Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European study on glycogen storage disease type I (ESGSD I)
- 1 October 2002
- journal article
- research article
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 161 (1), S20-S34
- https://doi.org/10.1007/bf02679990
Abstract
No abstract availableKeywords
This publication has 77 references indexed in Scilit:
- Increased lipogenesis and resistance of lipoproteins to oxidative modification in two patients with glycogen storage disease type 1aThe Journal of Pediatrics, 2002
- Direct Evidence for the Involvement of Two Glucose 6-Phosphate-binding Sites in the Glucose-6-phosphatase Activity of Intact Liver MicrosomesPublished by Elsevier ,1998
- The Gene for Glycogen-Storage Disease Type 1b Maps to Chromosome 11q23American Journal of Human Genetics, 1998
- Glycogen storage disease I and hepatocellular tumoursEuropean Journal of Pediatrics, 1993
- Type I glycogen storage disease: Kidney involvement, pathogenesis and its treatmentPediatric Nephrology, 1991
- Hyperfiltration and renal disease in glycogen storage disease, type IKidney International, 1989
- The Serum Apolipoprotein Profile of Patients with Glucose-6-Phosphatase DeficiencyPediatric Research, 1985
- Cornstarch Therapy in Type I Glycogen-Storage DiseaseNew England Journal of Medicine, 1984
- On the involvement of a glucose 6-phosphate transport system in the function of microsomal glucose 6-phosphataseMolecular and Cellular Biochemistry, 1975
- Effect of Diet on Iron Absorption in Iron-deficient RatsJournal of Nutrition, 1971