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Metabolites|May 28, 2022
Understanding Inborn Errors of Metabolism through MetabolomicsKaren Driesen, Peter WittersACS Omega|September 29, 2025
Resolving Hexose-Phosphates by LC-MS Leads to New Insights in PGM1-CDG PathophysiologyKaren Driesen, Sam De Craemer, Eva Morava, et al.Molecular Genetics and Metabolism|January 22, 2026
Multi-omics analysis reveals ER stress as a main feature in two endothelial cell models of N-linked congenital disorders of glycosylationKaren Driesen, Veronika Holubová, Pedro Magalhães, et al.Metabolites|July 27, 2022
TraVis Pies: A Guide for Stable Isotope Metabolomics Interpretation Using an Intuitive VisualizationSam De Craemer, Karen Driesen, Bart GhesquièreMolecular Genetics and Metabolism|September 29, 2018
Central nervous involvement is common in PGM1-CDGSilvia Radenkovic, Peter Witters, Eva MoravaNutrients|November 8, 2017
Nutritional Therapies in Congenital Disorders of Glycosylation (CDG)Peter Witters, David Cassiman, Eva MoravaCardiology in the Young|September 21, 2016
A rare cause of persisting anaemia in a patient with a failing Fontan circulationLoes Lambrecht, Bjorn Cools, Peter WittersMolecular Genetics and Metabolism|March 15, 2024
Glycosphingolipids in congenital disorders of glycosylation (CDG)Andrea Jáñez Pedrayes, Daisy Rymen, Bart Ghesquière, et al.European Journal of Pediatrics|April 9, 2016
Beyond pancreatic insufficiency and liver disease in cystic fibrosisStephanie Demeyer, Kris De Boeck, Peter Witters, et al.Molecular Genetics and Metabolism Reports|June 12, 2025
Adrenal insufficiency in inborn errors of metabolism and vice versa: Case reports and review of the literatureAriane De Preter, Anne Rochtus, Peter Witters, et al.Pageof 8