Miyamoto Yoshihiro | Division Of Arteriosclerosis Metabolism And Clinical Nutrition Department Of Internal Medicine National Cardiovascular Center

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著作論文

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))
Leptin Gene and Leptin Receptor Gene Polymorphisms Are Associated with Sweet Preference and Obesity
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
OJ-061 Association analysis between autosomal recessive hypercholesterolemia (ARH) gene and hypercholesterolemia(Lipid Disorders 1 (H) : OJ8)(Oral Presentation (Japanese))
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
Epinephrine Test for Genotyping LQT1 and LQT2 Forms of Congenital Long QT Syndrome
Increased Risk of Coronary Spasm Due to the Combination of T^ to C Mutation in the eNOS Gene and Smoking

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