Irene W. Keularts-Korver
Maastricht, LI, Netherlands
Last Updated: 09/26/2026
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Found 13 publications
Liberal versus restrictive transfusion in haemato-oncological patients undergoing autologous stem cell transplantation: A single-centre experience.
Journal: Transfusion medicine (Oxford, England)
Published: December 16, 2025
Clinical evaluation of red cell concentrates in non-DEHP plasticized containers compared with standard DEHP plasticized containers: A quasi-randomized observational multicentre study.
Journal: Vox sanguinis
Published: December 12, 2024
Diagnosing, discarding, or de-VUSsing: A practical guide to (un)targeted metabolomics as variant-transcending functional tests.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 04, 2022
Identification of Δ-1-pyrroline-5-carboxylate derived biomarkers for hyperprolinemia type II.
Journal: Communications biology
Published: April 06, 2022
Targeted urine metabolomics with a graphical reporting tool for rapid diagnosis of inborn errors of metabolism.
Journal: Journal of inherited metabolic disease
Published: February 08, 2021
Impaired iloprost-induced platelet inhibition and phosphoproteome changes in patients with confirmed pseudohypoparathyroidism type Ia, linked to genetic mutations in GNAS.
Journal: Scientific reports
Published: February 07, 2020
Monitoring phenylalanine concentrations in the follow-up of phenylketonuria patients: An inventory of pre-analytical and analytical variation.
Journal: JIMD reports
Published: February 01, 2020
Fast and accurate quantitative organic acid analysis with LC-QTOF/MS facilitates screening of patients for inborn errors of metabolism.
Journal: Journal of inherited metabolic disease
Published: August 29, 2017
Allelic Expression Imbalance Promoting a Mutant PEX6 Allele Causes Zellweger Spectrum Disorder.
Journal: American journal of human genetics
Published: August 18, 2017
Neurocognitive outcome in tyrosinemia type 1 patients compared to healthy controls.
Journal: Orphanet journal of rare diseases
Published: December 23, 2015
Two Novel Mutations in the SLC25A4 Gene in a Patient with Mitochondrial Myopathy.
Journal: JIMD reports
Published: May 20, 2014
Last Updated: 09/26/2026