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Drs. E.A. Nannenberg

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

Inherited Cardiovascular Diseases

Key publications
  • Christiaans I, Nannenberg EA, Dooijes D, Jongbloed RJE, Michels M, Postema PG, Majoor-Krakauer D, van den Wijngaard A, Mannens MMAM, van Tintelen JP, van Langen IM, Wilde AAM, Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands. NETH HEART J 2011;19 (Suppl. S):32-37
  • Nannenberg EA, Michels M, Christiaans I, Majoor-Krakauer D, Hoedemaekers YM, van Tintelen JP, Lombardi MP, ten Cate FJ, Schinkel AFL, Tijssen JGP, van Langen IM, Wilde AAM, Sijbrands EJG, Mortality risk of untreated myosin-binding protein C-related hypertrophic cardiomyopathy: insight into the natural history. J AM COLL CARDIOL 2011;58 (23):2406-2414 [PubMed]
  • Christiaans I, Nannenberg EA, Dooijes D, Jongbloed RJE, Michels M, Postema PG, Majoor-Krakauer D, van den Wijngaard A, Mannens MMAM, van Tintelen JP, van Langen IM, Wilde AAM, Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands. NETH HEART J 2010;18 (5):248-254 [PubMed]
  • Postema PG, van den Berg M, van Tintelen JP, van den Heuvel F, Grundeken M, Hofman N, van der Roest WP, Nannenberg EA, Krapels IPC, Bezzina CR, 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. NETH HEART J 2009;17 (11):422-428 [PubMed]
All Publications