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125篇 您的检索式：作者名="Priori S"

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	题名	作者	年代	出处	被引量
1	HRS/EHRA/ APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013显示文摘	PRIORI S G WILDE A A HORIE M	2013	Heart Rhythm2013，10，12：	1
2	HRS/ EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association(EHRA) 显示文摘	ACKERMAN M J PRIORI S G WILLEMS S	2011	Heart Rhythm2011，8，8：	1
3	Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia显示文摘	Marks A R Priori S Memmi M		0，，01：	1
4	The European Cardiac Resynchronization Therapy Survey:comparison of outcomes between de novo cardiac resynchronization therapy implantations and upgrades 显示文摘	Bogale N Witte K Priori S	2011	Eur J Heart Fail2011，13，：	1
5	Dispersion of the QT interval:a marker of therapeutic efficacy in the idiopathic long QT syndrome显示文摘	Priori S G Napolitano C Diehl L	1994	Circulation1994，89，：	1
6	Clinical and molecular characterizati0n of patients with catecholaminergic polymorphic ventricular tachycardia显示文摘	Priori S G Napolitano C M emmi M		0，，01：	1
7	A Genetic Algorithm Approach to Image Reconstruction in Electrical Impedance Tomngraphy显示文摘	OLMI R BINI M PRIORI S	2000	IEEE Trans on Evolutionary Computation2000，4，1：	1
8	The long QT syndrome 显示文摘	Priori S Bloise R Crotti L	2001	Europace2001，3，1：	1
9	Update of the guidelines on sudden cardiac death of European Society of Cardiology显示文摘	Priori S G Aliot E Blomstrom-Lundqvist C	2003	Eur Heart J2003，24，1：	1
10	Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia显示文摘	Marks A R Priori S Memmi M	2002	J Cell Physiol2002，190，1：	1
11	HRS/EHRA expert consensus statement on the state of genetic testing for the ehan- nelopathies and cardiomyopathies : this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Association (EHRA)显示文摘	Aekermen MJ Priori SG Willems S	2011	Europace2011，13，8：	1
12	Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia显示文摘	Priori S G Napolitano C Memmi M		0，，01：	1
13	Clinical and molecular characterization of patients with catecholaminergie polymorphic ventricular tachycardia 显示文摘	Priori S G Napolitano C Memmi M	2002	Circulation2002，106，1：	1
14	HRS/EHRA expert consensus statement on the state of genetic testing for the channelop- athies and cardiomyopathies this document was developed as a part- nership between the heart rhythm society (HRS) and the european heart rhythm association (EHRA) 显示文摘	Ackerman M J Priori SG Willems S	2011	Heart Rhythm2011，8，8：	1
15	A novel form of short QT syndrome(SQT3)is caused by a mutation in the KCNJ2 gene显示文摘	PRIORI G S PANDIT S V RIVOLTA I	2005	Circ Res2005，96，7：	1
16	Clinical spectrum of patients with a Brugada ECG显示文摘	FOWLER S J PRIORI S G	2009	Curr Opin Cardiol2009，24，1：	1
17	HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies:This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)显示文摘	Ackerman MJ Priori SG Willems S Berul C Brugada R Calkins H Camm AJ Ellinor PT Gollob M Hamilton R Hershberger RE Judge DP Le Marec H McKenna W J Schulze-Bahr E Semsarian C Towbin JA Watkins H Wilde A Wolpert C Zipes DP	2011	Europace2011，13，8：	1
18	Genetics of cardiac arrhythmia显示文摘	Cummings S Priori S	2011	Minerva Med2011，102，20：	1
19	Role of genetic analyses in cardiology:Part I:Mendelian diseases:Cardiac channelopathies显示文摘	Priori S G Napolitano C		0，，08：	1
20	Natural history of Brugada syndrome : insights for risk stratification and management显示文摘	PRIORI S G NAPOL1TANO C GASPARINI M	2002	Circulation2002，105，11：	1

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