Oono Seiko | Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine

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著作論文

ECG Findings in Andersen's Syndrome : Action Potential Simulation Study
PE-106 SCN5A and Lamin A/C Gene Mutations are Highly Prevalent in Patients with Familial Bradyarrhythmic Disorders(PE018,Arrhythmia, Others (Clinical/Pathophysiology) (A),Poster Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulat
FRS-149 Mutation Site-Specific Differences in Arrhythmic Risk and Sensitivity to Sympathetic Stimulation in Japanese Families with Congenital LQT1 Syndrome(Sudden Cardiac Death (A) : FRS18)(Featured Research Session (English))
Molecular and Genetic Basis for the Treatment of Long QT-Related Lethal Ventricular Arrhythmias
PE-104 Severer Phenotypes of Long QT Syndrome are Associated with Compound Mutations : A Multicenter Study(PE018,Arrhythmia, Others (Clinical/Pathophysiology) (A),Poster Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Soci
2 Latent Genetic Backgrounds and Molecular Pathogenesis of Drug-induced Long QT Syndrome(Proarrhythmic Risk of Drugs and Their Evaluation,Symposium 7 (SY-07) (I),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
1 A Novel Genetic Marker for Potential Risk of QT Prolongation and Cardiac Sudden Death : KCNE1-D85N Polymorphism(Biomarkers, Genetic Polymorphism, and Risk Estimation,Symposium 1 (SY-01) (H),The 73rd Annual Scientific Meeting of The Japanese Circulation
PE-251 Mutation analysis of the Glycerol-3 Phosphate Dehydrogenase-1 Like (GPD1L) Gene in Japanese Patients with Brugada Syndrome(Arrhythmia, diagnosis/Pathophysiology/EPS(07)(A),Poster Session(English),The 72nd Annual Scientific Meeting of the Japanese C
OE-391 Cardiac sodium channel gene mutations are prevalent in Japanese patients with familial sick sinus syndrome(Arrhythmia, diagnosis/Pathophysiology/EPS(02)(A),Oral Presentation(English),The 72nd Annual Scientific Meeting of the Japanese Circulation So
OE-276 Familial Dilated Cardiomyopathy with Conduction Disease Caused by Lamin A/C Mutations : Efficacy of the Cardiac Resynchronization Therapy with a Defibrillator(Cardiomyopathy, basic/clinical(01)(M),Oral Presentation(English),The 72nd Annual Scientif
FRS-109 A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation(New Horizon in Diagnosis and Pathophysiology of Arrhythmia(A),Featured Research Session,The 72nd Annual Scientific Meeting of the Japanese Circulation Soci
1 Brugada Syndrome and Diverse Phenotypes of Cardiac Sodium Channelopathies(Symposium 5 (SY-05) (A) New Findings of Mechanism and Therapeutic Strategies of Idiopathic Ventricular Fibrillation,Special Program,The 72nd Annual Scientific Meeting of the Japan
PJ-046 Genotype-Phenotype Correlations of KCNJ2 Mutations in Japanese Patients with Andersen-Tawil Syndrome(Arrhythmia, diagnosis/pathophysiology/EPS-10, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
PJ-043 Clinical Characteristics for Japanese Patients with Genotyped Long-QT Syndrome(Arrhythmia, diagnosis/pathophysiology/EPS-10, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
OJ-007 Variable Genetic Backgrounds Between Congenital and Acquired Long-QT Syndromes(Arrhythmia, diagnosis/pathophysiology/EPS-03, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
FRS-078 Spectrum and Prevalence of Cardiac Sodium Channel (SCN5A) Mutations in a Cohort of 194 Unrelated Patients Referred for Inherited Arrhythmias(Arrhythmia (basic), The 71st Annual Scientific Meeting of the Japanese Circulation Society)
Genetic Analysis of PRKAG2 in a Family with Inherited Wolff-Parkinson-White Syndrome (Arrhythmia, Diagnosis/Pathophysiology/EPS 8 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
High-risk for Bradyarrhythmic Complications in Patients with Brugada Syndrome Caused by SCN5A Gene Mutations(Arrhythmia, Basic (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Quantitative Analysis of Aberrant Splicing Caused by a Splice-site Mutation in KCNQ1 Gene of a Patient with Long QT Syndrome (Genetics/Genetically Engineered Models (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
SCN5A Gene Silencing by Adenovirus-mediated Short Interfering RNA Delivery in Neonatal Rat Ventricular Myocytes(Arrhythmia, Basic 2 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)

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