Brugada syndrome and sudden cardiac death in children

Lancet

Volumn 355, Issue 9206, 2000, Pages 808-809

  Priori, Silvia G ^a   Napolitano, Carlo ^a   Giordano, Umberto ^b   Collisani, Giuseppe ^b   Memmi, Mirella ^a  

^a IRCCS   (Italy)

^b Nephrology and Dialysis Unit   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

SODIUM CHANNEL;

ARTICLE; BRUGADA SYNDROME; CAUSE OF DEATH; CLINICAL ARTICLE; ELECTROCARDIOGRAM; FAMILY; FEMALE; GENE MUTATION; HUMAN; INFANT; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; SUDDEN DEATH;

EID: 0034603445     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(99)05277-0     Document Type: Article

References (5)

1. Brugada J, Brugada R, Brugada P. Right bundle-branch block and ST segment elevation in leads V1 through V3: a marker for sudden death in patients without demonstrable structural heart disease. Circulation 1998; 97: 457-60.
2. Grace AA. Brugada syndrome. Lancet 1999; 354: 445-46.
3. Chen Q, Kirsch GE, Zhang D, et al. Genetic basis and molecular mechanisms for idiopathic ventricular fibrillation. Nature 1998; 392: 393-96.
4. Priori SG, Barhanin J, Hauer RN, et al. Genetic and molecular basis of cardiac arrhythmias: impact on clinical management, Part I and II. Circulation 1999; 99: 518-28.
5. Priori SG, Napolitano C, Terreni L, et al. Incomplete penetrance and variable response to sodium channel blockade in Brugada syndrome. Eur Heart J 1999; 20: 465.