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1
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T wave peak-to-end interval and QT dispersion in acquired long QT syndrome: a new index for arrhythmogenicity.
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Clin Sci (Lond)
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2003
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1.86
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2
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T-peak to T-end interval may be a better predictor of high-risk patients with hypertrophic cardiomyopathy associated with a cardiac troponin I mutation than QT dispersion.
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Clin Cardiol
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2002
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1.72
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3
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Impact of severe earthquake on the occurrence of acute coronary syndrome and stroke in a rural area of Japan.
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Circ J
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2009
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1.55
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|
4
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An enhanced device for transluminal retrieval of vascular stents without surgical procedures: experimental studies.
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J Interv Cardiol
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2010
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1.50
|
|
5
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A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome.
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Heart Rhythm
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2012
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1.44
|
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6
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Changes in cardiac tissue characterization in carriers with gene mutations associated with hypertrophic cardiomyopathy.
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Int J Cardiol
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2005
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1.38
|
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7
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Impact of anti-apoptotic and anti-oxidative effects of bone marrow mesenchymal stem cells with transient overexpression of heme oxygenase-1 on myocardial ischemia.
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Am J Physiol Heart Circ Physiol
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2010
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1.15
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8
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Brugada syndrome with ventricular tachycardia and fibrillation related to hypokalemia.
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Circ J
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2003
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1.07
|
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9
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Differentiation between patients with takotsubo cardiomyopathy and those with anterior acute myocardial infarction.
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Circ J
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2005
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1.05
|
|
10
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Current perspectives in genetic cardiovascular disorders: from basic to clinical aspects.
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Heart Vessels
|
2013
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1.02
|
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11
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Assessment of QT intervals and prevalence of short QT syndrome in Japan.
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Clin Cardiol
|
2008
|
0.98
|
|
12
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High incidence of sudden cardiac death with conduction disturbances and atrial cardiomyopathy caused by a nonsense mutation in the STA gene.
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Circulation
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2005
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0.98
|
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13
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Marked aortic valve stenosis progression after receiving long-term aggressive cholesterol-lowering therapy using low-density lipoprotein apheresis in a patient with familial hypercholesterolemia.
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Circ J
|
2008
|
0.97
|
|
14
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Long QT syndrome and associated gene mutation carriers in Japanese children: results from ECG screening examinations.
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Clin Sci (Lond)
|
2009
|
0.94
|
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15
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Increased circulating matrix metalloproteinase-2 in patients with hypertrophic cardiomyopathy with systolic dysfunction.
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Circ J
|
2004
|
0.93
|
|
16
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A novel mutation Lys273Glu in the cardiac troponin T gene shows high degree of penetrance and transition from hypertrophic to dilated cardiomyopathy.
|
Am J Cardiol
|
2002
|
0.91
|
|
17
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Intravascular ultrasound appearance of scattered necrotic core as an index for deterioration of coronary flow during intervention in acute coronary syndrome.
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Heart Vessels
|
2011
|
0.89
|
|
18
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Gene mutations in adult Japanese patients with dilated cardiomyopathy.
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Circ J
|
2005
|
0.89
|
|
19
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Probucol aggravates long QT syndrome associated with a novel missense mutation M124T in the N-terminus of HERG.
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Clin Sci (Lond)
|
2004
|
0.89
|
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20
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Diagnostic value of abnormal Q waves for identification of preclinical carriers of hypertrophic cardiomyopathy based on a molecular genetic diagnosis.
|
Eur Heart J
|
2004
|
0.87
|
|
21
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Compound heterozygosity for mutations Asp611-->Tyr in KCNQ1 and Asp609-->Gly in KCNH2 associated with severe long QT syndrome.
|
Clin Sci (Lond)
|
2005
|
0.84
|
|
22
|
Differences in diagnostic value of four electrocardiographic voltage criteria for hypertrophic cardiomyopathy in a genotyped population.
|
Am J Cardiol
|
2005
|
0.84
|
|
23
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Expression and function of ephrin-B1 and its cognate receptor EphB2 in human atherosclerosis: from an aspect of chemotaxis.
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Clin Sci (Lond)
|
2008
|
0.83
|
|
24
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Characterization of a novel missense mutation E637K in the pore-S6 loop of HERG in a patient with long QT syndrome.
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Cardiovasc Res
|
2002
|
0.83
|
|
25
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Impact of QT variables on clinical outcome of genotyped hypertrophic cardiomyopathy.
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Ann Noninvasive Electrocardiol
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2009
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0.83
|
|
26
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A novel missense mutation in the myosin binding protein-C gene is responsible for hypertrophic cardiomyopathy with left ventricular dysfunction and dilation in elderly patients.
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J Am Coll Cardiol
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2003
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0.82
|
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27
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Effects of gender on the number of diseased vessels and clinical outcome in Japanese patients with acute coronary syndrome.
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Circ J
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2002
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0.82
|
|
28
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Heterogeneity of cardiac sympathetic nerve activity and systolic dysfunction in patients with hypertrophic cardiomyopathy.
