A molecular link between the sudden infant death syndrome and the long-QT syndrome.

被引:252
作者
Schwartz, PJ
Priori, SG
Dumaine, R
Napolitano, C
Antzelevitch, C
Stramba-Badiale, M
Richard, TA
Berti, MR
Bloise, R
机构
[1] Policlin San Matteo, IRCCS, Dept Cardiol, I-27100 Pavia, Italy
[2] Univ Pavia, Dept Cardiol, I-27100 Pavia, Italy
[3] Fdn Salvatore Maugeri, IRCCS, Mol Crdiol & Eletrophysiol Lab, Pavia, Italy
[4] Masonic Med Res Lab, Dept Mol Biol, Utica, NY USA
[5] Univ Milan, IRCCS, Ctr Fisiol Clin & Ipertens, Milan, Italy
[6] Osped San Luca, Ist Auxol, IRCCS, Milan, Italy
[7] Osped S Chiara, Unite Operat Neonatol, Trento, Italy
关键词
D O I
10.1056/NEJM200007273430405
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:262 / 267
页数:6
相关论文
共 33 条
[1]   Genetic basis and molecular mechanism for idiopathic: ventricular fibrillation [J].
Chen, QY ;
Kirsch, GE ;
Zhang, DM ;
Brugada, R ;
Brugada, J ;
Brugada, P ;
Potenza, D ;
Moya, A ;
Borggrefe, M ;
Breithardt, G ;
Ortiz-Lopez, R ;
Wang, Z ;
Antzelevitch, C ;
O'Brien, RE ;
Schulze-Bahr, E ;
Keating, MT ;
Towbin, JA ;
Wang, Q .
NATURE, 1998, 392 (6673) :293-296
[2]   Multiple mechanisms of Na+ channel-linked long-QT syndrome [J].
Dumaine, R ;
Wang, Q ;
Keating, MT ;
Hartmann, HA ;
Schwartz, PJ ;
Brown, AM ;
Kirsch, GE .
CIRCULATION RESEARCH, 1996, 78 (05) :916-924
[3]   THE CONTRIBUTION OF CHANGES IN THE PREVALENCE OF PRONE SLEEPING POSITION TO THE DECLINE IN SUDDEN-INFANT-DEATH-SYNDROME IN TASMANIA [J].
DWYER, T ;
PONSONBY, AL ;
BLIZZARD, L ;
NEWMAN, NM ;
COCHRANE, JA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1995, 273 (10) :783-789
[4]   PRIMARY STRUCTURE AND FUNCTIONAL EXPRESSION OF THE HUMAN CARDIAC TETRODOTOXIN-INSENSITIVE VOLTAGE-DEPENDENT SODIUM-CHANNEL [J].
GELLENS, ME ;
GEORGE, AL ;
CHEN, LQ ;
CHAHINE, M ;
HORN, R ;
BARCHI, RL ;
KALLEN, RG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (02) :554-558
[5]   The long QT syndrome with impaired atrioventricular conduction: A malignant variant in infants [J].
Gorgels, APM ;
Al Fadley, F ;
Zaman, LQ ;
Kantoch, MJ ;
Al Halees, Z .
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 1998, 9 (11) :1225-1232
[6]   EFFECTS OF III-IV LINKER MUTATIONS ON HUMAN HEART NA+ CHANNEL INACTIVATION GATING [J].
HARTMANN, HA ;
TIEDEMAN, AA ;
CHEN, SF ;
BROWN, AM ;
KIRSCH, GE .
CIRCULATION RESEARCH, 1994, 75 (01) :114-122
[7]   SUDDEN UNEXPECTED DEATH 12 YEARS AFTER NEAR-MISS SUDDEN-INFANT-DEATH-SYNDROME IN INFANCY [J].
MARON, BJ ;
BARBOUR, DJ ;
MARRACCINI, JV ;
ROBERTS, WC .
AMERICAN JOURNAL OF CARDIOLOGY, 1986, 58 (11) :1104-1105
[8]  
MYERBURG RJ, 1999, MIAMI HERALD 0317
[9]   DETECTION OF POLYMORPHISMS OF HUMAN DNA BY GEL-ELECTROPHORESIS AS SINGLE-STRAND CONFORMATION POLYMORPHISMS [J].
ORITA, M ;
IWAHANA, H ;
KANAZAWA, H ;
HAYASHI, K ;
SEKIYA, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (08) :2766-2770
[10]   Genetic and molecular basis of cardiac arrhythmias: Impact on clinical management parts I and II [J].
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, AM .
CIRCULATION, 1999, 99 (04) :518-528