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27篇 您的检索式：作者名="GOLLOB M H"

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	题名	作者	年代	出处	被引量
1	Long-term follow-up of a pediatric cohort with short QT syndrome显示文摘	Villafane J Atallah J Gollob M H	2013	J Am Coll Cardiol2013，61，11：	1
2	Transgenic mouse model of ventricular preexcitation and atrioventricular reentrant tachycardia induced by an AMP-activated protein kinase loss-of-function mutation responsible for Wolff-Parkinson-White syndrome显示文摘	Sidhu J S Rajawat Y S Rami T G Gollob M H Wang Z Yuan R	2005	Circulation2005，111，：	1
3	The short QT syndrome:proposed diagnostic criteria显示文摘	GOLLOB M H REDPATH C J ROBERTS J D	2011	J Am Coll Cardiol2011，57，7：	1
4	Current status of the implantable cardioverter - defibrillator显示文摘	GOLLOB M H SEGER J j	2001	Chest2001，119，4：	1
5	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
6	I- dentification of a gene responsible for familial Wolff- Parkinson-White syndrome显示文摘	GOLLOB M H GREEN M S TANG A S	2001	N Engl J Med2001，344，：	1
7	Cardiac connexins as candidate genes for idiopathic atrial fibrillation显示文摘	Gollob M H		0，，：	1
8	Identification of a gene responsible for familial Wolff-Parkinson-White syndrome显示文摘	GOLLOB M H GREEN M S TANG A	2001	N Engl J Med2001，344，：	1
9	Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy显示文摘	GOLLOB M H SEGER J J GOLLOB T N	2001	Circulation2001，104，：	1
10	PRKAG2 car- diac syndrome:Familial ventricular preexcitation, conduc- tion system disease, and cardiac hypertrophy 显示文摘	Gollob M H Green M S Tang A S	2002	Curt Opin Cardiol2002，17，3：	1
11	AMP-activated protein kinase and familial Wolff-Parkinson-White syndrome:new perspectives on heart development and arrhythmogenesis显示文摘	GOLLOB M H ROBERTS R	2002	Eur Heart J2002，23，：	1
12	Somatic mutaitons in the connexion 40 gene (GJA5) in atrial fibrillation显示文摘	GOLLOB M H JONES D L KRAHN A D	2006	N Engl J Med2006，354，：	1
13	A contemporary review on the genetic basis of atrial fibrillation显示文摘	Roberts J D Gollob M H	2014	Methodist Debakey Cardiovasc J2014，10，1：	1
14	Impact of genetic discoveries on the classification of lone atrial fibrillation显示文摘	Roberts J D Gollob M H	2010	J Am Coll Cardiol2010，55，8：	1
15	Sudden death in a young man with catecholaminergic polymorphic ventricular tachycardia and paroxysmal atrial fibrillation 显示文摘	PIZZALE S GOLLOB M H GOW R	2008	J Cardiovasc Electrophysiol2008，19，12：	1
16	PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac hypertrophy显示文摘	Gollob M H Green M S Tang A S Roberts R	2002	Curr Opin Cardiol2002，17，：	1
17	Glycogen storage disease as a unifying mechanism of disease in the PRKAG2 cardiac syndrome显示文摘	Gollob M H	2003	Biochem Soc Trans2003，31，：	1
18	Somatic mutations in the connexin 40 gene(GJA5) in atrial fibrillation显示文摘	GOLLOB M H JONES D L KRAHN A D	2006	N Engl J Med2006，354，：	1
19	Glycogen storage disease as a unifying mechanism of disease in the PRKAG2 cardiac syndrome显示文摘	GOLLOB M H	2003	Biochem Soc Trans2003，31，1：	1
20	Sudden cardiac death despite an implantable cardioverter-defibrillator in a young female with catecholaminergic ventricular tachycardia 显示文摘	MOHAMED U GOLLOB M H GOW R M	2006	Heart Rhythm2006，3，12：	1

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