PJ-600 Lidocaine Prevents Brugada Syndrome with the N406S Mutation of SCN5A from Going into the Intermediate Inactivation(Arrhythmia, basic-5 (A) PJ101,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation So

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概要

• 論文の詳細を見る
• 社団法人日本循環器学会の論文
• 2006-03-01

著者

• HORIE Minoru

  Department of Cardiovascular and Respiratory Medicine, Shiga University of Medical Science

• Itoh Hideki

  Department Of Cardiovascular And Respiratory Medicine Shiga University Of Medical Science

• Ito Masahiro

  新潟大学 医歯学総合研究科循環器学

• ITO Makoto

  Department of Cardiovascular Medicine, Shiga University of Medical Science

• Ito Makoto

  Department Of Cardiovascular And Respiratory Medicine Shiga University Of Medical Science

• IMOTO Keiji

  Department of Information Physiology, National Institute for Physiological Sciences

• Horie Minoru

  Department Of Cardiac Physiology National Cardiovascular Center Research Institute

• Imoto Keiji

  Department Of Information Physiology National Institute For Physiological Sciences

• Itoh Hideki

  Department Of Respiratory And Cardiovascular Medicine Shiga University Of Medical Science

• Itoh Hideki

  Sakurabashi Watanabe Hospital

• Itoh Hideki

  Department Of Anesthesiology And Critical Care Medicine Yokohama City University Graduate School Of

• Ito Makoto

  Department Of Bioscience And Biotechnology Graduate School Of Bioresource And Bioenvironmental Scien

• ITO Makoto

  Department of Bioresources, Faculty of Agriculture, Ehime University

関連論文

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• ECG Findings in Andersen's Syndrome : Action Potential Simulation Study
• ECG Findings in Andersen's Syndrome : Action Potential Simulation Study
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• Hydroxyzine, a First Generation H_1-Receptor Antagonist, Inhibits Human Ether-a-go-go-Related Gene (HERG) Current and Causes Syncope in a Patient With the HERG Mutation
• 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
• Association of Atrial Arrhythmia and Sinus Node Dysfunction in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia
• Whole-Body Periodic Acceleration Enhances Brachial Endothelial Function
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• Relationship between Metabolic Syndrome and Trp64Arg Polymorphism of the β3-Adrenergic Receptor Gene in a General Sample : The Shigaraki Study
• The Association between Morning Hypertension and Metabolic Syndrome in Hypertensive Patients
• Impact of Paraoxonase Polymorphism (Q192R) on Endothelial Function in Intact Coronary Circulation
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