The analysis of plasma and urinary organic acids during prolonged fasting differentiates between systemic carnitine deficiency and a defect of fatty acid oxidation
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF01810357
Reference7 articles.
1. Bartlett, K. and Gompertz, D. The specificity of glycine-N-acylase and acylglycine excretion in the organicacidaemias.Biochem. Med. 10 (1974) 15–23
2. Gregersen, N., Lauritzen, R. and Rasmussen, K. Suberylglycine excretion in the urine from a patient with dicarboxylic aciduria.Clin. Chim. Acta 70 (1976) 417–425
3. Kamerling, J. P., Brouwer, M., Ketting, D. and Wadman, S. K. Gas chromatography of urinaryN-phenylacetylglutamine.J. Chromatog. 164 (1979) 217–221
4. Mortensen, P. B. and Gregersen, N. The biological origin of ketotic dicarboxylic aciduria.In vivo andin vitro investigations of theω-oxidation of C6–C16 monocarboxylic acids in unstarved, starved and diabetic rats.Biochim. Biophys. Acta 666 (1981) 394–404
5. Pearson, D. J., Tubbs, P. K. and Chase, J. F. A. Carnitine and acylcarnitines.Methods Enzymol. 14 (1969) 1758–1771
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