Testing of Adrenal Axis Function in Patients With Combined Pituitary Hormone Deficiency Caused by PROP1 Mutation

Background: The mechanism of adrenal axis deterioration in PROP1 mutation remains uncertain and challenging. Aim: The aim of the project was to investigate the adrenal axis function in patients with combined pituitary function deficiency and PROP1 mutation. Methods: We performed the corticotrophin (...

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Dettagli Bibliografici
Pubblicato in:J Endocr Soc
Autori principali: Gilis-Januszewska, Aleksandra, Rogoziński, Damian, Nowak, Andrzej Jerzy, Piwońska-Solska, Beata, Zygmunt-Górska, Agata, Wójcik, Małgorzata, Starzyk, Jerzy, Hubalewska-Dydejczyk, Alicja
Natura: Artigo
Lingua:Inglês
Pubblicazione: Oxford University Press 2021
Soggetti:
Neuroendocrinology and Pituitary
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC8090037/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvab048.1293
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