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383 related items for PubMed ID: 19808437
1. Cost-effectiveness of genotyping in inherited arrhythmia syndromes: are we getting value for the money? Wilde AA, Pinto YM. Circ Arrhythm Electrophysiol; 2009 Feb; 2(1):1-3. PubMed ID: 19808437 [No Abstract] [Full Text] [Related]
2. Yield of genetic screening in inherited cardiac channelopathies: how to prioritize access to genetic testing. Bai R, Napolitano C, Bloise R, Monteforte N, Priori SG. Circ Arrhythm Electrophysiol; 2009 Feb; 2(1):6-15. PubMed ID: 19808439 [Abstract] [Full Text] [Related]
3. [Hereditary risk of sudden cardiac death--genetic investigation of the family]. Lundin C, Platonov P, Kristoffersson U. Lakartidningen; 2009 Feb; 106(15-16):1089-93. PubMed ID: 19492675 [No Abstract] [Full Text] [Related]
7. Importance of Dedicated Units for the Management of Patients With Inherited Arrhythmia Syndromes. Conte G, Wilde A, Behr ER, Scherr D, Lenarczyk R, Gandjbachkh E, Crotti L, Brugada-Sarquella G, Potpara T. Circ Genom Precis Med; 2021 Apr; 14(2):e003313. PubMed ID: 33797288 [No Abstract] [Full Text] [Related]
8. A clinical approach to inherited arrhythmias. Cerrone M, Cummings S, Alansari T, Priori SG. Circ Cardiovasc Genet; 2012 Oct 01; 5(5):581-90. PubMed ID: 23074337 [No Abstract] [Full Text] [Related]
10. Sudden death: managing the family, the role of genetics. Brugada R. Heart; 2011 Apr 16; 97(8):676-81. PubMed ID: 21421602 [No Abstract] [Full Text] [Related]
12. [Postmortem genetic testing in sudden cardiac death due to ion channelopathies]. Guan DW, Zhao R. Fa Yi Xue Za Zhi; 2010 Apr 16; 26(2):120-7. PubMed ID: 20653139 [Abstract] [Full Text] [Related]
13. [Sudden cardiac death in athletes with an apparently normal heart: the channelopathies]. Giustetto C, Gaita F. G Ital Cardiol (Rome); 2008 Oct 16; 9(10 Suppl 1):78S-82S. PubMed ID: 19195312 [Abstract] [Full Text] [Related]
14. The long QT syndrome and catecholaminergic polymorphic ventricular tachycardia. Monteforte N, Priori SG. Pacing Clin Electrophysiol; 2009 Jul 16; 32 Suppl 2():S52-7. PubMed ID: 19602163 [Abstract] [Full Text] [Related]
15. [Genetic aspects of the etiology of arrhythmia]. Thierfelder L. Z Kardiol; 2000 Jul 16; 89 Suppl 3():1-5. PubMed ID: 10810779 [Abstract] [Full Text] [Related]
16. Screening for, and management of, possible arrhythmogenic syndromes (channelopathies/ion channel diseases). Svendsen JH, Geelen P, EHRA Scientific Initiative Commitee. Europace; 2010 May 16; 12(5):741-2. PubMed ID: 20421225 [Abstract] [Full Text] [Related]
17. Brugada syndrome with marked conduction disease: dual implications of a SCN5A mutation. Vorobiof G, Kroening D, Hall B, Brugada R, Huang D. Pacing Clin Electrophysiol; 2008 May 16; 31(5):630-4. PubMed ID: 18439184 [Abstract] [Full Text] [Related]
18. Cardiac evaluation of pediatric relatives in sudden arrhythmic death syndrome: a 2-center experience. Wong LC, Roses-Noguer F, Till JA, Behr ER. Circ Arrhythm Electrophysiol; 2014 Oct 16; 7(5):800-6. PubMed ID: 25194972 [Abstract] [Full Text] [Related]
19. 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 16; 4(6):958-64. PubMed ID: 22203660 [No Abstract] [Full Text] [Related]
20. Repolarization syndromes. Bhatia A, Sra J, Akhtar M. Curr Probl Cardiol; 2012 Aug 16; 37(8):317-62. PubMed ID: 22749026 [Abstract] [Full Text] [Related] Page: [Next] [New Search]