|
1
|
Assessment of QT intervals and prevalence of short QT syndrome in Japan.
|
Clin Cardiol
|
2008
|
0.98
|
|
2
|
Long QT syndrome and associated gene mutation carriers in Japanese children: results from ECG screening examinations.
|
Clin Sci (Lond)
|
2009
|
0.94
|
|
3
|
Gene mutations in adult Japanese patients with dilated cardiomyopathy.
|
Circ J
|
2005
|
0.89
|
|
4
|
Differences in diagnostic value of four electrocardiographic voltage criteria for hypertrophic cardiomyopathy in a genotyped population.
|
Am J Cardiol
|
2005
|
0.84
|
|
5
|
Heterogeneity of clinical manifestation of hypertrophic cardiomyopathy caused by deletion of lysine 183 in cardiac troponin I gene.
|
Int Heart J
|
2010
|
0.78
|
|
6
|
Differences in the diagnostic value of various criteria of negative T waves for hypertrophic cardiomyopathy based on a molecular genetic diagnosis.
|
Clin Sci (Lond)
|
2007
|
0.78
|
|
7
|
A KCR1 variant implicated in susceptibility to the long QT syndrome.
|
J Mol Cell Cardiol
|
2010
|
0.76
|
|
8
|
Perfect correspondence of mitral valve perforation using real-time 3-dimensional transesophageal echocardiography.
|
J Am Coll Cardiol
|
2012
|
0.75
|
|
9
|
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
|
|
10
|
Occult aneurysms in aorto-coronary saphenous vein grafts.
|
Intern Med
|
2010
|
0.75
|