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机构 日期 题名 作者
臺大學術典藏 2022-09-20T06:49:21Z 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 2022-09-20T06:49:14Z 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 2022-09-20T06:49:12Z 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, JUEY-JEN; Chiang F.-T.; Lin J.-L.; Chen P.-C.
臺大學術典藏 2022-09-20T06:49:10Z 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 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 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 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 2022-09-20T06:48:35Z Application of the newest European Association of Cardiovascular Imaging Recommendation regarding the long-term prognostic relevance of left ventricular diastolic function in heart failure with preserved ejection fraction Lin T.-T.; Wang Y.-C.; Juang J.-M.J.; HWANG, JUEY-JEN; Wu C.-K.
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 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 2022-09-20T06:48:27Z Long-term outcomes and left ventricular diastolic function of sarcomere mutation-positive and mutation-negative patients with hypertrophic cardiomyopathy: a prospective cohort study Chen C.-Y.J.; Su M.-Y.M.; Liao Y.-C.; Chang F.-L.; Wu C.-K.; Lin L.-Y.; Chen Y.-S.; Lin Y.-H.; HWANG, JUEY-JEN; Yu S.-L.; Kao H.-L.; Chen W.-J.; Lu T.-P.; Shih C.-Y.; Yeh S.-F.S.; Yang D.-H.; Lai L.-P.; Juang J.-M.J.
臺大學術典藏 2022-09-13T08:18:54Z Atrial fibrillation and the risk of sudden cardiac arrest in patients with hypertrophic cardiomyopathy - A nationwide cohort study Liao M.-T.; Wu C.-K.; Juang J.-M.J.; Lin T.-T.; CHIH-CHENG WU; Lin L.-Y.
臺大學術典藏 2022-09-06T02:42:33Z 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 2022-09-06T02:42:26Z 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 2022-09-06T02:42:23Z 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 2022-09-06T02:42:21Z 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 2022-09-06T02:42:21Z 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 2022-09-06T02:42:19Z 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 2022-09-06T02:42:17Z Statin therapy lowers the risk of new-onset atrial fibrillation in patients with end-stage renal disease 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 2022-09-06T02:42:15Z 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.; LIAN-YU LIN; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Chen P.-C.; Lin J.-L.
臺大學術典藏 2022-09-06T02:42:14Z 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 2022-09-06T02:42:05Z 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 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 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 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 2022-09-06T02:41:44Z CMR-derived ECVs vary with myocardial region and associate with the regional wall thickness Su M.-Y.; Hou K.-Y.; Liu M.-H.; Lin T.-M.; Juang J.-M.J.; LIAN-YU LIN; Wu C.-K.; Yu H.-Y.; Yang S.-C.; Huang Y.-S.; Niisato E.; Chang Y.-C.

显示项目 1-25 / 212 (共9页)
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