prof. dr. J.B.M. (Jan) Kuks

Professor

prof. dr. J.B.M. (Jan) Kuks
E-mail:
j.b.m.kuks umcg.nl

Research

  1. 2020
  2. Lipka, A. F., Boldingh, M. I., van Zwet, E. W., Schreurs, M. W. J., Kuks, J. B. M., Tallaksen, C. M., Titulaer, M. J., & Verschuuren, J. J. G. M. (2020). Long-term follow-up, quality of life, and survival of patients with Lambert-Eaton myasthenic syndrome. Neurology, 94(5), E511-E520. https://doi.org/10.1212/WNL.0000000000008747
  3. 2019
  4. ten Dam, L., Frankhuizen, W. S., Linssen, W. H. J. P., Straathof, C. S., Niks, E. H., Faber, K., Fock, A., Kuks, J. B., Brusse, E., de Coo, R., Voermans, N., Verrips, A., Hoogendijk, J. E., van Der Pol, L., Westra, D., de Visser, M., van der Kooi, A. J., & Ginjaar, I. (2019). Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients. Clinical Genetics, 96(2), 126-133. https://doi.org/10.1111/cge.13544
  5. 2018
  6. Kuks, J. B. M., & Snoek, J. (Eds.) (2018). Textbook of Clinical Neurology. (1 ed.) Bohn, Stafleu, Van Loghum.
  7. 2017
  8. 2016
  9. Deenen, J. C. W., van Doorn, P. A., Faber, C. G., van der Kooi, A. J., Kuks, J. B. M., Notermans, N. C., Visser, L. H., Horlings, C. G. C., Verschuuren, J. J. G. M., Verbeek, A. L. M., & van Engelen, B. G. M. (2016). The epidemiology of neuromuscular disorders: Age at onset and gender in the Netherlands. Neuromuscular disorders, 26(7), 447-452. https://doi.org/10.1016/j.nmd.2016.04.011
  10. Huijbers, M. G., Niks, E. H., Klooster, R., de Visser, M., Kuks, J. B., Veldink, J. H., Klarenbeek, P., Van Damme, P., de Baets, M. H., van der Maarel, S. M., van den Berg, L. H., & Verschuuren, J. J. (2016). Myasthenia gravis with muscle specific kinase antibodies mimicking amyotrophic lateral sclerosis. Neuromuscular disorders, 26(6), 350-353. https://doi.org/10.1016/j.nmd.2016.04.004
  11. Huijbers, M. G., Vink, A-F. D., Niks, E. H., Westhuis, R. H., van Zwet, E. W., de Meel, R. H., Rojas-Garcia, R., Diaz-Manera, J., Kuks, J. B., Klooster, R., Straasheijm, K., Evoli, A., Illa, I., van der Maarel, S. M., & Verschuuren, J. J. (2016). Longitudinal epitope mapping in MuSK myasthenia gravis: implications for disease severity. Journal of Neuroimmunology, 291, 82-88. https://doi.org/10.1016/j.jneuroim.2015.12.016
  12. Groen, R., Kuks, J., & Snoek, J. (2016). Neurologische pijnsyndromen. In J. B. M. Kuks, & J. W. Snoek (Eds.), Leerboek klinische neurologie (18th ed., pp. 169-179). Bohn, Stafleu, Van Loghum. https://www.bsl.nl/shop/leerboek-klinische-neurologie-9789036813334.html
  13. Groen, R., Kuks, J., & Snoek, J. (2016). Ziekten van het ruggenmerg. In J. B. M. Kuks, & J. W. Snoek (Eds.), Leerboek klinische neurologie (18th ed., pp. 181-196). Bohn, Stafleu, Van Loghum. https://doi.org/10.1007/9789036813341_15
  14. 2015
  15. Keijzers, M., de Baets, M., Hochstenbag, M., Abdul-Hamid, M., zur Hausen, A., van der Linden, M., Kuks, J., Verschuuren, J., Kessels, F., Dingemans, A-M. C., & Maessen, J. (2015). Robotic thymectomy in patients with myasthenia gravis: neurological and surgical outcomes. EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 48(1), 40-45. https://doi.org/10.1093/ejcts/ezu352
  16. 2014
  17. 2013
  18. 2012
