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- W2018135068 abstract "Many lysosomal storage diseases are characterized by an increased urinary excretion of glycoconjugates and oligosaccharides that are characteristic for the underlying enzymatic defect. Here, we have used capillary high-performance anion-exchange chromatography (HPAEC) hyphenated to mass spectrometry to analyze free oligosaccharides from urine samples of patients suffering from the lysosomal storage disorders fucosidosis, α-mannosidosis, G(M1)-gangliosidosis, G(M2)-gangliosidosis, and sialidosis. Glycan fingerprints were registered, and the patterns of accumulated oligosaccharides were found to reflect the specific blockages of the catabolic pathway. Our analytical approach allowed structural analysis of the excreted oligosaccharides and revealed several previously unpublished oligosaccharides. In conclusion, using online coupling of HPAEC with mass spectrometric detection, our study provides characteristic urinary oligosaccharide fingerprints with diagnostic potential for lysosomal storage disorders." @default.
- W2018135068 created "2016-06-24" @default.
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- W2018135068 date "2012-04-20" @default.
- W2018135068 modified "2023-10-06" @default.
- W2018135068 title "Analysis of urinary oligosaccharides in lysosomal storage disorders by capillary high-performance anion-exchange chromatography–mass spectrometry" @default.
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- W2018135068 doi "https://doi.org/10.1007/s00216-012-5968-9" @default.
- W2018135068 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3354319" @default.
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