Search research articles
Contact Us
Filters
Showing results (121-130 of 222) with videos related to
Page
of 23
Sort By:
British Journal of Clinical Pharmacology
|
February 20, 2018
Population pharmacokinetics and pharmacogenomics of apixaban in Japanese adult patients with atrial fibrillation
Satoshi Ueshima, Daiki Hira, Yuuma Kimura, et al.
Heart Rhythm
|
August 19, 2015
Cardiac sodium channel mutation associated with epinephrine-induced QT prolongation and sinus node dysfunction
Jiarong Chen, Takeru Makiyama, Yimin Wuriyanghai, et al.
Brain Research
|
December 23, 2018
Novel roles of Drosophila FUS and Aub responsible for piRNA biogenesis in neuronal disorders
Keiko Tsuji Wakisaka, Ryo Tanaka, Tomoki Hirashima, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
June 30, 2015
A Common Mutation of Long QT Syndrome Type 1 in Japan
Hideki Itoh, Kenichi Dochi, Wataru Shimizu, 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.
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. 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.
JACC. Clinical Electrophysiology
|
March 25, 2022
Association Between Deleterious SCN5A Variants and Ventricular Septal Defect in Young Patients With Brugada Syndrome
Keisuke Suzuki, Keiko Sonoda, Hisaaki Aoki, et al.
Journal of Cardiovascular Electrophysiology
|
March 19, 2004
Additional gene variants reduce effectiveness of beta-blockers in the LQT1 form of long QT syndrome
Atsushi Kobori, Nobuaki Sarai, Wataru Shimizu, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
May 14, 2025
Congenital Short QT Syndrome - Review Focused on KCNQ1 p.Val141Met Variant
Minoru Horie, Hirofumi Saiki, Takanori Aizawa, et al.
Page
of 23
Search research articles
Search
Showing results (121-130 of 222) with videos related to
Sort By:
Page
of 23
British Journal of Clinical Pharmacology
|
February 20, 2018
Population pharmacokinetics and pharmacogenomics of apixaban in Japanese adult patients with atrial fibrillation
Satoshi Ueshima, Daiki Hira, Yuuma Kimura, et al.
Heart Rhythm
|
August 19, 2015
Cardiac sodium channel mutation associated with epinephrine-induced QT prolongation and sinus node dysfunction
Jiarong Chen, Takeru Makiyama, Yimin Wuriyanghai, et al.
Brain Research
|
December 23, 2018
Novel roles of Drosophila FUS and Aub responsible for piRNA biogenesis in neuronal disorders
Keiko Tsuji Wakisaka, Ryo Tanaka, Tomoki Hirashima, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
June 30, 2015
A Common Mutation of Long QT Syndrome Type 1 in Japan
Hideki Itoh, Kenichi Dochi, Wataru Shimizu, 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.
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. 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.
JACC. Clinical Electrophysiology
|
March 25, 2022
Association Between Deleterious SCN5A Variants and Ventricular Septal Defect in Young Patients With Brugada Syndrome
Keisuke Suzuki, Keiko Sonoda, Hisaaki Aoki, et al.
Journal of Cardiovascular Electrophysiology
|
March 19, 2004
Additional gene variants reduce effectiveness of beta-blockers in the LQT1 form of long QT syndrome
Atsushi Kobori, Nobuaki Sarai, Wataru Shimizu, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
May 14, 2025
Congenital Short QT Syndrome - Review Focused on KCNQ1 p.Val141Met Variant
Minoru Horie, Hirofumi Saiki, Takanori Aizawa, et al.
Page
of 23