Misaki Takuro | The First Department Of Surgery Toyama Medical And Pharmaceutical University

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著作論文

PE-108 Histologic Variation within the Koch's Triangle : Histologic Study Relevant to Atrioventricular Nodal Reentrant Tachycardia(PE018,Arrhythmia, Others (Clinical/Pathophysiology) (A),Poster Session (English),The 73rd Annual Scientific Meeting of The J
PJ-571 Multiple Mechanisms underlie Long QT Syndrome by the Change of Amino Acid R259 in the Intracellular S4-S5 Linker of KCNQ1(PJ096,Arrhythmia, Others (Clinical/Pathophysiology) 4 (A),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The
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
PE-240 Histopathological Analysis as Predictive Markers of Recovery from End Stage Heart Failure in Patients with Left Ventricular Assist Device(PE041,Transplantation/LVAD (M),Poster Session (English),The 73rd Annual Scientific Meeting of The Japanese Cir
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
FRS-052 Identification and Functional Characterization of a Novel Intronic Splicing Mutation in KCNQ1 Associated with Long QT Syndrome(FRS11,New Insights into Basic Mechanisms of Arrhythmia (A),Featured Research Session (English),The 73rd Annual Scientifi
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
Dynamic Change in ST-Segment and Spontaneous Occurrence of Ventricular Fibrillation in Brugada Syndrome With a Novel Nonsense Mutation in the SCN5A Gene During Long-Term Follow-up
Mutation Analysis of the Glycerol-3 Phosphate Dehydrogenase-1 Like (GPD1L) Gene in Japanese Patients With Brugada Syndrome
Mutation Site Dependent Variability of Cardiac Events in Japanese LQT2 Form of Congenital Long-QT Syndrome
A Novel Mutation Associated With Jervell and Lange-Nielsen Syndrome in a Japanese Family
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
OJ-009 A Common KCNE1 Polymorphism, D85N, is a Genetic Modifier of Long QT Syndrome(Arrhythmia, diagnosis/ Pathophysiology/ EPS(03)(A),Oral Presentation(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
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
PJ-743 Analysis of 1710 Cases of Endomyocardial Biopsy in a Single Center(PJ125,Preventive Medicine/Epidemiology/Education 3 (H),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
FRS-019 Plakophilin-2 Mutations are Common in Japanese Arrhythmogenic Right Ventricular Cardiomyopathy(New Insights into Basic Mechanism of Arrhythmia(A),Featured Research Session,The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
P396 ELECTROPHYSIOLOGICAL MECHANISMS OF FRAGMENTED ELECTRICAL ACTIVITY DURING ATRIAL FIBRILLATION : OBSERVATIONS FROM VAGALLY INDUCED CANINE ATRIAL FIBRILLATION AND OPEN HEART SURGERY
0593 CONDUCTION AT THE NARROW ISTHMUS DURING ATRIAL FLUTTER : OBSERVATIONS FROM CATHTER ABLATION AND OPEN HEART SURGERY
-0914-BASIC STUDY OF SURGICAL LASER TREATMENT FOR ARRHYTHMIA : THE 54th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY
Long-Term Usefulness of Percutaneous Intrapericardial Fibrin-Glue Fixation Therapy for Oozing Type of Left Ventricular Free Wall Rupture : A Case Report
P141 Radio frequency Catheter Ablation of Typical Atrial Flutter : Different Optimal Target Site Depending on the Direction of Excitation Wavefront
TWO DIFFERENT MECHANISMS OF CANINE ATRIAL FIBRILLATION:VAGAL STIMULATION AND PERICARDITIS
Total Anomalous Pulmonary Venous Connection With Bronchogenic Cyst in Neonatal Period
EVALUATION OF CARDIAC SURFACE PHASE MAP IN PATIENTS WITH EPICARDIAL PACING : Arrhythmias, Clinical : PROCEEDINGS OF THE 50th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY
Complex Atrial Reentrant Circuits Evaluated by Entrainment Mapping Using a Multielectrode Basket Catheter
Guidelines for Risks and Prevention of Sudden Cardiac Death (JCS 2010) : Digest Version

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