Glycogen Storage Disease Type 1b: Microsomal Glucose-6-Phosphatase System in Two Patients with Different Clinical Findings
- 30 June 1983
- journal article
- research article
- Published by Springer Nature in Pediatric Research
- Vol. 17 (7) , 545-549
- https://doi.org/10.1203/00006450-198307000-00006
Abstract
Pediatric Research publishes original papers, invited reviews, and commentaries on the etiologies of diseases of children and disorders of development, extending from molecular biology to epidemiology. Use of model organisms and in vitro techniques relevant to developmental biology and medicine are acceptable, as are translational human studies.Keywords
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- Clinical and Biochemical Findings Before and After Portacaval Shunt in a Girl with Type Ib Glycogen Storage DiseasePediatric Research, 1981
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- Type Ib glycogen storage disease is caused by a defect in the glucose-6-phosphate translocase of the microsomal glucose-6-phosphatase system.Journal of Biological Chemistry, 1980
- A new variant of glycogen storage disease Type I probably due to a defect in the glucose-6-phosphate transport systemBiochemical and Biophysical Research Communications, 1978
- STUDIES OF GLYCOGEN METABOLISM IN LIVER GLYCOGEN DISEASE (VON GIERKE'S DISEASE): SIX CASES WITH SIMILAR METABOLIC ABNORMALITIES AND RESPONSES TO GLUCAGON*Journal of Clinical Investigation, 1961