(Q45272373)

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N-acetylglutamate synthetase deficiency: diagnosis, management and follow-up of a rare disorder of ammonia detoxication

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Europe PubMed Central

PubMed publication ID

11 December 2017

N-acetylglutamate synthetase deficiency: diagnosis, management and follow-up of a rare disorder of ammonia detoxication (English)

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Europe PubMed Central

PubMed publication ID

11 December 2017

author name string

G Schubiger

1

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Europe PubMed Central

PubMed publication ID

11 December 2017

C Bachmann

2

1 reference

Europe PubMed Central

PubMed publication ID

11 December 2017

P Barben

3

1 reference

Europe PubMed Central

PubMed publication ID

11 December 2017

J P Colombo

4

1 reference

Europe PubMed Central

PubMed publication ID

11 December 2017

O Tönz

5

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Europe PubMed Central

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11 December 2017

D Schüpbach

6

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11 December 2017

publication date

1 March 1991

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Europe PubMed Central

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11 December 2017

European Journal of Pediatrics

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Europe PubMed Central

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11 December 2017

150

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Europe PubMed Central

PubMed publication ID

11 December 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

11 December 2017

353-356

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Europe PubMed Central

PubMed publication ID

11 December 2017

N-Acetylglutamate synthetase: enzyme assay in human liver

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acute and chronic effects of carbamyl glutamate on blood urea and ammonia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ammonia Intoxication in Rats: Protection by N -Carbamoyl-L-Glutamate Plus L-Arginine

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

N-acetylglutamate synthetase (NAGS) deficiency: diagnosis, clinical observations and treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044610

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/2044610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New pathways of nitrogen excretion in inborn errors of urea synthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Treatment of congenital hyperammonemias

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044610

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/2044610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of urea cycle disorders.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044610

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/2044610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretion

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01955939

1 reference

Europe PubMed Central

PubMed publication ID

11 December 2017

Dimensions Publication ID

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 December 2017

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