(Q46577337)

English

Late-onset form of partial N-acetylglutamate synthetase deficiency

scientific article published in June 1990

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/2373115

Late-onset form of partial N-acetylglutamate synthetase deficiency (English)

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/2373115

author name string

O N Elpeleg

1

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/2373115

J P Colombo

2

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/2373115

N Amir

3

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/2373115

C Bachmann

4

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/2373115

H Hurvitz

5

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/2373115

publication date

1 June 1990

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/2373115

European Journal of Pediatrics

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/2373115

149

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/2373115

634-636

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/2373115

9

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/2373115

https://scigraph.springernature.com/pub.10.1007/bf02034751

0 references

N-Acetylglutamate synthetase: enzyme assay in human liver

1 reference

https://pubmed.ncbi.nlm.nih.gov/2373115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Liver pathology in a new congenital disorder of urea synthesis: N-acetylglutamate synthetase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/2373115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2373115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determination of medium chain fatty acids in serum

1 reference

https://pubmed.ncbi.nlm.nih.gov/2373115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

N-acetylglutamate synthetase deficiency, a second patient

1 reference

https://pubmed.ncbi.nlm.nih.gov/2373115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determination of orotic acid in children's urine

1 reference

https://pubmed.ncbi.nlm.nih.gov/2373115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human carbamylphosphate synthetase I. Stabilization, purification, and partial characterization of the enzyme from human liver

1 reference

https://pubmed.ncbi.nlm.nih.gov/2373115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

N-acetylglutamate synthetase deficiency: a disorder of ammonia detoxication

1 reference

https://pubmed.ncbi.nlm.nih.gov/2373115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2373115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02034751

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/2373115

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/2373115

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