Disturbed lipid metabolism in glycogen storage disease type 1
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/BF02679998.pdf
Reference42 articles.
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2. Binkiewicz A, Senior B (1973) Decreased ketogenesis in von Gierke's disease (type I glycogenosis). J Pediatr 83: 973–978
3. Brown AM, Wiggins D, Gibbons GF (1999) Glucose phosphorylation is essential for the turnover of neutral lipid and the second stage assembly of triacylglycerol-rich ApoB-containing lipoproteins in primary hepatocyte cultures. Arterioscler Thromb Vasc Biol 19: 321–329
4. Chen YT, Cornblath M, Sidbury JB (1984) Cornstarch therapy in type I glycogen-storage disease. N Engl J Med 310: 171–175
5. Doiron B, Cuif MH, Chen R, Kahn A (1996) Transcriptional glucose signaling through the glucose response element is mediated by the pentose phosphate pathway. J Biol Chem 271: 5321–5324
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