| 臺大學術典藏 |
2021-03-11T04:29:17Z |
Circulating chemerin levels, but not the RARRES2 polymorphisms, predict the long-term outcome of angiographically confirmed coronary artery disease
|
Er L.K.;Hsu L.-A.;Juang J.-M.J.;Fu-Tien Chiang;Teng M.-S.;Tzeng I.-S.;Wu S.;Lin J.-F.;Ko Y.-L.; Er L.K.; Hsu L.-A.; Juang J.-M.J.; FU-TIEN CHIANG; Teng M.-S.; Tzeng I.-S.; Wu S.; Lin J.-F.; Ko Y.-L. |
| 臺大學術典藏 |
2021-03-11T04:29:17Z |
Osteoprotegerin and osteopontin levels, but not gene polymorphisms, predict mortality in cardiovascular diseases
|
Lin J.-F.;Wu S.;Juang J.-M.J.;Fu-Tien Chiang;Hsu L.-A.;Teng M.-S.;Cheng S.-T.;Huang H.-L.;Ko Y.-L.; Lin J.-F.; Wu S.; Juang J.-M.J.; FU-TIEN CHIANG; Hsu L.-A.; Teng M.-S.; Cheng S.-T.; Huang H.-L.; Ko Y.-L. |
| 臺大學術典藏 |
2021-03-11T04:29:15Z |
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.;Fu-Tien Chiang;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; 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.; FU-TIEN CHIANG; 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 |
2021-03-11T04:29:13Z |
Genetic determinants of circulating galectin-3 levels in patients with coronary artery disease
|
Liao Y.-H.; Teng M.-S.; Juang J.-M.J.; FU-TIEN CHIANG; Er L.-K.; Wu S.; Ko Y.-L. |
| 臺大學術典藏 |
2021-03-10T08:55:46Z |
The risk of osteonecrosis of the jaws in taiwanese osteoporotic patients treated with oral alendronate or raloxifene
|
Chiu W.-Y.;Chien J.-Y.;Yang W.-S.;Juang J.-M.J.;Lee J.-J.;Keh-Sung Tsai; Chiu W.-Y.; Chien J.-Y.; Yang W.-S.; Juang J.-M.J.; Lee J.-J.; KEH-SUNG TSAI |
| 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 |
2020-12-31T02:57:06Z |
Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan
|
Juang J.M.J.; Tsai C.-T.; Lin L.-Y.; Liu Y.-B.; Yu C.-C.; Hwang J.-J.; Chen J.-J.; Chiu F.-C.; Chen W.-J.; Tseng C.-D.; Chiang F.-T.; Yeh H.-M.; Sherri Yeh S.-F.; LING-PING LAI; Lin J.-L. |
| 臺大學術典藏 |
2020-12-30T08:47:48Z |
Next-generation sequencing in the genetics of human atrial fibrillation
|
Hsieh C.-S.; Chuang E.Y.; Juang J.-M.J.; Hwang J.-J.; Tseng C.-D.; Chiang F.-T.; Lai L.-P.; Lin J.-L.; CHIA-TI TSAI |
| 臺大學術典藏 |
2020-12-30T08:47:47Z |
Prevalence of atrial fibrillation in patients with brugada syndrome in Taiwan
|
Lin L.-Y.; Chen W.-J.; Lai L.-P.; CHIA-TI TSAI; Lin J.-L.; Juang J.-M.J.; Chen C.-Y.; Liu Y.B. |
| 臺大學術典藏 |
2020-12-30T08:47:45Z |
Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations
|
Juang J.-M.J.; Chen C.-Y.; Yeh H.-M.; Chiu W.-Y.; Yu C.-C.; Liu Y.-B.; CHIA-TI TSAI; Lo L.-W.; Yeh S.-F.S.; Lai L.-P. |
| 臺大學術典藏 |
2020-12-30T08:47:44Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
|
Chiang F.-T.; Hwang J.-J.; Lin L.-Y.; Yu C.-C.; CHIA-TI TSAI; Liu Y.-B.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-30T08:47:43Z |
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
|
Lin J.-L.; Chuang E.Y.; Lai L.-P.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Ho C.-C.; Liu Y.-B.; CHIA-TI TSAI; Lin L.-Y.; Yu C.-C.; Chen W.-J.; Chiang F.-T.; Yeh S.-F.S. |
| 臺大學術典藏 |
2020-12-30T08:47:42Z |
Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan
|
Juang J.M.J.; CHIA-TI TSAI; Lin L.-Y.; Liu Y.-B.; Yu C.-C.; Hwang J.-J.; Chen J.-J.; Chiu F.-C.; Chen W.-J.; Tseng C.-D.; Chiang F.-T.; Yeh H.-M.; Sherri Yeh S.-F.; Lai L.-P.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-30T08:47:42Z |
