(Q71397004)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7439194%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

title

Diagnostic value of orotic acid excretion in heritable disorders of the urea cycle and in hyperammonemia due to organic acidurias (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7439194%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

author name string

C Bachmann

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7439194%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

J P Colombo

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7439194%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

publication date

1 August 1980

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7439194%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Pediatrics

18 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7439194%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

volume

134

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18 October 2019

issue

2

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18 October 2019

page(s)

109-113

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https://scigraph.springernature.com/pub.10.1007/bf01846026

18 October 2019

exact match

0 references

cites work

Propionic acidemia and hyperlysinemia in a case with ornithine transcarbamylase (OTC) deficiency

1 reference

12 December 2020

Enzymatic synthesis of acetylglutamate by mammalian liver preparations and its stimulation by arginine

1 reference

12 December 2020

Treatment of Carbamyl Phosphate Synthetase Deficiency with Keto Analogues of Essential Amino Acids

1 reference

12 December 2020

Evidence for x-linked dominant inheritance of ornithine transcarbamylase deficiency

1 reference

12 December 2020

1 reference

12 December 2020

Hereditary metabolic disorders of the urea cycle

1 reference

12 December 2020

Comparison of plasma creatinine determined with the Greiner Selective Analyser GSA II and the glomerular filtration rate.

1 reference

12 December 2020

New pathways of nitrogen excretion in inborn errors of urea synthesis

1 reference

12 December 2020

Metabolic and genetic studies of a family with ornithine transcarbamylase deficiency

1 reference

12 December 2020

Variants of citrullinaemia

1 reference

12 December 2020

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

1 reference

12 December 2020

X-chromosome inactivation in human liver: confirmation of X-linkage of ornithine transcarbamylase

1 reference

12 December 2020

The simulation of the urea cycle: correlation of effects due to inborn errors in the catalytic properties of the enzymes with clinical-biochemical observations

1 reference

12 December 2020

Effect of propionate and pyruvate on citrulline synthesis and ATP content in rat liver mitochondria

1 reference

12 December 2020

Detection of female carriers of ornithine-carbamyl-transferase deficiency by measurement of orotic acid in the urine

1 reference

12 December 2020

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

1 reference

12 December 2020

Short chain fatty acids in plasma and brain: Quantitative determination by gas chromatography

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01846026

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7439194%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

1 reference