The genetic background of arrhythmogenic right ventricular cardiomyopathy

por Ohno, Seiko
Publicado 2016

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

por Ohno, Seiko, Hasegawa, Kanae, Horie, Minoru
Publicado 2015

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

por Ohno, Seiko, Hasegawa, Kanae, Horie, Minoru
Publicado 2021

Unique genetic background and outcome of non‐Caucasian Japanese probands with arrhythmogenic right ventricular dysplasia/cardiomyopathy

por Wada, Yuko, Ohno, Seiko, Aiba, Takeshi, Horie, Minoru
Publicado 2017

Bradycardia Is a Specific Phenotype of Catecholaminergic Polymorphic Ventricular Tachycardia Induced by RYR2 Mutations

por Miyata, Kazuaki, Ohno, Seiko, Itoh, Hideki, Horie, Minoru
Publicado 2018

Case report of a ventricular fibrillation storm with a cardiac conduction disorder and HCN4 variant 18 years after ablation of atrial flutter

por Nakamura, Toshihiro, Fukuzawa, Koji, Aiba, Takeshi, Ohno, Seiko
Publicado 2022

Diversity of P-element piRNA production among M' and Q strains and its association with P-M hybrid dysgenesis in Drosophila melanogaster

por Wakisaka, Keiko Tsuji, Ichiyanagi, Kenji, Ohno, Seiko, Itoh, Masanobu
Publicado 2017

Association of zygotic piRNAs derived from paternal P elements with hybrid dysgenesis in Drosophila melanogaster

por Wakisaka, Keiko Tsuji, Ichiyanagi, Kenji, Ohno, Seiko, Itoh, Masanobu
Publicado 2018

Computerized misinterpretation of QT interval in 12‐lead electrocardiogram and its clinical consequences: A case of recurrent syncope

por Hasegawa, Kanae, Fukuoka, Yoshitomo, Ohno, Seiko, Horie, Minoru, Tada, Hiroshi
Publicado 2023

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

por Aoki, Hisaaki, Nakamura, Yoshihide, Ohno, Seiko, Makiyama, Takeru, Horie, Minoru
Publicado 2017

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

por Kato, Koichi, Ozawa, Tomoya, Ohno, Seiko, Nakagawa, Yoshihisa, Horie, Minoru
Publicado 2020

Three cases of catecholaminergic polymorphic ventricular tachycardia with prolonged QT intervals including two cases of compound mutations

por Saito, Aki, Ohno, Seiko, Nuruki, Norihito, Nomura, Yuichi, Horie, Minoru, Yoshinaga, Masao
Publicado 2018

A novel CACNA1C mutation identified in a patient with Timothy syndrome without syndactyly exerts both marked loss- and gain-of-function effects

por Ozawa, Junichi, Ohno, Seiko, Saito, Hideki, Saitoh, Akihiko, Matsuura, Hiroshi, Horie, Minoru
Publicado 2018

A tryptophan residue in the caffeine-binding site of the ryanodine receptor regulates Ca(2+) sensitivity

por Murayama, Takashi, Ogawa, Haruo, Kurebayashi, Nagomi, Ohno, Seiko, Horie, Minoru, Sakurai, Takashi
Publicado 2018

Familial sick sinus syndrome possibly associated with novel SCN5A mutation diagnosed in pregnancy

por Abe, Ichitaro, Wang, Pu, Takahashi, Masaki, Ohno, Seiko, Ono, Katsushige, Takahashi, Naohiko
Publicado 2020

Arrhythmogenic right-ventricular cardiomyopathy with plakophilin-2 genetic variant concomitant with early manifestation of ventricular tachyarrhythmia: a case series

por Kawano, Kyoko, Kondo, Hidekazu, Takahashi, Masaki, Shinohara, Tetsuji, Ohno, Seiko, Horie, Minoru, Takahashi, Naohiko
Publicado 2022

Identification of a novel exon3 deletion of RYR2 in a family with catecholaminergic polymorphic ventricular tachycardia

por Dharmawan, Tommy, Nakajima, Tadashi, Ohno, Seiko, Iizuka, Takashi, Tamura, Shuntaro, Kaneko, Yoshiaki, Horie, Minoru, Kurabayashi, Masahiko
Publicado 2019

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

por Kashiwa, Asami, Hosaka, Yukio, Takahashi, Kazuyoshi, Ohno, Seiko, Wada, Yuko, Makiyama, Takeru, Oda, Hirotaka, Horie, Minoru
Publicado 2021

Successful Management of a Young Athlete with Type 2 Long QT Syndrome by Genotype-specific Risk Stratification and Bridging Therapy with a Wearable Cardioverter Defibrillator

por Kojima, Katsumi, Kato, Koichi, Fujii, Yusuke, Okuyama, Yusuke, Ohno, Seiko, Ozawa, Tomoya, Horie, Minoru, Nakagawa, Yoshihisa
Publicado 2022

Investigation on the optimal implantation site and setting of Reveal LINQ(®) avoiding interference with performance of transthoracic echocardiography

por Tada, Shizuka, Shibata, Masayoshi, Ohno, Seiko, Haruki, Yasunobu, Murakami, Hironori, Hotta, Daisuke, Nojima, Masanori, Ruhnke, Gregory W.
Publicado 2018