Author:
Leonard J. V.,Heales S. J. R.
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Reference14 articles.
1. Bremer HJ, Neumann W (1966) Tolerance of phenylalanine after intravenous administration in phenylketonurias, heterozygous carriers and normal adults. Nature 209:1148–1149
2. Clarke JTR, Bier DM (1982) The conversion of phenylalanine to tyrosine in man. Direct measurement by continuous intravenous tracer infusions of L-[2H5] phenylalanine and L-[1-13C] tyrosine in the post absorptive state. Metab Clin Exp 31:999–1005
3. Heales SJR, Leonard JV, Halliday D, Thompson GN (1991) In vivo oxidation of octanoate in medium chain Acyl CoA dehydrogenase deficiency. Abstracts of the 29th SSIEM Annual Symposium (London) SSIEM, Pinner, p 59
4. Lehmann WD, Theobald N, Heinrich HC, Clemens P, Gruttner R (1984) Detection of heterozygous carriers of phenylketonuria by a L-[2H5] phenylalanine stable isotope loading test. Clin Chim Acta 138:59–71
5. Matthews DE, Young RD, Bier DM, Young VR (1985) What is whole body alanine when studied with labelled alanine tracers? In: Garrow JS, Halliday D (eds) Substrate and energy metabolism in man. J Libbey, London, pp 187–193
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