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93篇 您的检索式:作者名="Denjoy"
    题名 作者 年代 出处 被引量
1Comparison of the safety and efficacy of flecamide versus propafenone in hospital out-patients with symptomatic paroxysmal atrial fibrillation/flutter显示文摘Etienne Allot Isabelle Denjoy 1996The American Journal of Cardiology1996,,3:1
2High efficacy of β-blocker in long-QT syndrome type I显示文摘VINCENT G M SCHWARTZ P J DENJOY I 2009Circulation2009,119,:1
3Catecholaminergicpolymorphic ventricular tachycardia 显示文摘Leenhardt A Denjoy I Guicheney P 2012Circ ArrhythmElectrophysiol2012,5,:1
4Anovel mutation in the potassium channel gene KVLQTl causes the Jervell and Lange?Nielsen cardioauditory syndrome显示文摘NeyroudN TessonF Denjoy I 1997Nat Genet1997,15,2:1
5Absence of calsequestrin 2 causes severe forms of catecholam inergic polymorphic ventricular tachycardia显示文摘Postma A V Denjoy I Hoorntje T M 0,,08:1
6The Jervell and Lange-Nielsen Syndrome: Natural History, Molecular Basis, and Clinical Outcome显示文摘Peter J. Schwartz Carla Spazzolini Lia Crotti J?rn Bathen Jan P. Amlie Katherine Timothy Maria Shkolnikova Charles I. Berul Maria Bitner-Glindzicz Lauri Toivonen Minoru Horie Eric Schulze-Bahr Isabelle Denjoy 2006Circulation2006,,6:1
7The effect of atropine onrhythm and conduction disturbances during 322 critical care in-tubations 显示文摘Jones P Dauger S Denjoy I 2013Pediatr Crit Care Med2013,14,6:1
8A novel mutation in the potassiumchannel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditorysyndrome显示文摘Neyroud N Tesson F Denjoy I 1997Nat Genet1997,15,2:1
9Hydroquinidine therapy in Brugada syndrome显示文摘Hermida JS Denjoy I Clerc J 2004J Am Coll Cardiol2004,43,10:1
10High efficacy of beta-blockers in long-QT syndrome type 1:contribution of noncompliance and QT-prolonging drugs to the occurrence of beta-blocker treatment 'failures'显示文摘Vincent GM Schwartz PJ Denjoy I 2009Circulation2009,119,2:1
11Mutational spectrum in the Caz+-activated cation channel gene TRPM4 in patients with car- diac conductance disturbances 显示文摘Stallmeyer B Zumhagen S Denjoy 1 2012Hum Mutat2012,33,:1
12Catecholaminergic poly- morphic ventricular tachycardia in children : a 7-year follow-up of 21 patients显示文摘Leenhardt A Lucet V Denjoy I 1995Circulation1995,91,5:1
13KvLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome显示文摘Donger C Denjoy I Berthet M 1997Circulation1997,96,9:1
14A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and LangeNielsen cardioauditory syndrome显示文摘Neyroud N Tesson F Denjoy I 0,,2:1
15A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome 显示文摘Neyroud N Tesson F Denjoy I 1997Nat Genet1997,15,2:1
16KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome显示文摘 Denjoy I Berthet M 1997Circulation1997,96,9:1
17Novel mechanism for Bruga- da syndrome: defective surface localization of an SCN5A mutant (R1432G)显示文摘Baroudi G Pouliot V Denjoy I 2001CircRes2001,88,:1
18Catecholaminergic polymor- phic ventricular tachycardia 显示文摘Leenhardt A Denjoy I Guicheney P 2012Circ Arrhythm Electrophysiol2012,5,:1
19Novel mechanism for Brugada syndrome:defective surface localization of an SCN5A mutant (R1432G)显示文摘Baroudi G Pouliot V Denjoy I 0,,12:1
20Impact of the control of symptomatic paroxysmal atrial fibrillation on health- related quality of life 显示文摘Gu6don-Moreau L Capucci A Denjoy I 2010Europace2010,12,5:1
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