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Heart and Vessels
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July 10, 2013
Successful control of life-threatening polymorphic ventricular tachycardia by radiofrequency catheter ablation in an infant
Yuriko Abe, Naokata Sumitomo, Hiromi Okuma, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
October 28, 2016
Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes
Mari Ichikawa, Takeshi Aiba, Seiko Ohno, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
September 27, 2007
Association of atrial arrhythmia and sinus node dysfunction in patients with catecholaminergic polymorphic ventricular tachycardia
Naokata Sumitomo, Harumizu Sakurada, Kazuo Taniguchi, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
June 11, 2016
Relationship of Insulin Resistance to Prevalence and Progression of Coronary Artery Calcification Beyond Metabolic Syndrome Components: Shiga Epidemiological Study of Subclinical Atherosclerosis
Masahiro Yamazoe, Takashi Hisamatsu, Katsuyuki Miura, et al.
Journal of Cardiovascular Electrophysiology
|
April 1, 2008
Age- and genotype-specific triggers for life-threatening arrhythmia in the genotyped long QT syndrome
Tomoko Sakaguchi, Wataru Shimizu, Hideki Itoh, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
July 13, 2012
Seasonal and circadian distributions of cardiac events in genotyped patients with congenital long QT syndrome
Masateru Takigawa, Mihoko Kawamura, Takashi Noda, et al.
Circulation. Arrhythmia and Electrophysiology
|
April 16, 2011
KCNE5 (KCNE1L) variants are novel modulators of Brugada syndrome and idiopathic ventricular fibrillation
Seiko Ohno, Dimitar P Zankov, Wei-Guang Ding, et al.
Biological & Pharmaceutical Bulletin
|
July 3, 2007
Protective mechanism of adenosine to the rat arterial endothelial dysfunction induced by hydrogen peroxide
Jun Lu, Shu-Ming Zhu, Wei-Jin Zang, et al.
International Journal of Cardiology
|
August 12, 2008
A novel KCNH2 mutation as a modifier for short QT interval
Hideki Itoh, Tomoko Sakaguchi, Takashi Ashihara, et al.
Journal of Pharmacological Sciences
|
December 6, 2008
Hydroxyzine, a first generation H(1)-receptor antagonist, inhibits human ether-a-go-go-related gene (HERG) current and causes syncope in a patient with the HERG mutation
Tomoko Sakaguchi, Hideki Itoh, Wei-Guang Ding, et al.
Page
of 43
Search research articles
Search
Showing results (271-280 of 428) with videos related to
Sort By:
Page
of 43
Heart and Vessels
|
July 10, 2013
Successful control of life-threatening polymorphic ventricular tachycardia by radiofrequency catheter ablation in an infant
Yuriko Abe, Naokata Sumitomo, Hiromi Okuma, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
October 28, 2016
Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes
Mari Ichikawa, Takeshi Aiba, Seiko Ohno, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
September 27, 2007
Association of atrial arrhythmia and sinus node dysfunction in patients with catecholaminergic polymorphic ventricular tachycardia
Naokata Sumitomo, Harumizu Sakurada, Kazuo Taniguchi, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
June 11, 2016
Relationship of Insulin Resistance to Prevalence and Progression of Coronary Artery Calcification Beyond Metabolic Syndrome Components: Shiga Epidemiological Study of Subclinical Atherosclerosis
Masahiro Yamazoe, Takashi Hisamatsu, Katsuyuki Miura, et al.
Journal of Cardiovascular Electrophysiology
|
April 1, 2008
Age- and genotype-specific triggers for life-threatening arrhythmia in the genotyped long QT syndrome
Tomoko Sakaguchi, Wataru Shimizu, Hideki Itoh, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
July 13, 2012
Seasonal and circadian distributions of cardiac events in genotyped patients with congenital long QT syndrome
Masateru Takigawa, Mihoko Kawamura, Takashi Noda, et al.
Circulation. Arrhythmia and Electrophysiology
|
April 16, 2011
KCNE5 (KCNE1L) variants are novel modulators of Brugada syndrome and idiopathic ventricular fibrillation
Seiko Ohno, Dimitar P Zankov, Wei-Guang Ding, et al.
Biological & Pharmaceutical Bulletin
|
July 3, 2007
Protective mechanism of adenosine to the rat arterial endothelial dysfunction induced by hydrogen peroxide
Jun Lu, Shu-Ming Zhu, Wei-Jin Zang, et al.
International Journal of Cardiology
|
August 12, 2008
A novel KCNH2 mutation as a modifier for short QT interval
Hideki Itoh, Tomoko Sakaguchi, Takashi Ashihara, et al.
Journal of Pharmacological Sciences
|
December 6, 2008
Hydroxyzine, a first generation H(1)-receptor antagonist, inhibits human ether-a-go-go-related gene (HERG) current and causes syncope in a patient with the HERG mutation
Tomoko Sakaguchi, Hideki Itoh, Wei-Guang Ding, et al.
Page
of 43