Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Janna Mittnacht"'
Publikováno v:
Endocrinology, Diabetes & Metabolism, Vol 7, Iss 4, Pp n/a-n/a (2024)
ABSTRACT Objective During the process of transition from paediatric to adult health care, counselling concerning fertility is an important issue and is based mainly on serum markers of gonadal function. Here, we analysed these markers in adolescents
Externí odkaz:
https://doaj.org/article/71f471b7f41b43f299d99fe5a09a4795
Autor:
Corinna Grasemann, Jakob Höppner, Peter Burgard, Michael M. Schündeln, Nora Matar, Gabriele Müller, Heiko Krude, Reinhard Berner, Min Ae Lee-Kirsch, Fabian Hauck, Kerstin Wainwright, Sylvana Baumgarten, Janet Atinga, Jens J. Bauer, Eva Manka, Julia Körholz, Cordula Kiewert, André Heinen, Tanita Kretschmer, Tobias Kurth, Janna Mittnacht, Christoph Schramm, Christoph Klein, Holm Graessner, Olaf Hiort, Ania C. Muntau, Annette Grüters, Georg F. Hoffmann, Daniela Choukair
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-9 (2023)
Abstract Purpose The transition process from paediatric/adolescent to adult medical care settings is of utmost importance for the future health of adolescents with chronic diseases and poses even more difficulties in the context of rare diseases (RDs
Externí odkaz:
https://doaj.org/article/ef5f9b76b7484569ab9e82d3e5536374
Autor:
Daniela Choukair, Annette Hückmann, Janna Mittnacht, Thomas Breil, Jens Peter Schenk, Abdulsattar Alrajab, Lorenz Uhlmann, Markus Bettendorf
Publikováno v:
Indian journal of pediatrics. 89(7)
Objectives To validate adult height predictions (BX) using automated and Greulich–Pyle bone age determinations in children with chronic endocrine diseases. Methods Heights and near-adult heights were measured in 82 patients (48 females) with chroni
Autor:
Abdul Alrajab, Janna Mittnacht, Daniela Klose, Ioana Inta, Egbert Schulze, Jürgen Grulich-Henn, Daniela Choukair, Vira Yakovenko, Thomas Breil, Markus Bettendorf
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEMReferences. 32(3)
Background 11β-hydroxylase deficiency (11βOHD) is a rare disease representing the second most common cause of congenital adrenal hyperplasia (CAH) (5–8%) with an incidence of about 1:100,000. In contrast to 21-hydroxylase deficiency (21OHD), 11β
Autor:
Egbert Schulze, Catherine Lorz, Daniela Klose, Daniela Choukair, Markus Bettendorf, Janna Mittnacht, Jessica Jesser, Thomas Breil, Ioana Inta
Publikováno v:
Hormone research in paediatrics. 89(3)
Background: Paediatric prolactinomas are rare. The aim of this study was to investigate the clinical features and outcome of paediatric patients with prolactinomas. Methods: In this single-centre retrospective analysis, clinical, biochemical, and rad
Autor:
Matthias Gorenflo, Markus Bettendorf, Romuald Brunner, Carolin Kneppo, Janna Mittnacht, Peter Parzer, Daniela Choukair
Publikováno v:
Hormone Research in Paediatrics. 84:130-136
Background: Transient thyroid dysfunction occurs in children after cardiopulmonary bypass (CPB). We demonstrated significant benefits of acute postoperative tri-iodothyronine (T3) treatment for recovery and myocardial function. Now we report the long
Publikováno v:
European journal of pediatrics. 166(8)
Acquired primary hypothyroidism in infancy can be related to autoimmune thyroiditis and can present with unusual symptoms, such as muscle pseudohypertrophy and pituitary tumor. This condition can cause permanent deficits in psychomotor development an