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Minoru Horie

Showing results (341-350 of 428) 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|January 9, 2018
Different responses to exercise between Andersen-Tawil syndrome and catecholaminergic polymorphic ventricular tachycardiaYuko Y Inoue, Takeshi Aiba, Hiro Kawata, et al.
International Journal of Cardiology|August 12, 2008
Prevalence of atrial fibrillation in the general population of Japan: an analysis based on periodic health examinationHiroshi Inoue, Akira Fujiki, Hideki Origasa, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 17, 2020
Identification of transmembrane protein 168 mutation in familial Brugada syndromeAkio Shimizu, Dimitar P Zankov, Akira Sato, et al.
Heart Rhythm|January 5, 2013
Effects of flecainide on exercise-induced ventricular arrhythmias and recurrences in genotype-negative patients with catecholaminergic polymorphic ventricular tachycardiaHiroshi Watanabe, Christian van der Werf, Ferran Roses-Noguer, et al.
Neurology|February 28, 2014
A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1Yosuke Kokunai, Tomohiko Nakata, Mitsuru Furuta, 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|June 28, 2021
Novel electrocardiographic criteria for short QT syndrome in children and adolescentsHiroshi Suzuki, Minoru Horie, Junichi Ozawa, et al.
Heart Rhythm|May 6, 2014
Sudden cardiac arrest recorded during Holter monitoring: prevalence, antecedent electrical events, and outcomesEiichi Watanabe, Teruhisa Tanabe, Motohisa Osaka, et al.
Human Mutation|January 16, 2007
Genotype-phenotype correlations of KCNJ2 mutations in Japanese patients with Andersen-Tawil syndromeYoshisumi Haruna, Atsushi Kobori, Takeru Makiyama, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|May 29, 2015
Clinical and Pathological Impact of Tissue Fibrosis on Lethal Arrhythmic Events in Hypertrophic Cardiomyopathy Patients With Impaired Systolic FunctionYuko Wada, Takeshi Aiba, Taka-aki Matsuyama, et al.
Circulation|November 7, 2007
The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratificationLia Crotti, Carla Spazzolini, Peter J Schwartz, et al.
Pageof 43

Showing results (341-350 of 428) with videos related to

Sort By:
Pageof 43
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|January 9, 2018
Different responses to exercise between Andersen-Tawil syndrome and catecholaminergic polymorphic ventricular tachycardiaYuko Y Inoue, Takeshi Aiba, Hiro Kawata, et al.
International Journal of Cardiology|August 12, 2008
Prevalence of atrial fibrillation in the general population of Japan: an analysis based on periodic health examinationHiroshi Inoue, Akira Fujiki, Hideki Origasa, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 17, 2020
Identification of transmembrane protein 168 mutation in familial Brugada syndromeAkio Shimizu, Dimitar P Zankov, Akira Sato, et al.
Heart Rhythm|January 5, 2013
Effects of flecainide on exercise-induced ventricular arrhythmias and recurrences in genotype-negative patients with catecholaminergic polymorphic ventricular tachycardiaHiroshi Watanabe, Christian van der Werf, Ferran Roses-Noguer, et al.
Neurology|February 28, 2014
A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1Yosuke Kokunai, Tomohiko Nakata, Mitsuru Furuta, 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|June 28, 2021
Novel electrocardiographic criteria for short QT syndrome in children and adolescentsHiroshi Suzuki, Minoru Horie, Junichi Ozawa, et al.
Heart Rhythm|May 6, 2014
Sudden cardiac arrest recorded during Holter monitoring: prevalence, antecedent electrical events, and outcomesEiichi Watanabe, Teruhisa Tanabe, Motohisa Osaka, et al.
Human Mutation|January 16, 2007
Genotype-phenotype correlations of KCNJ2 mutations in Japanese patients with Andersen-Tawil syndromeYoshisumi Haruna, Atsushi Kobori, Takeru Makiyama, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|May 29, 2015
Clinical and Pathological Impact of Tissue Fibrosis on Lethal Arrhythmic Events in Hypertrophic Cardiomyopathy Patients With Impaired Systolic FunctionYuko Wada, Takeshi Aiba, Taka-aki Matsuyama, et al.
Circulation|November 7, 2007
The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratificationLia Crotti, Carla Spazzolini, Peter J Schwartz, et al.
Pageof 43