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Seiko Ohno

Showing results (71-80 of 222) with videos related to

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Clinical Biochemistry|November 7, 2017
Macro-pro-B-type natriuretic peptide (proBNP) and hidden macro-N-terminal proBNP: Case reportYasuaki Nakagawa, Toshio Nishikimi, Hiroshi Sakai, et al.
Circulation. Cardiovascular Genetics|April 16, 2011
A novel KCNJ2 nonsense mutation, S369X, impedes trafficking and causes a limited form of Andersen-Tawil syndromeTakahiro Doi, Takeru Makiyama, Takeshi Morimoto, et al.
Journal of Electrocardiology|October 17, 2021
Sudden death after inappropriate shocks of implantable cardioverter defibrillator in a catecholaminergic polymorphic ventricular tachycardia case with a novel RyR2 mutationHideki Itoh, Takashi Murayama, Nagomi Kurebayashi, et al.
International Journal of Cardiology|August 24, 2016
Early repolarization and risk of arrhythmia events in long QT syndromeKanae Hasegawa, Hiroshi Watanabe, Takashi Hisamatsu, et al.
Heart Rhythm|February 17, 2024
Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variantsAsami Kashiwa, Hideki Itoh, Takeru Makiyama, et al.
International Heart Journal|December 7, 2018
Medical Castration is a Rare but Possible Trigger of Torsade de Pointes and Ventricular FibrillationKanae Hasegawa, Tetsuji Morishita, Dai Miyanaga, et al.
Internal Medicine (Tokyo, Japan)|March 3, 2024
Cardiomyopathy with an LMNA Genetic Variant Affecting Three Consecutive Generations: A Case SeriesNaoko Ogawa, Hidekazu Kondo, Yumi Ishii, et al.
Journal of Human Genetics|November 4, 2025
Functional and pharmacological investigation of novel and de novo KCND3 variants identified in patients with neurodevelopmental disordersByambajav Tserenlkham, Koichiro Takayama, Dimitar P Zankov, et al.
Journal of the American College of Cardiology|November 5, 2013
A molecular mechanism for adrenergic-induced long QT syndromeJie Wu, Nobu Naiki, Wei-Guang Ding, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|September 19, 2012
KCNE3 T4A as the genetic basis of Brugada-pattern electrocardiogramTadashi Nakajima, Jie Wu, Yoshiaki Kaneko, et al.
Pageof 23

Showing results (71-80 of 222) with videos related to

Sort By:
Pageof 23
Clinical Biochemistry|November 7, 2017
Macro-pro-B-type natriuretic peptide (proBNP) and hidden macro-N-terminal proBNP: Case reportYasuaki Nakagawa, Toshio Nishikimi, Hiroshi Sakai, et al.
Circulation. Cardiovascular Genetics|April 16, 2011
A novel KCNJ2 nonsense mutation, S369X, impedes trafficking and causes a limited form of Andersen-Tawil syndromeTakahiro Doi, Takeru Makiyama, Takeshi Morimoto, et al.
Journal of Electrocardiology|October 17, 2021
Sudden death after inappropriate shocks of implantable cardioverter defibrillator in a catecholaminergic polymorphic ventricular tachycardia case with a novel RyR2 mutationHideki Itoh, Takashi Murayama, Nagomi Kurebayashi, et al.
International Journal of Cardiology|August 24, 2016
Early repolarization and risk of arrhythmia events in long QT syndromeKanae Hasegawa, Hiroshi Watanabe, Takashi Hisamatsu, et al.
Heart Rhythm|February 17, 2024
Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variantsAsami Kashiwa, Hideki Itoh, Takeru Makiyama, et al.
International Heart Journal|December 7, 2018
Medical Castration is a Rare but Possible Trigger of Torsade de Pointes and Ventricular FibrillationKanae Hasegawa, Tetsuji Morishita, Dai Miyanaga, et al.
Internal Medicine (Tokyo, Japan)|March 3, 2024
Cardiomyopathy with an LMNA Genetic Variant Affecting Three Consecutive Generations: A Case SeriesNaoko Ogawa, Hidekazu Kondo, Yumi Ishii, et al.
Journal of Human Genetics|November 4, 2025
Functional and pharmacological investigation of novel and de novo KCND3 variants identified in patients with neurodevelopmental disordersByambajav Tserenlkham, Koichiro Takayama, Dimitar P Zankov, et al.
Journal of the American College of Cardiology|November 5, 2013
A molecular mechanism for adrenergic-induced long QT syndromeJie Wu, Nobu Naiki, Wei-Guang Ding, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|September 19, 2012
KCNE3 T4A as the genetic basis of Brugada-pattern electrocardiogramTadashi Nakajima, Jie Wu, Yoshiaki Kaneko, et al.
Pageof 23