维普期刊资源整合服务平台（V6.5）

83篇 您的检索式：作者名="Denjoy I"

选中清除导出查看参考文献查看引证文献引用追踪共5页首页上一页第1页下一页末页 /5 跳转

	题名	作者	年代	出处	被引量
1	High efficacy of β-blocker in long-QT syndrome type I显示文摘	VINCENT G M SCHWARTZ P J DENJOY I	2009	Circulation2009，119，：	1
2	Catecholaminergicpolymorphic ventricular tachycardia 显示文摘	Leenhardt A Denjoy I Guicheney P	2012	Circ ArrhythmElectrophysiol2012，5，：	1
3	Anovel mutation in the potassium channel gene KVLQTl causes the Jervell and Lange?Nielsen cardioauditory syndrome显示文摘	NeyroudN TessonF Denjoy I	1997	Nat Genet1997，15，2：	1
4	Absence 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
5	The effect of atropine onrhythm and conduction disturbances during 322 critical care in-tubations 显示文摘	Jones P Dauger S Denjoy I	2013	Pediatr Crit Care Med2013，14，6：	1
6	A novel mutation in the potassiumchannel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditorysyndrome显示文摘	Neyroud N Tesson F Denjoy I	1997	Nat Genet1997，15，2：	1
7	Hydroquinidine therapy in Brugada syndrome显示文摘	Hermida JS Denjoy I Clerc J	2004	J Am Coll Cardiol2004，43，10：	1
8	High 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	2009	Circulation2009，119，2：	1
9	Catecholaminergic poly- morphic ventricular tachycardia in children : a 7-year follow-up of 21 patients显示文摘	Leenhardt A Lucet V Denjoy I	1995	Circulation1995，91，5：	1
10	KvLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome显示文摘	Donger C Denjoy I Berthet M	1997	Circulation1997，96，9：	1
11	A 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
12	A 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	1997	Nat Genet1997，15，2：	1
13	KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome显示文摘	Denjoy I Berthet M	1997	Circulation1997，96，9：	1
14	Novel mechanism for Bruga- da syndrome: defective surface localization of an SCN5A mutant (R1432G)显示文摘	Baroudi G Pouliot V Denjoy I	2001	CircRes2001，88，：	1
15	Catecholaminergic polymor- phic ventricular tachycardia 显示文摘	Leenhardt A Denjoy I Guicheney P	2012	Circ Arrhythm Electrophysiol2012，5，：	1
16	Novel 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
17	Impact 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	2010	Europace2010，12，5：	1
18	KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome显示文摘	Donger C Denjoy I Berthet M	1997	Circulation1997，96，9：	1
19	Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia显示文摘	Postma A V Denjoy I Hoorntje T M	2002	Circ Res2002，91，8：	1
20	Practical attitude toward arrhythmia in the neonate and infant 显示文摘	Lupoglazoff JM Denjoy I	2004	Arch Pediatr2004，11，10：	1

返回顶部每页显示：

共5页首页上一页第1页下一页末页 /5 跳转

互联网出版许可证新出网证(渝)字10号全国400电话 - 免长途话费

用户提示