DICARBOXYLIC ACIDURIA DURING KETOTIC PHASES IN VARIOUS TYPES OF GLYCOGEN STORAGE DISEASE
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1981.tb16557.x/fullpdf
Reference15 articles.
1. Ketosis in Hepatic Glycogenosis
2. Urinary excretion of C6–C10 dicarboxylic acids in glycogen storage disease types I and III
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Improvements of hypertriglyceridemia and hyperlacticemia in Japanese children with glycogen storage disease type Ia by medium-chain triglyceride milk;European Journal of Pediatrics;2007-01-06
2. Dicarboxylicaciduria and secondary carnitine deficiency in glycogenosis type IV.;Archives of Disease in Childhood;1987-10-01
3. DICARBOXYLIC ACIDURIA DUE TO MEDIUM CHAIN ACYL CoA DEHYDROGENASE DEFECT.;Acta Paediatrica;1983-11
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