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Seiko Ohno

Showing results (41-50 of 222) with videos related to

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European Heart Journal. Case Reports|October 13, 2022
Arrhythmogenic right-ventricular cardiomyopathy with plakophilin-2 genetic variant concomitant with early manifestation of ventricular tachyarrhythmia: a case seriesKyoko Kawano, Hidekazu Kondo, Masaki Takahashi, et al.
Circulation. Genomic and Precision Medicine|August 21, 2020
<i>LMNA</i> Missense Mutation Causes Nonsense-Mediated mRNA Decay and Severe Dilated CardiomyopathyKoichi Kato, Seiko Ohno, Keiko Sonoda, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|January 30, 2016
Pediatric Cohort With Long QT Syndrome　- KCNH2 Mutation Carriers Present Late Onset But Severe SymptomsJunichi Ozawa, Seiko Ohno, Takashi Hisamatsu, et al.
Journal of Arrhythmia|August 13, 2021
<i>Pueraria mirifica</i>, an estrogenic tropical herb, unveiled the severity of Type 1 LQTS caused by <i>KCNQ1</i>-T587MAsami Kashiwa, Yukio Hosaka, Kazuyoshi Takahashi, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|March 22, 2013
Age-dependent clinical and genetic characteristics in Japanese patients with arrhythmogenic right ventricular cardiomyopathy/dysplasiaSeiko Ohno, Iori Nagaoka, Megumi Fukuyama, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|October 26, 2020
Age-Dependent Clinical and Genetic Characteristics in Japanese Patients with Arrhythmogenic Right Ventricular Cardiomyopathy/DysplasiaSeiko Ohno, Iori Nagaoka, Megumi Fukuyama, et al.
European Heart Journal. Case Reports|April 23, 2026
A diagnostic challenge of advanced-stage cardiac Fabry disease without left ventricular hypertrophy: a case reportMasataka Suzuki, Yuko Yoshigai, Hiromi Hashimura, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|April 12, 2013
L-type calcium channel mutations in Japanese patients with inherited arrhythmiasMegumi Fukuyama, Seiko Ohno, Qi Wang, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|December 3, 2023
Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT SyndromeMasao Yoshinaga, Yumiko Ninomiya, Yuji Tanaka, et al.
Journal of Cardiology|December 2, 2015
LMNA cardiomyopathy detected in Japanese arrhythmogenic right ventricular cardiomyopathy cohortKoichi Kato, Naohiko Takahashi, Yusuke Fujii, et al.
Pageof 23

Showing results (41-50 of 222) with videos related to

Sort By:
Pageof 23
European Heart Journal. Case Reports|October 13, 2022
Arrhythmogenic right-ventricular cardiomyopathy with plakophilin-2 genetic variant concomitant with early manifestation of ventricular tachyarrhythmia: a case seriesKyoko Kawano, Hidekazu Kondo, Masaki Takahashi, et al.
Circulation. Genomic and Precision Medicine|August 21, 2020
<i>LMNA</i> Missense Mutation Causes Nonsense-Mediated mRNA Decay and Severe Dilated CardiomyopathyKoichi Kato, Seiko Ohno, Keiko Sonoda, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|January 30, 2016
Pediatric Cohort With Long QT Syndrome　- KCNH2 Mutation Carriers Present Late Onset But Severe SymptomsJunichi Ozawa, Seiko Ohno, Takashi Hisamatsu, et al.
Journal of Arrhythmia|August 13, 2021
<i>Pueraria mirifica</i>, an estrogenic tropical herb, unveiled the severity of Type 1 LQTS caused by <i>KCNQ1</i>-T587MAsami Kashiwa, Yukio Hosaka, Kazuyoshi Takahashi, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|March 22, 2013
Age-dependent clinical and genetic characteristics in Japanese patients with arrhythmogenic right ventricular cardiomyopathy/dysplasiaSeiko Ohno, Iori Nagaoka, Megumi Fukuyama, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|October 26, 2020
Age-Dependent Clinical and Genetic Characteristics in Japanese Patients with Arrhythmogenic Right Ventricular Cardiomyopathy/DysplasiaSeiko Ohno, Iori Nagaoka, Megumi Fukuyama, et al.
European Heart Journal. Case Reports|April 23, 2026
A diagnostic challenge of advanced-stage cardiac Fabry disease without left ventricular hypertrophy: a case reportMasataka Suzuki, Yuko Yoshigai, Hiromi Hashimura, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|April 12, 2013
L-type calcium channel mutations in Japanese patients with inherited arrhythmiasMegumi Fukuyama, Seiko Ohno, Qi Wang, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|December 3, 2023
Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT SyndromeMasao Yoshinaga, Yumiko Ninomiya, Yuji Tanaka, et al.
Journal of Cardiology|December 2, 2015
LMNA cardiomyopathy detected in Japanese arrhythmogenic right ventricular cardiomyopathy cohortKoichi Kato, Naohiko Takahashi, Yusuke Fujii, et al.
Pageof 23