  19. van der Beek, N. A. M. E., de Vries, J. M., Hagemans, M. L. C., Hop, W. C. J., Kroos, M. A., Wokke, J. H. J., de Visser, M., van Engelen, B. G. M., Kuks, J. B. M., van der Kooi, A. J., Notermans, N. C., Faber, K. G., Verschuuren, J. J. G. M., Reuser, A. J. J., van der Ploeg, A. T., & van Doorn, P. A. (2012). Clinical features and predictors for disease natural progression in adults with Pompe disease: a nationwide prospective observational study. Orphanet journal of rare diseases, 7, [88]. https://doi.org/10.1186/1750-1172-7-88
  20. de Vries, J. M., van der Beek, N. A. M. E., Hop, W. C. J., Karstens, F. P. J., Wokke, J. H., de Visser, M., van Engelen, B. G. M., Kuks, J. B. M., van der Kooi, A. J., Notermans, N. C., Faber, C. G., Verschuuren, J. J. G. M., Kruijshaar, M. E., Reuser, A. J. J., van Doorn, P. A., & van der Ploeg, A. T. (2012). Effect of enzyme therapy and prognostic factors in 69 adults with Pompe disease: an open-label single-center study. Orphanet journal of rare diseases, 7, [73]. https://doi.org/10.1186/1750-1172-7-73
  21. 2011
  22. Titulaer, M. J., Maddison, P., Sont, J. K., Wirtz, P. W., Hilton-Jones, D., Klooster, R., Willcox, N., Potman, M., Smitt, P. A. E. S., Kuks, J. B. M., Roep, B. O., Vincent, A., van der Maarel, S. M., van Dijk, J. G., Lang, B., & Verschuuren, J. J. G. M. (2011). Clinical Dutch-English Lambert-Eaton Myasthenic Syndrome (LEMS) Tumor Association Prediction Score Accurately Predicts Small-Cell Lung Cancer in the LEMS. Journal of Clinical Oncology, 29(7), 902-908. https://doi.org/10.1200/JCO.2010.32.0440
  23. 2010
  24. Cats, E. A., van der Pol, W. -L., Piepers, S., Franssen, H., Jacobs, B. C., van den Berg-Vos, R. M., Kuks, J. B., van Doorn, P. A., van Engelen, B. G., Verschuuren, J. J., Wokke, J. H., Veldink, J. H., & van den Berg, L. H. (2010). Correlates of outcome and response to IVIg in 88 patients with multifocal motor neuropathy. Neurology, 75(9), 818-825. https://doi.org/10.1212/WNL.0b013e3181f0738e
  25. Niks, E. H., Kuks, J. B. M., Wokke, J. H. J., Veldman, H., Bakker, E., Verschuuren, J. J. G. M., & Plomp, J. J. (2010). PRE- AND POSTSYNAPTIC NEUROMUSCULAR JUNCTION ABNORMALITIES IN MuSK MYASTHENIA. MUSCLE & NERVE, 42(2), 283-288. https://doi.org/10.1002/mus.21642
  26. 2009
  27. van Tintelen, J. P., Van Gelder, I. C., Asimaki, A., Suurmijer, A. J. H., Wiesfeld, A. C. P., Jongbloed, J. D. H., van den Wijngaard, A., Kuks, J. B. M., van Spaendonck-Zwarts, K. Y., Notermans, N., Boven, L., van den Heuvel, F., Veenstra-Knol, H. E., Saffitz, J. E., Hofstra, R. M. W., & van den Berg, M. P. (2009). Severe cardiac phenotype with right ventricular predominance in a large cohort of patients with a single missense mutation in the DES gene. Heart Rhythm, 6(11), 1574-1583. https://doi.org/10.1016/j.hrthm.2009.07.041
  28. Faber, C. G., Molenaar, P. C., Vles, J. S. H., Bonifati, D. M., Verschuuren, J. J. G. M., van Doorn, P. A., Kuks, J. B. M., Wokke, J. H. J., Beeson, D., & 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
  29. Brugman, F., Veldink, J. H., Franssen, H., de Visser, M., de Jong, J. M. B. V., Faber, C. G., Kremer, B. H. P., Schelhaas, H. J., van Doorn, P. A., Verschuuren, J. J. G. M., Bruyn, R. P. M., Kuks, J. B. M., Robberecht, W., Wokke, J. H. J., & van den Berg, L. H. (2009). Differentiation of Hereditary Spastic Paraparesis From Primary Lateral Sclerosis in Sporadic Adult-Onset Upper Motor Neuron Syndromes. Archives of Neurology, 66(4), 509-514. https://doi.org/10.1001/archneurol.2009.19
Previous 1 2 Next

ID: 105973