Art

J-GLOBAL ID：201502239025718293   Reference number：15A0733360

Unveiling Specific Triggers and Precipitating Factors for Fatal Cardiac Events in Inherited Arrhythmia Syndromes

遺伝性不整脈症候群における致命的心臓イベントへの特異的トリガーと増悪因子の解明

Author (3)： NAKAJIMA Tadashi (Dep. of Medicine and Biological Sci., Gunma Univ. Graduate School of Medicine) ,  KANEKO Yoshiaki (Dep. of Medicine and Biological Sci., Gunma Univ. Graduate School of Medicine) ,  KURABAYASHI Masahiko (Dep. of Medicine and Biological Sci., Gunma Univ. Graduate School of Medicine)
Material： Circulation Journal  (Circ J)
Volume： 79  Issue： 6  Page： 1185-1192 (J-STAGE)  Publication year： 2015 
JST Material Number： F0908A  ISSN： 1346-9843  Document type： Article
Article type： 解説  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： human(primates) ,...
Semi thesaurus term： genotype-phenotype correlation ,...

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JST classification (2)： Cardiovascular system diseases  (GJ03000C) ,  Congenital diseases,deformities in general.  (GD03010V)

Reference (78)：

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• 2. Curran ME, Splawski I, Timothy KW, Vincent GM, Green ED, Keating MT. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome. Cell 1995; 80: 795-803.
• 3. Wang Q, Shen J, Splawski I, Atkinson D, Li Z, Robinson JL, et al. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell 1995; 80: 805-811.
• 4. Shimizu W. Update of diagnosis and management of inherited cardiac arrhythmias. Circ J 2013; 77: 2867-2872.
• 5. Schwartz PJ, Ackerman MJ, George AL Jr, Wilde AA. Impact of genetics on the clinical management of channelopathies. J Am Coll Cardiol 2013; 62: 169-180.

Terms in the title (6)： 遺伝性不整脈 ,  症候群 ,  心臓 ,  イベント ,  トリガー ,  増悪因子