Effects of angiotensin converting enzyme inhibition or angiotensin receptor blockade in dialysis patients: A nationwide data survey and propensity analysis
|
Wu C.-K.; Yang Y.-H.; Juang J.-M.J.; Wang Y.-C.; CHIA-TI TSAI; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Chen P.-C.; Lin J.-L.; Lin L.-Y. |
| 臺大學術典藏 |
2020-12-30T08:47:41Z |
Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation
|
Lin L.-Y.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L.; CHIA-TI TSAI; Hsieh C.-S.; Chang S.-N.; Chuang E.Y.; Juang J.-M.J. |
| 臺大學術典藏 |
2020-12-30T08:47:40Z |
Statin therapy lowers the risk of new-onset atrial fibrillation in patients with end-stage renal disease
|
Chen P.-C.; Lin J.-L.; Ho L.-T.; Lin L.-Y.; Yang Y.-H.; Wu C.-K.; Juang J.-M.J.; Wang Y.-C.; CHIA-TI TSAI; Lai L.-P.; Hwang J.-J.; Chiang F.-T. |
| 臺大學術典藏 |
2020-12-30T08:47:38Z |
Spironolactone is associated with reduced risk of new-onset atrial fibrillation in patients receiving renal replacement therapy
|
Juang J.-M.J.; Wang Y.-C.; CHIA-TI TSAI; 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. |
| 臺大學術典藏 |
2020-12-30T08:47:34Z |
The Taiwan Heart Registries: Its Influence on Cardiovascular Patient Care
|
Wu C.-K.; Juang J.-M.J.; Chiang J.-Y.; Li Y.-H.; CHIA-TI TSAI; Chiang F.-T. |
| 臺大學術典藏 |
2020-12-30T07:47:51Z |
Prevalence of atrial fibrillation in patients with brugada syndrome in Taiwan
|
Juang J.-M.J.; Chen C.-Y.; YEN BIN LIU; Lin L.-Y.; Chen W.-J.; Lai L.-P.; Tsai C.-T.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-30T07:47:50Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
|
Chuang E.Y.; Lai L.-P.; Lin J.-L.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; YEN BIN LIU; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Hwang J.-J.; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P. |
| 臺大學術典藏 |
2020-12-30T07:47:50Z |
Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations
|
YEN BIN LIU; Yu C.-C.; Yeh H.-M.; Chiu W.-Y.; Chen C.-Y.; Juang J.-M.J.; Tsai C.-T.; Lo L.-W.; Yeh S.-F.S.; Lai L.-P. |
| 臺大學術典藏 |
2020-12-30T07:47:49Z |
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
|
Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Ho C.-C.; YEN BIN LIU; 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 |
2020-12-30T07:47:49Z |
Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan
|
Juang J.M.J.; Tsai C.-T.; Lin L.-Y.; YEN BIN LIU; Yu C.-C.; Hwang J.-J.; Chen J.-J.; Chiu F.-C.; Chen W.-J.; Tseng C.-D.; Chiang F.-T.; Yeh H.-M.; Sherri Yeh S.-F.; Lai L.-P.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-30T07:47:47Z |
Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry
|
SADS-TW BrS Registry; 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.; Chen C.-Y.J.; Juang J.-M.J.; Lin L.-Y.; YEN BIN LIU; 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. |
| 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 |
2020-12-28T12:04:07Z |
Next-generation sequencing in the genetics of human atrial fibrillation
|
Hsieh C.-S.; Chuang E.Y.; Juang J.-M.J.; HWANG, JUEY-JEN; Tseng C.-D.; Chiang F.-T.; Lai L.-P.; Lin J.-L.; Tsai C.-T. |
| 臺大學術典藏 |
