Yoshida Hidetada | Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine

スポンサーリンク

概要

関連著者

もっと見る

著作論文

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
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
A single mutation of cardiac sodium channel gene confers phenotypes of both Brugada and long QT syndromes
Ion channel mutations and polymorphisms in Japanese patients with acquired 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)
OJ-009 N- And C-terminal KCNE1 Mutations Cause Distinct Phenotypes of Long QT Syndrome(Arrhythmia, diagnosis/pathophysiology/EPS-03, The 71st Annual Scientific Meeting of the Japanese Circulation Society)

スポンサーリンク