(Q70467684)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6422148%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

title

The mechanism of hyperammonaemia and hyperornithinaemia in the syndrome of hyperornithinaemia, hyperammonaemia with homocitrullinuria (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6422148%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

author name string

K Oyanagi

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6422148%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

A Tsuchiyama

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6422148%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

Y Itakura

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6422148%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

H Sogawa

4

1 reference

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11 October 2019

K Wagatsuma

5

1 reference

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11 October 2019

T Nakao

6

1 reference

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11 October 2019

S Sakamoto

7

1 reference

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11 October 2019

A Yachi

8

1 reference

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11 October 2019

publication date

1 January 1983

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6422148%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

11 October 2019

published in

1 reference

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11 October 2019

volume

6

1 reference

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11 October 2019

issue

3

1 reference

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11 October 2019

page(s)

133-134

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf01800748

11 October 2019

exact match

0 references

cites work

Decreased transport of ornithine across the inner mitochondrial membrane as a cause of hyperornithinaemia

1 reference

12 December 2020

Defective ornithine metabolism in cultured skin fibroblasts from patients with the syndrome of hyperornithinemia, hyperammonemia and homocitrullinuria.

1 reference

12 December 2020

Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation

1 reference

12 December 2020

Psychomotor Retardation, Epileptic and Stuporous Attacks, Irritability and Ataxia Associated with Ammonia Intoxication, High Blood Ornithine Levels and Increased Homocitrulline in the Urine

1 reference

12 December 2020

Hyperornithinemia, Hyperammonemia, and Homocitrullinuria Associated with Decreased Carbamyl Phosphate Synthetase I Activity

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01800748

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6422148%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

1 reference