(Q67353674)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:668733%20AND%20SRC:MED&resulttype=core&format=json

12 September 2019

title

Attempted dietary treatment of a boy with hyperammonemia due to ornithine transferase deficiency (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:668733%20AND%20SRC:MED&resulttype=core&format=json

ornithine carbamoyltransferase deficiency

12 September 2019

main subject

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A668733

19 July 2022

author name string

C. van der Heiden

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A668733

19 July 2022

H. D. Bakker

2

1 reference

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19 July 2022

J. Desplanque

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A668733

19 July 2022

M. Brink

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A668733

19 July 2022

P. K. de Bree

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A668733

19 July 2022

S. K. Wadman

6

1 reference

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19 July 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=668733

19 July 2022

publication date

1 July 1978

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:668733%20AND%20SRC:MED&resulttype=core&format=json

12 September 2019

19 July 1978

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=668733

European Journal of Pediatrics

19 July 2022

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:668733%20AND%20SRC:MED&resulttype=core&format=json

12 September 2019

volume

128

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:668733%20AND%20SRC:MED&resulttype=core&format=json

12 September 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:668733%20AND%20SRC:MED&resulttype=core&format=json

12 September 2019

page(s)

261-272

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:668733%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00445611

12 September 2019

exact match

0 references

cites work

Hyperammonaemia due to ornithine transcarbamylase deficiency

1 reference

12 December 2020

Hyperammonemia due to a defect in hepatic ornithine transcarbamylase

1 reference

12 December 2020

Rapid, high-resolution, two-dimensional amino acid chromatography on micro scale chromatograms

1 reference

12 December 2020

Direct determination of ammonium in blood and tissue extracts by means of the phenol by chlorite reaction

1 reference

12 December 2020

Biochemical investigations of hyperammonaemia

1 reference

12 December 2020

Urinary excretion of 3 -methylxanthine and related compounds in children

1 reference

12 December 2020

Chronic hyperammonemia with orotic aciduria: evidence of pyrimidine pathway stimulation (author's transl)

1 reference

12 December 2020

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

1 reference

12 December 2020

Arginosuccinicaciduria. The hair abnormality

1 reference

12 December 2020

Evidence for x-linked dominant inheritance of ornithine transcarbamylase deficiency

1 reference

12 December 2020

The therapy of hyperammonemia due to ornithine transcarbamylase defiency in a male neonate

1 reference

12 December 2020

Saccharopine cleavage by a dehydrogenase of human liver.

1 reference

12 December 2020

Hereditary ornithine-carbamyl-transferase deficiency with qualitative enzyme abnormality. Report of a form with neonatal revelation and fatal course in a boy

1 reference

12 December 2020

Clinical and biochemical studies on periodic hyperammonemia with hyperlysinemia and homocitrullinuria

1 reference

12 December 2020

N-EPSILON-(CARBOXYMETHYL)LYSINE, A CONSTITUENT OF HUMAN URINE

1 reference

12 December 2020

Ornithine transcarbamylase deficiency: a cause of lethal neonatal hyperammonemia in males

1 reference

12 December 2020

X-linked transmission of ornithine-transcarbamylase deficiency

1 reference

12 December 2020

Metabolic and genetic studies of a family with ornithine transcarbamylase deficiency

1 reference

12 December 2020

Hyperammonemia through deficiency of ornithine carbamyl transferase

1 reference

12 December 2020

Peritoneal clearance of ammonia and creatinine in a neonate

1 reference

12 December 2020

Hereditary ornithine transcarbamylase deficiency. Report of two male cases with residual enzymatic activity

1 reference

12 December 2020

Ornithine transcarbamylase deficiency. Unsuccessful therapy of neonatal hyperammonemia with N-carbamyl-L-glutamate and L-arginine

1 reference

12 December 2020

Congenital hyperammoniemia caused by ornithine carbamoyl-transferase and carbamyl phosphate synthetase deficiency

1 reference

12 December 2020

Periodic attacks of lethargy in a baby with ammonia intoxication due to a congenital defect in ureogenesis

1 reference

12 December 2020

[Hereditary hyperammonemia due to qualitative abnormality of hepatic and intestinal ornithine carbamoyl-transferase]

1 reference

12 December 2020

PROTEIN AND AMINO ACID REQUIREMENTS OF INFANTS AND CHILDREN

1 reference

12 December 2020

Peritoneal dialysis and exchange transfusion in a neonate with argininosuccinic aciduria

1 reference

12 December 2020

Protein measurement with the Folin phenol reagent

1 reference

12 December 2020

Hyperammonemia due to a mutant enzyme of ornithine transcarbamylase

1 reference

12 December 2020

Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase

1 reference

12 December 2020

Peritoneal dialysis in the reduction of blood ammonia levels in a case of hyperammonaemia

1 reference

12 December 2020

Hyperammonemia: a deficiency of liver ornithine transcarbamylase

1 reference

12 December 2020

[Chromosome X transmission of the ornithine-carbamyl-transferase structural gene. A study of 3 families]

1 reference

12 December 2020

Early dietary management in an infant with argininosuccinase deficiency: Preliminary report

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

Lethal neonatal argininosuccinate lyase deficiency in four children from one sibship

1 reference

12 December 2020

Ornitbine transcarbamylase deficiency in the newborn infant

1 reference

12 December 2020

Treatment of hyperammonemia

1 reference

12 December 2020