Molecular aspects of sudden cardiac death

被引:3
作者
Escande, D [1 ]
机构
[1] CHU Hotel Dieu, Fac Med, INSERM, U533,Inst Thorax, F-44093 Nantes 1, France
来源
M S-MEDECINE SCIENCES | 2004年 / 20卷 / 6-7期
关键词
D O I
10.1051/medsci/2004206-7623
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
引用
收藏
页码:623 / 625
页数:3
相关论文
共 18 条
[1]
Bezzina C, 1999, CIRC RES, V85, P1206
[2]
GENE FOR PROGRESSIVE FAMILIAL HEART-BLOCK TYPE-I MAPS TO CHROMOSOME 19Q13 [J].
BRINK, PA ;
FERREIRA, A ;
MOOLMAN, JC ;
WEYMAR, HW ;
VANDERMERWE, PL ;
CORFIELD, VA .
CIRCULATION, 1995, 91 (06) :1633-1640
[3]
RIGHT BUNDLE-BRANCH BLOCK, PERSISTENT ST SEGMENT ELEVATION AND SUDDEN CARDIAC DEATH - A DISTINCT CLINICAL AND ELECTROCARDIOGRAPHIC SYNDROME - A MULTICENTER REPORT [J].
BRUGADA, P ;
BRUGADA, J .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1992, 20 (06) :1391-1396
[4]
KCNQ1 gain-of-function mutation in familial atrial fibrillation [J].
Chen, YH ;
Xu, SJ ;
Bendahhou, S ;
Wang, XL ;
Wang, Y ;
Xu, WY ;
Jin, HW ;
Sun, H ;
Su, XY ;
Zhuang, QN ;
Yang, YQ ;
Li, YB ;
Liu, Y ;
Xu, HJ ;
Li, XF ;
Ma, N ;
Mou, CP ;
Chen, Z ;
Barhanin, J ;
Huang, W .
SCIENCE, 2003, 299 (5604) :251-254
[5]
Genetics of arrhythmogenic right ventricular cardiomyopathy [J].
Danieli, GA ;
Rampazzo, A .
CURRENT OPINION IN CARDIOLOGY, 2002, 17 (03) :218-221
[6]
Dessertenne F, 1966, Arch Mal Coeur Vaiss, V59, P263
[7]
Out-of-hospital cardiac arrest in the 1990s: A population-based study in the Maastricht area on incidence, characteristics and survival [J].
deVreedeSwagemakers, JJM ;
Gorgels, APM ;
DuboisArbouw, WI ;
vanRee, JW ;
Daemen, MJAP ;
Houben, LGE ;
Wellens, HJJ .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1997, 30 (06) :1500-1505
[8]
Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation [J].
Grant, AO ;
Carboni, MP ;
Neplioueva, V ;
Starmer, CF ;
Memmi, M ;
Napolitano, C ;
Priori, S .
JOURNAL OF CLINICAL INVESTIGATION, 2002, 110 (08) :1201-1209
[9]
Decreased energetics in murine hearts bearing the R92Q mutation in cardiac troponin T [J].
Javadpour, MM ;
Tardiff, JC ;
Pinz, I ;
Ingwall, JS .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (05) :768-775
[10]
Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family [J].
Kyndt, F ;
Probst, V ;
Potet, F ;
Demolombe, S ;
Chevallier, JC ;
Baro, I ;
Moisan, JP ;
Boisseau, P ;
Schott, JJ ;
Escande, D ;
Le Marec, H .
CIRCULATION, 2001, 104 (25) :3081-3086