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  1. 2002

  2. Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidism

    Moreno, J. C., Bikker, H., Kempers, M. J. E., van Trotsenburg, A. S. P., Baas, F., de Vijlder, J. J. M., Vulsma, T. & Ris-Stalpers, C., 2002, In: New England journal of medicine. 347, 2, p. 95-102

    Research output: Contribution to journal › Article › Academic › peer-review

  3. Longitudinal analysis of growth and puberty in 21-hydroxylase deficiency patients

    van der Kamp, H. J., Otten, B. J., Buitenweg, N., de Muinck Keizer-Schrama, S. M. P. F., Oostdijk, W., Jansen, M., Delemarre-de Waal, H. A., Vulsma, T. & Wit, J. M., 2002, In: Archives of disease in childhood. 87, 2, p. 139-144

    Research output: Contribution to journal › Article › Academic › peer-review

  4. Thyroid disease in newborns, infants, and children

    van Trotsenburg, A. S. P. & Vulsma, T., 2002, Oxford textbook of endocrinology and diabetes. Wass, J. A. H. & Shalet, S. M. (eds.). S.l.: Oxford University Press, p. 557-571

    Research output: Chapter in Book/Report/Conference proceeding › Chapter › Academic › peer-review

  5. 1989

  6. Antibodies to 'second colloid antigen.' A study on the prevalence in sporadic forms of congenital hypothyroidism

    van Trotsenburg, P., Vulsma, T., Bloot, A. M., van der Gaag, R. D., Lens, J. W., Drexhage, H. A. & de Vijlder, J. J., 1989, In: Acta endocrinologica. 121, 5, p. 659-665

    Research output: Contribution to journal › Article › Academic › peer-review

  7. The long-term outcome of thyroidectomy for sporadic non-toxic goitre

    Berghout, A., Wiersinga, W. M., Drexhage, H. A., van Trotsenburg, P., Smits, N. J., van der Gaag, R. D. & Touber, J. L., 1989, In: Clinical endocrinology. 31, 2, p. 193-199

    Research output: Contribution to journal › Article › Academic › peer-review

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