(Q52116870)

22 April 2018

title

Argininosuccinic aciduria: investigation of an affected family. (English)

1 reference

22 April 2018

argininosuccinic aciduria

main subject

1 reference

Billmeier GJ Jr

1

1 reference

22 April 2018

Molinary SV

2

1 reference

22 April 2018

Wilroy RS Jr

3

1 reference

22 April 2018

Duenas DA

4

1 reference

22 April 2018

Brannon ME

5

1 reference

22 April 2018

language of work or name

English

0 references

publication date

1 January 1974

1 reference

22 April 2018

The Journal of Pediatrics

published in

1 reference

22 April 2018

volume

84

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22 April 2018

issue

1

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22 April 2018

page(s)

85-89

1 reference

22 April 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2874%2980558-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2874%2980558-5

Argininosuccinic aciduria: identification and reactions of the abnormal metabolite in a newly described form of mental disease, with some preliminary metabolic studies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2874%2980558-5

Metabolic Abnormalities Detected in a Survey of Mentally Backward Individuals in Northern Ireland

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2874%2980558-5

The electroencephalogram in phenylpyruvic oligophrenia.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2874%2980558-5

Deficient argininosuccinase activity in brain in argininosuccinicaciduria.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2874%2980558-5

10.1016/S0022-3476(74)80558-5

7 January 2021

Identifiers

DOI

1 reference

22 April 2018

1 reference

22 April 2018