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Seiko Ohno

Showing results (111-120 of 222) with videos related to

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Circulation. Cardiovascular Imaging|August 28, 2019
Response by Sakamoto et al to Letter Regarding Article, "Left-Dominant Arrhythmogenic Cardiomyopathy With Heterozygous Mutations in DSP and MYBPC3"Naka Sakamoto, Shunsuke Natori, Shohei Hosoguchi, et al.
Journal of Molecular and Cellular Cardiology|February 13, 2007
Mechanistic basis for the pathogenesis of long QT syndrome associated with a common splicing mutation in KCNQ1 geneKeiko Tsuji, Masaharu Akao, Takahiro M Ishii, et al.
Cardiovascular Research|December 14, 2011
A novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currentsTetsuhisa Hattori, Takeru Makiyama, Masaharu Akao, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|December 22, 2012
Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5Taisuke Ishikawa, Naohiko Takahashi, Seiko Ohno, et al.
Journal of Medical Case Reports|April 29, 2023
Meningitis caused by Chromobacterium haemolyticum suspected to be derived from a canal in Japan: a case reportKumi Iwamoto, Masaki Yamamoto, Atsushi Yamamoto, et al.
Heart Rhythm|October 8, 2013
A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channelsKanae Hasegawa, Seiko Ohno, Takashi Ashihara, et al.
BMC Cardiovascular Disorders|December 19, 2019
Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac deathTetsuro Yokokawa, Shohei Ichimura, Naoko Hijioka, et al.
Journal of the American College of Cardiology|October 22, 2008
A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillationTakeru Makiyama, Masaharu Akao, Satoshi Shizuta, et al.
Journal of Cardiology Cases|July 23, 2025
Atypical Holt-Oram syndrome: Early-onset sick sinus syndrome in a Japanese family with a novel <i>TBX5</i> mutation, Q469Yoshihiro Nomura, Taisuke Ishikawa, Seiko Ohno, et al.
Journal of the American Heart Association|February 18, 2021
Impact of Medical Castration on Malignant Arrhythmias in Patients With Prostate CancerKanae Hasegawa, Hideaki Ito, Kenichi Kaseno, et al.
Pageof 23

Showing results (111-120 of 222) with videos related to

Sort By:
Pageof 23
Circulation. Cardiovascular Imaging|August 28, 2019
Response by Sakamoto et al to Letter Regarding Article, "Left-Dominant Arrhythmogenic Cardiomyopathy With Heterozygous Mutations in DSP and MYBPC3"Naka Sakamoto, Shunsuke Natori, Shohei Hosoguchi, et al.
Journal of Molecular and Cellular Cardiology|February 13, 2007
Mechanistic basis for the pathogenesis of long QT syndrome associated with a common splicing mutation in KCNQ1 geneKeiko Tsuji, Masaharu Akao, Takahiro M Ishii, et al.
Cardiovascular Research|December 14, 2011
A novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currentsTetsuhisa Hattori, Takeru Makiyama, Masaharu Akao, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|December 22, 2012
Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5Taisuke Ishikawa, Naohiko Takahashi, Seiko Ohno, et al.
Journal of Medical Case Reports|April 29, 2023
Meningitis caused by Chromobacterium haemolyticum suspected to be derived from a canal in Japan: a case reportKumi Iwamoto, Masaki Yamamoto, Atsushi Yamamoto, et al.
Heart Rhythm|October 8, 2013
A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channelsKanae Hasegawa, Seiko Ohno, Takashi Ashihara, et al.
BMC Cardiovascular Disorders|December 19, 2019
Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac deathTetsuro Yokokawa, Shohei Ichimura, Naoko Hijioka, et al.
Journal of the American College of Cardiology|October 22, 2008
A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillationTakeru Makiyama, Masaharu Akao, Satoshi Shizuta, et al.
Journal of Cardiology Cases|July 23, 2025
Atypical Holt-Oram syndrome: Early-onset sick sinus syndrome in a Japanese family with a novel <i>TBX5</i> mutation, Q469Yoshihiro Nomura, Taisuke Ishikawa, Seiko Ohno, et al.
Journal of the American Heart Association|February 18, 2021
Impact of Medical Castration on Malignant Arrhythmias in Patients With Prostate CancerKanae Hasegawa, Hideaki Ito, Kenichi Kaseno, et al.
Pageof 23