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Circulation Journal : Official Journal of the Japanese Circulation Society
|
February 24, 2025
Screening of 1-Month-Old Infants With Prolonged QT Interval and Its Cutoff Value
Masao Yoshinaga, Hiroya Ushinohama, Seiichi Sato, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
June 23, 2017
Development of a Patient-Derived Induced Pluripotent Stem Cell Model for the Investigation of SCN5A-D1275N-Related Cardiac Sodium Channelopathy
Mamoru Hayano, Takeru Makiyama, Tsukasa Kamakura, et al.
International Journal of Cardiology
|
May 4, 2017
Heart failure in patients with arrhythmogenic right ventricular cardiomyopathy: What are the risk factors?
Yoshitaka Kimura, Takashi Noda, Taka-Aki Matsuyama, et al.
Journal of the American Heart Association
|
October 30, 2018
Sex-Dependent Phenotypic Variability of an SCN5A Mutation: Brugada Syndrome and Sick Sinus Syndrome
Yoshiyasu Aizawa, Taishi Fujisawa, Yoshinori Katsumata, et al.
The EMBO Journal
|
November 25, 2003
NRSF regulates the fetal cardiac gene program and maintains normal cardiac structure and function
Koichiro Kuwahara, Yoshihiko Saito, Makoto Takano, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
October 19, 2020
Improved Risk Stratification of Patients With Brugada Syndrome by the New Japanese Circulation Society Guideline - A Multicenter Validation Study
Akinori Wakamiya, Tsukasa Kamakura, Tetsuji Shinohara, et al.
Heart Rhythm
|
December 16, 2014
Efficacy and safety of flecainide for ventricular arrhythmias in patients with Andersen-Tawil syndrome with KCNJ2 mutations
Koji Miyamoto, Takeshi Aiba, Hiromi Kimura, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
August 7, 2018
Clinical Manifestations and Long-Term Mortality in Lamin A/C Mutation Carriers From a Japanese Multicenter Registry
Kenzaburo Nakajima, Takeshi Aiba, Takeru Makiyama, et al.
Circulation. Arrhythmia and Electrophysiology
|
January 17, 2012
A connexin40 mutation associated with a malignant variant of progressive familial heart block type I
Naomasa Makita, Akiko Seki, Naokata Sumitomo, et al.
Heart Rhythm
|
August 25, 2022
Disrupted Ca<sub>V</sub>1.2 selectivity causes overlapping long QT and Brugada syndrome phenotypes in the CACNA1C-E1115K iPS cell model
Asami Kashiwa, Takeru Makiyama, Hirohiko Kohjitani, et al.
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of 43
Search research articles
Search
Showing results (361-370 of 428) with videos related to
Sort By:
Page
of 43
Circulation Journal : Official Journal of the Japanese Circulation Society
|
February 24, 2025
Screening of 1-Month-Old Infants With Prolonged QT Interval and Its Cutoff Value
Masao Yoshinaga, Hiroya Ushinohama, Seiichi Sato, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
June 23, 2017
Development of a Patient-Derived Induced Pluripotent Stem Cell Model for the Investigation of SCN5A-D1275N-Related Cardiac Sodium Channelopathy
Mamoru Hayano, Takeru Makiyama, Tsukasa Kamakura, et al.
International Journal of Cardiology
|
May 4, 2017
Heart failure in patients with arrhythmogenic right ventricular cardiomyopathy: What are the risk factors?
Yoshitaka Kimura, Takashi Noda, Taka-Aki Matsuyama, et al.
Journal of the American Heart Association
|
October 30, 2018
Sex-Dependent Phenotypic Variability of an SCN5A Mutation: Brugada Syndrome and Sick Sinus Syndrome
Yoshiyasu Aizawa, Taishi Fujisawa, Yoshinori Katsumata, et al.
The EMBO Journal
|
November 25, 2003
NRSF regulates the fetal cardiac gene program and maintains normal cardiac structure and function
Koichiro Kuwahara, Yoshihiko Saito, Makoto Takano, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
October 19, 2020
Improved Risk Stratification of Patients With Brugada Syndrome by the New Japanese Circulation Society Guideline - A Multicenter Validation Study
Akinori Wakamiya, Tsukasa Kamakura, Tetsuji Shinohara, et al.
Heart Rhythm
|
December 16, 2014
Efficacy and safety of flecainide for ventricular arrhythmias in patients with Andersen-Tawil syndrome with KCNJ2 mutations
Koji Miyamoto, Takeshi Aiba, Hiromi Kimura, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
August 7, 2018
Clinical Manifestations and Long-Term Mortality in Lamin A/C Mutation Carriers From a Japanese Multicenter Registry
Kenzaburo Nakajima, Takeshi Aiba, Takeru Makiyama, et al.
Circulation. Arrhythmia and Electrophysiology
|
January 17, 2012
A connexin40 mutation associated with a malignant variant of progressive familial heart block type I
Naomasa Makita, Akiko Seki, Naokata Sumitomo, et al.
Heart Rhythm
|
August 25, 2022
Disrupted Ca<sub>V</sub>1.2 selectivity causes overlapping long QT and Brugada syndrome phenotypes in the CACNA1C-E1115K iPS cell model
Asami Kashiwa, Takeru Makiyama, Hirohiko Kohjitani, et al.
Page
of 43