Maaike H Oosterveer
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Explore the profile of Maaike H Oosterveer including associated specialties, affiliations and a list of published articles.
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49
Citations
2189
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Recent Articles
1.
Kiyuna L, Krishnamurthy K, Homan E, Langelaar-Makkinje M, Gerding A, Bos T, et al.
Commun Biol
. 2024 Nov;
7(1):1479.
PMID: 39521914
Fasting hypoglycemia is a severe and incompletely understood symptom of various inborn errors of metabolism (IEM). Precision-cut liver slices (PCLS) represent a promising model for studying glucose production ex vivo....
2.
Rossi A, Ruoppolo M, Fedele R, Pirozzi F, Rosano C, Auricchio R, et al.
J Lipid Res
. 2024 Sep;
65(10):100651.
PMID: 39306041
Glycogen storage disease type Ia (GSDIa) is a rare, inherited glucose-6-phosphatase-α (G6Pase-α) deficiency-induced carbohydrate metabolism disorder. Although hyperlipidemia is a hallmark of GSDI, the extent of lipid metabolism disruption remains...
3.
Buziau A, Oosterveer M, Wouters K, Bos T, Tolan D, Agius L, et al.
Mol Metab
. 2024 Jul;
87:101984.
PMID: 38972375
Objective: Stable isotope studies have shown that hepatic de novo lipogenesis (DNL) plays an important role in the pathogenesis of intrahepatic lipid (IHL) deposition. Furthermore, previous research has demonstrated that...
4.
Liu F, Tol A, Kuipers F, Oosterveer M, van der Beek E, van Leeuwen S
Heliyon
. 2024 Feb;
10(3):e24539.
PMID: 38317966
Oligosaccharides and sialic acids (Sia) are bioactive components in milk that contribute to newborn development and health. Hyperglycemia in pregnancy (HIP) can have adverse effects on both mother and infant....
5.
Rossi A, Oosterveer M, van Dijk T, Bleeker A, Koehorst M, Weinstein D, et al.
J Clin Endocrinol Metab
. 2023 Sep;
109(2):389-401.
PMID: 37690115
Context: Glycogen storage disease type Ia (GSDIa) is an inborn metabolic disorder characterized by impaired endogenous glucose production (EGP). Monitoring of patients with GSDIa is prioritized because of ongoing treatment...
6.
Geiger M, Oppi S, Nusser-Stein S, Costantino S, Mohammed S, Gorica E, et al.
Cardiovasc Diabetol
. 2023 Jun;
22(1):144.
PMID: 37349757
Background: The nuclear receptor corepressor 1 (NCOR1) plays an important role in the regulation of gene expression in immunometabolic conditions by connecting chromatin-modifying enzymes, coregulators and transcription factors. NCOR1 has...
7.
Rutten M, Lei Y, Hoogerland J, Bloks V, Yang H, Bos T, et al.
Cancer Metab
. 2023 Apr;
11(1):5.
PMID: 37085901
Background: Glycogen storage disease type 1a (GSD Ia) is an inborn error of metabolism caused by a defect in glucose-6-phosphatase (G6PC1) activity, which induces severe hepatomegaly and increases the risk...
8.
Tol A, Hribar K, Kruit J, Bongiovanni L, Vieira-Lara M, Koster M, et al.
J Physiol
. 2023 Apr;
601(10):1761-1780.
PMID: 37010236
Hyperglycaemia in pregnancy (HIP) is a pregnancy complication characterized by mild to moderate hyperglycaemia that negatively impacts short- and long-term health of mother and child. However, relationships between severity and...
9.
Haring M, Peeks F, Oosterveer M, Brouwers M, Hollak C, Janssen M, et al.
JHEP Rep
. 2022 Jul;
4(8):100512.
PMID: 35811762
Background & Aims: Glycogen storage disease type Ia (GSDIa) is an inborn error of carbohydrate metabolism caused by pathogenic variants in the glucose-6-phosphatase catalytic subunit 1 () gene and is...
10.
Rossi A, Rutten M, van Dijk T, Bakker B, Reijngoud D, Oosterveer M, et al.
Front Endocrinol (Lausanne)
. 2022 Jul;
13:858832.
PMID: 35789807
Hypoglycemia results from an imbalance between glucose entering the blood compartment and glucose demand, caused by a defect in the mechanisms regulating postprandial glucose homeostasis. Hypoglycemia represents one of the...