Tolerance of Phenylalanine after Intravenous Administration in Phenylketonurics, Heterozygous Carriers, and Normal Adults-Reference-Cited by-同舟云学术

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Tolerance of Phenylalanine after Intravenous Administration in Phenylketonurics, Heterozygous Carriers, and Normal Adults

Published:1966-03 Issue:5028 Volume:209 Page:1148-1149
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

BREMER H. J.,NEUMANN W.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/2091148a0.pdf

Reference7 articles.

1. Dost, F. H., Der Blutspiegel. Kinetik der Konzentrationsabläufe (Leipzig, 1953).

2. Hsia, D. Y. Y., and Paine, R. S., J. Ment. Defic. Res., 1, 53 (1957).

3. Berry, H., Sutherland, B., and Guest, G. M., Amer. J. Hum. Genet., 9, 310 (1957).

4. Nelson, E., Nature, 205, 1024 (1965).

5. La Du, B. N., Howell, R. R., Michael, P. J., and Sober, E. K., Pediatrics, 31, 39 (1963).

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1. Heterozygous carriers in the relatives of a case of phenylketonuria;Hereditas;2009-02-12

2. Contribution of genetic factors to neonatal transient hypothyroidism;Archives of Disease in Childhood - Fetal and Neonatal Edition;2005-01-01

3. The investigation of inborn errors in vivo using stable isotopes;European Journal of Pediatrics;1994-01

4. Techniques for studying hepatic metabolismin vivo;Journal of Inherited Metabolic Disease;1991-07

5. Plasma amino acid concentrations and amino acid ratios in normal adults and adults heterozygous for phenylketonuria ingesting a hamburger and milk shake meal;The American Journal of Clinical Nutrition;1991-03-01

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