2020-12-28T12:04:03Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
|
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 |
2020-12-28T12:04:00Z |
Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan
|
Juang J.M.J.; Tsai C.-T.; Lin L.-Y.; Liu Y.-B.; Yu C.-C.; HWANG, JUEY-JEN; Chen J.-J.; Chiu F.-C.; Chen W.-J.; Tseng C.-D.; Chiang F.-T.; Yeh H.-M.; Sherri Yeh S.-F.; Lai L.-P.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-28T12:03:59Z |
Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation
|
Tsai C.-T.; Hsieh C.-S.; Chang S.-N.; Chuang E.Y.; Juang J.-M.J.; Lin L.-Y.; Lai L.-P.; HWANG, JUEY-JEN; Chiang F.-T.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-28T12:03:59Z |
Effects of angiotensin converting enzyme inhibition or angiotensin receptor blockade in dialysis patients: A nationwide data survey and propensity analysis
|
Wu C.-K.; Yang Y.-H.; Juang J.-M.J.; Wang Y.-C.; Tsai C.-T.; Lai L.-P.; HWANG, JUEY-JEN; Chiang F.-T.; Chen P.-C.; Lin J.-L.; Lin L.-Y. |
| 臺大學術典藏 |
2020-12-28T12:03:58Z |
Prevalence and prognosis of Brugada electrocardiogram patterns in an elderly Han Chinese population: A nation-wide community-based study (HALST cohort)
|
Hsiung C.A.; Juang J.-M.J.; Chen C.-Y.J.; Chen Y.-H.; Wu I.-C.; Hsu C.-C.; Chen L.-N.; Tang F.-C.; Wang C.-C.; Juan C.-C.; Chiu H.-C.; Lo H.-M.; Chang I.-S.; HWANG, JUEY-JEN; Lai L.-P.; Chiang F.-T.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-28T12:03:55Z |
Spironolactone is associated with reduced risk of new-onset atrial fibrillation in patients receiving renal replacement therapy
|
Chung Y.-W.; Yang Y.-H.; Wu C.-K.; Yu C.-C.; Juang J.-M.J.; Wang Y.-C.; Tsai C.-T.; Lin L.-Y.; Lai L.-P.; HWANG, JUEY-JEN; Chiang F.-T.; Chen P.-C.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-28T12:03:53Z |
Myocardial Regional Interstitial Fibrosis is Associated with Left Intra-Ventricular Dyssynchrony in Patients with Heart Failure: A Cardiovascular Magnetic Resonance Study
|
Lin L.-Y.; Wu C.-K.; Juang J.-M.J.; Wang Y.-C.; Su M.-Y.M.; Lai L.-P.; HWANG, JUEY-JEN; Chiang F.-T.; Tseng W.-Y.I.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-28T12:03:50Z |
Genome-wide methylation profiles in coronary artery ectasia
|
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, JUEY-JEN; Lin L.-Y.; Yeh S.-F.S.; Chien K.-L.; Juang J.-M.J. |
| 臺大學術典藏 |
2020-12-28T12:03:36Z |
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 Y.-H.; Wu I.-C.; Hsu C.-C.; Wu R.-C.; Chen K.-C.; Liaw W.-J.; Tsai T.-L.; Lin L.-Y.; HWANG, JUEY-JEN; 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.; Chen C.-Y.J.; Juang J.-M.J. |
| 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 |
2020-12-28T12:03:27Z |
Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry
|
Li C.-H.; Hsieh Y.-C.; Chua S.-K.; Lin M.-T.; Chiu S.-N.; Liu J.-F.; Hsia C.-P.; Chiang M.-C.; Lo H.-M.; Chang C.-J.; 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.; 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.; Li P.-T.; Stephen Huang S.K.; SADS-TW BrS Registry; 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. |
| 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 |
2020-12-28T10:02:42Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
|
Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; CHIH-CHIEH YU; 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.; Lu T.-P.; Lai L.-C.; Hsueh C.-H. |
| 臺大學術典藏 |
2020-12-28T10:02:42Z |
Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations
|
Yeh S.-F.S.; Lai L.-P.; Juang J.-M.J.; Chen C.-Y.; Yeh H.-M.; Chiu W.-Y.; CHIH-CHIEH YU; Liu Y.-B.; Tsai C.-T.; Lo L.-W. |
| 臺大學術典藏 |
2020-12-28T10:02:41Z |
Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan
|
Juang J.M.J.; Tsai C.-T.; Lin L.-Y.; Liu Y.-B.; CHIH-CHIEH YU; Hwang J.-J.; Chen J.-J.; Chiu F.-C.; Chen W.-J.; Tseng C.-D.; Chiang F.-T.; Yeh H.-M.; Sherri Yeh S.-F.; Lai L.-P.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-28T10:02:41Z |
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
|
Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; CHIH-CHIEH YU; 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 |
2020-12-28T10:02:40Z |
Spironolactone is associated with reduced risk of new-onset atrial fibrillation in patients receiving renal replacement therapy
|
CHIH-CHIEH YU; Yang Y.-H.; Wu C.-K.; Chung Y.-W.; Juang J.-M.J.; Wang Y.-C.; Tsai C.-T.; Lin L.-Y.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Chen P.-C.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-24T06:16:20Z |
Fabry disease cardiac variant IVS4+919 G>A is associated with multiple cardiac gene variants in patients with severe cardiomyopathy and fatal arrhythmia
|
YIN-HSIU CHIEN; Chen N.-Q.; Tsai W.-H.; Juang J.-M.J.; Shun C.-T.; Chen Y.-S.; Hwu W.-L.; Lee N.-C. |
| 臺大學術典藏 |
2020-12-21T08:16:30Z |
Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan
|
Juang J.M.J.;Tsai C.-T.;Lin L.-Y.;Liu Y.-B.;Yu C.-C.;Hwang J.-J.;Chen J.-J.;Chiu F.-C.;Wen-Jone Chen;Tseng C.-D.;Chiang F.-T.;Yeh H.-M.;Sherri Yeh S.-F.;Lai L.-P.;Lin J.-L.; Juang J.M.J.; Tsai C.-T.; Lin L.-Y.; Liu Y.-B.; Yu C.-C.; Hwang J.-J.; Chen J.-J.; Chiu F.-C.; WEN-JONE CHEN; Tseng C.-D.; Chiang F.-T.; Yeh H.-M.; Sherri Yeh S.-F.; Lai L.-P.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-21T08:16:30Z |
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
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Lin J.-L.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; WEN-JONE CHEN; Chiang F.-T.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y. |
| 臺大學術典藏 |
2020-12-21T02:54:55Z |
Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry
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Chen S.-A.; Wu T.-J.; Wu M.-H.; Horie M.; Lai L.-P.; Lin J.-L.; Chiang F.-T.; Yang D.-H.; Yeh S.-F.S.; Chen W.-J.; Hwang J.-J.; Chen J.-J.; Liao M.-C.; Lin T.-T.; Huang H.-C.; Yu C.-C.; Ho L.-T.; 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.;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.;Ming-Tai Lin;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; Chen C.-Y.J.; Juang J.-M.J.; Lin L.-Y.; Liu Y.-B.; Tsai T.-N.; Lin J.-Y.; Luo J.-L.; Chen W.-D.; Li K.-T.; Huang B.-X.; Kuo C.-T.; Kong C.-W.; Ko W.-C.; Lei M.-H.; Chang S.-X.; Feng W.-J.; Chang J.-R.; Chiu W.-R.; Ye G.-H.; 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.; MING-TAI LIN; Chua S.-K.; Hsieh Y.-C.; Li C.-H.; Liao Y.-C.; Lin H.-H.; Liu Z.-Z.; Hsu C.-T.; Lin L.-R.; Chen R.-Y.; Li P.-T.; Stephen Huang S.K.; SADS-TW BrS Registry |
