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E.A. Nannenberg

Position
Medical Specialist
Main activities
Patient care, Research
Specialisation
Clinical Geneticist
Focus of research

Inherited Cardiovascular Diseases

Key publications
  • Christiaans I., Nannenberg E. A., Dooijes D., Jongbloed R. J. E., Michels M., Postema P. G., Majoor-Krakauer D., van den Wijngaard A., Mannens M. M. A. M., van Tintelen J. P., van Langen I. M., Wilde A. A. M. Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands Netherlands heart journal 2011;19 (Suppl. S):32-37
  • Nannenberg Eline A., Michels Michelle, Christiaans Imke, Majoor-Krakauer Danielle, Hoedemaekers Yvonne M., van Tintelen J. Peter, Lombardi M. Paola, ten Cate Folkert J., Schinkel Arend F. L., Tijssen Jan G. P., van Langen Irene M., Wilde Arthur A. M., Sijbrands Eric J. G. Mortality risk of untreated myosin-binding protein C-related hypertrophic cardiomyopathy: insight into the natural history Journal of the American College of Cardiology 2011;58 (23):2406-2414 [PubMed]
  • Christiaans I., Nannenberg E. A., Dooijes D., Jongbloed R. J. E., Michels M., Postema P. G., Majoor-Krakauer D., van den Wijngaard A., Mannens M. M. A. M., van Tintelen J. P., van Langen I. M., Wilde A. A. M. Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands Netherlands heart journal 2010;18 (5):248-254 [PubMed]
  • Postema P. G., van den Berg M., van Tintelen J. P., van den Heuvel F., Grundeken M., Hofman N., van der Roest W. P., Nannenberg E. A., Krapels I. P. C., Bezzina C. R., Wilde A. Founder mutations in the Netherlands SCN5a 1795insD, the first described arrhythmia overlap syndrome and one of the largest and best characterised families worldwide Netherlands heart journal 2009;17 (11):422-428 [PubMed]
All Publications