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Seiko Ohno

Showing results (81-90 of 222) with videos related to

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Journal of Cardiothoracic Surgery|December 21, 2017
Refractory ventricular fibrillations after surgical repair of atrial septal defects in a patient with CACNA1C gene mutation - case reportAi Kojima, Fumiaki Shikata, Toru Okamura, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 30, 2018
Catecholaminergic polymorphic ventricular tachycardia managed as orthostatic dysregulation and epilepsy in 11- and 15-year-old sistersShuhei Fujita, Keigo Nishida, Hitoshi Irabu, et al.
The Journal of General Physiology|April 21, 2022
Cytosolic Ca2+-dependent Ca2+ release activity primarily determines the ER Ca2+ level in cells expressing the CPVT-linked mutant RYR2Nagomi Kurebayashi, Takashi Murayama, Ryosaku Ota, et al.
Internal Medicine (Tokyo, Japan)|February 3, 2016
Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese FamilyMari Ichikawa, Seiko Ohno, Yusuke Fujii, et al.
Journal of Arrhythmia|October 19, 2019
Genetic variants of alcohol-metabolizing enzymes in Brugada syndrome: Insights into syncope after drinking alcoholQi Wu, Hideki Hayashi, Daiki Hira, et al.
Biochimica Et Biophysica Acta|August 4, 2011
Identification and functional characterization of KCNQ1 mutations around the exon 7-intron 7 junction affecting the splicing processKeiko Tsuji-Wakisaka, Masaharu Akao, Takahiro M Ishii, et al.
Journal of Arrhythmia|June 29, 2018
Electrical storm in an infant with short-coupled variant of torsade de pointesHiroaki Kise, Seiko Ohno, Yosuke Kono, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|October 19, 2025
Characterization of a Splice-Altering Variant in SCN5A Associated With Brugada Syndrome　- Insights Into Splice Error CorrectionHideyuki Jinzai, Koichi Kato, Yuichi Sawayama, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|October 5, 2025
Novel Loss-of-Function Variant, Cys1384Phe, in SCN5A Is Associated With an Overlapping Phenotype of Brugada Syndrome, Sick Sinus Syndrome, and Dilated CardiomyopathyKohei Yamauchi, Koichi Kato, Seiko Ohno, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|December 26, 2019
Co-Phenotype of Left Ventricular Non-Compaction Cardiomyopathy and Atypical Catecholaminergic Polymorphic Ventricular Tachycardia in Association With R169Q, a Ryanodine Receptor Type 2 Missense MutationYoshihiro Nozaki, Yoshiaki Kato, Kiyoshi Uike, et al.
Pageof 23

Showing results (81-90 of 222) with videos related to

Sort By:
Pageof 23
Journal of Cardiothoracic Surgery|December 21, 2017
Refractory ventricular fibrillations after surgical repair of atrial septal defects in a patient with CACNA1C gene mutation - case reportAi Kojima, Fumiaki Shikata, Toru Okamura, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 30, 2018
Catecholaminergic polymorphic ventricular tachycardia managed as orthostatic dysregulation and epilepsy in 11- and 15-year-old sistersShuhei Fujita, Keigo Nishida, Hitoshi Irabu, et al.
The Journal of General Physiology|April 21, 2022
Cytosolic Ca2+-dependent Ca2+ release activity primarily determines the ER Ca2+ level in cells expressing the CPVT-linked mutant RYR2Nagomi Kurebayashi, Takashi Murayama, Ryosaku Ota, et al.
Internal Medicine (Tokyo, Japan)|February 3, 2016
Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese FamilyMari Ichikawa, Seiko Ohno, Yusuke Fujii, et al.
Journal of Arrhythmia|October 19, 2019
Genetic variants of alcohol-metabolizing enzymes in Brugada syndrome: Insights into syncope after drinking alcoholQi Wu, Hideki Hayashi, Daiki Hira, et al.
Biochimica Et Biophysica Acta|August 4, 2011
Identification and functional characterization of KCNQ1 mutations around the exon 7-intron 7 junction affecting the splicing processKeiko Tsuji-Wakisaka, Masaharu Akao, Takahiro M Ishii, et al.
Journal of Arrhythmia|June 29, 2018
Electrical storm in an infant with short-coupled variant of torsade de pointesHiroaki Kise, Seiko Ohno, Yosuke Kono, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|October 19, 2025
Characterization of a Splice-Altering Variant in SCN5A Associated With Brugada Syndrome　- Insights Into Splice Error CorrectionHideyuki Jinzai, Koichi Kato, Yuichi Sawayama, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|October 5, 2025
Novel Loss-of-Function Variant, Cys1384Phe, in SCN5A Is Associated With an Overlapping Phenotype of Brugada Syndrome, Sick Sinus Syndrome, and Dilated CardiomyopathyKohei Yamauchi, Koichi Kato, Seiko Ohno, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|December 26, 2019
Co-Phenotype of Left Ventricular Non-Compaction Cardiomyopathy and Atypical Catecholaminergic Polymorphic Ventricular Tachycardia in Association With R169Q, a Ryanodine Receptor Type 2 Missense MutationYoshihiro Nozaki, Yoshiaki Kato, Kiyoshi Uike, et al.
Pageof 23