View graph of relations
  1. 2019
  2. Published
  3. Published
  4. Published
    Snoeijen-Schouwenaars, F. M., van Ool, J. S., Verhoeven, J. S., van Mierlo, P., Braakman, H. M. H., Smeets, E. E., ... Willemsen, M. H. (2019). Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability. Epilepsia, 60(1), 155-164. https://doi.org/10.1111/epi.14618
  5. 2018
  6. Published
  7. Published
  8. Published
  9. Published
  10. Published
  11. Published
  12. Published
    DDD Study, Reijnders, M. R. F., Janowski, R., Alvi, M., Self, J. E., van Essen, T. J., ... Niessing, D. (2018). PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature. Journal of Medical Genetics, 55(2), 104-113. https://doi.org/10.1136/jmedgenet-2017-104946
  13. Published
  14. Published
  15. Published
  16. Published
  17. Published
  18. 2017
  19. Published
  20. Published
  21. Published
  22. Published
  23. Published
  24. Published
  25. Published
    Rouhl, R., Schelhaas, H. J., & Willemsen, M. (2017). Epilepsie en genetica. Neuron, 22, 22-27.
  26. 2016
  27. Published
  28. Published
  29. Published
  30. Published
    Rouhl, R., Wagner, G. L., & Vonck, K. (2016). Handboek diepe hersenstimulatie bij neurologische en psychiatrische aandoeningen. In Y. Temel, A. F. G. Leenthens, & R. M. A. de Bie (Eds.), Handboek diepe hersenstimulatie bij neurologische en psychiatrische aandoeningen (pp. 119-124). Houten: Bohn Stafleu van Loghum.
  31. 2015
  32. Published
  33. Published
  34. Published
  35. Published
  36. 2013
  37. Published
  38. Published
  39. Published
  40. Published
  41. 2012
  42. Published
  43. Published
  44. Published
  45. Published
  46. 2011
  47. Published
  48. Published
  49. 2010
  50. Published
  51. Published
  52. Published