|
1
|
A novel KCNH2 mutation as a modifier for short QT interval.
|
Int J Cardiol
|
2008
|
1.57
|
|
2
|
Age- and genotype-specific triggers for life-threatening arrhythmia in the genotyped long QT syndrome.
|
J Cardiovasc Electrophysiol
|
2008
|
1.50
|
|
3
|
A paradoxical effect of lidocaine for the N406S mutation of SCN5A associated with Brugada syndrome.
|
Int J Cardiol
|
2007
|
1.42
|
|
4
|
Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndrome.
|
Circ Arrhythm Electrophysiol
|
2009
|
1.33
|
|
5
|
A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation.
|
J Am Coll Cardiol
|
2008
|
1.22
|
|
6
|
Mutation site dependent variability of cardiac events in Japanese LQT2 form of congenital long-QT syndrome.
|
Circ J
|
2008
|
0.99
|
|
7
|
Cardioverter defibrillator implantation in a patient with double chambered right ventricle.
|
Int J Cardiovasc Imaging
|
2006
|
0.92
|
|
8
|
Hydroxyzine, a first generation H(1)-receptor antagonist, inhibits human ether-a-go-go-related gene (HERG) current and causes syncope in a patient with the HERG mutation.
|
J Pharmacol Sci
|
2008
|
0.81
|
|
9
|
Evaluation of meat meal, chicken meal, and corn gluten meal as dietary sources of protein in dry cat food.
|
Can J Vet Res
|
2005
|
0.80
|