Art

J-GLOBAL ID：201402208794633209   Reference number：14A1466976

Genetic and Clinical Advances in Congenital Long QT Syndrome

先天性QT延長症候群の遺伝的および臨床進行

Author (4)： MIZUSAWA Yuka (The Heart Failure Res. Center, Dep. of Clinical and Experimental Cardiology, Academic Medical Center, Univ. of Amsterdam) ,  HORIE Minoru (Dep. of Cardiovascular and Respiratory Medicine, Shiga Univ. of Medical Sci.) ,  WILDE Arthur AM (The Heart Failure Res. Center, Dep. of Clinical and Experimental Cardiology, Academic Medical Center, Univ. of Amsterdam) ,  WILDE Arthur AM (Princess Al-Jawhara Al-Brahim Centre of Excellence in Res. of Hereditary Disorders, King Abdulaziz Univ.)
Material： Circulation Journal  (Circ J)
Volume： 78  Issue： 12  Page： 2827-2833 (J-STAGE)  Publication year： 2014 
JST Material Number： F0908A  ISSN： 1346-9843  Document type： Article
Article type： 文献レビュー  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： *congenital disease ,...
Semi thesaurus term： Jervell and Lange-Nielsen syndrome ,...

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JST classification (2)： Cardiovascular system diagnosis  (GJ02000V) ,  Research methods in genetics  (EC01020N)

Reference (92)：

• 1. Jervell A, Lange-Nielsen F. Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death. Am Heart J 1957; 54: 59-68.
• 2. 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.
• 3. Shimizu W, Horie M. Phenotypic manifestations of mutations in genes encoding subunits of cardiac potassium channels. Circ Res 2011; 109: 97-109.
• 4. Wilde AA, Brugada R. Phenotypical manifestations of mutations in the genes encoding subunits of the cardiac sodium channel. Circ Res 2011; 108: 884-897.
• 5. Schwartz PJ, Stramba-Badiale M, Crotti L, Pedrazzini M, Besana A, Bosi G, et al. Prevalence of the congenital long-QT syndrome. Circulation 2009; 120: 1761-1767.

Terms in the title (3)： 先天性QT延長症候群 ,  遺伝 ,  臨床