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

Publikationen

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
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
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. 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
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
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
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