Bas P H Adriaansen
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Explore the profile of Bas P H Adriaansen including associated specialties, affiliations and a list of published articles.
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8
Citations
17
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Recent Articles
1.
Claahsen-van der Grinten H, Adriaansen B, Falhammar H
J Clin Endocrinol Metab
. 2025 Jan;
110(Supplement_1):S25-S36.
PMID: 39836620
Classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency results in severe cortisol and aldosterone deficiency, leading to persistent adrenal stimulation and excess production of ACTH and adrenal androgens. This...
2.
Free cortisol and free 21-deoxycortisol in the clinical evaluation of congenital adrenal hyperplasia
Adriaansen B, Utari A, Olthaar A, van der Steen R, Pijnenburg-Kleizen K, Berkenbosch L, et al.
J Clin Endocrinol Metab
. 2024 Aug;
PMID: 39183148
Context: Some patients with classic congenital adrenal hyperplasia (CAH) survive without glucocorticoid treatment. Increased precursor concentrations in these patients might lead to higher free (biological active) cortisol concentrations by influencing...
3.
Adriaansen B, Utari A, Westra D, Juniarto A, Ariani M, Ediati A, et al.
Front Endocrinol (Lausanne)
. 2024 Aug;
15:1410122.
PMID: 39175568
Introduction: Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21OHD) or 11-hydroxylase deficiency (11OHD) is characterized by underproduction of cortisol and overproduction of adrenal androgens. These androgens lead to a...
4.
Adriaansen B, Oude Alink S, Swinkels D, Schroder M, Span P, Sweep F, et al.
Eur J Endocrinol
. 2024 Jan;
PMID: 38243909
Objective: Classic androgens such as dehydroepiandrosterone, androstenedione, and testosterone are generally measured for diagnosis and treatment monitoring in children and adolescents with hyperandrogenism, as can occur in congenital adrenal hyperplasia,...
5.
Schroder M, Neacsu M, Adriaansen B, Sweep F, Ahmed S, Ali S, et al.
Eur J Endocrinol
. 2023 Oct;
189(4):460-468.
PMID: 37837609
Importance: Testicular adrenal rest tumors (TARTs), often found in male patients with congenital adrenal hyperplasia (CAH), are benign lesions causing testicular damage and infertility. We hypothesize that chronically elevated adrenocorticotropic...
6.
Adriaansen B, van Herwaarden A, Sweep F, Claahsen-van der Grinten H
Horm Res Paediatr
. 2023 Oct;
97(4):416-418.
PMID: 37778327
No abstract available.
7.
Shafaay E, Aldriweesh M, Aljahdali G, Babiker A, Alomar A, Alharbi K, et al.
Front Endocrinol (Lausanne)
. 2023 Jun;
14:1122435.
PMID: 37347111
Background: Congenital Adrenal Hyperplasia (CAH) is a chronic disease that requires lifelong treatment. Patients may face stigmatization, which may affect their quality of life (QoL). Therefore, we assessed the clinical...
8.
Adriaansen B, Schroder M, Span P, Sweep F, van Herwaarden A, Claahsen-van der Grinten H
Front Endocrinol (Lausanne)
. 2022 Dec;
13:1064024.
PMID: 36578966
Congenital adrenal hyperplasia (CAH) due to 21α-hydroxylase deficiency (21OHD) or 11β-hydroxylase deficiency (11OHD) are congenital conditions with affected adrenal steroidogenesis. Patients with classic 21OHD and 11OHD have a (nearly) complete...
9.
Adriaansen B, Kamphuis J, Schroder M, Olthaar A, Bock C, Brandt A, et al.
Clin Endocrinol (Oxf)
. 2022 Feb;
97(1):36-42.
PMID: 35150157
Objective: Treatment of congenital adrenal hyperplasia (CAH) patients with glucocorticoids is often challenging since there is a delicate balance between over- and undertreatment. Treatment can be monitored noninvasively by measuring...