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Page 1
Short QT syndrome: pharmacological treatment.
Gaita F, Giustetto C, Bianchi F, Schimpf R, Haissaguerre M, Calò L, Brugada R, Antzelevitch C, Borggrefe M, Wolpert C. Gaita F, et al. Among authors: antzelevitch c. J Am Coll Cardiol. 2004 Apr 21;43(8):1494-9. doi: 10.1016/j.jacc.2004.02.034. J Am Coll Cardiol. 2004. PMID: 15093889 Free article. Clinical Trial.
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation.
Chen Q, Kirsch GE, Zhang D, 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. Chen Q, et al. Among authors: antzelevitch c. Nature. 1998 Mar 19;392(6673):293-6. doi: 10.1038/32675. Nature. 1998. PMID: 9521325
The Brugada syndrome: clinical, electrophysiologic and genetic aspects.
Gussak I, Antzelevitch C, Bjerregaard P, Towbin JA, Chaitman BR. Gussak I, et al. Among authors: antzelevitch c. J Am Coll Cardiol. 1999 Jan;33(1):5-15. doi: 10.1016/s0735-1097(98)00528-2. J Am Coll Cardiol. 1999. PMID: 9935001 Free article. Review.
The Brugada syndrome.
Naccarelli GV, Antzelevitch C, Wolbrette DL, Luck JC. Naccarelli GV, et al. Among authors: antzelevitch c. Curr Opin Cardiol. 2002 Jan;17(1):19-23. doi: 10.1097/00001573-200201000-00003. Curr Opin Cardiol. 2002. PMID: 11790929 Review.
Novel mutations in domain I of SCN5A cause Brugada syndrome.
Vatta M, Dumaine R, Antzelevitch C, Brugada R, Li H, Bowles NE, Nademanee K, Brugada J, Brugada P, Towbin JA. Vatta M, et al. Among authors: antzelevitch c. Mol Genet Metab. 2002 Apr;75(4):317-24. doi: 10.1016/S1096-7192(02)00006-9. Mol Genet Metab. 2002. PMID: 12051963
440 results