Bi-directional Ventricular Tachycardia Revised

by Minoru Horie
Published 2010-01-01

Molecular genetics have opened a new era for arrhythmia research, but also Pandora׳s box?

by Minoru Horie, MD, PhD
Published 2016-10-01

Correction: Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients.

by Seiko Ohno, Kanae Hasegawa, Minoru Horie
Published 2021-01-01

Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients.

by Seiko Ohno, Kanae Hasegawa, Minoru Horie
Published 2015-01-01

Association between Progressive Intraventricular Conduction Disturbance and Cardiovascular Events.

by Hideki Hayashi, Qi Wu, Minoru Horie
Published 2016-01-01

Postoperative supraventricular tachycardia and polymorphic ventricular tachycardia due to a novel SCN5A variant: a case report of a rare comorbidity that is difficult to diagnose

by Koichi Kato, Tomoya Ozawa, Seiko Ohno, Yoshihisa Nakagawa, Minoru Horie
Published 2020-07-01

Biphasic P wave in inferior leads and the development of atrial fibrillation

by Hideki Hayashi, MD, PhD, Minoru Horie, MD, PhD
Published 2015-12-01

Genetic basis of Brugada syndrome

by Minoru Horie, MD, PhD, Seiko Ohno, MD, PhD
Published 2013-04-01

Genetics of Brugada syndrome

by Jyh-Ming Jimmy Juang, M.D., MS2, Ph.D., Minoru Horie
Published 2016-10-01

Assessment of disease-associated missense variants in RYR2 on transcript splicing

by Damilola Olubando, Huw Thomas, Minoru Horie, Raymond T. O’Keefe, Luigi Venetucci, William Newman
Published 2020-06-01

Irbesartan-mediated AT receptor blockade attenuates hyposmotic-induced enhancement of current and prevents shortening of action potential duration in atrial myocytes

by Jie Wu, Wei-Guang Ding, Jin Zhao, Wei-Jin Zang, Hiroshi Matsuura, Minoru Horie
Published 2014-12-01

Genetic Background of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Time to Start Asian Registry!

by Minoru Horie, MD, Katsuya Ishida, MD, Yukiko Nishio, MD, Iori Nagaoka, MD, Keiji Matsui, MD
Published 2008-01-01

Molecular pathogenesis of long QT syndrome type 1

by Jie Wu, PhD, Wei-Guang Ding, MD, PhD, Minoru Horie, MD, PhD
Published 2016-10-01

Pueraria mirifica, an estrogenic tropical herb, unveiled the severity of Type 1 LQTS caused by KCNQ1‐T587M

by Asami Kashiwa, Yukio Hosaka, Kazuyoshi Takahashi, Seiko Ohno, Yuko Wada, Takeru Makiyama, Hirotaka Oda, Minoru Horie
Published 2021-08-01

Not all rotors, effective ablation targets for nonparoxysmal atrial fibrillation, are included in areas suggested by conventional indirect indicators of atrial fibrillation drivers...

by Kensuke Sakata, Yusuke Okuyama, Tomoya Ozawa, Ryo Haraguchi, Kazuo Nakazawa, Takeshi Tsuchiya, Minoru Horie, Takashi Ashihara
Published 2018-04-01

A Novel SCN5A Mutation Associated with Drug Induced Brugada Type ECG.

by Isik Turker, Takeru Makiyama, Matteo Vatta, Hideki Itoh, Takeshi Ueyama, Akihiko Shimizu, Tomohiko Ai, Minoru Horie
Published 2016-01-01

Erratum to “Optical Recording of Action Potentials in Human Induced Pluripotent Stem Cell-Derived Cardiac Single Cells and Monolayers Generated from Long QT Syndrome Type 1 Patient...

by Tadashi Takaki, Azusa Inagaki, Kazuhisa Chonabayashi, Keiji Inoue, Kenji Miki, Seiko Ohno, Takeru Makiyama, Minoru Horie, Yoshinori Yoshida
Published 2020-01-01

Optical Recording of Action Potentials in Human Induced Pluripotent Stem Cell-Derived Cardiac Single Cells and Monolayers Generated from Long QT Syndrome Type 1 Patients

by Tadashi Takaki, Azusa Inagaki, Kazuhisa Chonabayashi, Keiji Inoue, Kenji Miki, Seiko Ohno, Takeru Makiyama, Minoru Horie, Yoshinori Yoshida
Published 2019-01-01

Late presentation of arrhythmogenic right ventricular cardiomyopathy in an octogenarian associated with a pathogenic variant in the plakophilin 2 gene: a case report

by Yusuke Adachi, Takekuni Hayashi, Takeshi Mitsuhashi, Kenichi Sakakura, Yoko Yamada, Yuko Wada, Minoru Horie, Shin-ichi Momomura, Hideo Fujita
Published 2019-02-01

Cardiac conduction defects and Brugada syndrome: A family with overlap syndrome carrying a nonsense SCN5A mutation

by Hisaaki Aoki, MD, PHD, Yoshihide Nakamura, MD, Seiko Ohno, MD, PHD, Takeru Makiyama, MD, PHD, Minoru Horie, MD, PHD
Published 2017-02-01