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Hideki Itoh

Showing results (61-70 of 117) with videos related to

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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 1, 2010
Heart rate-dependent variability of cardiac events in type 2 congenital long-QT syndromeIori Nagaoka, Wataru Shimizu, Yuka Mizusawa, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|October 27, 2010
Atrioventricular block-induced Torsades de Pointes with clinical and molecular backgrounds similar to congenital long QT syndromeYuko Oka, Hideki Itoh, Wei-Guang Ding, et al.
Heart Rhythm|August 23, 2011
Clinical and electrocardiographic characteristics of patients with short QT interval in a large hospital-based populationAkashi Miyamoto, Hideki Hayashi, Tomohide Yoshino, 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|April 15, 2014
Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypesMegumi Fukuyama, Qi Wang, Koichi Kato, et al.
Circulation. Arrhythmia and Electrophysiology|February 28, 2022
Novel <i>CALM3</i> Variant Causing Calmodulinopathy With Variable Expressivity in a 4-Generation FamilyKoichi Kato, Holly M Isbell, Véronique Fressart, et al.
Journal of the American College of Cardiology|October 22, 2008
A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillationTakeru Makiyama, Masaharu Akao, Satoshi Shizuta, et al.
Cardiovascular Research|December 14, 2011
A novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currentsTetsuhisa Hattori, Takeru Makiyama, Masaharu Akao, et al.
Heart Rhythm|October 8, 2013
A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channelsKanae Hasegawa, Seiko Ohno, Takashi Ashihara, et al.
British Journal of Clinical Pharmacology|February 20, 2018
Population pharmacokinetics and pharmacogenomics of apixaban in Japanese adult patients with atrial fibrillationSatoshi Ueshima, Daiki Hira, Yuuma Kimura, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|June 30, 2015
A Common Mutation of Long QT Syndrome Type 1 in JapanHideki Itoh, Kenichi Dochi, Wataru Shimizu, et al.
Pageof 12

Showing results (61-70 of 117) with videos related to

Sort By:
Pageof 12
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 1, 2010
Heart rate-dependent variability of cardiac events in type 2 congenital long-QT syndromeIori Nagaoka, Wataru Shimizu, Yuka Mizusawa, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|October 27, 2010
Atrioventricular block-induced Torsades de Pointes with clinical and molecular backgrounds similar to congenital long QT syndromeYuko Oka, Hideki Itoh, Wei-Guang Ding, et al.
Heart Rhythm|August 23, 2011
Clinical and electrocardiographic characteristics of patients with short QT interval in a large hospital-based populationAkashi Miyamoto, Hideki Hayashi, Tomohide Yoshino, 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|April 15, 2014
Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypesMegumi Fukuyama, Qi Wang, Koichi Kato, et al.
Circulation. Arrhythmia and Electrophysiology|February 28, 2022
Novel <i>CALM3</i> Variant Causing Calmodulinopathy With Variable Expressivity in a 4-Generation FamilyKoichi Kato, Holly M Isbell, Véronique Fressart, et al.
Journal of the American College of Cardiology|October 22, 2008
A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillationTakeru Makiyama, Masaharu Akao, Satoshi Shizuta, et al.
Cardiovascular Research|December 14, 2011
A novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currentsTetsuhisa Hattori, Takeru Makiyama, Masaharu Akao, et al.
Heart Rhythm|October 8, 2013
A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channelsKanae Hasegawa, Seiko Ohno, Takashi Ashihara, et al.
British Journal of Clinical Pharmacology|February 20, 2018
Population pharmacokinetics and pharmacogenomics of apixaban in Japanese adult patients with atrial fibrillationSatoshi Ueshima, Daiki Hira, Yuuma Kimura, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|June 30, 2015
A Common Mutation of Long QT Syndrome Type 1 in JapanHideki Itoh, Kenichi Dochi, Wataru Shimizu, et al.
Pageof 12