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Brugada syndrome: two decades of progress.
Veerakul G, Nademanee K. Veerakul G, et al. Among authors: nademanee k. Circ J. 2012;76(12):2713-22. doi: 10.1253/circj.cj-12-1352. Epub 2012 Nov 14. Circ J. 2012. PMID: 23149437 Free article. Review.
Arrhythmogenic marker for the sudden unexplained death syndrome in Thai men.
Nademanee K, Veerakul G, Nimmannit S, Chaowakul V, Bhuripanyo K, Likittanasombat K, Tunsanga K, Kuasirikul S, Malasit P, Tansupasawadikul S, Tatsanavivat P. Nademanee K, et al. Circulation. 1997 Oct 21;96(8):2595-600. doi: 10.1161/01.cir.96.8.2595. Circulation. 1997. PMID: 9355899
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: nademanee k. Mol Genet Metab. 2002 Apr;75(4):317-24. doi: 10.1016/S1096-7192(02)00006-9. Mol Genet Metab. 2002. PMID: 12051963
Proposed diagnostic criteria for the Brugada syndrome: consensus report.
Wilde AA, Antzelevitch C, Borggrefe M, Brugada J, Brugada R, Brugada P, Corrado D, Hauer RN, Kass RS, Nademanee K, Priori SG, Towbin JA; Study Group on the Molecular Basis of Arrhythmias of the European Society of Cardiology. Wilde AA, et al. Among authors: nademanee k. Circulation. 2002 Nov 5;106(19):2514-9. doi: 10.1161/01.cir.0000034169.45752.4a. Circulation. 2002. PMID: 12417552 Review. No abstract available.
170 results