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Research Output 2008 2019

Biochemically Silent Sympathetic Paraganglioma, Pheochromocytoma, or Metastatic Disease in SDHD Mutation Carriers

Dreijerink, K. M. A., Rijken, J. A., Compaijen, C. J., Timmers, H. J. L. M., van der Horst-Schrivers, A. N. A., van Leeuwaarde, R. S., van Dam, P. S., Leemans, C. R., van Dam, E. W. C. M., Dickhoff, C., Dommering, C. J., de Graaf, P., Zwezerijnen, G. J. C., van der Valk, P., Menke-van der Houven van Oordt, C. W., Hensen, E. F., Corssmit, E. P. M. & Eekhoff, E. M. W., 2019, In : The Journal of clinical endocrinology and metabolism. 104, 11, p. 5421-5426

Research output: Contribution to journalArticleAcademicpeer-review

Familial Paget's disease of bone: Long-term follow-up of unaffected relatives with and without Sequestosome 1 mutations

Peeters, J. J. M., de Ridder, R., Hamoen, E. C., Eekhoff, E. M. W., Smit, F., Boudin, E., van Hul, W., Papapoulos, S. E. & Appelman-Dijkstra, N. M., 2019, In : Bone. 128, 115044.

Research output: Contribution to journalArticleAcademicpeer-review

Relative importance of four functional measures as predictors of 15-year mortality in the older Dutch population

Eekhoff, E. M. W., Van Schoor, N. M., Biedermann, J. S., Oosterwerff, M. M., De Jongh, R., Bravenboer, N., Van Poppel, M. N. M. & Deeg, D. J. H., 25 Mar 2019, In : BMC Geriatrics. 19, 1

Research output: Contribution to journalArticleAcademicpeer-review

The first family with adult osteogenesis imperfecta caused by a novel homozygous mutation in CREB3L1

Cayami, FK., Maugeri, A., Treurniet, S., Setijowati, E. D., Teunissen, B., Eekhoff, EMW., Pals, G., Faradz, S. M. & Micha, D., 2019, In : Molecular Genetics and Genomic Medicine.

Research output: Contribution to journalArticleAcademicpeer-review