Flecainide for recurrent malignant ventricular arrhythmias in two siblings with Andersen-Tawil syndrome

被引：40
作者：
Boekenkamp, Regina
Wilde, Arthur A.
Schalij, Martin J.
Blom, Nico A.
机构：
[1] Leiden Univ, Med Ctr, Dept Pediat Cardiol, NL-2300 RC Leiden, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
来源：
HEART RHYTHM | 2007年 / 4卷 / 04期
关键词：
D O I：
10.1016/j.hrthm.2006.12.031
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
[No abstract available]
引用
收藏
页码：508 / 511
页数：4
相关论文
共 15 条
  • [1] Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia
    Ai, T
    Fujiwara, Y
    Tsuji, K
    Otani, H
    Nakano, S
    Kubo, Y
    Horie, M
    [J]. CIRCULATION, 2002, 105 (22) : 2592 - 2594
  • [2] Canún S, 1999, AM J MED GENET, V85, P147, DOI 10.1002/(SICI)1096-8628(19990716)85:2<147::AID-AJMG9>3.0.CO
  • [3] 2-0
  • [4] CONARD GJ, 1984, CLIN THER, V6, P643
  • [5] Suppression of bidirectional ventricular tachycardia and unmasking of prolonged QT interval with verapamil in Andersen's syndrome
    Kannankeril, PJ
    Roden, DM
    Fish, FA
    [J]. JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2004, 15 (01) : 119 - 119
  • [6] Functional role of inward rectifier current in heart probed by Kir2.1 overexpression and dominant-negative suppression
    Miake, J
    Marbán, E
    Nuss, HB
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (10) : 1529 - 1536
  • [7] Long QT syndrome: from channels to cardiac arrhythmias
    Moss, AJ
    Kass, RS
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (08) : 2018 - 2024
  • [8] Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome
    Plaster, NM
    Tawil, R
    Tristani-Firouzi, M
    Canún, S
    Bendahhou, S
    Tsunoda, A
    Donaldson, MR
    Iannaccone, ST
    Brunt, E
    Barohn, R
    Clark, J
    Deymeer, F
    George, AL
    Fish, FA
    Hahn, A
    Nitu, A
    Ozdemir, C
    Serdaroglu, P
    Subramony, SH
    Wolfe, G
    Fu, YH
    Ptácek, LJ
    [J]. CELL, 2001, 105 (04) : 511 - 519
  • [9] Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome
    Preisig-Müller, R
    Schlichthörl, G
    Goerge, T
    Heinen, S
    Brüggemann, A
    Rajan, S
    Derst, C
    Veh, RW
    Daut, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (11) : 7774 - 7779
  • [10] Smith CR, 2006, J INSECT SCI, V6, DOI 10.1673/2006_06_32.1
12