Walinka Van Tol
Nijmegen, GE 6525GA, Netherlands
Last Updated: 09/26/2026
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Found 8 publications
Dynamic tracing of sugar metabolism reveals the mechanisms of action of synthetic sugar analogs.
Journal: Glycobiology
Published: February 23, 2021
A mutation in mannose-phosphate-dolichol utilization defect 1 reveals clinical symptoms of congenital disorders of glycosylation type I and dystroglycanopathy.
Journal: JIMD reports
Published: April 09, 2019
Cytidine Diphosphate-Ribitol Analysis for Diagnostics and Treatment Monitoring of Cytidine Diphosphate-l-Ribitol Pyrophosphorylase A Muscular Dystrophy.
Journal: Clinical chemistry
Published: April 09, 2019
Toward understanding tissue-specific symptoms in dolichol-phosphate-mannose synthesis disorders; insight from DPM3-CDG.
Journal: Journal of inherited metabolic disease
Published: February 01, 2019
O-glycosylation disorders pave the road for understanding the complex human O-glycosylation machinery.
Journal: Current opinion in structural biology
Published: September 28, 2018
Corrigendum to "A homozygous DPM3 mutation in a patient with alpha-dystroglycan-related limb girdle muscular dystrophy" [Neuromuscular disorders 27/11 (2017) 1043-1046].
Journal: Neuromuscular disorders : NMD
Published: December 17, 2017
A homozygous DPM3 mutation in a patient with alpha-dystroglycan-related limb girdle muscular dystrophy.
Journal: Neuromuscular disorders : NMD
Published: April 19, 2017
Human ISPD Is a Cytidyltransferase Required for Dystroglycan O-Mannosylation.
Journal: Chemistry & biology
Published: June 30, 2015
Showing 1-8 of 8
Last Updated: 09/26/2026