Genetic and molecular basis of cardiac arrhythmias - Impact on clinical management

被引：102
作者：
Priori, SG
Barhanin, J
Hauer, RNW
Haverkamp, W
Jongsma, HJ
Kleber, AG
McKenna, WJ
Roden, DM
Rudy, Y
Schwartz, K
Schwartz, PJ
Towbin, JA
Wilde, A
机构：
[1] IRCCS, Fdn S Maugeri, Mol Cardiol & Electrophysiol Lab, I-27100 Pavia, Italy
[2] CNRS, Inst Pharmacol Mol & Cellulaire, Lab Genet Neurotransmiss, F-06560 Valbonne, France
[3] Univ Utrecht Hosp, Heart Lung Inst, Utrecht, Netherlands
[4] Univ Munster, Med Klin & Poliklin, D-4400 Munster, Germany
[5] Univ Utrecht, Physiol Lab, Utrecht, Netherlands
[6] Univ Bern, Dept Physiol, CH-3012 Bern, Switzerland
[7] Univ London St Georges Hosp, Sch Med, Dept Cardiol Sci, London SW17 0RE, England
[8] Vanderbilt Univ, Med Ctr, Div Med & Pharmacol, Nashville, TN USA
[9] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44106 USA
[10] Grp Hosp Pitie Salpetriere, INSERM, U153, F-75634 Paris, France
[11] IRCCS, Policlin San Matteo, Dipartimento Cardiol, Pavia, Italy
[12] Texas Childrens Hosp, Baylor Coll Med, Houston, TX 77030 USA
[13] Univ Amsterdam, Acad Med Ctr, Dept Clin & Expt Cardiol, NL-1105 AZ Amsterdam, Netherlands
来源：
EUROPEAN HEART JOURNAL | 1999年 / 20卷 / 03期
关键词：
sudden cardiac death; genetics; arrhythmia; molecular diagnosis; basic electrophysiology;
D O I：
10.1053/euhj.1998.1220
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：174 / 195
页数：22
相关论文
共 160 条
[1]   INDUCTION OF RHYTHM ABNORMALITIES IN THE FETAL-RAT HEART - A TENTATIVE MECHANISM FOR THE EMBRYOTOXIC EFFECT OF THE CLASS-III ANTIARRHYTHMIC AGENT ALMOKALANT [J].
ABRAHAMSSON, C ;
PALMER, M ;
LJUNG, B ;
DUKER, G ;
BAARNHIELM, C ;
CARLSSON, L ;
DANIELSSON, B .
CARDIOVASCULAR RESEARCH, 1994, 28 (03) :337-344
[2]   PROTEINS THAT INTERACT WITH THE PORE-FORMING SUBUNITS OF VOLTAGE-GATED ION CHANNELS [J].
ADELMAN, JP .
CURRENT OPINION IN NEUROBIOLOGY, 1995, 5 (03) :286-295
[3]   HETEROGENEITY WITHIN THE VENTRICULAR WALL - ELECTROPHYSIOLOGY AND PHARMACOLOGY OF EPICARDIAL, ENDOCARDIAL, AND M-CELLS [J].
ANTZELEVITCH, C ;
SICOURI, S ;
LITOVSKY, SH ;
LUKAS, A ;
KRISHNAN, SC ;
DIDIEGO, JM ;
GINTANT, GA ;
LIU, DW .
CIRCULATION RESEARCH, 1991, 69 (06) :1427-1449
[4]   GAP JUNCTIONAL CHANNELS IN ADULT MAMMALIAN SINUS NODAL CELLS - IMMUNOLOCALIZATION AND ELECTROPHYSIOLOGY [J].
ANUMONWO, JMB ;
WANG, HZ ;
TRABKAJANIK, E ;
DUNHAM, B ;
VEENSTRA, RD ;
DELMAR, M ;
JALIFE, J .
CIRCULATION RESEARCH, 1992, 71 (02) :229-239
[5]   K(v)LQT1 and IsK (minK) proteins associate to form the I-Ks cardiac potassium current [J].
Barhanin, J ;
Lesage, F ;
Guillemare, E ;
Fink, M ;
Lazdunski, M ;
Romey, G .
NATURE, 1996, 384 (6604) :78-80
[6]   Arrhythmogenic right ventricular cardiomyopathy - Dysplasia, dystrophy, or myocarditis? [J].
Basso, C ;
Thiene, G ;
Corrado, D ;
Angelini, A ;
Nava, A ;
Valente, M .
CIRCULATION, 1996, 94 (05) :983-991
[7]   MOLECULAR MECHANISM FOR AN INHERITED CARDIAC-ARRHYTHMIA [J].
BENNETT, PB ;
YAZAWA, K ;
MAKITA, N ;
GEORGE, AL .
NATURE, 1995, 376 (6542) :683-685
[8]   A novel X-linked gene, G4.5. is responsible for Barth syndrome [J].
Bione, S ;
DAdamo, P ;
Maestrini, E ;
Gedeon, AK ;
Bolhuis, PA ;
Toniolo, D .
NATURE GENETICS, 1996, 12 (04) :385-389
[9]   CARDIAC MYOSIN BINDING PROTEIN-C GENE SPLICE ACCEPTOR SITE MUTATION IS ASSOCIATED WITH FAMILIAL HYPERTROPHIC CARDIOMYOPATHY [J].
BONNE, G ;
CARRIER, L ;
BERCOVICI, J ;
CRUAUD, C ;
RICHARD, P ;
HAINQUE, B ;
GAUTEL, M ;
LABEIT, S ;
JAMES, M ;
BECKMANN, J ;
WEISSENBACH, J ;
VOSBERG, HP ;
FISZMAN, M ;
KOMAJDA, M ;
SCHWARTZ, K .
NATURE GENETICS, 1995, 11 (04) :438-440
[10]   Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 1Oq21-23 [J].
Bowles, KR ;
Gajarski, R ;
Porter, P ;
Goytia, V ;
Bachinski, L ;
Roberts, R ;
Pignatelli, R ;
Towbin, JA .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (06) :1355-1360
12345678910