臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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顯示項目 321-345 / 727 (共30頁)
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機構	日期	題名	作者
臺大學術典藏	2020-12-30T08:47:38Z	Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation	Chiang F.-T.; Lin J.-L.; Hwang J.-J.; Tseng C.-D.; CHIA-TI TSAI; Hsieh C.-S.; Chang S.-N.; Chuang E.Y.; Ueng K.-C.; Tsai C.-F.; Lin T.-H.; Wu C.-K.; Lee J.-K.; Lin L.-Y.; Wang Y.-C.; Yu C.-C.; Lai L.-P.
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	2020-12-30T08:47:38Z	Repolarization alternans and ventricular arrhythmia in a repaired tetralogy of Fallot animal model	Chiu S.-N.; CHIA-TI TSAI; Lin L.-Y.; Huang S.-C.; Chen Y.-S.; Wang J.-K.; Wu M.-H.; Lai L.-P.; Lin J.-L.
臺大學術典藏	2020-12-30T08:47:36Z	Atrial flutter/fibrillation in patients receiving transcatheter closure of atrial septal defect	Chiu S.-N.; Wu M.-H.; CHIA-TI TSAI; Lai L.-P.; Lin J.-L.; Lin M.-T.; Lu C.-W.; Wang J.-K.
臺大學術典藏	2020-12-30T08:47:36Z	C-reactive protein gene polymorphism predicts the risk of thromboembolic stroke in patients with atrial fibrillation: a more than 10-year prospective follow-up study	Chang S.-N.; Lai L.-P.; Chiang F.-T.; Lin J.-L.; Hwang J.-J.; CHIA-TI TSAI
臺大學術典藏	2020-12-30T08:47:36Z	Renal Denervation Decreases Susceptibility to Arrhythmogenic Cardiac Alternans and Ventricular Arrhythmia in a Rat Model of Post-Myocardial Infarction Heart Failure	Chang S.-N.; Chang S.-H.; Yu C.-C.; Wu C.-K.; Lai L.-P.; Chiang F.-T.; Hwang J.-J.; Lin J.-L.; CHIA-TI TSAI
臺大學術典藏	2020-12-30T08:47:35Z	Biomarkers and echocardiography for evaluating the improvement of the ventricular diastolic function after surgical relief of hydronephrosis	Yeh H.-M.; Lin T.-T.; Yeh C.-F.; Huang H.-S.; Chang S.-N.; Lin J.-W.; CHIA-TI TSAI; Lai L.-P.; Huang Y.-Y.; Chu C.-L.
臺大學術典藏	2020-12-30T08:47:32Z	The effect and molecular mechanism of statins on the expression of human anti-coagulation genes	CHIA-TI TSAI; Chang S.-N.; Wu C.-K.; Lai L.-P.; Chiang F.-T.; Hwang J.-J.
臺大學術典藏	2020-12-30T07:47:57Z	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	Ko Y.-L.; Wang C.-C.; Chen W.-J.; Yeh S.-J.; Ho Y.-L.; YEN BIN LIU; Lai L.-P.; Su Y.-N.; Chiang F.-T.; Juang J.-M.; 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	2020-12-30T07:47:57Z	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)	Lin J.-L.; Lai L.-P.; Su Y.-N.; Hsieh F.-J.; Chiang F.-T.; Juang J.-M.; YEN BIN LIU; Ho Y.-L.; 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.
臺大學術典藏	2020-12-30T07:47:54Z	Functional studies on three novel HCNH2 mutations in Taiwan: Identification of distinct mechanisms of channel defect and dissociation between glycosylation defect and assembly defect	Hsueh C.-H.; Chen W.-P.; Lin J.-L.; YEN BIN LIU; Su M.-J.; Lai L.-P.
臺大學術典藏	2020-12-30T07:47:53Z	Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations	Hsueh C.-H.; Chen W.-P.; Lin J.-L.; Tsai C.-T.; YEN BIN LIU; Juang J.-M.; Tsao H.-M.; Su M.-J.; Lai L.-P.
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	2020-12-30T07:47:46Z	Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry	Jyh-Ming J.-J.; YEN BIN LIU; 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.; Lu T.-P.; Chuang E.Y.; Ackerman M.J.
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	2020-12-28T12:19:10Z	Antiphospholipid antibody syndrome with severe Libman-Sacks endocarditis - A case report	Lai L.-P.; HWANG, JUEY-JEN; Wang C.-R.; Chen J.-J.; Cheng J.-J.; Lin F.-Y.; Lien W.-P.
臺大學術典藏	2020-12-28T12:19:06Z	Transesophageal echocardiographic findings of left atrial floating thrombus	Tsai C.-H.; Li Y.-H.; HWANG, JUEY-JEN; Shyu K.-G.; Ma H.-M.; Lai L.-P.; Chiang F.-T.; Lien W.-P.
臺大學術典藏	2020-12-28T12:19:05Z	Clinical implications of left atrial appendage flow patterns in nonrheumatic atrial fibrillation	Li Y.-H.; Lai L.-P.; Shyu K.-G.; HWANG, JUEY-JEN; Kuan P.; Lien W.-P.
臺大學術典藏	2020-12-28T12:04:48Z	Transesophageal echocardiographic assessment of mitral valve position and pulmonary venous flow during cardiopulmonary resuscitation in humans	HWANG, JUEY-JEN; Ma M.H.-M.; Lien W.-P.; Tseng Y.-Z.; Kuan P.; Chen J.-J.; Hsu K.-L.; Lai L.-P.; Wang S.-M.; Huang G.-T.; Shyu K.-G.; Ko Y.-L.; Lin J.-L.; Chen W.-J.

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