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Researcher
Peter Witters
- Disciplines:Laboratory medicine, Palliative care and end-of-life care, Regenerative medicine, Other basic sciences, Other health sciences, Nursing, Other paramedical sciences, Other translational sciences, Other medical and health sciences
Affiliations
- Woman and Child (Division)
Member
From1 Oct 2014 → Today - Hepatology (Division)
Member
From1 Oct 2006 → 30 Sep 2010
Projects
1 - 10 of 11
- Reconstruction and Computational Modelling for Inherited Metabolic DiseasesFrom1 Jun 2023 → TodayFunding: HORIZON.2.1 - Health
- A novel hybrid metabolomics platform combining the power of gas chromatography separation with highresolution, high-accuracy mass spectrometry of full precursor masses.From1 May 2022 → TodayFunding: FWO Medium Size Research Infrastructure
- Towards treatments of Congenital Disorders of GlycosylationFrom1 Oct 2021 → TodayFunding: FWO fundamental clinical research fellowship
- Metabolomics as a tool for developing therapies in an endothelial cell model of congenital disorders of glycosylationFrom20 Sep 2021 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- The endothelium is a central mediator of cystic fibrosis lung diseaseFrom20 Nov 2020 → 24 May 2022Funding: Own budget, for example: patrimony, inscription fees, gifts
- Studying congenital disorders of glycosylation and their potential treatments using tracer metabolomicsFrom24 Sep 2020 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Vascular & immune microenvironments in patients with CF-associated liver disease.From3 Sep 2020 → 31 Aug 2023Funding: Other federal public and semi-governmental institutions
- Galactose rewires metabolism in the treatment of congenital disorders of glycosylation.From1 Jan 2020 → 31 Dec 2023Funding: FWO research project (including WEAVE projects)
- Mapping and treating metabolic rewiring in mitochondrial diseaseFrom1 Oct 2018 → 13 Jan 2023Funding: Own budget, for example: patrimony, inscription fees, gifts
- DE ROL VAN HET ENDOTHEEL IN MUCOVISCIDOSE GEASSOCIEERDE LEVERZIEKTEFrom1 Dec 2017 → 24 Nov 2021Funding: Own budget, for example: patrimony, inscription fees, gifts
Publications
31 - 40 of 95
- Use of a mobile application for self-management of pancreatic enzyme replacement therapy is associated with improved gastro-intestinal related quality of life in children with Cystic Fibrosis(2020)
Authors: Mieke Boon, Peter Witters, Christiane De Boeck
Pages: 562 - 568 - Novel GAA Variants and Mosaicism in Pompe Disease Identified by Extended Analyses of Patients with an Incomplete DNA Diagnosis(2020)
Authors: David Cassiman, Peter Witters
Pages: 337 - 348 - Clinical and biochemical improvement with galactose supplementation in SLC35A2-CDG(2020)
Authors: Peter Witters
Pages: 1102 - 1107 - Efficacy and safety of D,L-3-hydroxybutyrate (D,L-3-HB) treatment in multiple acyl-CoA dehydrogenase deficiency(2020)
Authors: Peter Witters
Pages: 908 - 916 - RANGE OF NORMAL LIVER STIFFNESS AND FACTORS ASSOCIATED WITH INCREASED STIFFNESS MEASUREMENTS IN APPARENTLY HEALTHY CHILDREN: AN INDIVIDUAL PATIENT DATA META-ANALYSIS(2020)
Authors: Darrick K Li, Muhammad Rehan Khan, Katryn Furuya, Luz Helena Gutierrez Sanchez, Zhen Wang, Mohammad Murad, Ulrike Teufel, Guido Engelmann, Grant A Ramm, Peter J Lewindon, et al.
Pages: S606 - S607 - Two cases of non-alcoholic fatty liver disease caused by biallelic ABHD5 mutations(2020)
Authors: Isabelle Adant, Mathias Declercq, Matthew Bird, Nancy Boeckx, Koenraad Devriendt, David Cassiman, Peter Witters
Pages: 1030 - 1032 - Consensus guideline for the diagnosis and management of mannose phosphate isomerase-congenital disorder of glycosylation (MPI-CDG)(2020)
Authors: Silvia Radenkovic, Peter Witters
Pages: 671 - 693 - Congenital Extrahepatic Portosystemic Shunts (Abernethy Malformation): An International Observational Study(2020)
Authors: Frederik Nevens, Peter Witters, Wim Laleman
Pages: 658 - 669 - Therapeutic approaches in Congenital Disorders of Glycosylation (CDG) involving N-linked glycosylation: an update(2020)
Authors: Peter Witters, Eva Morava
Pages: 268 - 279 - Hypoglycemia in CDG patients due to PMM2 mutations: Follow up on hyperinsulinemic patients.(2020)
Authors: Peter Witters
Pages: 76 - 81