FluvoxamineProvocation of Brugada syndrome ECG in a patient with an SCN5A p.W822X nonsense mutation: case report

被引：0
|
作者：
机构：
来源：
Reactions Weekly | 2010年 / 1301卷 / 1期
关键词：
Ventricular Arrhythmia; Depressive Episode; Implantable Cardioverter Defibrillator; Fluvoxamine; Outpatient Visit;
D O I：
10.2165/00128415-201013010-00084
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：24 / 24
相关论文
共 50 条
  • [21] A Novel SCN5A Mutation Associated With Brugada Type ECG And Intraventricular Conduction Defects
    Samani, Kaveh
    Ai, Tomohiko
    Towbin, Jeffrey A.
    Brugada, Ramon
    Xi, Yutao
    Cheng, Jie
    Vatta, Matteo
    BIOPHYSICAL JOURNAL, 2009, 96 (03) : 263A - 263A
  • [22] SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families
    Wijeyeratne, Yanushi D.
    Tanck, Michael W.
    Mizusawa, Yuka
    Batchvarov, Velislav
    Barc, Julien
    Crotti, Lia
    Bos, J. Martijn
    Tester, David J.
    Muir, Alison
    Veltmann, Christian
    Ohno, Seiko
    Page, Stephen P.
    Galvin, Joseph
    Tadros, Rafik
    Muggenthaler, Martina
    Raju, Hariharan
    Denjoy, Isabelle
    Schott, Jean-Jacques
    Gourraud, Jean-Baptiste
    Skoric-Milosavljevic, Doris
    Nannenberg, Eline A.
    Redon, Richard
    Papadakis, Michael
    Kyndt, Florence
    Dagradi, Federica
    Castelletti, Silvia
    Torchio, Margherita
    Meitinger, Thomas
    Lichtner, Peter
    Ishikawa, Taisuke
    Wilde, Arthur A. M.
    Takahashi, Kazuhiro
    Sharma, Sanjay
    Roden, Dan M.
    Borggrefe, Martin M.
    McKeown, Pascal P.
    Shimizu, Wataru
    Horie, Minoru
    Makita, Naomasa
    Aiba, Takeshi
    Ackerman, Michael J.
    Schwartz, Peter J.
    Probst, Vincent
    Bezzina, Connie R.
    Behr, Elijah R.
    CIRCULATION-GENOMIC AND PRECISION MEDICINE, 2020, 13 (06): : 599 - 608
  • [23] Drug-induced Brugada ECG Changes Associated With A Novel SCN5A Mutation In A Patient With Atrial Arrhythmias
    Samani, Kaveh
    Ai, Tomohiko
    Ueyama, Takeshi
    Makiyama, Takeru
    Vatta, Matteo
    Sohma, Yoshiro
    Xi, Yutao
    Itoh, Hideki
    Horie, Minoru
    Shimizu, Akihiko
    Cheng, Jie
    BIOPHYSICAL JOURNAL, 2009, 96 (03) : 665A - 665A
  • [24] A Nonsense SCN5A Mutation Associated with Brugada-Type Electrocardiogram and Intraventricular Conduction Defects
    Samani, Kaveh
    Ai, Tomohiko
    Towbin, Jeffrey A.
    Brugada, Ramon
    Shuraih, Mossaab
    Xi, Yutao
    Wu, Geru
    Cheng, Jie
    Vatta, Matteo
    PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY, 2009, 32 (09): : 1231 - 1236
  • [25] A novel SCN5A mutation associated with idiopathic ventricular fibrillation without typical ECG findings of Brugada syndrome
    Akai, J
    Makita, N
    Sakurada, H
    Shirai, N
    Ueda, K
    Kitabatake, A
    Nakazawa, K
    Kimura, A
    Hiraoka, M
    FEBS LETTERS, 2000, 479 (1-2) : 29 - 34
  • [26] SCN5A polymorphism restores trafficking of a Brugada syndrome mutation on a separate gene
    Poelzing, Steven
    Forleo, Cinzia
    Samodell, Melissa
    Dudash, Lynn
    Sorrentino, Sandro
    Anaclerio, Matteo
    Troccoli, Rossella
    Iacoviello, Massimo
    Romito, Roberta
    Guida, Pietro
    Chahine, Mohamed
    Pitzalis, Mariavittoria
    Deschenes, Isabelle
    CIRCULATION, 2006, 114 (05) : 368 - 376
  • [27] A newly characterized SCN5A mutation underlying Brugada syndrome unmasked by hyperthermia
    Mok, NS
    Priori, SG
    Napolitano, C
    Chan, NY
    Chahine, M
    Baroudi, G
    JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2003, 14 (04) : 407 - 411
  • [28] A new SCN5A mutation associate Brugada syndrome and sinus node dysfunction
    Kyndt, F
    Schott, JJ
    Probst, V
    Chevallier, JC
    Le Marec, H
    JOURNAL OF MOLECULAR MEDICINE-JMM, 2000, 78 (03): : B13 - B13
  • [29] Brugada syndrome with marked conduction disease: Dual implications of a SCN5A mutation
    Vorobiof, Gabriel
    Kroening, Daniel
    Hall, Burr
    Brugada, Ramon
    Huang, David
    PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY, 2008, 31 (05): : 630 - 634
  • [30] SCN5A polymorphism restores trafficking of a Brugada syndrome mutation on a separate gene
    Chen, Peng-Sheng
    HEART RHYTHM, 2006, 3 (11) : 1393 - 1393
12345