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Journal Abstract Search
1529 related items for PubMed ID: 21135804
1. Arrhythmogenic hereditary syndromes: Brugada Syndrome, long QT syndrome, short QT syndrome and CPVT. Schimpf R, Veltmann C, Wolpert C, Borggrefe M. Minerva Cardioangiol; 2010 Dec; 58(6):623-36. PubMed ID: 21135804 [Abstract] [Full Text] [Related]
2. The genetic and clinical features of cardiac channelopathies. Roberts JD, Gollob MH. Future Cardiol; 2010 Jul; 6(4):491-506. PubMed ID: 20608822 [Abstract] [Full Text] [Related]
3. Mechanisms and clinical management of inherited channelopathies: long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome. Kaufman ES. Heart Rhythm; 2009 Aug; 6(8 Suppl):S51-5. PubMed ID: 19631908 [Abstract] [Full Text] [Related]
4. Channelopathies: Brugada syndrome, long QT syndrome, short QT syndrome, and CPVT. Schimpf R, Veltmann C, Wolpert C, Borggrefe M. Herz; 2009 Jun; 34(4):281-8. PubMed ID: 19575158 [Abstract] [Full Text] [Related]
9. Sudden cardiac death in Long QT syndrome (LQTS), Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia (CPVT). Singh M, Morin DP, Link MS. Prog Cardiovasc Dis; 2019 Jun; 62(3):227-234. PubMed ID: 31078562 [Abstract] [Full Text] [Related]
10. [Postmortem genetic testing in sudden cardiac death due to ion channelopathies]. Guan DW, Zhao R. Fa Yi Xue Za Zhi; 2010 Apr; 26(2):120-7. PubMed ID: 20653139 [Abstract] [Full Text] [Related]
15. [Prevention of sudden death in congenital long-QT syndrome]. Oliveira M, Antunes E, da Silva MN. Rev Port Cardiol; 1999 Jun; 18(6):627-33. PubMed ID: 10422460 [Abstract] [Full Text] [Related]
16. How to perform and interpret provocative testing for the diagnosis of Brugada syndrome, long-QT syndrome, and catecholaminergic polymorphic ventricular tachycardia. Obeyesekere MN, Klein GJ, Modi S, Leong-Sit P, Gula LJ, Yee R, Skanes AC, Krahn AD. Circ Arrhythm Electrophysiol; 2011 Dec; 4(6):958-64. PubMed ID: 22203660 [No Abstract] [Full Text] [Related]