Journal of Neurology, 0340-5354

Journal

  1. 2020
  2. 2019
  3. 2018
  4. de Mol, C. L., Wong, Y. Y. M., van Pelt, E. D., Ketelslegers, I. A., Bakker, D. P., Boon, M., ... Neuteboom, R. F. (2018). Incidence and outcome of acquired demyelinating syndromes in Dutch children: update of a nationwide and prospective study. Journal of Neurology, 265(6), 1310-1319. https://doi.org/10.1007/s00415-018-8835-6
  5. 2017
  6. Visser, A. E., Pazoki, R., Pulit, S. L., van Rheenen, W., Raaphorst, J., van der Kooi, A. J., ... van den Berg, L. H. (2017). No association between gluten sensitivity and amyotrophic lateral sclerosis. Journal of Neurology, 264(4), 694-700. https://doi.org/10.1007/s00415-017-8400-8
  7. 2016
  8. Govaarts, R., Beeldman, E., Kampelmacher, M. J., van Tol, M-J., van den Berg, L. H., van der Kooi, A. J., ... Raaphorst, J. (2016). The frontotemporal syndrome of ALS is associated with poor survival. Journal of Neurology, 263(12), 2476-2483. https://doi.org/10.1007/s00415-016-8290-1
  9. Lehn, A., Gelauff, J., Hoeritzauer, I., Ludwig, L., McWhirter, L., Williams, S., ... Stone, J. (2016). Functional neurological disorders: Mechanisms and treatment. Journal of Neurology, 263(3), 611-620. https://doi.org/10.1007/s00415-015-7893-2
  10. 2015
  11. Nibbeling, E., Schaake, S., Tijssen, M. A., Weissbach, A., Groen, J. L., Altenmueller, E., ... Lohmann, K. (2015). Accumulation of rare variants in the arylsulfatase G (ARSG) gene in task-specific dystonia. Journal of Neurology, 262(5), 1340-1343. https://doi.org/10.1007/s00415-015-7718-3
  12. Aerts, M. B., Esselink, R. A. J., Abdo, W. F., Meijer, F. J. A., Drost, G., Norgren, N., ... Verbeek, M. M. (2015). Ancillary investigations to diagnose parkinsonism: a prospective clinical study. Journal of Neurology, 262(2), 346-356. https://doi.org/10.1007/s00415-014-7568-4
  13. 2014
  14. Contarino, M. F., Van den Munckhof, P., Tijssen, M. A. J., de Bie, R. M. A., Bosch, D. A., Schuurman, P. R., & Speelman, J. D. (2014). Selective peripheral denervation: comparison with pallidal stimulation and literature review. Journal of Neurology, 261(2), 300-308. https://doi.org/10.1007/s00415-013-7188-4
  15. 2013
  16. de Bot, S. T., Vermeer, S., Buijsman, W., Heister, A., Voorendt, M., Verrips, A., ... Kamsteeg, E-J. (2013). Pure adult-onset Spastic Paraplegia caused by a novel mutation in the KIAA0196 (SPG8) gene. Journal of Neurology, 260(7), 1765-1769. https://doi.org/10.1007/s00415-013-6870-x
  17. de Bot, S. T., Veldink, J. H., Vermeer, S., Mensenkamp, A. R., Brugman, F., Scheffer, H., ... van de Warrenburg, B. P. (2013). ATL1 and REEP1 mutations in hereditary and sporadic upper motor neuron syndromes. Journal of Neurology, 260(3), 869-875. https://doi.org/10.1007/s00415-012-6723-z
  18. 2012
  19. Ketelslegers, I. A., Catsman-Berrevoets, C. E., Neuteboom, R. F., Boon, M., van Dijk, K. G. J., Eikelenboom, M. J., ... Hintzen, R. Q. (2012). Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide study. Journal of Neurology, 259(9), 1929-1935. https://doi.org/10.1007/s00415-012-6441-6
  20. 2011
  21. Visser, N. A., Braun, K. P. J., Leijten, F. S. S., van Nieuwenhuizen, O., Wokke, J. H. J., & van den Bergh, W. M. (2011). Magnesium treatment for patients with refractory status epilepticus due to POLG1-mutations. Journal of Neurology, 258(2), 218-22. https://doi.org/10.1007/s00415-010-5721-2
  22. 2010
  23. van der Salm, S. M. A., Koelman, J. H. T. M., Henneke, S., van Rootselaar, A-F., & Tijssen, M. A. J. (2010). Axial jerks: A clinical spectrum ranging from propriospinal to psychogenic myoclonus. Journal of Neurology, 257(8), 1349-1355. https://doi.org/10.1007/s00415-010-5531-6
  24. 2009
  25. Maliepaard, M., Hekster, Y. A., Kappelle, A., van Puijenbroek, E. P., Elferink, A. J., Welink, J., ... Lekkerkerker, F. J. F. (2009). Requirements for generic anti-epileptic medicines: a regulatory perspective. Journal of Neurology, 256(12), 1966-1971. https://doi.org/10.1007/s00415-009-5231-2
  26. Faber, C. G., Molenaar, P. C., Vles, J. S. H., Bonifati, D. M., Verschuuren, J. J. G. M., van Doorn, P. A., ... De Baets, M. (2009). AChR deficiency due to epsilon-subunit mutations: two common mutations in the Netherlands. Journal of Neurology, 256(10), 1719-1723. https://doi.org/10.1007/s00415-009-5190-7
  27. Trip, J., de Vries, J., Drost, G., Ginjaar, H. B., van Engelen, B. G. M., & Faber, C. G. (2009). Health status in non-dystrophic myotonias: close relation with pain and fatigue. Journal of Neurology, 256(6), 939-947. https://doi.org/10.1007/s00415-009-5049-y
  28. Zschiedrich, K., Koenig, I. R., Bruggemann, N., Kock, N., Kasten, M., Leenders, K. L., ... Lohmann, K. (2009). MDR1 variants and risk of Parkinson disease. Journal of Neurology, 256(1), 115-120. https://doi.org/10.1007/s00415-009-0089-x
  29. 2008
  30. 2007
  31. Smits, B. W., Hol, F. A., van den Heuvel, L. P., Drost, G., Rodenburg, R. J. T., ter Laak, H. J., & van Engelen, B. G. M. (2007). Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNA(Ile). Journal of Neurology, 254(11), 1614-1615. https://doi.org/10.1007/s00415-007-0608-6
  32. Vermeer, S., Kremer, H. P. H., Leijten, Q. H., Scheffer, H., Matthijs, G., Wevers, R. A., ... Lefeber, D. J. (2007). Cerebellar ataxia and congenital disorder of glycosylation Ia (CDG-Ia) with normal routine CDG screening. Journal of Neurology, 254(10), 1356-1358. https://doi.org/10.1007/s00415-007-0546-3
  33. 2006
  34. Voermans, NC., Drost, G., van Kampen, A., Gabreels-Festen, AA., Lammens, M., Hamel, BC., ... van Engelen, BG. (2006). Recurrent neuropathy associated with Ehlers-Danlos syndrome. Journal of Neurology, 253(5), 670-671. https://doi.org/10.1007/s00415-005-0056-0
  35. 2005
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