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The American Journal of Cardiology
|
August 28, 2014
Effect of preinfarction angina pectoris on long-term survival in patients with ST-segment elevation myocardial infarction who underwent primary percutaneous coronary intervention
Tomohiko Taniguchi, Hiroki Shiomi, Toshiaki Toyota, et al.
Journal of Cardiology
|
November 18, 2017
Novel intracellular transport-refractory mutations in KCNH2 identified in patients with symptomatic long QT syndrome
Daisuke Fukumoto, Wei-Guang Ding, Yuko Wada, et al.
Heart (British Cardiac Society)
|
November 18, 2017
Single-session versus staged procedures for elective multivessel percutaneous coronary intervention
Toshiaki Toyota, Takeshi Morimoto, Hiroki Shiomi, et al.
Stem Cell Reports
|
August 6, 2019
Phenotype-Based High-Throughput Classification of Long QT Syndrome Subtypes Using Human Induced Pluripotent Stem Cells
Daisuke Yoshinaga, Shiro Baba, Takeru Makiyama, et al.
Heart Rhythm
|
March 9, 2010
High prevalence of early repolarization in short QT syndrome
Hiroshi Watanabe, Takeru Makiyama, Taku Koyama, et al.
Frontiers in Physiology
|
August 5, 2024
Novel <i>KCNQ1</i> Q234K variant, identified in patients with long QT syndrome and epileptiform activity, induces both gain- and loss-of-function of slowly activating delayed rectifier potassium currents
Tadashi Nakajima, Shuntaro Tamura, Reika Kawabata-Iwakawa, et al.
Scientific Reports
|
February 17, 2018
A hERG mutation E1039X produced a synergistic lesion on I<sub>Ks</sub> together with KCNQ1-R174C mutation in a LQTS family with three compound mutations
Jie Wu, Yuka Mizusawa, Seiko Ohno, et al.
Circulation
|
February 8, 2006
The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome
Peter J Schwartz, Carla Spazzolini, Lia Crotti, et al.
Human Mutation
|
March 24, 2009
Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome
Seiko Ohno, Futoshi Toyoda, Dimitar P Zankov, et al.
Journal of the American Heart Association
|
August 20, 2020
Cardiac Conduction Disorders as Markers of Cardiac Events in Myotonic Dystrophy Type 1
Hideki Itoh, Takashi Hisamatsu, Takuhisa Tamura, et al.
Page
of 43
Search research articles
Search
Showing results (291-300 of 428) with videos related to
Sort By:
Page
of 43
The American Journal of Cardiology
|
August 28, 2014
Effect of preinfarction angina pectoris on long-term survival in patients with ST-segment elevation myocardial infarction who underwent primary percutaneous coronary intervention
Tomohiko Taniguchi, Hiroki Shiomi, Toshiaki Toyota, et al.
Journal of Cardiology
|
November 18, 2017
Novel intracellular transport-refractory mutations in KCNH2 identified in patients with symptomatic long QT syndrome
Daisuke Fukumoto, Wei-Guang Ding, Yuko Wada, et al.
Heart (British Cardiac Society)
|
November 18, 2017
Single-session versus staged procedures for elective multivessel percutaneous coronary intervention
Toshiaki Toyota, Takeshi Morimoto, Hiroki Shiomi, et al.
Stem Cell Reports
|
August 6, 2019
Phenotype-Based High-Throughput Classification of Long QT Syndrome Subtypes Using Human Induced Pluripotent Stem Cells
Daisuke Yoshinaga, Shiro Baba, Takeru Makiyama, et al.
Heart Rhythm
|
March 9, 2010
High prevalence of early repolarization in short QT syndrome
Hiroshi Watanabe, Takeru Makiyama, Taku Koyama, et al.
Frontiers in Physiology
|
August 5, 2024
Novel <i>KCNQ1</i> Q234K variant, identified in patients with long QT syndrome and epileptiform activity, induces both gain- and loss-of-function of slowly activating delayed rectifier potassium currents
Tadashi Nakajima, Shuntaro Tamura, Reika Kawabata-Iwakawa, et al.
Scientific Reports
|
February 17, 2018
A hERG mutation E1039X produced a synergistic lesion on I<sub>Ks</sub> together with KCNQ1-R174C mutation in a LQTS family with three compound mutations
Jie Wu, Yuka Mizusawa, Seiko Ohno, et al.
Circulation
|
February 8, 2006
The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome
Peter J Schwartz, Carla Spazzolini, Lia Crotti, et al.
Human Mutation
|
March 24, 2009
Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome
Seiko Ohno, Futoshi Toyoda, Dimitar P Zankov, et al.
Journal of the American Heart Association
|
August 20, 2020
Cardiac Conduction Disorders as Markers of Cardiac Events in Myotonic Dystrophy Type 1
Hideki Itoh, Takashi Hisamatsu, Takuhisa Tamura, et al.
Page
of 43