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Detection of Urinary Exosomal HSD11B2 mRNA Expression: A Useful Novel Tool for the Diagnostic Approach of Dysfunctional 11β-HSD2-Related Hypertension
OBJECTIVE: Apparent mineralocorticoid excess (AME) is an autosomal recessive disorder caused by the 11β-hydroxysteroid dehydrogenase type 2 (11β-HSD2) enzyme deficiency, traditionally assessed by measuring either the urinary cortisol metabolites ratio (tetrahydrocortisol+allotetrahydrocortisol/tetra...
Autores principales: | De Santis, Domenica, Castagna, Annalisa, Danese, Elisa, Udali, Silvia, Martinelli, Nicola, Morandini, Francesca, Veneri, Mariangela, Bertolone, Lorenzo, Olivieri, Oliviero, Friso, Simonetta, Pizzolo, Francesca |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419411/ https://www.ncbi.nlm.nih.gov/pubmed/34497581 http://dx.doi.org/10.3389/fendo.2021.681974 |
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