Contact information
Research groups
Danielle Taylor-te Vruchte
Research Assistant in Lysosomal Storage Diseases
Recent publications
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Effects of N-Acetyl-Leucine and its enantiomers in Niemann-Pick disease type C cells
Journal article
TE VRUCHTE D. and TAYLOR-TE VRUCHTE D., (2025), ?
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Analysis of glycosphingolipids from cell lines v1
Preprint
A Priestman D. et al, (2024)
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Plasma phosphorylated-tau217 is increased in Niemann-Pick disease type C.
Journal article
Gonzalez-Ortiz F. et al, (2024), Brain Commun, 6
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Analysis of glycosphingolipids from human cerebrospinal fluid v1
Preprint
A Priestman D. et al, (2022)
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Analysis of glycosphingolipids from animal tissues v1
Preprint
A Priestman D. et al, (2022)
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Glycosphingolipid Changes in Plasma in Parkinson's Disease Independent of Glucosylceramide Levels.
Journal article
Te Vruchte D. et al, (2022), Mov Disord, 37, 2129 - 2134
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Glycosphingolipid metabolism and its role in ageing and Parkinson's disease.
Journal article
Wallom K-L. et al, (2022), Glycoconj J, 39, 39 - 53
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Annual severity increment score as a tool for stratifying patients with Niemann-Pick disease type C and for recruitment to clinical trials.
Journal article
Cortina-Borja M. et al, (2018), Orphanet J Rare Dis, 13
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NMR analysis reveals significant differences in the plasma metabolic profiles of Niemann Pick C1 patients, heterozygous carriers, and healthy controls.
Journal article
Probert F. et al, (2017), Sci Rep, 7
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A novel approach to analyze lysosomal dysfunctions through subcellular proteomics and lipidomics: the case of NPC1 deficiency.
Journal article
Tharkeshwar AK. et al, (2017), Sci Rep, 7