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Minoru Horie

Showing results (381-390 of 428) with videos related to

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European Heart Journal|July 5, 2021
Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndromeTaisuke Ishikawa, Hiroki Kimoto, Hiroyuki Mishima, et al.
Circulation|March 26, 2017
Genotype-Phenotype Correlation of <i>SCN5A</i> Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese Multicenter RegistryKenichiro Yamagata, Minoru Horie, Takeshi Aiba, et al.
Journal of the American College of Cardiology|July 15, 2017
Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 MutationAkiko Seki, Taisuke Ishikawa, Xavier Daumy, 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|February 11, 2025
SCN5A variant type-dependent risk prediction in Brugada syndromeTakanori Aizawa, Takeru Makiyama, Hai Huang, et al.
The American Journal of Cardiology|June 23, 2012
Comparison of long-term outcome after percutaneous coronary intervention versus coronary artery bypass grafting in patients with unprotected left main coronary artery disease (from the CREDO-Kyoto PCI/CABG Registry Cohort-2)Hiroki Shiomi, Takeshi Morimoto, Mamoru Hayano, et al.
Plos Genetics|April 18, 2013
A nonsynonymous polymorphism in semaphorin 3A as a risk factor for human unexplained cardiac arrest with documented ventricular fibrillationYukiko Nakano, Kazuaki Chayama, Hidenori Ochi, et al.
Circulation. Cardiovascular Genetics|December 15, 2017
Gene-Based Risk Stratification for Cardiac Disorders in <i>LMNA</i> Mutation CarriersSuguru Nishiuchi, Takeru Makiyama, Takeshi Aiba, et al.
Plos One|December 3, 2024
Correction: Targeted deep sequencing analyses of long QT syndrome in a Japanese populationYuki Nagata, Ryo Watanabe, Christian Eichhorn, et al.
Plos One|December 8, 2022
Targeted deep sequencing analyses of long QT syndrome in a Japanese populationYuki Nagata, Ryo Watanabe, Christian Eichhorn, et al.
Circulation. Genomic and Precision Medicine|September 16, 2020
Systematic Evaluation of <i>KCNQ1</i> Variant Using ACMG/AMP Guidelines and Risk Stratification in Long QT Syndrome Type 1Asami Kashiwa, Takeshi Aiba, Hisaki Makimoto, et al.
Pageof 43

Showing results (381-390 of 428) with videos related to

Sort By:
Pageof 43
European Heart Journal|July 5, 2021
Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndromeTaisuke Ishikawa, Hiroki Kimoto, Hiroyuki Mishima, et al.
Circulation|March 26, 2017
Genotype-Phenotype Correlation of <i>SCN5A</i> Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese Multicenter RegistryKenichiro Yamagata, Minoru Horie, Takeshi Aiba, et al.
Journal of the American College of Cardiology|July 15, 2017
Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 MutationAkiko Seki, Taisuke Ishikawa, Xavier Daumy, 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|February 11, 2025
SCN5A variant type-dependent risk prediction in Brugada syndromeTakanori Aizawa, Takeru Makiyama, Hai Huang, et al.
The American Journal of Cardiology|June 23, 2012
Comparison of long-term outcome after percutaneous coronary intervention versus coronary artery bypass grafting in patients with unprotected left main coronary artery disease (from the CREDO-Kyoto PCI/CABG Registry Cohort-2)Hiroki Shiomi, Takeshi Morimoto, Mamoru Hayano, et al.
Plos Genetics|April 18, 2013
A nonsynonymous polymorphism in semaphorin 3A as a risk factor for human unexplained cardiac arrest with documented ventricular fibrillationYukiko Nakano, Kazuaki Chayama, Hidenori Ochi, et al.
Circulation. Cardiovascular Genetics|December 15, 2017
Gene-Based Risk Stratification for Cardiac Disorders in <i>LMNA</i> Mutation CarriersSuguru Nishiuchi, Takeru Makiyama, Takeshi Aiba, et al.
Plos One|December 3, 2024
Correction: Targeted deep sequencing analyses of long QT syndrome in a Japanese populationYuki Nagata, Ryo Watanabe, Christian Eichhorn, et al.
Plos One|December 8, 2022
Targeted deep sequencing analyses of long QT syndrome in a Japanese populationYuki Nagata, Ryo Watanabe, Christian Eichhorn, et al.
Circulation. Genomic and Precision Medicine|September 16, 2020
Systematic Evaluation of <i>KCNQ1</i> Variant Using ACMG/AMP Guidelines and Risk Stratification in Long QT Syndrome Type 1Asami Kashiwa, Takeshi Aiba, Hisaki Makimoto, et al.
Pageof 43