.-L.; Wu T.-J.; Ueng K.-C.; Lei M.-H.; Tsao H.-M.; Chen S.-A.; Lin T.-K.; Wu M.-H.; Lo H.-M.; Huang S.K.S.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-01T07:10:28Z |
Erratum: Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms (Journal of Human Genetics (2005) 50 (490-496) DOI: 10.1007/s10038-005-0283-3)
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Lai L.-P.;Su Y.-N.;Hsieh F.-J.;Chiang F.-T.;Juang J.-M.;Liu Y.-B.;Yi-Lwun Ho;Chen W.-J.;Yeh S.-J.;Wang C.-C.;Ko Y.-L.;Wu T.-J.;Ueng K.-C.;Lei M.-H.;Tsao H.-M.;Chen S.-A.;Lin T.-K.;Wu M.-H.;Lo H.-M.;Huang S.K.S.;Lin J.-L.; Lai L.-P.; Su Y.-N.; Hsieh F.-J.; Chiang F.-T.; Juang J.-M.; Liu Y.-B.; YI-LWUN HO; Chen W.-J.; Yeh S.-J.; Wang C.-C.; Ko Y.-L.; Wu T.-J.; Ueng K.-C.; Lei M.-H.; Tsao H.-M.; Chen S.-A.; Lin T.-K.; Wu M.-H.; Lo H.-M.; Huang S.K.S.; Lin J.-L. |
| 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
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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, 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 |
2020-11-17T02:45:34Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
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Lin J.-L.; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Hwang J.-J.; Juang J.-M.J.;Tzu-Pin Lu;Lai L.-C.;Hsueh C.-H.;Liu Y.-B.;Tsai C.-T.;Lin L.-Y.;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.; Juang J.-M.J.; TZU-PIN LU; Lai L.-C.; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C. |
| 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
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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 |
2020-11-17T02:45:22Z |
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
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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 |
2020-11-17T02:45:19Z |
Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry
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Jyh-Ming J.-J.; 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 J.-J.; Lin T.-T.; Liao M.-T.; Chen J.-J.; Sherri Yeh S.-F.; Chuang J.-Y.; Yang D.-H.; Lin J.-L.; TZU-PIN LU; Chuang E.Y.; Ackerman M.J. |
| 臺大學術典藏 |
2020-10-26T11:34:50Z |
Characteristics of Chinese patients with symptomatic Brugada syndrome in Taiwan
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Ueng K.-C.; Kong C.-W.; Ko W.-C.; Lei M.-H.; Tsao H.-M.; Kuo C.-T.; Wang C.-C.; Lai L.-P.; Lin J.-L.; Chiang F.-T.; Tsai C.-T.; Huang S.K.S.; JYH-MING JIMMY JUANG |
| 臺大學術典藏 |
2020-10-26T11:34:49Z |
Brugada syndrome in the elderly in Taiwan - Report of two cases
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JYH-MING JIMMY JUANG; Lai L.-P.; Lin J.-L.; Chiang F.-T. |
| 臺大學術典藏 |
2020-10-26T11:34:49Z |
Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms
|
Lo H.-M.; Huang S.K.S.; Lin J.-L.; Wu M.-H.; Lin T.-K.; Chen S.-A.; Lei M.-H.; Tsao H.-M.; Wu T.-J.; Ueng K.-C.; JYH-MING JIMMY JUANG; Su Y.-N.; Chiang F.-T.; Lai L.-P.; Ko Y.-L.; Wang C.-C.; Chen W.-J.; Yeh S.-J.; Ho Y.-L.; Liu Y.-B. |
| 臺大學術典藏 |
2020-10-26T11:34:47Z |
Rupture of mitral chordae tendineae: Adding to the list of hypertension complications
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Lai L.-P.; Lin Y.-T.; JYH-MING JIMMY JUANG; Ke S.-R.; Lin J.-L.; Hwang J.-J.; Hsu K.-L.; Chiang F.-T.; Tseng C.-D.; Tseng Y.-Z.; Chen J.-J.; Hu F.-C. |
| 臺大學術典藏 |
2020-10-26T11:34:47Z |
Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations
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Chen W.-P.; Hsueh C.-H.; Lin J.-L.; Tsai C.-T.; Liu Y.-B.; JYH-MING JIMMY JUANG; Tsao H.-M.; Su M.-J.; Lai L.-P. |
| 臺大學術典藏 |
2020-10-26T11:34:47Z |
Erratum: Arrhythmogenic right ventricular dysplasia: Clinical characteristics and identification of novel desmosome gene mutations (Journal of the Formosan Medical Association (2008) vol. 107 (7) (548-558))
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Yu C.H.; Hsueh C.H.; Yang C.T.; JYH-MING JIMMY JUANG; Hwang J.J.; Lai L.P.; Lin J.L.; Yu C.C. |
| 臺大學術典藏 |
2020-10-26T11:34:47Z |
Renin-angiotensin system gene polymorphisms and diastolic heart failure
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Chiang F.-T.; Lin J.-L.; Tseng C.-D.; Hsu K.-L.; Lai L.-P.; JYH-MING JIMMY JUANG; Luo J.-L.; Tsai C.-T.; Hwang J.-J.; Wu C.-K. |
| 臺大學術典藏 |
2020-10-26T11:34:46Z |
Brugada-type electrocardiogram in the Taiwanese population-Is it a risk factor for sudden death?
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Lin J.-W.; Cheng P.-H.; Chiu W.-Y.; Cheng B.-W.; Hwang J.-J.; Tseng C.-D.; Hsu K.-L.; Tseng Y.-Z.; Lin J.-L.; Chiang F.-T.; Tsai M.-H.; Lai L.-P.; Chen P.-C.; Phan W.-L.; Jimmy JYH-MING JIMMY JUANG |
| 臺大學術典藏 |
2020-10-26T11:34:44Z |
Prevalence of atrial fibrillation in patients with brugada syndrome in Taiwan
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Chen C.-Y.; JYH-MING JIMMY JUANG; Liu Y.B.; Lin L.-Y.; Chen W.-J.; Lai L.-P.; Tsai C.-T.; Lin J.-L. |
| 臺大學術典藏 |
2020-10-26T11:34:43Z |
Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations
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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
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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 |
2020-10-26T11:34:41Z |
Prevalence and prognosis of Brugada electrocardiogram patterns in an elderly Han Chinese population: A nation-wide community-based study (HALST cohort)
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Hsiung C.A.; Chiang F.-T.; Lin J.-L.; Lai L.-P.; Hwang J.-J.; Chang I.-S.; Lo H.-M.; Chiu H.-C.; Wang C.-C.; Juan C.-C.; Tang F.-C.; JYH-MING JIMMY JUANG; Chen C.-Y.J.; Chen Y.-H.; Wu I.-C.; Hsu C.-C.; Chen L.-N. |
