KETOTIC HYPOGLYCAEMIA ASSOCIATED WITH TRANSIENT BRANCHED-CHAIN AMINOACIDEMIA
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1972.tb15906.x/fullpdf
Reference33 articles.
1. FAMILIAL HYPOGLYCEMIA PRECIPITATED BY AMINO ACIDS
2. Ketotic hypoglycemia
3. Metabolism of the white blood cells in maple-syrup-urine disease
4. Intermittent Branched-Chain Ketonuria
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1. Hypoglycemia in association with various organic and amino acid disorders;Seminars in Perinatology;2000-04
2. Significance of l-Alloisoleucine in Plasma for Diagnosis of Maple Syrup Urine Disease;Clinical Chemistry;1999-10-01
3. Serum branched-chain amino acids in the diagnosis of hyperinsulinism in infancy;The Journal of Pediatrics;1980-12
4. Zur Abklärung der Hypoglykämien im Kindesalter;Klinische Pädiatrie;1980-07
5. The occurrence of 2-hydroxyisovaleric acid in patients with lactic acidosis and ketoacidosis;Clinica Chimica Acta;1977-08
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