Læknaneminn - 01.01.2017, Blaðsíða 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.