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Seiko Ohno

Showing results (131-140 of 222) with videos related to

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Heart Rhythm|June 15, 2010
Long QT syndrome with compound mutations is associated with a more severe phenotype: a Japanese multicenter studyHideki Itoh, Wataru Shimizu, Kenshi Hayashi, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|June 28, 2023
Calmodulinopathy in Japanese Children　- Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and InfancyMegumi Fukuyama, Minoru Horie, Koichi Kato, et al.
Journal of Cardiology|November 18, 2017
Novel intracellular transport-refractory mutations in KCNH2 identified in patients with symptomatic long QT syndromeDaisuke Fukumoto, Wei-Guang Ding, Yuko Wada, 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 mutationsJie Wu, Yuka Mizusawa, Seiko Ohno, et al.
Human Mutation|March 24, 2009
Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndromeSeiko Ohno, Futoshi Toyoda, Dimitar P Zankov, et al.
JACC. Clinical Electrophysiology|October 10, 2024
Clinical Features, Long-Term Prognosis, and Clinical Management of Genotype-Negative Long QT Syndrome PatientsKeiko Shimamoto, Federica Dagradi, Seiko Ohno, et al.
American Journal of Physiology. Cell Physiology|July 19, 2013
Pharmacological correction of long QT-linked mutations in KCNH2 (hERG) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulumJennifer L Smith, Allison R Reloj, Parvathi S Nataraj, et al.
Journal of the American College of Cardiology|December 6, 2005
High risk for bradyarrhythmic complications in patients with Brugada syndrome caused by SCN5A gene mutationsTakeru Makiyama, Masaharu Akao, Keiko Tsuji, et al.
Journal of Cardiology Cases|July 23, 2025
SCN5A mutation-associated sick sinus syndrome revealed by atrial flutter in a pediatric patientYoshikatsu Takeda, Shuhei Fujita, Yusuke Yachi, et al.
Heart and Vessels|January 26, 2021
Diagnostic value of P-waves in children with idiopathic restrictive cardiomyopathyShota Muraji, Naokata Sumitomo, Tomohiko Imamura, et al.
Pageof 23

Showing results (131-140 of 222) with videos related to

Sort By:
Pageof 23
Heart Rhythm|June 15, 2010
Long QT syndrome with compound mutations is associated with a more severe phenotype: a Japanese multicenter studyHideki Itoh, Wataru Shimizu, Kenshi Hayashi, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|June 28, 2023
Calmodulinopathy in Japanese Children　- Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and InfancyMegumi Fukuyama, Minoru Horie, Koichi Kato, et al.
Journal of Cardiology|November 18, 2017
Novel intracellular transport-refractory mutations in KCNH2 identified in patients with symptomatic long QT syndromeDaisuke Fukumoto, Wei-Guang Ding, Yuko Wada, 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 mutationsJie Wu, Yuka Mizusawa, Seiko Ohno, et al.
Human Mutation|March 24, 2009
Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndromeSeiko Ohno, Futoshi Toyoda, Dimitar P Zankov, et al.
JACC. Clinical Electrophysiology|October 10, 2024
Clinical Features, Long-Term Prognosis, and Clinical Management of Genotype-Negative Long QT Syndrome PatientsKeiko Shimamoto, Federica Dagradi, Seiko Ohno, et al.
American Journal of Physiology. Cell Physiology|July 19, 2013
Pharmacological correction of long QT-linked mutations in KCNH2 (hERG) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulumJennifer L Smith, Allison R Reloj, Parvathi S Nataraj, et al.
Journal of the American College of Cardiology|December 6, 2005
High risk for bradyarrhythmic complications in patients with Brugada syndrome caused by SCN5A gene mutationsTakeru Makiyama, Masaharu Akao, Keiko Tsuji, et al.
Journal of Cardiology Cases|July 23, 2025
SCN5A mutation-associated sick sinus syndrome revealed by atrial flutter in a pediatric patientYoshikatsu Takeda, Shuhei Fujita, Yusuke Yachi, et al.
Heart and Vessels|January 26, 2021
Diagnostic value of P-waves in children with idiopathic restrictive cardiomyopathyShota Muraji, Naokata Sumitomo, Tomohiko Imamura, et al.
Pageof 23