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Results: 7
Number of items: 7
  • Open Access
    van den Heuvel, L. M. (2021). Informing relatives at risk of inherited (cardiac) conditions: On our way towards the best approach. [Thesis, fully internal, Universiteit van Amsterdam].
  • Open Access
    Vermeer, A. M. C. (2019). Inherited cardiomyopathies and phenocopies. [Thesis, fully internal, Universiteit van Amsterdam].
  • Open Access
    Nannenberg, E. A. (2014). Mortality in inherited cardiac diseases: directing care in affected families. [Thesis, fully internal, Universiteit van Amsterdam].
  • Open Access
    van Rijsingen, I. A. W. (2013). Dilated cardiomyopathy: Translating genetic defects into clinical care. Towards personalized medicine in dilated cardiomyopathy. [Thesis, fully internal, Universiteit van Amsterdam].
  • Open Access
    Christiaans, I., Kenter, S. B., Brink, H. C., van Os, T. A. M., Baas, F., van den Munckhof, P., Kidd, A. M. J., & Hulsebos, T. J. M. (2011). Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomas. Journal of Medical Genetics, 48(2), 93-97. https://doi.org/10.1136/jmg.2010.082420
  • Open Access
    Christiaans, I., & Wilde, A. A. M. (2011). The patient with hypertrophic cardiomyopathy has a family. Heart, 97(3), 262-263. https://doi.org/10.1136/hrt.2010.216762
  • Open Access
    Christiaans, I. (2010). Hypertrophic cardiomyopathy: towards an optimal strategy. [Thesis, fully internal, Universiteit van Amsterdam].
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