(Q68250128)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1017595%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

title

Sibling cases of chronic recurrent hepatocerebral disease with hypercitrullinemia (English)

1 reference

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23 September 2019

author name string

T. Tsujii

1

1 reference

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14 August 2022

T. Morita

2

1 reference

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14 August 2022

Y. Matsuyama

3

1 reference

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14 August 2022

T. Matsui

4

1 reference

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14 August 2022

M. Tamura

5

1 reference

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14 August 2022

Y. Matsuoka

6

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14 August 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=1017595

14 August 2022

publication date

1 January 1976

1 reference

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Gastroenterologia Japonica

23 September 2019

published in

1 reference

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23 September 2019

volume

11

1 reference

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23 September 2019

issue

4

1 reference

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23 September 2019

page(s)

328-340

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1017595%20AND%20SRC:MED&resulttype=core&format=json

[An autopsy case of juvenile hepato-cerebral degeneration (non-Wilsonian Inose-type) with mental retardation, with special reference to ammonia and amino acids metabolism (author's transl)]

23 September 2019

cites work

1 reference

12 December 2020

Protein intolerance with deficient transport of basic aminoacids. Another inborn error of metabolism

1 reference

12 December 2020

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

1 reference

12 December 2020

Hepatocerebral degeneration, a special type

1 reference

12 December 2020

Argininosuccinic aciduria. Report of two new cases and demonstration of intermittent elevation of blood ammonia

1 reference

12 December 2020

Chronic porto-hepatic encephalopathy.

1 reference

12 December 2020

[An autopsied case of the "pseudoulegyria type" of the hepatocerebral disease]

1 reference

12 December 2020

Citrullinemia: Elevated serum citrulline levels in healthy siblings

1 reference

12 December 2020

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

1 reference

12 December 2020

A vulnerable and rate-limiting step in urea synthesis in patients with hyperammoniaemia

1 reference

12 December 2020

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

1 reference

12 December 2020

Changes in free amino acids in the plasma during hepatic coma

1 reference

12 December 2020

Hyperammonaemia. A new instance of an inborn enzymatic defect of the biosynthesis of urea

1 reference

12 December 2020

Lethal neonatal deficiency of carbamyl phosphate synthetase.

1 reference

12 December 2020

Portal-systemic encephalopathy; neurological complications of liver disease

1 reference

12 December 2020

Familial hyperargininemia

1 reference

12 December 2020

Hyperglucagonemia in Laennec's cirrhosis. The role of portal-systemic shunting

1 reference

12 December 2020

CONGENITAL LYSINE INTOLERANCE WITH PERIODIC AMMONIA INTOXICATION

1 reference

12 December 2020

Citrullinemia with defective urea production

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02777374

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1017595%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

1 reference