Læknaneminn - 01.01.2017, Side 49

Læknaneminn - 01.01.2017, Side 49
Ri trý nt ef ni 4848 10. Cooper LT, Jr. Myocarditis. The New England journal of medicine 2009;360:1526­38. 11. Fung G, Luo H, Qiu Y, Yang D, McManus B. Myocarditis. Circulation research 2016;118:496­514. 12. Kindermann I, Barth C, Mahfoud F, Ukena C, Lenski M, Yilmaz A, et al. Update on myocarditis. Journal of the American College of Cardiology 2012;59:779­92. 13. Kandolin R, Lehtonen J, Salmenkivi K, Raisanen­Sokolowski A, Lommi J, Kupari M. Diagnosis, treatment, and outcome of giant­cell myocarditis in the era of combined immunosuppression. Circulation Heart failure 2013;6:15­22. 14. Houston BA, Stevens GR. Hypertrophic cardiomyopathy: a review. Clinical Medicine Insights Cardiology 2014;8:53­65. 15. Maron BJ. Hypertrophic cardiomyopathy: a systematic review. Jama 2002;287:1308­20. 16. O’Mahony C, Elliott P, McKenna W. Sudden cardiac death in hypertrophic cardiomyopathy. Circulation Arrhythmia and electrophysiology 2013;6:443­51. 17. Maron BJ, Casey SA, Poliac LC, Gohman TE, Almquist AK, Aeppli DM. Clinical course of hypertrophic cardiomyopathy in a regional United States cohort. Jama 1999;281:650­5. 18. Maron BJ, McKenna WJ, Danielson GK, Kappenberger LJ, Kuhn HJ, Seidman CE, et al. American College of Cardiology/European Society of Cardiology clinical expert consensus document on hypertrophic cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the European Society of Cardiology Committee for Practice Guidelines. Journal of the American College of Cardiology 2003;42:1687­713. 19. Gemayel C, Pelliccia A, Thompson PD. Arrhythmogenic right ventricular cardiomyopathy. Journal of the American College of Cardiology 2001;38:1773­81. 20. Corrado D, Wichter T, Link MS, Hauer R, Marchlinski F, Anastasakis A, et al. Treatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: an international task force consensus statement. European heart journal 2015;36:3227­37. 21. Corrado D, Link MS, Calkins H. Arrhythmogenic Right Ventricular Cardiomyopathy. The New England journal of medicine 2017;376:61­72. 22. Mizusawa Y, Wilde AA. Brugada syndrome. Circulation Arrhythmia and electrophysiology 2012;5:606­16. 23. Antzelevitch C, Brugada P, Borggrefe M, Brugada J, Brugada R, Corrado D, et al. Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association. Circulation 2005;111:659­70. 24. Brugada J, Brugada R, Antzelevitch C, Towbin J, Nademanee K, Brugada P. Long­ term follow­up of individuals with the electrocardiographic pattern of right bundle­ branch block and ST­segment elevation in precordial leads V1 to V3. Circulation 2002;105:73­8. 25. Goldenberg I, Moss AJ. Long QT syndrome. Journal of the American College of Cardiology 2008;51:2291­300. 26. Roden DM. Clinical practice. Long­QT syndrome. The New England journal of medicine 2008;358:169­76. 27. Schwartz PJ, Crotti L, Insolia R. Long­QT syndrome: from genetics to management. Circulation Arrhythmia and electrophysiology 2012;5:868­77. 28. Sauer AJ, Newton­Cheh C. Clinical and genetic determinants of torsade de pointes risk. Circulation 2012;125:1684­94. 29. Khan IA. Clinical and therapeutic aspects of congenital and acquired long QT syndrome. The American journal of medicine 2002;112:58­66. 30. Priori SG, Schwartz PJ, Napolitano C, Bloise R, Ronchetti E, Grillo M, et al. Risk stratification in the long­QT syndrome. The New England journal of medicine 2003;348:1866­74. 31. Morita H, Wu J, Zipes DP. The QT syndromes: long and short. Lancet 2008;372:750­63. Beinin eru lifandi vefur og þú styrkir þau með hverju skrefi sem þú tekur. Sparaðu ekki sporin, þannig standa þau lengur undir þér. Látum beinin ganga fyrir – fyrir framtíðina. beinvernd.is . Læknanemar Hafið þið áhuga á að starfa með öldruðum? Við höfum áhuga á að fá ykkur til starfa. Ýmsir vaktamöguleikar í boði.Sjálfstæð vinna á deildum. Mjög góð reynsla sem nýtist ykkur í áframhaldandi námi. Nánari upplýsingar um störfin, starfshlutfall, vaktir og launakjör veitir Helga J. Karlsdóttir starfsmannastjóri í síma 530-6165 og 560-1719 eða með tölvupósti á netfangið helga@grund.is Einnig er hægt að sækja beint um á heimasíðunum www.grund.is og www. morkhjukrunarheimili.is Trúnaður, traust og umhyggja eru höfð að leiðarljósi í samskiptum og lögð áhersla á góðan vinnuanda, sjálfstæð vinnubrögð og heimilislegt umhverfi.
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