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Endocrine Connections|June 14, 2022
The impact of Klinefelter syndrome on socioeconomic status: a multicenter studySebastian Franik, Kathrin Fleischer, Barbara Kortmann, et al.
Endocrine Connections|August 14, 2023
Quality of life in men with Klinefelter syndrome: a multicentre studySebastian Franik, Kathrin Fleischer, Barbara Kortmann, et al.
Endocrine Connections|June 27, 2024
Comparison of modified-release hydrocortisone capsules versus prednisolone in the treatment of congenital adrenal hyperplasiaDafydd Aled Rees, Deborah P Merke, Wiebke Arlt, et al.
Hepatology (Baltimore, Md.)|August 19, 2014
Polymorphisms in melanoma differentiation-associated gene 5 link protein function to clearance of hepatitis C virusFranziska S Hoffmann, Andreas Schmidt, Meike Dittmann Chevillotte, et al.
Frontiers in Endocrinology|September 11, 2023
Integration of clinical parameters and CT-based radiomics improves machine learning assisted subtyping of primary hyperaldosteronismNabeel Mansour, Andreas Mittermeier, Roman Walter, et al.
Frontiers in Immunology|January 3, 2025
Sex-dependent modulation of T and NK cells and gut microbiome by low sodium diet in patients with primary aldosteronismHanna F Nowotny, Tingting Zheng, Thomas Marchant Seiter, et al.
The Journal of Clinical Endocrinology and Metabolism|February 2, 2021
Modified-Release Hydrocortisone in Congenital Adrenal HyperplasiaDeborah P Merke, Ashwini Mallappa, Wiebke Arlt, et al.
The Journal of Clinical Endocrinology and Metabolism|January 22, 2010
Functional consequences of seven novel mutations in the CYP11B1 gene: four mutations associated with nonclassic and three mutations causing classic 11{beta}-hydroxylase deficiencySilvia Parajes, Lourdes Loidi, Nicole Reisch, et al.
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