prof. dr. O.F. (Oebo) Brouwer

Professor Neurology

E-mail:
o.f.brouwer umcg.nl

Research

  1. 2019
  2. Arts, W. F., Geerts, A. T., Brouwer, O. F., van Donselaar, C. A., Stroink, H., Peters, B. A. C., ... Camfield, C. (2019). Childhood epilepsy with a small number of seizures may be left untreated: an international prospective study. Epileptic disorders, 21(2), 141-153. https://doi.org/10.1684/epd.2019.1040
  3. GRIN2A Study Grp, Strehlow, V., Heyne, H. O., Vlaskamp, D. R. M., Marwick, K. F. M., Rudolf, G., ... Lemke, J. R. (2019). GRIN2A-related disorders: genotype and functional consequence predict phenotype. Brain, 142(1), 80-92. https://doi.org/10.1093/brain/awy304
  4. 2018
  5. van Diessen, E., Lamberink, H. J., Otte, W. M., Doornebal, N., Brouwer, O. F., Jansen, F. E., & Braun, K. P. J. (2018). A Prediction Model to Determine Childhood Epilepsy After 1 or More Paroxysmal Events. Pediatrics, 142(6), [20180931]. https://doi.org/10.1542/peds.2018-0931
  6. Goselink, R. J. M., van Kernebeek, C. R., Mul, K., Lemmers, R. J. L. F., van der Maarel, S. M., Brouwer, O. F., ... van Engelen, B. G. M. (2018). A 22-year follow-up reveals a variable disease severity in early-onset facioscapulohumeral dystrophy. European Journal of Paediatric Neurology, 22(5), 782-785. https://doi.org/10.1016/j.ejpn.2018.04.013
  7. Brouwer, O. (2018). Neurologie. In G. Derksen-Lubsen, H. A. Moll, A. M. Oudesluys-Murphy, A. J. Sprij, J. W. Bolt-Wieringa, A. P. M. van den Elzen, W. G. Leeuwenburgh-Pronk, F. G. Ropers, ... J. J. Verhoeven (Eds.), Compendium Kindergeneeskunde : Diagnostiek en behandeling (5 ed., pp. 597-616). Bohn, Stafleu, Van Loghum.
  8. 2017
  9. Goselink, R. J. M., Voermans, N. C., Okkersen, K., Brouwer, O. F., Padberg, G. W., Nikolic, A., ... Erasmus, C. E. (2017). Early onset facioscapulohumeral dystrophy - a systematic review using individual patient data. Neuromuscular disorders, 27(12), 1077-1083. https://doi.org/10.1016/j.nmd.2017.09.007
  10. de Lange, I. M., Rump, P., Neuteboom, R. F., Augustijn, P. B., Hodges, K., Kistemaker, A. I., ... Brilstra, E. H. (2017). Male patients affected by mosaic PCDH19 mutations: five new cases. Neurogenetics, 18(3), 147-153. https://doi.org/10.1007/s10048-017-0517-5
  11. 2016
  12. Wright, S., Geerts, A. T., Jol-van der Zijde, C. M., Jacobson, L., Lang, B., Waters, P., ... Vincent, A. (2016). Neuronal antibodies in pediatric epilepsy: Clinical features and long-term outcomes of a historical cohort not treated with immunotherapy. Epilepsia, 57(5), 823-831. https://doi.org/10.1111/epi.13356
  13. 2015
  14. Verbeek, N. E., van der Maas, N. A. T., Sonsma, A. C. M., Ippel, E., Bondt, P. E. V., Hagebeuk, E., ... Brilstra, E. H. (2015). Effect of vaccinations on seizure risk and disease course in Dravet syndrome. Neurology, 85(7), 596-603. https://doi.org/10.1212/WNL.0000000000001855
  15. 2014
  16. Fleurke-Rozema, J. H., Vogel, T. A., Voskamp, B. J., Pajkrt, E., van den Berg, P. P., Beekhuis, J. R., ... Snijders, R. J. M. (2014). Impact of introduction of mid-trimester scan on pregnancy outcome of open spina bifida in The Netherlands. Ultrasound in Obstetrics & Gynecology, 43(5), 553-556. https://doi.org/10.1002/uog.12546
  17. 2013
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