Hair cortisol-a method to detect chronic cortisol levels in patients with Prader-Willi syndrome

BACKGROUND: Prader-Willi syndrome (PWS) is a multisymptomatic, rare, genetic, neurodevelopmental disorder in adults mainly characterized by hyperphagia, cognitive dysfunction, behavioral problems and risk of morbid obesity. Although endocrine insufficiencies are common, hypocortisolism is rare and k...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:BMC Endocr Disord
Päätekijät: Shukur, Hasanain Hamid, de Rijke, Yolanda B., van Rossum, Elisabeth F. C., Hussain-Alkhateeb, Laith, Höybye, Charlotte
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2020
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7654170/
https://ncbi.nlm.nih.gov/pubmed/33167936
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12902-020-00646-w
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