prof. dr. T.P. Links

E-mail:
t.p.links umcg.nl

Research

  1. 2019
  2. van der Tuin, K., Garcia, M. V., Corver, W. E., Khalifa, M. N., Neto, D. R., Corssmit, E. P. M., ... Morreau, H. (2019). Targetable gene fusions identified in radioactive iodine refractory advanced thyroid carcinoma. European Journal of Endocrinology, 180(4), 235-241. https://doi.org/10.1530/EJE-18-0653
  3. 2018
  4. de Vries, L. H., Lodewijk, L., Willems, S. M., Dreijerink, K. M. A., de Keizer, B., van Diest, P. J., ... Vriens, M. R. (2018). SSTR2A expression in medullary thyroid carcinoma is correlated with longer survival. Endocrine, 62(3), 639-647. https://doi.org/10.1007/s12020-018-1706-1
  5. Lodewijk, L., Willems, S. M., Dreijerink, K. M. A., de Keizer, B., van Diest, P. J., Schepers, A., ... Vriens, M. R. (2018). The theranostic target prostate-specific membrane antigen is expressed in medullary thyroid cancer. Human Pathology, 81, 245-254. https://doi.org/10.1016/j.humpath.2018.06.035
  6. Krauss, T., Ferrara, A. M., Links, T. P., Wellner, U., Bancoss, I., Kvachenyuk, A., ... Daerr, R. (2018). Preventive medicine of von Hippel-Lindau disease-associated pancreatic neuroendocrine tumors. Endocrine-Related cancer, 25(9), 783-793. https://doi.org/10.1530/ERC-18-0100
  7. Neumann, H. P., Young, W. F., Krauss, T., Bayley, J-P., Schiavi, F., Opocher, G., ... Eng, C. (2018). 65 YEARS OF THE DOUBLE HELIX Genetics informs precision practice in the diagnosis and management of pheochromocytoma. Endocrine-Related cancer, 25(8), T201-T219. https://doi.org/10.1530/ERC-18-0085
  8. Eijkelenkamp, K., Olderode-Berends, M. J. W., van der Luijt, R. B., Robledo, M., van Dooren, M., Feelders, R. A., ... van der Horst-Schrivers, A. N. A. (2018). Homozygous TMEM127 mutations in 2 patients with bilateral pheochromocytomas. Clinical Genetics, 93(5), 1049-1056. https://doi.org/10.1111/cge.13202
  9. Stunnenberg, B. C., Raaphorst, J., Deenen, J. C. W., Links, T. P., Wilde, A. A., Verbove, D. J., ... Ginjaar, H. B. (2018). Prevalence and mutation spectrum of skeletal muscle channelopathies in the Netherlands. Neuromuscular disorders, 28(5), 402-407. https://doi.org/10.1016/j.nmd.2018.03.006
  10. 2017
  11. Castinetti, F., Maia, A. L., Peczkowska, M., Barontini, M., Hasse-Lazar, K., Links, T. P., ... Neumann, H. P. H. (2017). The penetrance of MEN2 pheochromocytoma is not only determined by RET mutations. Endocrine-Related cancer, 24(8), L63-L67. https://doi.org/10.1530/ERC-17-0189
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