Acta Paediatrica · 1997 · 48 citations · 14 references
Life SciencesBiochemistryNutritional SciencesCarbohydrate BiochemistryClinical NutritionHuman NutritionCarbohydrate MetabolismCarbohydrate Metabolism DisordersGalactose MetabolismMalabsorption SyndromesProtein GlycosylationCarbohydrate-deficient TransferrinClassical GalactosemiaGalactose AvailabilityGalactose Metabolic DisordersGalactose-1-phosphate Uridylyltransferase DeficiencyInborn Errors Of Galactose MetabolismMetabolic Consequences Of GalactosemiaTransferrin Deficiency
Carbohydrate-deficient isoforms of transferrin (CDT) were examined in Guthrie cards from patients with galactosaemia before and during dietary treatment for up to 9 y. In untreated patients the CDT values were elevated due to abnormal asialo- and/or disialotransferrin. During treatment, the CDT levels were normal except on a few temporary occasions. Galactose or its close metabolites did not inhibit two relevant glycosyltransferases in vitro, and their levels were not correlated to the CDT values. The transferrin isoform changes in untreated patients were similar to, but less pronounced than in CDG syndrome type I.
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A community‐based prospective incidence study of epileptic seizures in children
Ragnar Sidenvall, Lars Forsgren, Hans K son Blomquist et al. · Acta Paediatrica · 1993 · 145 citations
Medicine, Child Health, Pediatrics +13
Deficit of uridine diphosphate galactose in galactosaemia
W.G. Ng, Y Xu, Francine Kaufman et al. · Journal of Inherited Metabolic Disease · 1989 · 106 citations