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Seiko Ohno

Showing results (171-180 of 196) with videos related to

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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 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.
Circulation. Genomic and Precision Medicine|July 26, 2021
Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare <i>KCNH2</i> VariantsKrystian Kozek, Yuko Wada, Luca Sala, et al.
Journal of the American Heart Association|September 15, 2016
Variants in the SCN5A Promoter Associated With Various Arrhythmia PhenotypesNobue Yagihara, Hiroshi Watanabe, Phil Barnett, et al.
Heart (British Cardiac Society)|March 16, 2017
Arrhythmia risk and β-blocker therapy in pregnant women with long QT syndromeKohei Ishibashi, Takeshi Aiba, Chizuko Kamiya, et al.
JAMA Cardiology|February 14, 2019
Association of Genetic and Clinical Aspects of Congenital Long QT Syndrome With Life-Threatening Arrhythmias in Japanese PatientsWataru Shimizu, Hisaki Makimoto, Kenichiro Yamagata, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|March 30, 2025
Clinical Impact of Genetic Testing for Long QT Syndrome　- Evidence From a Nationwide LQTS Registry in JapanTakeshi Aiba, Seiko Ohno, Misa Takegami, et al.
Circulation|February 16, 2019
Mutant KCNJ3 and KCNJ5 Potassium Channels as Novel Molecular Targets in Bradyarrhythmias and Atrial FibrillationNoriaki Yamada, Yoshihiro Asano, Masashi Fujita, et al.
European Heart Journal|May 15, 2024
Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk lociTaisuke Ishikawa, Tatsuo Masuda, Tsuyoshi Hachiya, et al.
Pageof 20

Showing results (171-180 of 196) with videos related to

Sort By:
Pageof 20
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 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.
Circulation. Genomic and Precision Medicine|July 26, 2021
Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare <i>KCNH2</i> VariantsKrystian Kozek, Yuko Wada, Luca Sala, et al.
Journal of the American Heart Association|September 15, 2016
Variants in the SCN5A Promoter Associated With Various Arrhythmia PhenotypesNobue Yagihara, Hiroshi Watanabe, Phil Barnett, et al.
Heart (British Cardiac Society)|March 16, 2017
Arrhythmia risk and β-blocker therapy in pregnant women with long QT syndromeKohei Ishibashi, Takeshi Aiba, Chizuko Kamiya, et al.
JAMA Cardiology|February 14, 2019
Association of Genetic and Clinical Aspects of Congenital Long QT Syndrome With Life-Threatening Arrhythmias in Japanese PatientsWataru Shimizu, Hisaki Makimoto, Kenichiro Yamagata, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|March 30, 2025
Clinical Impact of Genetic Testing for Long QT Syndrome　- Evidence From a Nationwide LQTS Registry in JapanTakeshi Aiba, Seiko Ohno, Misa Takegami, et al.
Circulation|February 16, 2019
Mutant KCNJ3 and KCNJ5 Potassium Channels as Novel Molecular Targets in Bradyarrhythmias and Atrial FibrillationNoriaki Yamada, Yoshihiro Asano, Masashi Fujita, et al.
European Heart Journal|May 15, 2024
Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk lociTaisuke Ishikawa, Tatsuo Masuda, Tsuyoshi Hachiya, et al.
Pageof 20