Type I Glycogen Storage Disease: A Metabolic Basis for Advances In Treatment
Top Cited Papers
- 28 November 2022
- journal article
- review article
- Published by Elsevier in Advances in Pediatrics
- Vol. 26 (1) , 63-92
- https://doi.org/10.1016/s0065-3101(22)00671-5
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- Abnormalities of Cell-Membrane Fluidity in the Pathogenesis of DiseaseNew England Journal of Medicine, 1977
- Glycogen metabolism: The integrated cellular response to a bi-directional metabolic stimulusBiochemical and Biophysical Research Communications, 1977
- Glycogen synthase-“R”: The occurrence and significance of a previously unknown form of GS, found in metabolically active human leucocytesBiochemical and Biophysical Research Communications, 1977
- Comparison of the effects of total parenteral nutrition, continuous intragastric feeding, and portacaval shunt on a patient with type I glycogen storage diseaseThe Journal of Pediatrics, 1974
- Impaired platelet function in glucose-6-phosphatase deficiencyThe Journal of Pediatrics, 1974
- Studies in Type I glycogenosis of the liver: The genesis and disposition of lactateThe Journal of Pediatrics, 1974
- Decreased ketogenesis in von Gierke's disease (Type I glycogenosis)The Journal of Pediatrics, 1973
- Studies of uric acid metabolism in glycogen storage disease associated with gouty arthritisArthritis & Rheumatism, 1967
- The interrelationship of glycogen storage disease and goutArthritis & Rheumatism, 1965
- Phosphofructokinase deficiency in skeletal muscle. A new type of glycogenosisBiochemical and Biophysical Research Communications, 1965