Discrimination of phenylketonurics from persistent hyperphenylalaninemia patients using a simple phenylalanine loading test-Reference-Cited by-同舟云学术

Discrimination of phenylketonurics from persistent hyperphenylalaninemia patients using a simple phenylalanine loading test

Published:1985-12 Issue:2 Volume:153 Page:137-142
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Blitzer Miriam G.,Bailey-Wilson Joan E.,Shapira Emmanuel

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference14 articles.

1. Phenylketonuria and hyperphenylalaninemia;Tourian,1983

2. Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood;Güttier;Acta Paediatr Scand [Suppl],1980

3. Diagnosis of phenylalanine hydroxylase deficiency (phenylketonuria);Berry;Am J Dis Child,1982

4. Serum tyrosine within the first hour after an oral load of phenylalanine;Güttler;Scand J Clin Lab Invest,1977

5. The diagnosis of phenylketonuria;O'Flynn;Am J Dis Child,1980

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1. The advantage of phenylalanine to tyrosine ratio for the early detection of phenylketonuria;Clinica Chimica Acta;1998-02

2. Rapid automated quantitation of isoleucine, leucine, tyrosine and phenylalanine from dried blood filter paper specimens;Clinica Chimica Acta;1991-12

3. Genetic analysis of treated and untreated phenylketonuria in one family.;Journal of Medical Genetics;1990-09-01

4. In vivo enzyme activity in inborn errors of metabolism;Metabolism;1990-08

5. Significant phenylalanine hydroxylation in vivo in patients with classical phenylketonuria.;Journal of Clinical Investigation;1990-07-01