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Seiko Ohno

Showing results (141-150 of 222) with videos related to

Pageof 23
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Journal of Arrhythmia|October 8, 2021
Prevalence and characteristics of the Brugada electrocardiogram pattern in patients with arrhythmogenic right ventricular cardiomyopathyNobuhiko Ueda, Satoshi Nagase, Naoya Kataoka, et al.
Journal of Cardiovascular Electrophysiology|January 10, 2014
Gain-of-function KCNH2 mutations in patients with Brugada syndromeQ I Wang, Seiko Ohno, Wei-Guang Ding, et al.
Nutrients|December 3, 2020
Association of Red Meat Intake with the Risk of Cardiovascular Mortality in General Japanese Stratified by Kidney Function: NIPPON DATA80Hiroyoshi Segawa, Keiko Kondo, Aya Kadota, et al.
International Journal of Cardiology|September 3, 2020
Impact of the T-wave characteristics on distinguishing arrhythmogenic right ventricular cardiomyopathy from healthy childrenTomohiko Imamura, Naokata Sumitomo, Shota Muraji, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 2, 2023
Non-missense variants of KCNH2 show better outcomes in type 2 long QT syndromeTakanori Aizawa, Yuko Wada, Kanae Hasegawa, et al.
Journal of Cardiology|November 7, 2016
Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano-Ward syndrome under double mutations and acquired long QT syndrome under heterozygoteYusuke Fujii, Yuichi Matsumoto, Kenshi Hayashi, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|October 18, 2021
Loss-of-function mutations in cardiac ryanodine receptor channel cause various types of arrhythmias including long QT syndromeSayako Hirose, Takashi Murayama, Naoyuki Tetsuo, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|April 29, 2008
Mutation site dependent variability of cardiac events in Japanese LQT2 form of congenital long-QT syndromeIori Nagaoka, Wataru Shimizu, Hideki Itoh, et al.
Heart Rhythm|October 21, 2016
A type 2 ryanodine receptor variant associated with reduced Ca<sup>2+</sup> release and short-coupled torsades de pointes ventricular arrhythmiaYusuke Fujii, Hideki Itoh, Seiko Ohno, et al.
Journal of the American College of Cardiology|August 22, 2009
D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndromeYukiko Nishio, Takeru Makiyama, Hideki Itoh, et al.
Pageof 23

Showing results (141-150 of 222) with videos related to

Sort By:
Pageof 23
Journal of Arrhythmia|October 8, 2021
Prevalence and characteristics of the Brugada electrocardiogram pattern in patients with arrhythmogenic right ventricular cardiomyopathyNobuhiko Ueda, Satoshi Nagase, Naoya Kataoka, et al.
Journal of Cardiovascular Electrophysiology|January 10, 2014
Gain-of-function KCNH2 mutations in patients with Brugada syndromeQ I Wang, Seiko Ohno, Wei-Guang Ding, et al.
Nutrients|December 3, 2020
Association of Red Meat Intake with the Risk of Cardiovascular Mortality in General Japanese Stratified by Kidney Function: NIPPON DATA80Hiroyoshi Segawa, Keiko Kondo, Aya Kadota, et al.
International Journal of Cardiology|September 3, 2020
Impact of the T-wave characteristics on distinguishing arrhythmogenic right ventricular cardiomyopathy from healthy childrenTomohiko Imamura, Naokata Sumitomo, Shota Muraji, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 2, 2023
Non-missense variants of KCNH2 show better outcomes in type 2 long QT syndromeTakanori Aizawa, Yuko Wada, Kanae Hasegawa, et al.
Journal of Cardiology|November 7, 2016
Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano-Ward syndrome under double mutations and acquired long QT syndrome under heterozygoteYusuke Fujii, Yuichi Matsumoto, Kenshi Hayashi, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|October 18, 2021
Loss-of-function mutations in cardiac ryanodine receptor channel cause various types of arrhythmias including long QT syndromeSayako Hirose, Takashi Murayama, Naoyuki Tetsuo, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|April 29, 2008
Mutation site dependent variability of cardiac events in Japanese LQT2 form of congenital long-QT syndromeIori Nagaoka, Wataru Shimizu, Hideki Itoh, et al.
Heart Rhythm|October 21, 2016
A type 2 ryanodine receptor variant associated with reduced Ca<sup>2+</sup> release and short-coupled torsades de pointes ventricular arrhythmiaYusuke Fujii, Hideki Itoh, Seiko Ohno, et al.
Journal of the American College of Cardiology|August 22, 2009
D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndromeYukiko Nishio, Takeru Makiyama, Hideki Itoh, et al.
Pageof 23