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Hideki Itoh

Showing results (41-50 of 117) with videos related to

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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.
Biophysical Journal|July 23, 2015
Directional bleb formation in spherical cells under temperature gradientKotaro Oyama, Tomomi Arai, Akira Isaka, et al.
Neuroscience Research|October 5, 2010
Intrathecally administered Sema3A protein attenuates neuropathic pain behavior in rats with chronic constriction injury of the sciatic nerveMichiko Hayashi, Yoshinori Kamiya, Hideki Itoh, et al.
Clinical Cardiology|July 12, 2002
T-peak to T-end interval may be a better predictor of high-risk patients with hypertrophic cardiomyopathy associated with a cardiac troponin I mutation than QT dispersionMasami Shimizu, Hidekazu Ino, Kazuyasu Okeie, et al.
Internal Medicine (Tokyo, Japan)|February 3, 2016
Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese FamilyMari Ichikawa, Seiko Ohno, Yusuke Fujii, et al.
American Heart Journal|March 30, 2002
Septal wall thinning and systolic dysfunction in patients with hypertrophic cardiomyopathy caused by a cardiac troponin I gene mutationMasami Shimizu, Hidekazu Ino, Kazuyasu Okeie, et al.
European Journal of Pharmacology|November 23, 2007
Differential effects of isoflurane on A-type and delayed rectifier K channels in rat substantia nigraDai Ishiwa, Isao Nagata, Tatsuo Ohtsuka, et al.
Heart Rhythm|March 8, 2007
N- and C-terminal KCNE1 mutations cause distinct phenotypes of long QT syndromeSeiko Ohno, Dimitar P Zankov, Hidetada Yoshida, et al.
Pageof 12

Showing results (41-50 of 117) with videos related to

Sort By:
Pageof 12
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.
Biophysical Journal|July 23, 2015
Directional bleb formation in spherical cells under temperature gradientKotaro Oyama, Tomomi Arai, Akira Isaka, et al.
Neuroscience Research|October 5, 2010
Intrathecally administered Sema3A protein attenuates neuropathic pain behavior in rats with chronic constriction injury of the sciatic nerveMichiko Hayashi, Yoshinori Kamiya, Hideki Itoh, et al.
Clinical Cardiology|July 12, 2002
T-peak to T-end interval may be a better predictor of high-risk patients with hypertrophic cardiomyopathy associated with a cardiac troponin I mutation than QT dispersionMasami Shimizu, Hidekazu Ino, Kazuyasu Okeie, et al.
Internal Medicine (Tokyo, Japan)|February 3, 2016
Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese FamilyMari Ichikawa, Seiko Ohno, Yusuke Fujii, et al.
American Heart Journal|March 30, 2002
Septal wall thinning and systolic dysfunction in patients with hypertrophic cardiomyopathy caused by a cardiac troponin I gene mutationMasami Shimizu, Hidekazu Ino, Kazuyasu Okeie, et al.
European Journal of Pharmacology|November 23, 2007
Differential effects of isoflurane on A-type and delayed rectifier K channels in rat substantia nigraDai Ishiwa, Isao Nagata, Tatsuo Ohtsuka, et al.
Heart Rhythm|March 8, 2007
N- and C-terminal KCNE1 mutations cause distinct phenotypes of long QT syndromeSeiko Ohno, Dimitar P Zankov, Hidetada Yoshida, et al.
Pageof 12