ing. L.G. Boven

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E-mail:
l.g.boven umcg.nl

Research

  1. 2020
  2. 2019
  3. 2018
  4. Hoorntje, E. T., van Spaendonck-Zwarts, K. Y., Te Rijdt, W. P., Boven, L., Vink, A., van der Smagt, J. J., ... van Tintelen, J. P. (2018). The first titin (c.59926 + 1G > A) founder mutation associated with dilated cardiomyopathy. European Journal of Heart Failure, 20(4), 803-806. https://doi.org/10.1002/ejhf.1030
  5. 2017
  6. van der Linde, I. H. M., Hiemstra, Y. L., Bokenkamp, R., van Mil, A. M., Breuning, M. H., Ruivenkamp, C., ... Barge-Schaapveld, D. Q. C. M. (2017). A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defects. Netherlands Heart Hournal, 25(12), 675-681. https://doi.org/10.1007/s12471-017-1037-5
  7. 2016
  8. Almomani, R., Verhagen, J. M. A., Herkert, J. C., Brosens, E., van Spaendonck-Zwarts, K. Y., Asimaki, A., ... van de Laar, I. M. B. H. (2016). Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy. Journal of the American College of Cardiology, 67(5), 515-525. https://doi.org/10.1016/j.jacc.2015.10.093
  9. 2015
  10. 2014
  11. 2013
  12. 2012
  13. 2011
  14. 2009
  15. 2007
  16. 2006
  17. van Tintelen, JP., Entius, MM., Bhuiyan, ZA., Jongbloed, R., Wiesfeld, ACP., Wilde, AAM., ... Hauer, RNW. (2006). Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circulation, 113(13), 1650-1658. https://doi.org/10.1161/CIRCULATIONAHA.105.609719
  18. 2005

ID: 62167009