Cardiac dyssynchrony and response to cardiac resynchronisation therapy in heart failure: can genetic predisposition play a role?

por Lahrouchi, N., Bezzina, C.R.
Publicado 2015

Genomic approaches for the elucidation of genes and gene networks underlying cardiovascular traits

por Adriaens, M. E., Bezzina, C. R.
Publicado 2018

Genetic predisposition for sudden cardiac death in myocardial ischaemia: the Arrhythmia Genetics in the NEtherlandS study

por Marsman, R. F. J., Wilde, A. A. M., Bezzina, C. R.
Publicado 2011

Clinical and molecular findings in a Moroccan family with Jervell and Lange-Nielsen syndrome: a case report

por Adadi, N., Lahrouchi, N., Bouhouch, R., Fellat, I., Amri, R., Alders, M., Sefiani, A., Bezzina, C., Ratbi, I.
Publicado 2017

Founder mutations in the Netherlands: familial idiopathic ventricular fibrillation and DPP6

por Postema, P. G., Christiaans, I., Hofman, N., Alders, M., Koopmann, T. T., Bezzina, C. R., Loh, P., Zeppenfeld, K., Volders, P. G. A., Wilde, A. A. M.
Publicado 2011

The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardium

por Remme, C. A., Verkerk, A. O., Hoogaars, W. M. H., Aanhaanen, W. T. J., Scicluna, B. P., Annink, C., van den Hoff, M. J. B., Wilde, A. A. M., van Veen, T. A. B., Veldkamp, M. W., de Bakker, J. M. T., Christoffels, V. M., Bezzina, C. R.
Publicado 2009