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Showing items 36-60 of 94 (4 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2021-01-05T08:07:36Z	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)	Huang S.K.S.; Lo H.-M.; MEI-HWAN WU; Lin T.-K.; Chen S.-A.; Tsao H.-M.; Lei M.-H.; Lai L.-P.; Su Y.-N.; Hsieh F.-J.; Chiang F.-T.; Juang J.-M.; Liu Y.-B.; Ho Y.-L.; Chen W.-J.; Yeh S.-J.; Wang C.-C.; Ko Y.-L.; Wu T.-J.; Ueng K.-C.; Lin J.-L.
臺大學術典藏	2020-12-31T02:57:32Z	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	LING-PING LAI; Su Y.-N.; Chiang F.-T.; Juang J.-M.; Liu Y.-B.; 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.; Lin J.-L.
臺大學術典藏	2020-12-31T02:57:31Z	Brugada syndrome in the elderly in Taiwan - Report of two cases	Juang J.-M.; LING-PING LAI; Lin J.-L.; Chiang F.-T.
臺大學術典藏	2020-12-30T08:48:07Z	Characteristics of Chinese patients with symptomatic Brugada syndrome in Taiwan	Juang J.-M.; Huang S.K.S.; CHIA-TI TSAI; Chiang F.-T.; Lin J.-L.; Lai L.-P.; Wang C.-C.; Kuo C.-T.; Ueng K.-C.; Kong C.-W.; Ko W.-C.; Lei M.-H.; Tsao H.-M.
臺大學術典藏	2020-12-30T08:48:04Z	The association of human connexin 40 genetic polymorphisms with atrial fibrillation	Juang J.-M.; Chern Y.-R.; CHIA-TI TSAI; Chiang F.-T.; Lin J.-L.; Hwang J.-J.; Hsu K.-L.; Tseng C.-D.; Tseng Y.-Z.; Lai L.-P.
臺大學術典藏	2020-12-30T08:47:56Z	Rimonabant inhibits TNF-α-induced endothelial IL-6 secretion via CB1 receptor and cAMP-dependent protein kinase pathway	Hsueh C.-H.; Liang Y.-J.; Lin J.-L.; CHIA-TI TSAI; Lai L.-P.; Huang N.-L.; Juang J.-M.; Wang Y.-H.
臺大學術典藏	2020-12-30T08:47:56Z	Association between genetic polymorphisms in the renin-angiotensin system and systolic heart failure revised by a propensity score-based analysis	Chiang F.-T.; Hwang J.-J.; Chang S.-N.; Lin J.-W.; Juang J.-M.; CHIA-TI TSAI
臺大學術典藏	2020-12-30T08:47:49Z	Angiotensin II regulates the LARG/RhoA/MYPT1 axis in rat vascular smooth muscle in vitro	Chiu W.-C.; Juang J.-M.; Chang S.-N.; Wu C.-K.; CHIA-TI TSAI; Tseng Y.-Z.; Chiang F.-T.
臺大學術典藏	2020-12-30T08:47:37Z	Non-carriers of reduced-function CYP2C19 alleles are most susceptible to impairment of the anti-platelet effect of clopidogrel by proton-pump inhibitors: A pilot study	Lee J.-K.; Wu C.-K.; Juang J.-M.; CHIA-TI TSAI; Hwang J.-J.; Lin J.-L.; Chiang F.-T.
臺大學術典藏	2020-12-30T08:47:37Z	KCNN2 polymorphisms and cardiac tachyarrhythmias	Yu C.-C.; CHIA-TI TSAI; Chen P.-L.; Wu C.-K.; Chiu F.-C.; Chiang F.-T.; Chen P.-S.; Chen C.-L.; Lin L.-Y.; Juang J.-M.; Ho L.-T.; La L.-P.; Yang W.-S.; Lin J.-L.
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	2020-12-30T07:47:53Z	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	2020-12-28T12:04:30Z	The association of human connexin 40 genetic polymorphisms with atrial fibrillation	Chern Y.-R.; Juang J.-M.; Lai L.-P.; Tsai C.-T.; Chiang F.-T.; Lin J.-L.; HWANG, JUEY-JEN; Hsu K.-L.; Tseng C.-D.; Tseng Y.-Z.
