Hideki Itoh

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

Masami Shimizu, Hidekazu Ino, Kazuyasu Okeie et al. · Clinical Cardiology · 2002 · 262 citations · Full text

The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome

Naomasa Makita, Elijah R. Behr, Wataru Shimizu et al. · Journal of Clinical Investigation · 2008 · 235 citations · Full text

Long Qt Syndrome, Genetics, Genetic Epidemiology +17

The genetics underlying acquired long QT syndrome: impact for genetic screening

Hideki Itoh, Lia Crotti, Takeshi Aiba et al. · European Heart Journal · 2015 · 209 citations · Full text

A Novel SCN5A Gain-of-Function Mutation M1875T Associated With Familial Atrial Fibrillation

Takeru Makiyama, Masaharu Akao, Satoshi Shizuta et al. · Journal of the American College of Cardiology · 2008 · 201 citations

Genetic Disorder, Genetics, Familial Atrial Fibrillation +4

Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy

Fernande Freyermuth, Frédérique Rau, Yosuke Kokunai et al. · Nature Communications · 2016 · 198 citations · Full text