Type I glycogen storage disease: Nine years of management with cornstarch
- 1 January 1993
- journal article
- research article
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 152 (1) , 56-59
- https://doi.org/10.1007/bf02072090
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Glucose therapy for glycogenosis type 1 in infants: Comparison of intermittent uncooked cornstarch and continuous overnight glucose feedingsThe Journal of Pediatrics, 1990
- Glycogen Storage Disease Type I and III and Pyruvate Carboxylase Deficiency: Results of Long‐Term Treatment with Uncooked CornstarchActa Paediatrica, 1988
- Phytate in FoodsPublished by S. Karger AG ,1986
- Long‐term cornstarch therapy in glycogen storage disease types I, Ib and IIIJournal of Inherited Metabolic Disease, 1986
- Management of postoperative nesidioblastosis with zinc protamine glucagon and oral starchThe Journal of Pediatrics, 1986
- The Dietary Treatment of Children with Type I Glycogen Storage Disease with Slow Release CarbohydratePediatric Research, 1984
- Cornstarch Therapy in Type I Glycogen-Storage DiseaseNew England Journal of Medicine, 1984
- Effects of Changes in Cell Size and Ouabain Sensitive Respiration on Development of Brown Adipose Tissue Thermogenesis in the RabbitPediatric Research, 1983
- Continuous Nocturnal Intragastric Feeding for Management of Type 1 Glycogen-Storage DiseaseNew England Journal of Medicine, 1976
- Standards for Children's Height at Ages 2-9 Years Allowing for Height of ParentsArchives of Disease in Childhood, 1970