«1234›»Seite
4 articles with references, page 4 of 4

cme

Inherited Cardiac Arrhythmias: Diagnosis, Treatment, and Prevention

Dtsch Arztebl Int 2011; 108(37): 623-34; DOI: 10.3238/arztebl.2011.0623

Beckmann, B; Pfeufer, A; Kääb, S

1.Kauferstein S, Kiehne N, Neumann T, Pitschner H, Bratzke H: Cardiac gene defects can cause sudden cardiac death in young people. Dtsch Arztebl Int 2009; 106(4): 41–7. VOLLTEXT
2. Behr ER, Dalageorgou C, Christiansen M, et al.: Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families. Eur Heart J 2008; 29: 1670–80. CrossRef MEDLINE
3. Tan HL, Hofman N, van Langen IM, van der Wal AC, Wilde AA: Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives. Circulation 2005; 112: 207–13. CrossRef MEDLINE
4. Basso C, Burke M, Fornes P, et al.: Guidelines for autopsy investigation of sudden cardiac death. Virchows Arch 2008; 452: 11–8. CrossRef MEDLINE
5. Hofman N, Wilde AA, Tan HL. Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system? Eur Heart J 2007; 28: 1399. CrossRef MEDLINE
6. Ackerman MJ, Tester DJ, Porter CJ. Swimming, a gene-specific arrhythmogenic trigger for inherited long QT syndrome. Mayo Clin Proc 1999; 74: 1088–94. CrossRef MEDLINE
7. Moss AJ, Robinson JL, Gessman L, et al.: Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome. Am J Cardiol 1999; 84: 876–9. CrossRef MEDLINE
8. Schwartz PJ, Priori SG, Spazzolini C, et al.: Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias. Circulation 2001; 103: 89–95. MEDLINE
9. Vollmar C, Feddersen B, Beckmann BM, Kaab S, Noachtar S: Sei-zures on hearing the alarm clock. Lancet 2007; 370: 2172. CrossRef MEDLINE
10. Antzelevitch C, Brugada P, Borggrefe M, et al.: Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association. Circulation 2005; 111: 659–70. CrossRef MEDLINE
11. Peters S, Trummel M, Meyners W: Prevalence of right ventricular dysplasia-cardiomyopathy in a non-referral hospital. Int J Cardiol 2004; 97: 499–501. CrossRef MEDLINE
12. Schwartz PJ, Stramba-Badiale M, Crotti L, et al.: Prevalence of the congenital long-QT syndrome. Circulation 2009; 120: 1761–7. CrossRef MEDLINE
13. Beckmann BM, Wilde AA, Kaab S: Dual inheritance of sudden death from cardiovascular causes. N Engl J Med 2008; 358: 2077–8. CrossRef MEDLINE
14. Olson TM, Michels VV, Ballew JD, et al.: Sodium channel mutations and susceptibility to heart failure and atrial fibrillation. JAMA 2005; 293: 447–54. CrossRef MEDLINE
15. Smits JP, Koopmann TT, Wilders R, et al.: A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families. J Mol Cell Cardiol 2005; 38: 969–81. CrossRef MEDLINE
16. Meulenkamp TM, Tibben A, Mollema ED, et al.: Predictive genetic testing for cardiovascular diseases: impact on carrier children. Am J Med Genet A 2008;146A: 3136–46. CrossRef MEDLINE
17. Smets EM, Stam MM, Meulenkamp TM, et al.: Health-related quality of life of children with a positive carrier status for inherited cardiovascular diseases. Am J Med Genet A 2008; 146A: 700–7. CrossRef MEDLINE
18. Corrado D, Basso C, Rizzoli G, Schiavon M, Thiene G: Does sports activity enhance the risk of sudden death in adolescents and young adults? J Am Coll Cardiol 2003; 42: 1959–63. CrossRef MEDLINE
19. Schwartz PJ, Moss AJ, Vincent GM, Crampton RS: Diagnostic criteria for the long QT syndrome. An update. Circulation 1993; 88: 782–4. MEDLINE
20. Shimizu W: The long QT syndrome: therapeutic implications of a genetic diagnosis. Cardiovasc Res 2005; 67: 347–56. CrossRef MEDLINE
21. Zipes DP, Camm AJ, Borggrefe M, et al.: ACC/AHA/ESC 2006 Guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: a report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiology Committee for Practice
Guidelines (writing committee to develop Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death): developed in collaboration with the
European Heart Rhythm Association and the Heart Rhythm Society. Circulation 2006; 114: e385–484. CrossRef MEDLINE
22. Beckmann B, Holinski-Feder E, Walter M, et al.: Laminopathy presenting as familial atrial fibrillation. Int J Cardiology 2010; 145: 394–6. CrossRef MEDLINE
23. Meune C, Van Berlo JH, Anselme F, Bonne G, Pinto YM, Duboc D: Primary prevention of sudden death in patients with lamin A/C gene mutations. N Engl J Med 2006; 354: 209–10. CrossRef MEDLINE
24. Wilde AA, Bhuiyan ZA, Crotti L, et al.: Left cardiac sympathetic
denervation for catecholaminergic polymorphic ventricular
tachycardia. N Engl J Med 2008; 358: 2024–9. CrossRef MEDLINE
25. Tester D, Ackerman M: Genetic testing for potentially lethal, highly treatable inherited cardiomyopathies/channelopathies in clinical practice. Circulation 2011;123:1021–37. CrossRef MEDLINE