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96篇 您的检索式：作者名="Tester DJ"

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	题名	作者	年代	出处	被引量
1	Genotypic heterogeneity and phenotypie mimicry among unrelated patients referred for catecholaminergic polymorphic ventricular taehycardia genetic testing显示文摘	Tester DJ Arya P Will M	2006	Heart Rhythm2006，3，7：	1
2	Novel NOTCH1 mutations in patients with bicuspid aortic valve disease and thoracic aortic aneurysms显示文摘	McKellar SH Tester DJ Yagubyan M	2007	J Thorac Cardio- vase Surg2007，134，2：	1
3	Genetic testing for long-QT syndrome:distinguishing pathogenic mutations from benign variants显示文摘	Kapa S Tester DJ Salisbury BA	2009	Circulation2009，120，18：	1
4	Molecular autopsy of HERG defects in sudden infant death syndrome显示文摘	Ackerman MJ Anson BD Tester DJ	2002	J Am Coll Cardiol2002，39，3：	1
5	SCN4B-encoded sodiumchannel beta4 subunit in congenital long-QT syndrome显示文摘	Medeiros-Domingo A Kaku T Tester DJ	2007	Circulation2007，116，2：	1
6	SCN4B-encoded sodium channel subunit in congenital long-QT syndrome显示文摘	Domingo AM Kaku T Tester DJ	2007	Circulation2007，116，2：	1
7	Mutation of an A-kinase-anchoring protein causes long-QT syndrome显示文摘	Chen L Marquardt ML Tester DJ	2007	Proc Natl Acad Sci U S A2007，104，20：	1
8	Cardiac channelmolecular autopsy for sudden unexpected death in epilepsy 显示文摘	Johnson JN Tester DJ Bass NE	2010	JChild Neurol2010，25，：	1
9	Mutation of an ,A-ki-nase-anchoring protein causes long-QT syndrome 显示文摘	Chen L Marquardt ML Tester DJ	2007	Proc Nat Acad Sci2007，104，20：	1
10	The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative,exercise-induced long QT syndrome:a comprehensive open reading frame mutational analysis显示文摘	Medeiros-Domingo A Bhuiyan ZA Tester DJ	2009	J Am Coll Cardiol2009，54，22：	1
11	Genetics of long QT syndrome 显示文摘	Tester DJ Ackerman MJ	2014	Methodist De-bakey Cardiovasc J2014，10，1：	1
12	Catecholamine-provoked microvoltage T wave alternans in genotyped long QT syndrome 显示文摘	Nemec J Ackerman M J Tester DJ	2003	Pacing Clin Electrophysiol2003，26，：	1
13	Diagnostic miscues in congenital long-QT syndrome显示文摘	Taggart NW Haglund CM Tester DJ	2007	Circulation2007，115，20：	1
14	Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test显示文摘	Kapplinger JD Tester DJ Salisbury BA	2009	Heart Rhythm2009，6，9：	1
15	Molecular and functional characterization of common polymorphisms in HERG (KCNH2) potassium channels 显示文摘	Anson BD Ackerman MJ Tester DJ	2004	Am J Physiol Heart Circ Physiol2004，286，6：	1
16	Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome显示文摘	Van Norstrand DW Valdivia CR Tester DJ	2007	Circulation2007，116，20：	1
17	Effect of clinical phenotype on yield of long QT syndrome genetic testing显示文摘	Tester DJ Will ML Haglund CM	2006	J Am Coll Cardiol2006，47，4：	1
18	Identification of a common genetic substrate underlying postpartum cardiac events in congenital long QT syndrome 显示文摘	Khositseth A Tester DJ Will ML	2004	Heart Rhythm2004，1，：	1
19	Swimming,a gene-specific arrhythmogenic trigger for inherited long QT syndrome显示文摘	Ackerman MJ Tester DJ Porter CJ	1999	Mayo Clin Proc1999，74，11：	1
20	Effect of clinicalphenotype on yield of long QT syndrome genetic testing显示文摘	Tester DJ Will ML Haglund CM Ackerman MJ	2006	Am Coll Cardiol2006，47，：	1

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