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Institution Date Title Author
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 2020-12-30T07:20:31Z Atrial fibrillation screening in nonmetropolitan areas using a telehealth surveillance system with an embedded cloud-computing algorithm: Prospective pilot study Chen Y.-H.; Hung C.-S.; CHING-CHANG HUANG; Hung Y.-C.; Hwang J.-J.; Ho Y.-L.
臺大學術典藏 2020-12-30T02:43:37Z Relapse of SARS upon tapering corticosteroid Chien J.-Y.;Hsueh P.-R.;Shan-Chwen Chang;Hwang J.-J.;Yu C.-J.;Yang P.-C.; Chien J.-Y.; Hsueh P.-R.; SHAN-CHWEN CHANG; Hwang J.-J.; Yu C.-J.; Yang P.-C.
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 2020-12-28T10:52:55Z Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry Liu Y.-B.; Jyh-Ming J.-J.; Julius Chen C.-Y.; Yu Q.-Y.; Chattopadhyay A.; Lin L.-Y.; Chen W.-J.; Yu C.-C.; HUI-CHUN HUANG; 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 2020-12-28T10:52:54Z 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 2020-12-28T10:02:49Z Arrhythmogenic right ventricular dysplasia: Clinical characteristics and identification of novel desmosome gene mutations Yang C.-T.; Juang J.-M.; Hwang J.-J.; Lin J.-L.; Lai L.-P.; CHIH-CHIEH YU; Yu C.-H.; Hsueh C.-H.
臺大學術典藏 2020-12-28T10:02:49Z Provocation of Masked Left Ventricular Mechanical Dyssynchrony by Treadmill Exercise in Patients With Systolic Heart Failure and Narrow QRS Complex Lin J.-L.; Katra R.; Lin L.-C.; Tsai C.-T.; Wang Y.-C.; Hwang J.-J.; CHIH-CHIEH YU; Lai L.-P.

Showing items 556-565 of 1196  (120 Page(s) Totally)
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