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Department Of Atherosclerosis And Diabetes National Cerebral And Cardiovascular Center | 論文
- OE-389 Clinical Phenotype of Japanese LQT1 Form of Congenital Long QT Syndrome by Location and Coding Type From Japanese Multicenter Registry(Arrhythmia, diagnosis/Pathophysiology/EPS(02)(A),Oral Presentation(English),The 72nd Annual Scientific Meeting of
- OJ-011 Association of Obesity Related Factors with Plasma B-type Natriuretic Peptide Levels in General Japanese Population(OJ02,Obesity/SAS (H),Oral Presentation (Japanese),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
- Impact of Metabolic Syndrome Components on the Incidence of Cardiovascular Disease in a General Urban Japanese Population : The Suita Study
- Leptin Gene and Leptin Receptor Gene Polymorphisms Are Associated with Sweet Preference and Obesity
- FRS-076 A link between LDL Receptor (LDLR) Gene Mutation and Clinical Manifestations in Familial Hypercholesterolemia(FRS16,Basic Mechanisms of Lipid Disorders and Metabolic Syndrome (H),Featured Research Session (English),The 73rd Annual Scientific Meeti
- PJ-898 Predicting high risk patients of coronary artery disease in heterozygous familial hypercholesterolemia from clinical features(Lipid disorders(05)(H),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
- 3 Effects of Anti-postprandial Hyperglycemia Drugs on the Coronary Atherosclerosis in Early Stage Diabetic Patients with Coronary Artery Disease : A Study of the DIAbetes and Diffuse Coronary NArrowing (DIANA)(Late Breaking Clinical Trials I,The 73rd Annu
- 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
- Mutation Site Dependent Variability of Cardiac Events in Japanese LQT2 Form of Congenital Long-QT Syndrome
- 3 Mutant KCNE3 Reduces Repolarizing Potassium Current And Causes Long QT Syndrome(Plenary Session 4 (PL-4) (A) New Scientific Approaches to QT Prolongation,Special Program,The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
- PE-103 Clinical Phenotype of Japanese LQT3 Form of Congenital Long QT Syndrome by Location of Mutation from Japanese Multicenter Registry(PE018,Arrhythmia, Others (Clinical/Pathophysiology) (A),Poster Session (English),The 73rd Annual Scientific Meeting o
- FRS-117 Clinical and Electrocardiographic Characteristics of Japanese Probands with Brugada Syndrome with an SCN5A Mutation from Japanese Multicenter Registry(FRS24,Novel Mechanisms of Ventricular Arrhythmia (A),Featured Research Session (English),The 73r
- PJ-208 Impact of Frameshift Mutation and Nonsense-mediated mRNA Decay on Clinical Phenotype in LQT2 Form of Congenital Long QT Syndrome(Arrhythmia,diagnosis/Pathophysiology/EPS(13)(A),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japa
- 5 Cellular Mechanism, Gender and Ethnic Difference in the Brugada Syndrome(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 Japane
- 2 Mutation Location- or Mutation Type-Specific Clinical Severity and Therapy in LQT1 and LQT2 Forms of Congenital Long-QT Syndrome(Plenary Session 4 (PL-4) (A) New Scientific Approaches to QT Prolongation,Special Program,The 72nd Annual Scientific Meeting
- PJ-378 Decreased Circulating CD34-positive Cells are Associated with High Plasma BNP Concentration in Elderly Patients with Type 2 Diabetes Mellitus(Diabetes/Obesity/Metabolic syndrome-9 (H) PJ64,Poster Session (Japanese),The 70th Anniversary Annual Scien
- Obesity and Insulin Resistance Possibly Promotes Ischemic Heart Disease of the Patients with Familial Combined Hyperlipidemia (FCHL)(Lipid Disorders 4 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- 2 Future Challenge in Brugada syndrome : Gender and Ethnic Differences(Brugada Syndrome:From Cell to Bedside,Plenary Session 2 (PL2) (A),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- PJ-243 A Novel Mutation in the Autosomal Recessive Hypercholesterolemia Gene Leads to Hypercholesterolemia(Lipid disorders-3 (H) PJ41,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- Resistin Gene Polymorphism Positively Associated with the Metabolic Syndrome in Japanese Men(Gene Therapy/Genetic Engineering (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
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