臺大學術典藏	2020-12-28T12:04:15Z	Association between genetic polymorphisms in the renin-angiotensin system and systolic heart failure revised by a propensity score-based analysis	Juang J.-M.; Tsai C.-T.; HWANG, JUEY-JEN; Chiang F.-T.; Chang S.-N.; Lin J.-W.
臺大學術典藏	2020-12-28T12:03:53Z	Non-carriers of reduced-function CYP2C19 alleles are most susceptible to impairment of the anti-platelet effect of clopidogrel by proton-pump inhibitors: A pilot study	Lee J.-K.; Wu C.-K.; Juang J.-M.; Tsai C.-T.; HWANG, JUEY-JEN; Lin J.-L.; Chiang F.-T.
臺大學術典藏	2020-12-28T12:03:27Z	Prescription patterns of anti-diabetic medications and clinical outcomes in Asian patients with heart failure and diabetes mellitus	Erwinanto, Munawar M.; Martanto E.; Tedjokusumo P.; Purayil M.P.; Sharma M.K.; Sawhney J.; Gong X.; Wu Z.; Yu C.M.; Sastry B.K.S.; Gopi A.; Raghu K.; Sridevi C.; Kaur D.; Naik A.; Parikh K.; Chandarana A.; Shah U.; Chag M.; Baxi H.; Gupta S.; Bhatia J.; Khakhkhar V.; Sankhla V.; Patel T.; Kapoor V.; Wander G.S.; Tandon R.; Chopra V.; Kumar M.; Sethi H.J.S.; Verma R.; Mittal S.; Chia Y.M.F.; Teng T.-H.K.; Tay W.T.; Anand I.; MacDonald M.R.; Yap J.; Chandramouli C.; Richards A.M.; Tromp J.; Ouwerkerk W.; Ling L.H.; Lam C.S.P.; Hung C.-L.; Liew H.B.; Narasimhan C.; Ngarmukos T.; Park S.W.; Reyes E.; Siswanto B.B.; Shimizu W.; Zhang S.; Fan X.; Chen K.; Wu L.; Xie Y.; Jin Q.; Ling T.; Li X.; Zhou F.; Zhou Y.; Xu D.; Zhang H.; Su Y.; Chen X.; Qin S.; Wang J.; Shim J.; Kim D.-H.; Soo L.D.; Lee S.; Hong S.K.; Suzuki T.; Suzuki A.; Hagiwara N.; Kiuchi S.; Kabuki T.; Hisatake S.; Ikeda T.; Izumi Y.; Kubota Y.; Murai K.; Asai K.; Yasuoka R.; Pambudi J.A.; Lukito A.; Pardede I.; Thengker A.; Damay V.; Danny S.S.; Surarso R.; Noda T.; Nakajima I.; Wada M.; Ishibashi K.; Kurita T.; Sridhar G.S.; Sari N.A.M.; Zhudi A.S.B.M.; Abidin I.Z.; Azmee M.G.; Muhammad Z.; Hussin A.; Yap L.B.; Lee Y.W.; Yen C.H.; Othman M.K.; Augustine A.-A.; Asnawi M.H.M.; Mojolou R.A.; Tan Y.Z.; Arbain A.N.; Wong C.K.; Omar R.; Ghazi A.M.; Khelae S.K.; Chew D.S.P.; Park S.-M.; Roh S.-Y.; Kim Y.H.; Kim M.; Choi J.-I.; Na J.O.; Rha S.W.; Seo H.S.; Oh D.J.; Park C.G.; Kim E.J.; Joung B.; Uhm J.-S.; Lee M.H.; Cho I.-J.; Park H.-N.; Park H.-W.; Cho J.-G.; Yoon N.; Lee K.; Kim K.H.; Kim S.H.; Saharudin S.; Beh B.C.; Chao T.-F.; Hsu C.-N.; Yu W.-C.; Lin J.-W.; Chang S.-N.; Hung C.-S.; Lin P.-C.; Ling L.F.; Soon D.K.N.; Yeh H.-I.; Kuo J.-Y.; Yen C.-H.; HWANG, JUEY-JEN; Chien K.-L.; Su T.-C.; Lin L.-Y.; Juang J.-M.; Lin Y.-H.; Chiang F.-T.; Lin J.-L.; Ho Y.-L.; Lee C.