(Q41931497)

14 October 2017

An inborn defect in the metabolism of tyrosine in infants on a normal diet (English)

1 reference

14 October 2017

Bloxam HR

1

1 reference

14 October 2017

Day MG

series ordinal

2

1 reference

14 October 2017

Gibbs NK

series ordinal

3

1 reference

14 October 2017

Woolf LI

series ordinal

4

1 reference

14 October 2017

language of work or name

English

0 references

publication date

1 November 1960

1 reference

14 October 2017

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14 October 2017

77

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14 October 2017

2

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14 October 2017

320-326

1 reference

A new error of tyrosine metabolism: tyrosinosis. The intermediary metabolism of tyrosine and phenylalanine

14 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1204987

THE METABOLISM OF l-TYROSINE IN INFANTILE SCURVY.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1204987

A DEFECT IN THE METABOLISM OF TYROSINE AND PHENYLALANINE IN PREMATURE INFANTS. III. DEMONSTRATION OF THE IRREVERSIBLE CONVERSION OF PHENYLALANINE TO TYROSINE IN THE HUMAN ORGANISM.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1204987

A DEFECT IN THE METABOLISM OF TYROSINE AND PHENYLALANINE IN PREMATURE INFANTS. II. SPONTANEOUS OCCURRENCE AND ERADICATION BY VITAMIN C.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1204987

A DEFECT IN THE METABOLISM OF TYROSINE AND PHENYLALANINE IN PREMATURE INFANTS. I. IDENTIFICATION AND ASSAY OF INTERMEDIARY PRODUCTS.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1204987

The oxidation in liver of l-tyrosine to acetoacetate through p-hydroxyphenylpyruvate and homogentisic acid

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1204987

The metabolism of tyrosine and phenylalanine in premature infants; the effect of large doses

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1204987

Studies on sulphatases. 23. The enzymic desulphation of tyrosine O-sulphate

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1204987

Certain aspects of tyrosine metabolism in the young. II. The tyrosine oxidizing system of fetal rat liver

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1204987

Certain aspects of tyrosine metabolism in the young. I. The development of the tyrosine oxidizing system in human liver

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1204987

The phenolic acids of human urine; paper chromatography of phenolic acids

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1204987

Excretion of rho-oxyphenylacetic acid after administration rho-oxyphenylpyruvic acid in the guinea pig

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1204987

Synthesis of 35S-labelled arylsulphates byintact animals and by tissue preparations, with particular reference to L-tyrosine O-sulphate

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1204987

Tests for phenylketonuria: results of a one-year programme for its detection in infancy and among mental defectives.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1204987

Maple syrup urine disease; an inborn error of the metabolism of valine, leucine, and isoleucine associated with gross mental deficiency.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1204987

On the excretion of indole derivatives in phenylketonuria.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1204987

A DEFECT IN THE METABOLISM OF AROMATIC AMINO ACIDS IN PREMATURE INFANTS: THE ROLE OF VITAMIN C

18 August 2018

1 reference

12 December 2020

THE CONTROL OF EXPERIMENTAL ALCAPTONURIA BY MEANS OF VITAMIN C

1 reference

12 December 2020

The tyrosine oxidation system of liver. IV. Studies on the inhibition of p-hydroxyphenylpyruvic acid oxidase by excess substrate

1 reference

12 December 2020

Tyrosine-O-sulfate as a constituent of normal human urine

1 reference

12 December 2020

Paper chromatography of urinary indoles

1 reference

12 December 2020

Tryptophan peroxidase-oxidase, histidase, and transaminase activity in the liver of the developing rat

1 reference

12 December 2020

Development of phenylalanine hydroxylase in mammalian liver

1 reference

12 December 2020

Development of phenylalanine hydroxylase in liver of the rat

1 reference

12 December 2020

The urinary excretion of amino acids and sugars in early infancy

1 reference

12 December 2020

Estimation of Phenylpyruvic Acid

1 reference

12 December 2020

[Urinary excretion of p-oxyphenylpyruvic acid, pyruvic acid, phenol and diacetic acid following intake of p-oxyphenylpyruvic acid in the normal state and in liver disease.]

1 reference

12 December 2020

Identifiers

DOI

10.1042/BJ0770320

1 reference

14 October 2017

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14 October 2017

1 reference