Maaike C de Vries
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Explore the profile of Maaike C de Vries including associated specialties, affiliations and a list of published articles.
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53
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918
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Recent Articles
1.
Veldman A, Sikkema-Raddatz B, Derks T, van Karnebeek C, Kiewiet M, Mulder M, et al.
Int J Neonatal Screen
. 2025 Jan;
11(1.
PMID: 39846587
The biomarker-based Dutch Newborn Screening (NBS) panel (as of 2024) comprises 19 inherited metabolic disorders (IMDs). With the use of next-generation sequencing (NGS) as a first-tier screen, NBS could expand...
2.
de Vreugd A, Zimmermann F, Steinbrucker K, de Vries M, de Boer L, Janssen M, et al.
Immunol Lett
. 2024 Nov;
271:106946.
PMID: 39557131
We here explore adverse events following immunization (AEFI) in children with mitochondrial disease (MD) recruited from two expertise centers in Austria (SALK) and The Netherlands (RUMC). Parents completed a questionnaire...
3.
Broertjes J, Franz E, Friesema I, Jansen H, Reubsaet F, Rutjes S, et al.
Emerg Infect Dis
. 2023 Jun;
29(7):1-9.
PMID: 37347519
We provide incidences (cases/10 million persons) in the Netherlands during 2009-2019 for pathogens listed as potential bioterrorism agents. We included pathogens from the highest categories of the European Medicines Agency...
4.
de Vries M, Hoeve-Bakker B, van den Beld M, Hendriks A, Harpal A, Noomen R, et al.
Microorganisms
. 2023 Apr;
11(4).
PMID: 37110328
is a zoonotic bacterium that is endemic in large parts of the world. It is absent in the standard library of the most applied matrix-assisted laser desorption ionization-time of flight...
5.
Savelkoel J, Oladele R, Ojide C, Peters R, Notermans D, Makinwa J, et al.
Emerg Infect Dis
. 2023 Apr;
29(5):1073-1075.
PMID: 37081606
Melioidosis, caused by the soil-dwelling bacterium Burkholderia pseudomallei, is predicted to be endemic in Nigeria but is only occasionally reported. This report documents the systematic identification of the presence of...
6.
Ferreira E, Veenvliet A, Engelke U, Kluijtmans L, Huigen M, Hoegen B, et al.
Genet Med
. 2022 Nov;
25(1):125-134.
PMID: 36350326
Purpose: For patients with inherited metabolic disorders (IMDs), any diagnostic delay should be avoided because early initiation of personalized treatment could prevent irreversible health damage. To improve diagnostic interpretation of...
7.
van de Loo K, Custers J, de Boer L, van Lieshout M, de Vries M, Janssen M, et al.
Orphanet J Rare Dis
. 2022 Oct;
17(1):368.
PMID: 36183138
Background: Studies regarding cognitive and mental health functioning in children with mitochondrial disease (MD) are scarce, while both are important issues given their impact on QoL. Knowledge on these aspects...
8.
Veenvliet A, Garrelfs M, Udink Ten Cate F, Ferdinandusse S, Denis S, Fuchs S, et al.
Mol Genet Metab Rep
. 2022 Jul;
31:100873.
PMID: 35782614
Isolated long-chain 3-keto-acyl CoA thiolase (LCKAT) deficiency is a rare long-chain fatty acid oxidation disorder caused by mutations in LCKAT is part of a multi-enzyme complex called the mitochondrial trifunctional...
9.
van Vliet K, van Ginkel W, Jahja R, Daly A, MacDonald A, Santra S, et al.
J Inherit Metab Dis
. 2022 Jun;
45(5):952-962.
PMID: 35722880
Tyrosinemia type 1 (TT1) and phenylketonuria (PKU) are both inborn errors of phenylalanine-tyrosine metabolism. Neurocognitive and behavioral outcomes have always featured in PKU research but received less attention in TT1...
10.
Schwantje M, Fuchs S, de Boer L, Bosch A, Cuppen I, Dekkers E, et al.
J Inherit Metab Dis
. 2022 Apr;
45(4):804-818.
PMID: 35383965
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) is included in many newborn screening (NBS) programs. Acylcarnitine-based NBS for LCHADD not only identifies LCHADD, but also the other deficiencies of the mitochondrial trifunctional...