-M.; Zuhdi A.S.M.; Ismail M.D.; Ong T.K.; Cham Y.L.; Khiew N.Z.; Said A.B.; Fong A.Y.Y.; Amin N.H.M.; Seng K.C.; Tan S.K.; Yew K.L.; Santos J.; Lim A.; Lapitan R.; Andal R.; Lopez E.; Sim K.L.D.; Tan B.Y.; Lim C.P.; Teo L.L.Y.; Chan L.L.H.; Chai P.; Wong C.C.R.; Poh K.K.; Yeo P.S.D.; Lee E.M.; Loh S.Y.; Ching M.E.; Khoo D.Z.L.; Yew M.S.; Huang W.; Leong K.T.G.; See J.H.J.; Lim Y.B.; Tan S.; Yeo C.; Chai S.C.; Jaufeerally F.R.; Tulsidas H.; Aung T.; Ong H.Y.; Phrommintikul A.; Tiyanon W.; Wongcharoen W.; Laothavorn P.; Lin Y.-N.; Chen K.-W.; Lo P.-H.; Hsu C.-H.; Hsieh L.-C.; Chandavimol M.; Yingchoncharoen T.; Sung S.-H.; Wang K.-L.; Leu H.-B.; Lin Y.-J.; Chang S.-L.; Huang P.-H.; Lo L.-W.; Wu C.-H.; Liang H.-Y.; Chang S.-S.; Hsiao L.-C.; Wang Y.-C.; Lu C.-R.; Wu H.-P.; on behalf of the ASIAN-HF Investigators
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	2020-12-28T10:02:48Z	Erratum: Arrhythmogenic right ventricular dysplasia: Clinical characteristics and identification of novel desmosome gene mutations (Journal of the Formosan Medical Association (2008) vol. 107 (7) (548-558))	CHIH-CHIEH YU; Yu C.H.; Hsueh C.H.; Yang C.T.; Juang J.M.; Hwang J.J.; Lin J.L.; Lai L.P.
臺大學術典藏	2020-12-25T08:38:50Z	The Impact of Lesion Length on Angiographic Restenosis after Vertebral Artery Origin Stenting	Hung C.S.; Lin J.W.; Juang J.M.; Lin Y.H.; Liu Y.C.; Tseng W.Y.I.; Jeng J.S.; Yip P.K.; Kao H.L.
臺大學術典藏	2020-12-25T08:32:21Z	The Impact of Lesion Length on Angiographic Restenosis after Vertebral Artery Origin Stenting	Kao H.L.; Yip P.K.; Lin Y.H.; Liu Y.C.; Tseng W.Y.I.; Juang J.M.; Hung C.S.; Lin J.W.; Jeng J.S.
臺大學術典藏	2020-12-25T08:24:25Z	The Impact of Lesion Length on Angiographic Restenosis after Vertebral Artery Origin Stenting	Lin Y.H.; Liu Y.C.; Tseng W.Y.I.; Juang J.M.; Hung C.S.; Lin J.W.; Jeng J.S.; Yip P.K.; Kao H.L.
臺大學術典藏	2020-12-23T08:28:49Z	Carotid artery stenosis: Routine predilatation or direct stenting?	Juang J.-M.; Lin Y.-H.; Lin, Lung-Chun; Lu C.-J.; Yip P.-K.; Kao H.-L.
臺大學術典藏	2020-12-21T08:16:55Z	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)	Liu Y.-B.; Juang J.-M.; Chiang F.-T.; Hsieh F.-J.; Su Y.-N.; Lai L.-P.; Lai L.-P.;Su Y.-N.;Hsieh F.-J.;Chiang F.-T.;Juang J.-M.;Liu Y.-B.;Ho Y.-L.;Wen-Jone Chen;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.;Lin J.-L.; Ho Y.-L.; WEN-JONE CHEN; 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.; Lin J.-L.
臺大學術典藏	2020-12-18T05:21:15Z	Symptomatic ostial vertebral artery stenosis treated with tubular coronary stents: Clinical results and restenosis analysis	YEN-HUNG LIN; Juang J.-M.; Jeng J.-S.; Yip P.-K.; Kao H.-L.

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