Man made disease: Clinical manifestations of low phenylalanine levels in an inadequately treated phenylketonuria patient and mouse study-Reference-Cited by-同舟云学术

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Man made disease: Clinical manifestations of low phenylalanine levels in an inadequately treated phenylketonuria patient and mouse study

Published:2013 Issue: Volume:110 Page:S66-S70
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Pode-Shakked Ben,Shemer-Meiri Lilach,Harmelin Alon,Stettner Noa,Brenner Ori,Abraham Smadar,Schwartz Gerard,Anikster Yair

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference15 articles.

1. Dietary and biochemical control of phenylketonuria;Brimblecombe;Br. Med. J.,1961

2. Phenylalanine deficiency syndrome;Rouse;J. Pediatr.,1966

3. Malnutrition caused by dietary treatment of phenylketonuria;Hanley;Pediatr. Res.,1970

4. Effect of phenylalanine deficient diet on bone marrow and amino acid metabolism;Cockburn;Exp. Biol. Med.,1965

5. Phenylalanine–tyrosine deficiency syndrome as a complication of the management of hereditary tyrosinemia;Cohn;Am. J. Clin. Nutr.,1977

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