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12篇 您的检索式:作者名="Koopmann TT"
    题名 作者 年代 出处 被引量
1Sodium channel betal subunit mutations associated with Brugada syndrome and cardi- ac conduction disease in humans显示文摘WatanabeH Koopmann TT le Scouarnec S 2008JCI2008,118,:1
2Sodium channel betal subunit mutations associated with Brugada syndrome and cardiac conduction disease in Humans 显示文摘Watanabe H Koopmann TT Le Scouarnec S 2008J Clin Invest2008,118,6:1
3Polymorphisms in the cardiac sodium channel promoler displaying variant in vitro expression activity 显示文摘Yang P Koopmann TT Pfeufer A 2008Eur J Hum Genet2008,16,5:1
4Sodium channel betal subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans 显示文摘Watanabe H Koopmann TT le Scouamec S 2008J Clin Invest2008,118,:1
5A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome,conduction disease and Brugada syndrome in two families显示文摘Smits JP Koopmann TT Wilders R 2005J Mol Cell Cardiol2005,38,:1
6A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome,conduction disease and Brugada syndrome in two families显示文摘Smits JP Koopmann TT Wilders R 2005J Mol Cell Cardiol2005,38,6:1
7Sodi- um channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans 显示文摘Watanabe H Koopmann TT Le Scouarnec S 2008J Clin Invest2008,118,6:1
8Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined eleetrophysiologieal, genetic, histopathologic, and computational study 显示文摘Coronel R Casini S Koopmann TT 2005Circulation2005,112,:1
9Sodium channel betal subunit mutations associated with brugada syndrome and cardiac conduction disease in humans 显示文摘Watanabe H Koopmann TT Le Scouarnec S 2008Clin Invest2008,118,6:1
10Sodium channel betal subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans 显示文摘Watanabe H Koopmann TT Le Scouarnec S 2008J Clin Invest2008,118,6:1
11A mutation in the human cardiac sodium channel (El 61 K) contributes to sick sinus syndrome,conduction disease and Bmgada syndrome in two families显示文摘Smits JP Koopmann TT Wilders R 2005J Mol Cell Cardiol2005,38,6:1
12Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current poly- merase chain reaction-based exon-scanning methodolo- gies显示文摘Koopmann TT Alders M Jongbloed RJ 2006Heart Rhythm2006,3,1:1
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