| 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. |
