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The Journal of Clinical Endocrinology and Metabolism|August 14, 2013
A diagnosis not to be missed: nonclassic steroid 11β-hydroxylase deficiency presenting with premature adrenarche and hirsutismNicole Reisch, Wolfgang Högler, Silvia Parajes, et al.
The Journal of Clinical Endocrinology and Metabolism|March 23, 2023
Interpretation of Steroid Biomarkers in 21-Hydroxylase Deficiency and Their Use in Disease ManagementKyriakie Sarafoglou, Deborah P Merke, Nicole Reisch, et al.
Journal of Clinical Medicine|July 27, 2022
Ectopic Prostate Tissue in the Uterine Cervix of a Female with Non-Classic Congenital Adrenal Hyperplasia-A Case ReportLea Tschaidse, Matthias K Auer, Ilja Dubinski, et al.
Journal of Clinical Research in Pediatric Endocrinology|May 23, 2023
Continuous Glucose Monitoring in Children and Adolescents with Congenital Adrenal HyperplasiaIlja Dubinski, Susanne Bechtold-Dalla Pozza, Belana Debor, et al.
The Journal of Steroid Biochemistry and Molecular Biology|February 10, 2023
Synthetic glucocorticoids instead of hydrocortisone do not increase mineralocorticoid needs in adult patients with salt wasting congenital adrenal hyperplasiaMatthias K Auer, Luisa Paizoni, Hanna Nowotny, et al.
The Journal of Clinical Endocrinology and Metabolism|July 9, 2004
Characterization of an adrenocorticotropin (ACTH) receptor promoter polymorphism leading to decreased adrenal responsiveness to ACTHMarc Slawik, Nicole Reisch, Oliver Zwermann, et al.
European Journal of Endocrinology|June 1, 2021
Altered endocannabinoid-dynamics in craniopharyngioma patients and their association with HPA-axis disturbancesMatthias K Auer, Dorothea Gebert, Sarah V Biedermann, et al.
European Journal of Endocrinology|May 22, 2015
A critical reappraisal of bilateral adrenalectomy for ACTH-dependent Cushing's syndromeMartin Reincke, Katrin Ritzel, Andrea Oßwald, et al.
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