Claus Hojbjerg Gravholt
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Explore the profile of Claus Hojbjerg Gravholt including associated specialties, affiliations and a list of published articles.
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101
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1813
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Recent Articles
1.
Just J, Ridder L, Johannsen E, Jensen J, Petersen M, Christensen H, et al.
NPJ Genom Med
. 2025 Feb;
10(1):9.
PMID: 39915521
Turner syndrome (TS) presents with multiple karyotypes, including 45,X monosomy and variants such as isochromosomes and mosaicism, and is characterized by several co-morbidities, including metabolic conditions and autoimmunity. Here, we...
2.
Berglund A, Gravholt C, Stochholm K
J Clin Endocrinol Metab
. 2025 Jan;
PMID: 39775857
Context: Few studies have reported on males with 45,X/46,XY mosaicism. Most studies stem from pediatric settings and knowledge of natural history and long-term health outcomes are therefore lacking. Objective: To...
3.
Kjaergaard K, Eriksen P, Nohr T, Pedersen S, Gravholt C, Vilstrup H, et al.
Metab Brain Dis
. 2024 Nov;
40(1):46.
PMID: 39607664
Hyperammonaemic encephalopathy in the absence of liver failure is a major diagnostic challenge. A rare cause is as a complication to previous gastric bypass surgery, a condition reported to be...
4.
Lind-Holst M, Hansen D, Main K, Juul A, Andersen M, Duno M, et al.
J Clin Endocrinol Metab
. 2024 Nov;
PMID: 39545512
Context: Clinical studies of psychiatric morbidity in patients with congenital adrenal hyperplasia (CAH) imply impaired mental health. Objective: To delineate psychiatric morbidity in a national CAH cohort by using complete...
5.
Ridder L, Mains Balle C, Skakkebaek A, Lind-Holst M, Nielsen M, Hermann P, et al.
Clin Endocrinol (Oxf)
. 2024 Apr;
100(6):515-526.
PMID: 38572909
Objective: To investigate the metabolic, cardiovascular, and neuropsychological phenotype, quality of life (QoL), and hormonal regulation in individuals with congenital adrenal hyperplasia (CAH), a group of autosomal recessive disorders characterized...
6.
Mains Balle C, Kassentoft C, van Heusden J, Knudsen M, Raaby L, Gravholt C
Sex Dev
. 2024 Jan;
17(4-6):203-210.
PMID: 38281483
Introduction: The presence of Y-chromosomal material in females with Turner syndrome (TS) is a well-established risk factor for developing gonadoblastoma and malignant transformations thereof. However, these events are rarely seen...
7.
Sandahl K, Just J, Erlandsen M, Mortensen K, Andersen N, Gravholt C
J Endocr Soc
. 2023 Oct;
7(11):bvad124.
PMID: 37822574
Context: Turner syndrome (TS) is a rare genetic syndrome with an increased mortality, mainly attributed to cardiovascular disease. Objective: This work aimed to investigate and correlate the lipid profile in...
8.
Skakkebaek A, Kjaer-Sorensen K, Matchkov V, Christensen L, Just J, Comert C, et al.
Sci Rep
. 2023 Jul;
13(1):12089.
PMID: 37495650
The genetic architecture of the QT interval, defined as the period from onset of depolarisation to completion of repolarisation of the ventricular myocardium, is incompletely understood. Only a minor part...
9.
Hagen C, Fischer M, Mola G, Mikkelsen T, Cleemann L, Gravholt C, et al.
Front Endocrinol (Lausanne)
. 2023 Jul;
14:1173600.
PMID: 37455919
Turner syndrome (TS) is a chromosomal disorder that affects about 1 in 2500 female births and is characterized by the partial or complete absence of the second X chromosome. Depending...
10.
Ridder L, Stochholm K, Mortensen K, Andersen N, Gravholt C
Clin Endocrinol (Oxf)
. 2023 Mar;
99(6):545-551.
PMID: 36890688
Objective: Cardiovascular complications and congenital malformations are known traits in Turner syndrome (TS), which increases mortality. Women with TS have varying phenotype and cardiovascular risks. A biomarker assessing the risk...