スポンサーリンク
Sohen Central Hospital | 論文
- Congenital atrial standstill associated with coinheritance of a novel SCN5A mutation and connexin 40 polymorphisms
- OJ-426 Enhanced Temporal and Spatial Cycle Length Variability during Ventricular Fibrillation in Hypertrophic Cardiomyopathy(ECG/Body Surface Potential Mapping/Holter 6 (A) : OJ52)(Oral Presentation (Japanese))
- Increased cycle length variability during ventricular fibrillation : a novel predictor of arrhythmia recurrence
- Altered repolarization dynamics during premature stimulation in Brugada syndrome with inducible ventricular fibrillation
- Prevalence and Clinical Characteristics of Patients With Atrial Fibrillation : Analysis of 20,000 Cases in Japan
- An SCN5A Mutation Associated With Idiopathic Ventricular Fibrillation Alters The Na^+ Channel Pore Structure And Responses To Antiarrhythmic Drugs
- Double SCN5A mutation underlying asymptomatic Brugada syndrome
- Single Nucleotide Polymorphisms of Cardiac Na^+ Channel Gene SCN5A : Allelic Prevalence in Brugada Syndrome and Their Biophysical Properties
- PE-307 Left Ventricular Noncompaction Associated With Mutations in Cardiac Na Channel Gene SCN5A(Cardiomyopathy, basic/clinical-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- OE-085 Genetic Factors Conferring Congenital Sick Sinus Syndrome in SCN5A Mutation Carriers(Arrhythmia, basic-1, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- Nonreentrant atrioventricular nodal tachycardia due to triple nodal pathways manifested by radiofrequency ablation at coronary sinus ostium