Intestinal absorption in type I glycogen storage disease
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference15 articles.
1. Glucose-6-phosphatase of the liver in glycogen storage disease;Cori;J. Biol. Chem.,1952
2. Liver and kidney glucose-6-phosphatase activity in children with normal and diseased organs;Harris;J. Clin. Invest.,1954
3. Studies in glycogen storage disease. I. Intestinal glucose-6-phosphatase activity in patients with von Gierke's disease and their parents;Fields;J. Clin. Invest.,1965
4. The photometric microdetermination of blood glucose with glucose oxidase;Saifer;J. Lab. & Clin. Med.,1958
5. A submicrodetermination of glucose;Park;J. Biol. Chem.,1949
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1. Effect of VSL#3 Probiotic in a Patient with Glycogen Storage Disease Type Ia and Irritable Bowel Disease-like Disease;Probiotics and Antimicrobial Proteins;2018-02-13
2. Lessons from new mouse models of glycogen storage disease type 1a in relation to the time course and organ specificity of the disease;Journal of Inherited Metabolic Disease;2014-08-28
3. Glycogenosis type I – Von Gierke disease;Atlas of Inherited Metabolic Diseases 3E;2011-12-30
4. Glycogenosis type I – Von Gierke disease;Atlas of Metabolic Diseases Second edition;2005-08-26
5. Intestinal glucose transport: Evidence for a membrane traffic–based pathway in humans;Gastroenterology;2003-01
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