Martin T. Vervaart
Amsterdam, NH, Netherlands
Last Updated: 09/26/2026
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Found 11 publications
Discovery of novel diagnostic biomarkers for Sjögren-Larsson syndrome by untargeted lipidomics.
Journal: Biochimica et biophysica acta. Molecular and cell biology of lipids
Published: October 03, 2023
A conserved complex lipid signature marks human muscle aging and responds to short-term exercise.
Journal: Nature aging
Published: December 23, 2022
An improved functional assay in blood spot to diagnose Barth syndrome using the monolysocardiolipin/cardiolipin ratio.
Journal: Journal of inherited metabolic disease
Published: June 29, 2021
Metabolomics and lipidomics in Caenorhabditis elegans using a single-sample preparation.
Journal: Disease models & mechanisms
Published: October 13, 2020
Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia.
Journal: Brain : a journal of neurology
Published: February 02, 2019
Plasma lipidomics as a diagnostic tool for peroxisomal disorders.
Journal: Journal of inherited metabolic disease
Published: August 16, 2017
Functional characterisation of peroxisomal β-oxidation disorders in fibroblasts using lipidomics.
Journal: Journal of inherited metabolic disease
Published: May 25, 2017
A sensitive mass spectrometry platform identifies metabolic changes of life history traits in C. elegans.
Journal: Scientific reports
Published: November 10, 2016
Lipidomic analysis of fibroblasts from Zellweger spectrum disorder patients identifies disease-specific phospholipid ratios.
Journal: Journal of lipid research
Published: February 26, 2016
Defining functional classes of Barth syndrome mutation in humans.
Journal: Human molecular genetics
Published: January 12, 2016
Showing 1-11 of 11
Last Updated: 09/26/2026