Peter Witters-Wang
Leuven, VLG 3000, Belgium
Last Updated: 09/26/2026
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Found 90 publications
Multi-omics analysis reveals ER stress as a main feature in two endothelial cell models of N-linked congenital disorders of glycosylation.
Journal: Molecular genetics and metabolism
Published: November 10, 2025
Classic galactosemia in the differential diagnosis of neonatal low gammaglutamyltransferase cholestasis.
Journal: Acta gastro-enterologica Belgica
Published: October 13, 2025
The complexome contextualizes proteomics data to fingerprint biological states and highlight perturbed functional modules in disease.
Journal: NPJ systems biology and applications
Published: September 07, 2025
Hearing rehabilitation in SERAC1 related MEGD(H)EL syndrome - implications from a multi-center retrospective cohort study.
Journal: Molecular genetics and metabolism
Published: May 31, 2025
Long-Term Safety and Clinical Outcomes With Olipudase Alfa Enzyme Replacement Therapy in Children and Adolescents With Acid Sphingomyelinase Deficiency.
Journal: Journal of inherited metabolic disease
Published: May 06, 2025
Adrenal insufficiency in inborn errors of metabolism and vice versa: Case reports and review of the literature.
Journal: Molecular genetics and metabolism reports
Published: February 06, 2025
Glycosphingolipid synthesis is impaired in SLC35A2-CDG and improves with galactose supplementation.
Journal: Cellular and molecular life sciences : CMLS
Published: February 06, 2025
Rare disorders, big challenges: Special issue on congenital disorders of glycosylation.
Journal: Molecular genetics and metabolism
Published: January 19, 2025
An unusual case of neuroblastoma presenting with prolonged watery diarrhea in a pediatric patient.
Journal: Biochemia medica
Published: November 05, 2024
Clinical severity and cardiac phenotype in phosphomannomutase 2-congenital disorders of glycosylation : Insights into genetics and management recommendations.
Journal: Journal of inherited metabolic disease
Published: July 02, 2024
Frontiers in congenital disorders of glycosylation consortium, a cross-sectional study report at year 5 of 280 individuals in the natural history cohort.
Journal: Molecular genetics and metabolism
Published: April 15, 2024
Quality of life in children with erythropoietic protoporphyria: a case-control study.
Journal: The Journal of dermatology
Published: April 15, 2024
Last Updated: 09/26/2026