Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ulla Döhnert"'
Autor:
Sabine Wiegmann, Ralph Schilling, Mirja Winter, Martina Ernst, Katja Wechsung, Ute Kalender, Barbara Stöckigt, Annette Richter-Unruh, Olaf Hiort, Ulla Döhnert, Louise Marshall, Julia Rohayem, Klaus-Peter Liesenkötter, Martin Wabitsch, Gloria Herrmann, Gundula Ernst, Stephanie Roll, Thomas Keil, Uta Neumann
Publikováno v:
PEC Innovation, Vol 5, Iss , Pp 100321- (2024)
Objective: Evaluation of the participant satisfaction with a newly developed interdisciplinary, modular education program for children, adolescents, and young adults with differences of sex development (DSD) and their parents. Methods: The two-day pr
Externí odkaz:
https://doaj.org/article/f4aeea3d5bf343b8916af0c2026eb7af
Publikováno v:
Monatsschrift Kinderheilkunde. 171:159-164
Autor:
Ulla Döhnert, Ute Thyen, Martine Cools, Faisal Ahmed, Marion Rapp, Martina Jürgensen, Olaf Hiort, Fabian-Simon Frielitz
Publikováno v:
ENDOCRINE
Endocrine
Endocrine
Purpose Health care requirements and perception of people with differences of sex development (DSD) have changed enormously since the “Chicago Consensus Conference” in 2005. Therefore, new standards of care and evaluation of care have to be devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6dd0f4bdb7ac319b84b158aae50c0d4
https://biblio.ugent.be/publication/8695715
https://biblio.ugent.be/publication/8695715
Autor:
Louise Marshall, Lutz Wünsch, Olaf Hiort, Ralf Werner, Ulla Döhnert, Wiebke Birnbaum, Paul-Martin Holterhus
Publikováno v:
Hormone Research in Paediatrics. 87:354-358
Background: 17β-hydroxysteroid dehydrogenase (17β-HSD) type 3 deficiency is an autosomal recessive disorder with diminished testosterone synthesis and consequently underandrogenisation. 46,XY patients with 17β-HSD type 3 deficiency are often assig
Autor:
Clemens Freiberg, Isabel Mönig, Ralf Lünstedt, Ulla Döhnert, Alexandra Kulle, Olaf Hiort, Annette Richter-Unruh, Lutz Wünsch, Julia August, Ralf Werner, Benedikt Reiz, Christoph Thorns, Stefan A. Wudy, Paul-Martin Holterhus
Publikováno v:
Sexual Development. 9:260-268
The differential diagnosis of 46,XY disorders of sex development (DSD) is based on the distinction between forms of gonadal dysgenesis and disorders of androgen biosynthesis and action. However, clinical and endocrine evaluations are often not conclu
Publikováno v:
Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation. 11(4)
Prophylactic gonadectomy has been recommended in complete androgen insensitivity syndrome (CAIS) because of an increased risk for the development of malignant germ cell tumors in the intra-abdominal gonads. No reliable screening parameters are availa
Autor:
Olaf Hiort, Louise Marshall, Wiebke Birnbaum, Lutz Wünsch, Paul-Martin Holterhus, Ulla Döhnert, Ralf Werner, Tatjana Schröder
Publikováno v:
Nature Reviews Endocrinology. 10:520-529
The medical term disorders of sex development (DSDs) is used to describe individuals with an atypical composition of chromosomal, gonadal and phenotypic sex, which leads to differences in the development of the urogenital tract and reproductive syste
Autor:
Ralf, Werner, Isabel, Mönig, Julia, August, Clemens, Freiberg, Ralf, Lünstedt, Benedikt, Reiz, Lutz, Wünsch, Paul-Martin, Holterhus, Alexandra, Kulle, Ulla, Döhnert, Stefan A, Wudy, Annette, Richter-Unruh, Christoph, Thorns, Olaf, Hiort
Publikováno v:
Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation. 9(5)
The differential diagnosis of 46,XY disorders of sex development (DSD) is based on the distinction between forms of gonadal dysgenesis and disorders of androgen biosynthesis and action. However, clinical and endocrine evaluations are often not conclu
Autor:
Stefan A. Wudy, Ralf Werner, Ulla Döhnert, Felix G. Riepe, H. Merz, Michaela F. Hartmann, Paul-Martin Holterhus, Alexandra Kulle, Olaf Hiort, I. Sommerfeld, Silvano Bertelloni
Publikováno v:
Sexual Development; Vol 6
17β-hydroxysteroid dehydrogenase 3 (17β-HSD 3) deficiency is a rare cause of 46,XY disorders of sex development (DSD). At puberty, these patients experience a surge of androstenedione and also testosterone, leading to substantial virilization. The