Frontiers in Endocrinology
ISSN: 1664-2392
Publisher: Frontiers Media
Publications (21)
The association between leptin, adiponectin levels and the ovarian reserve in women of reproductive age (2024)
Nikolettos K, Vlahos N, Pagonopoulou O, Nikolettos N, Zikopoulos K, Tsikouras P, Kontomanolis E, et al.
Journal article
Effects of allicin on human Simpson-Golabi-Behmel syndrome cells in mediating browning phenotype (2023)
Ali U, Wabitsch M, Tews D, Colitti M
Journal article, Original article
Health related Quality of Life over time in German sarcoma patients. An analysis of associated factors - results of the PROSa study (2023)
Eichler M, Hentschel L, Singer S, Hornemann B, Richter S, Hofbauer C, Hohenberger P, et al.
Journal article
Associations of incidental vertebral fractures and longitudinal changes of MR–based proton density fat fraction and T2* measurements of vertebral bone marrow (2022)
Leonhardt Y, Ketschau J, Ruschke S, Gassert FT, Glanz L, Feuerriegel GC, Gassert FG, et al.
Journal article
Distinct Metabolism of Bone Marrow Adipocytes and their Role in Bone Metastasis (2022)
Li Y, Cao S, Gaculenko A, Zhan Y, Bozec A, Chen X
Journal article, Review article
Differences in Hip Geometry Between Female Subjects With and Without Acute Hip Fracture: A Cross-Sectional Case-Control Study (2022)
Wang L, Yang M, Liu Y, Ge Y, Zhu S, Su Y, Cheng X, et al.
Journal article
Pubertal Timing and Growth Dynamics in Children With Severe Primary IGF-1 Deficiency: Results From the European Increlex® Growth Forum Database Registry (2022)
Bang P, Polak M, Perrot V, Sert C, Shaikh H, Wölfle J
Journal article
Hyperglycemia Is Not Associated With Higher Volumetric BMD in a Chinese Health Check-up Cohort (2022)
Wang L, Zhao K, Zha X, Ran L, Su H, Yang Y, Shuang Q, et al.
Journal article
Plasma Metabolome Profiling for the Diagnosis of Catecholamine Producing Tumors (2021)
März J, Kurlbaum M, Roche-Lancaster O, Deutschbein T, Peitzsch M, Prehn C, Weismann D, et al.
Journal article
Case Report: Consecutive Adrenal Cushing’s Syndrome and Cushing’s Disease in a Patient With Somatic CTNNB1, USP8, and NR3C1 Mutations (2021)
Detomas M, Altieri B, Schlötelburg W, Appenzeller S, Schlaffer SM, Coras R, Schirbel A, et al.
Journal article