Angela Huebner
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Explore the profile of Angela Huebner including associated specialties, affiliations and a list of published articles.
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104
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1747
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Recent Articles
1.
Rohayem J, Idkowiak J, Huss S, Balke T, Schurmann H, Heitkotter B, et al.
Endocr Connect
. 2024 Nov;
14(1.
PMID: 39565383
Human chorionic gonadotropin (hCG) has structural similarities with thyroid-stimulating hormone (TSH) and may stimulate TSH receptors at higher concentrations. During pregnancy, placental hCG causes TSH suppression, contributing to hyperemesis. However,...
2.
Cehic M, Mitrovic K, Vukovic R, Milenkovic T, Kovacevic G, Todorovic S, et al.
Front Endocrinol (Lausanne)
. 2024 Oct;
15:1431383.
PMID: 39387047
Triple A syndrome (TAS), also known as Allgrove syndrome (OMIM#231550), is a rare, autosomal recessive disorder characterized by the triad of alacrima, achalasia, and adrenal insufficiency. Additional neurological features may...
3.
Casey R, Hendriks E, Deal C, Waguespack S, Wiegering V, Redlich A, et al.
Nat Rev Endocrinol
. 2024 Aug;
20(12):760.
PMID: 39191988
No abstract available.
4.
Casey R, Hendriks E, Deal C, Waguespack S, Wiegering V, Redlich A, et al.
Nat Rev Endocrinol
. 2024 Aug;
20(12):729-748.
PMID: 39147856
Phaeochromocytomas and paragangliomas (PPGL) are rare neuroendocrine tumours that arise not only in adulthood but also in childhood and adolescence. Up to 70-80% of childhood PPGL are hereditary, accounting for...
5.
Smits D, Dekker J, Douben H, Schot R, Magee H, Bakhtiari S, et al.
HGG Adv
. 2024 Jul;
5(4):100327.
PMID: 39003500
Nuclear pore complexes (NPCs) regulate nucleocytoplasmic transport and are anchored in the nuclear envelope by the transmembrane nucleoporin NDC1. NDC1 is essential for post-mitotic NPC assembly and the recruitment of...
6.
Choukair D, Mittnacht J, Treiber D, Hoffmann G, Grasemann C, Huebner A, et al.
Clin Endocrinol (Oxf)
. 2024 Jul;
101(2):121-129.
PMID: 38979902
Objective: Structured transition of adolescents and young adults with a chronic endocrine disease from paediatric to adult care is important. Until now, no data on time and resources required for...
7.
Thirumalasetty S, Schubert T, Naumann R, Reichardt I, Rohm M, Landgraf D, et al.
Int J Mol Sci
. 2024 May;
25(10).
PMID: 38791102
Congenital Adrenal Hyperplasia (CAH) is an autosomal recessive disorder impairing cortisol synthesis due to reduced enzymatic activity. This leads to persistent adrenocortical overstimulation and the accumulation of precursors before the...
8.
Dumic K, Heinrichs C, Koehler K, Huebner A, Dumic M, Kusec V, et al.
Front Endocrinol (Lausanne)
. 2024 Mar;
15:1357084.
PMID: 38544685
Objective: Triple A syndrome, caused by autosomal recessively inherited mutations in the gene is characterized by alacrima, achalasia, adrenal insufficiency, and neurological impairment. To the best of our knowledge, no...
9.
Kunstreich M, Dunstheimer D, Mier P, Holterhus P, Wudy S, Huebner A, et al.
J Clin Endocrinol Metab
. 2024 Feb;
109(8):2053-2060.
PMID: 38318871
Context: Adrenocortical carcinomas are very rare malignancies in childhood associated with poor outcome in advanced disease. Most adrenocortical tumors (ACT) are functional, causing signs and symptoms of adrenal hormone excess....
10.
Eisenhofer G, Peitzsch M, Bechmann N, Huebner A
Front Endocrinol (Lausanne)
. 2022 Aug;
13:901760.
PMID: 35957826
Catecholamine-producing tumors of childhood include most notably neuroblastoma, but also pheochromocytoma and paraganglioma (PPGL). Diagnosis of the former depends largely on biopsy-dependent histopathology, but this is contraindicated in PPGL where...