Ausgabe 12/2009
Inhalt (10 Artikel)
Invasive treatment of patients with cardiomyopathy: CRT-ICD better than ICD alone
E. E. van der Wall
Hypertrophic cardiomyopathy family with double-heterozygous mutations; does disease severity suggest doubleheterozygosity?
I. A. W. van Rijsingen, J. F. Hermans-van Ast, Y. H. J. M. Arens, S. M. Schalla, C. E. M de Die-Smulders, A. van den Wijngaard, Y. M. Pinto
Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: Dutch cardiologists and the care of mutation carriers
J. T. Vehmeijer, I. Christiaans, I. M. van Langen, E. Birnie, G. J. Bonsel, E. M. A. Smets, A. A. M. Wilde
Reduced regional myocardial perfusion reserve is associated with impaired contractile performance in idiopathic dilated cardiomyopathy
R. A. Tio, R. H. J. A. Slart, R. A. de Boer, P. A. van der Vleuten, R. M. de Jong, L. M. van Wijk, T. Willems, D. D. Lubbers, A. A. Voors, D. J. van Veldhuisen
Left ventricular aneurysm in patients with idiopathic dilated cardiomyopathy: clinical analysis of six cases
Shudong Xia, Bifeng Wu, Xiaolian Zhang, Xiaosheng Hu
The importance of cardiac MRI as a diagnostic tool in viral myocarditis-induced cardiomyopathy
M. A. G. M. Olimulder, J. van Es, M. A. Galjee
A Dutch case of a takotsubo cardiomyopathy after pacemaker implantation
R. F. Kohnen, L. H. B. Baur
Leonardo da Vinci on atherosclerosis and the function of the sinuses of Valsalva
B. Boon