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Showing items 131-155 of 212 (9 Page(s) Totally)
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Institution	Date	Title	Author
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	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	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
臺大學術典藏	2020-12-18T06:22:08Z	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.;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.;Shuenn-Nan Chiu;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; Lin L.-R.; Huang B.-X.; Li K.-T.; Chen W.-D.; Luo J.-L.; Lin J.-Y.; Tsai T.-N.; Hsu C.-T.; Kong C.-W.; Kuo C.-T.; Ko W.-C.; Lei M.-H.; Chang S.-X.; 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.; SHUENN-NAN CHIU; 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.; 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.; Chen R.-Y.; Li P.-T.; Stephen Huang S.K.; SADS-TW BrS Registry
臺大學術典藏	2020-12-16T02:25:04Z	Fabry disease cardiac variant IVS4+919 G>A is associated with multiple cardiac gene variants in patients with severe cardiomyopathy and fatal arrhythmia	Juang J.-M.J.;Shun C.-T.;Chen Y.-S.;Wuh-Liang Hwu;Lee N.-C.;Tsai W.-H.;Chen N.-Q.;Chien Y.-H.; Juang J.-M.J.; Shun C.-T.; Chen Y.-S.; WUH-LIANG HWU; Lee N.-C.; Tsai W.-H.; Chen N.-Q.; Chien Y.-H.
臺大學術典藏	2020-12-09T01:38:10Z	Fabry disease cardiac variant IVS4+919 G>A is associated with multiple cardiac gene variants in patients with severe cardiomyopathy and fatal arrhythmia	Juang J.-M.J.; Shun C.-T.; Chen Y.-S.; Hwu W.-L.; NI-CHUNG LEE; Tsai W.-H.; Chen N.-Q.; Chien Y.-H.
臺大學術典藏	2020-12-04T07:45:01Z	Prevalence of atrial fibrillation in patients with brugada syndrome in Taiwan	Juang J.-M.J.; Chen C.-Y.; Liu Y.B.; LIAN-YU LIN; Chen W.-J.; Lai L.-P.; Tsai C.-T.; Lin J.-L.
臺大學術典藏	2020-12-04T07:44:55Z	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.; 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	2020-12-04T07:44:54Z	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 J.-J.; Chiang F.-T.; Chen P.-C.; Lin J.-L.; LIAN-YU LIN
臺大學術典藏	2020-12-04T07:44:54Z	Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan	Juang J.M.J.; Tsai C.-T.; LIAN-YU LIN; 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	2020-12-04T07:44:54Z	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.; 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	2020-12-04T07:44:53Z	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.; LIAN-YU LIN; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L.
臺大學術典藏	2020-12-04T07:44:50Z	Statin therapy lowers the risk of new-onset atrial fibrillation in patients with end-stage renal disease	Hwang J.-J.; Chiang F.-T.; Lin J.-L.; Chen P.-C.; 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.
臺大學術典藏	2020-12-04T07:44:49Z	Spironolactone is associated with reduced risk of new-onset atrial fibrillation in patients receiving renal replacement therapy	Chen P.-C.; Chung Y.-W.; Yang Y.-H.; Wu C.-K.; Yu C.-C.; Juang J.-M.J.; Wang Y.-C.; Tsai C.-T.; LIAN-YU LIN; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L.
臺大學術典藏	2020-12-04T07:44:48Z	Myocardial Regional Interstitial Fibrosis is Associated with Left Intra-Ventricular Dyssynchrony in Patients with Heart Failure: A Cardiovascular Magnetic Resonance Study	LIAN-YU LIN; Wu C.-K.; Juang J.-M.J.; Wang Y.-C.; Su M.-Y.M.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Tseng W.-Y.I.; Lin J.-L.
臺大學術典藏	2020-12-04T07:44:42Z	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 J.-J.; LIAN-YU LIN; Yeh S.-F.S.; Chien K.-L.; Juang J.-M.J.
臺大學術典藏	2020-12-04T07:44:40Z	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.; 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	2020-12-04T07:44:36Z	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.

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