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J Nucl Med
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2002
|
0.82
|
|
29
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A novel beta-myosin heavy chain gene mutation, p.Met531Arg, identified in isolated left ventricular non-compaction in humans, results in left ventricular hypertrophy that progresses to dilation in a mouse model.
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Clin Sci (Lond)
|
2008
|
0.82
|
|
30
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Hemodynamic changes and prognosis in patients with hypertrophic cardiomyopathy and abnormal blood pressure responses during exercise.
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Clin Cardiol
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2003
|
0.81
|
|
31
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Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome.
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Clin Sci (Lond)
|
2003
|
0.80
|
|
32
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Autopsy findings in siblings with hypertrophic cardiomyopathy caused by Arg92Trp mutation in the cardiac troponin T gene showing dilated cardiomyopathy-like features.
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Clin Cardiol
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2003
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0.80
|
|
33
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Cardiac sympathetic nerve activity in patients with hypertrophic cardiomyopathy with malignant ventricular tachyarrhythmias.
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J Nucl Cardiol
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2003
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0.80
|
|
34
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Analysis of ankyrin-B gene mutations in patients with long QT syndrome.
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Nan Fang Yi Ke Da Xue Xue Bao
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2006
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0.79
|
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35
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Multiple noncoding exons 1 of nuclear receptors NR4A family (nerve growth factor-induced clone B, Nur-related factor 1 and neuron-derived orphan receptor 1) and NR5A1 (steroidogenic factor 1) in human cardiovascular and adrenal tissues.
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J Hypertens
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2011
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0.79
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36
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Heterogeneity of clinical manifestation of hypertrophic cardiomyopathy caused by deletion of lysine 183 in cardiac troponin I gene.
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Int Heart J
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2010
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0.78
|
|
37
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Differences in the diagnostic value of various criteria of negative T waves for hypertrophic cardiomyopathy based on a molecular genetic diagnosis.
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Clin Sci (Lond)
|
2007
|
0.78
|
|
38
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Impact of out-stent plaque volume on in-stent intimal hyperplasia: results from serial volumetric analysis with high-gain intravascular ultrasound.
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Int J Cardiol
|
2011
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0.77
|
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39
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Q-T peak dispersion in congenital long QT syndrome: possible marker of mutation of HERG.
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Circ J
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2003
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0.77
|
|
40
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Septal wall thinning and systolic dysfunction in patients with hypertrophic cardiomyopathy caused by a cardiac troponin I gene mutation.
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Am Heart J
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2002
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0.77
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|
41
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Oxidative stress correlates with left ventricular volume after acute myocardial infarction.
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Jpn Heart J
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2002
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0.77
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|
42
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Impact of systolic dysfunction in genotyped hypertrophic cardiomyopathy.
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Clin Cardiol
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2012
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0.77
|
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43
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Impact of lesion morphology and associated procedures for left main coronary stenting on angiographic outcome after intervention: sub-analysis of Heart Research Group of Kanazawa, HERZ, Study.
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Cardiovasc Interv Ther
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2013
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0.76
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44
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Changes in cardiac sympathetic nerve innervation and activity in pathophysiologic transition from typical to end-stage hypertrophic cardiomyopathy.
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J Nucl Med
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2003
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0.76
|
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45
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A KCR1 variant implicated in susceptibility to the long QT syndrome.
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J Mol Cell Cardiol
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2010
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0.76
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46
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A rare type of alternating bundle branch block in a patient with cardiac sarcoidosis--a case report.
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Angiology
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2005
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0.76
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47
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Impact of renin-angiotensin system polymorphisms on development of systolic dysfunction in hypertrophic cardiomyopathy. Evidence from a study of genotyped patients.
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Circ J
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2010
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0.75
|
|
48
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Impact of bilateral internal thoracic-to-epigastric artery communications on salvaging total lower limb ischemia.
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J Am Coll Cardiol
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2011
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0.75
|
|
49
|
A novel mutation in the cardiac myosin-binding protein C gene is responsible for hypertrophic cardiomyopathy with severe ventricular hypertrophy and sudden death.
|
Clin Sci (Lond)
|
2006
|
0.75
|
|
50
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Images in cardiovascular medicine. Adult patient with isolated noncompaction of ventricular myocardium.
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Circulation
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2005
|
0.75
|
|
51
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Chronologic electrocardiographic changes in patients with hypertrophic cardiomyopathy associated with cardiac troponin 1 mutation.
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Am Heart J
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2002
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0.75
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52
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Low electrocardiogram voltage due to anasarca.
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Intern Med
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2010
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0.75
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53
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In-hospital outcome in octogenarians with acute coronary syndrome undergoing emergent coronary angiography.
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Jpn Heart J
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2003
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0.75
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54
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[Restrictive cardiomyopathy associated with heart failure].
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Nihon Rinsho
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2007
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0.75
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55
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Scintigraphic evaluation of regression of abnormal Q waves in myocardial infarction.
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Ann Nucl Med
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2005
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0.75
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