Genetic Defects of Amino Acid Metabolism

Author:

Nyhan William L.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference92 articles.

1. Neuropathological Findings in Phenylpyruvic Oligophrenia (Phenylketonuria);Alvord;J. Neuropath. & Exper. Neurol.,1950

2. Identification of Heterozygotes with Phenylketonuria on Basis of Tyrosine Response;Anderson;J. Pediat.,1962

3. Phenylketonuria. VIII. Relation between Age, Serum Phenylalanine Level and Phenylpyruvic Acid Excretion;Armstrong;Proc. Soc. Exper. Biol. & Med.,1957

4. Studies on Phenylketonuria. II. The Excretion of o-Hydroxyphenylacetic Acid in Phenylketonuria;Armstrong;J. Biol. Chem.,1955

5. Studies on Phenylketonuria. I. Restricted Phenylalanine Intake in Phenylketonuria;Armstrong;J. Clin. Invest.,1955

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The Aminoacidurias;Pediatric Clinics of North America;1967-11

2. Fenilcetonúria: estudo clínico e mediante biópsia cerebral;Arquivos de Neuro-Psiquiatria;1967-03

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