Prof. Dr. med. Olaf Hiort

Photo of Olaf  Hiort

Klinik für Kinder- und Jugendmedizin
Sektion für Pädiatrische Endokrinologie und Diabetologie


Universität zu Lübeck
Ratzeburger Allee 160
23562 Lübeck

Email: olaf.hiort(at)uksh.de
Phone: +49 451 500-42810

Publications

M. Al-Sharkawi, V. Calonga-Solis, F. Dressler, H. Busch, O. Hiort, and R. Werner,
Persistence of foetal testicular features in patients with defective androgen signalling, Eur J Endocrinol , vol. 188, no. 1, 2023.
DOI:10.1093/ejendo/lvad007
O. Hiort, M. Jurgensen, and C. Rehmann-Sutter,
Intersex, DSD, and the Child's Well-Being: Changing Perceptions, Hormone Research in Paediatrics , vol. 95, no. 1, pp. 21-24, 2022.
DOI:10.1159/000523876
M. Auer, W. Birnbaum, M. Hartmann, P. Holterhus, A. Kulle, A. Lux, L. Marshall, K. Rall, A. Richter-Unruh, R. Werner, S. Wudy, and O. Hiort,
Metabolic effects of estradiol versus testosterone in complete androgen insensitivity syndrome, Endocrine , vol. 76, no. 3, pp. 722-732, 2022.
DOI:10.1007/s12020-022-03017-8
M. Jurgensen, M. Rapp, U. Dohnert, F. Frielitz, F. Ahmed, M. Cools, U. Thyen, and O. Hiort,
Assessing the health-related management of people with differences of sex development, Endocrine , vol. 71, no. 3, pp. 675-680, 2021.
DOI:10.1007/s12020-021-02627-y
T. Eggermann, M. Elbracht, I. Kurth, A. Juul, T. Johannsen, I. Netchine, G. Mastorakos, G. Johannsson, T. Musholt, M. Zenker, D. Prawitt, A. Pereira, O. Hiort, and C. Rare Endocrine,
Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN), Orphanet J Rare Dis , vol. 15, no. 1, pp. 144, 2020.
DOI:10.1186/s13023-020-01420-w
O. Hiort, M. Cools, A. Springer, K. McElreavey, A. Greenfield, S. Wudy, A. Kulle, S. Ahmed, A. Dessens, A. Balsamo, M. Maghnie, M. Bonomi, M. Dattani, L. Persani, L. Audi, C. DSDnet, and R. Gn,
Addressing gaps in care of people with conditions affecting sex development and maturation, Nat Rev Endocrinol , vol. 15, no. 10, pp. 615-622, 2019.
DOI:10.1038/s41574-019-0238-y
C. Fluck, A. Nordenstrom, S. Ahmed, S. Ali, M. Berra, J. Hall, B. Kohler, V. Pasterski, R. Robeva, K. Schweizer, A. Springer, P. Westerveld, O. Hiort, and M. Cools,
Standardised data collection for clinical follow-up and assessment of outcomes in differences of sex development (DSD): recommendations from the COST action DSDnet, Eur J Endocrinol , vol. 181, no. 5, pp. 545-564, 2019.
DOI:10.1530/EJE-19-0363
L. Audi, S. Ahmed, N. Krone, M. Cools, K. McElreavey, P. Holterhus, A. Greenfield, A. Bashamboo, O. Hiort, S. Wudy, R. McGowan, and E. The,
GENETICS IN ENDOCRINOLOGY: Approaches to molecular genetic diagnosis in the management of differences/disorders of sex development (DSD): position paper of EU COST Action BM 1303 'DSDnet', Eur J Endocrinol , vol. 179, no. 4, pp. R197-R206, 2018.
DOI:10.1530/EJE-18-0256
W. Birnbaum, L. Marshall, R. Werner, A. Kulle, P. Holterhus, K. Rall, B. Kohler, A. Richter-Unruh, M. Hartmann, S. Wudy, M. Auer, A. Lux, S. Kropf, and O. Hiort,
Oestrogen versus androgen in hormone-replacement therapy for complete androgen insensitivity syndrome: a multicentre, randomised, double-dummy, double-blind crossover trial, Lancet Diabetes Endocrinol , vol. 6, no. 10, pp. 771-780, 2018.
DOI:10.1016/S2213-8587(18)30197-9
M. Cools, M. Simmonds, S. Elford, J. Gorter, S. Ahmed, F. D'Alberton, A. Springer, O. Hiort, S. European Cooperation in, and B. Technology Action,
Response to the Council of Europe Human Rights Commissioner's Issue Paper on Human Rights and Intersex People, Eur Urol , vol. 70, no. 3, pp. 407-9, 2016.
DOI:10.1016/j.eururo.2016.05.015