(Q36062035)

11 August 2017

Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child (English)

1 reference

11 August 2017

Levin B

1

1 reference

11 August 2017

Abraham JM

series ordinal

2

1 reference

11 August 2017

Oberholzer VG

series ordinal

3

1 reference

11 August 2017

Burgess EA

series ordinal

4

1 reference

11 August 2017

language of work or name

English

0 references

publication date

1 April 1969

1 reference

Archives of Disease in Childhood

11 August 2017

1 reference

11 August 2017

44

1 reference

11 August 2017

234

1 reference

11 August 2017

152-161

1 reference

Argininosuccinic Aciduria: An Inborn Error of Amino Acid Metabolism

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020046

Comparative biochemistry of urea synthesis. I. Methods for the quantitative assay of urea cycle enzymes in liver

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020046

L-Lysine dehydrogenase deficiency in a patient with congenital lysine intolerance

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020046

THE RENAL EXCRETION OF HYDROGEN IONS IN INFANTS AND CHILDREN.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020046

Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020046

A disease, probably hereditary characterised by severe mental deficiency and a constant gross abnormality of aminoacid metabolism.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020046

Protein intolerance with deficient transport of basic aminoacids. Another inborn error of metabolism

23 September 2018

1 reference

12 December 2020

Treatment of hyperammonemia

1 reference

12 December 2020

Arginosuccine aciduria

1 reference

12 December 2020

The free amino acids of human blood plasma

1 reference

12 December 2020

The estimation of plasma ammonia by ion exchange

1 reference

12 December 2020

Hyperammonaemia. A new instance of an inborn enzymatic defect of the biosynthesis of urea

1 reference

12 December 2020

1 reference

12 December 2020

A SIMPLE METHOD FOR THE QUANTITATIVE DETERMINATION OF URINARY PSEUDOURIDINE AND SOME NEW ULTRAVIOLET-ABSORBING METABOLITES

1 reference

12 December 2020

Identifiers

DOI

10.1136/ADC.44.234.152

1 reference

11 August 2017

1 reference

11 August 2017

PubMed publication ID

5779426

1 reference