Klassisk medfødt binyrebarkhyperplasi

A high frequency of de novo mutations strengthens the case for newborn screening for X-ALD, in order to provide timely treatment for adrenal failure, cerebral demyelination and

High frequency of adrenal myelolipomas and testicular adrenal rest tumours in adult Norwegian patients with classical congenital adrenal hyperplasia because of

By studying the well-established human adrenocortical carcinoma cell line NCI- H295R as a model of the adrenal cortex, adrenal cells were shown to respond to environmental factors

Keywords: adrenal insufficiency, congenital adrenal hyperplasia, 3β-hydroxysteroid dehydrogenase type 2 deficiency, autoimmune adrenalitis, autoimmune Addison’s

Diagnostic testing of autonomous cortisol secretion in adrenal incidentalomas Grethe Å Ueland1,2, Thea Grinde1, Paal Methlie1,2,3, Oskar Kelp4, Kristian Løvås2,3 and Eystein

The increased success rate is independent of whether cosyntropin is used, the cortisol gradient required to deem the sample representa- tive, the assay employed, and the number

In rats, inhibited weight gain, reduced pituitary POMC expression, adrenal Nr3c1 mRNA downregulation, as well as increased miR-146a, miR-30c and miR-223 in plasma were

In the present study, we used a new in vitro assay of 21OH enzyme activity and molecular computer modelling to predict the phenotypes of recently detected variants (p.L388R