(Q70762041)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228016%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

title

Ultrastructure of hepatic mitochondria in a child with hyperornithinemia, hyperammonemia, and homocitrullinuria (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228016%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

author name string

M. D. Haust

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7228016

13 March 2024

P. D. Gatfield

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7228016

13 March 2024

B. A. Gordon

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7228016

13 March 2024

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=7228016

13 March 2024

publication date

1 March 1981

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228016%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

13 October 2019

https://api.elsevier.com/content/article/PII:S0046817781801219?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0046-8177(81)80121-9

https://api.elsevier.com/content/article/PII:S0046817781801219?httpAccept=text/plain

13 March 2024

1 reference

https://api.crossref.org/works/10.1016/S0046-8177(81)80121-9

13 March 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228016%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

volume

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228016%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228016%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

page(s)

212-222

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228016%20AND%20SRC:MED&resulttype=core&format=json

Ammonia detoxication in liver from humans

13 October 2019

cites work

1 reference

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7 January 2021

Development of urea-synthesizing enzymes in human liver

1 reference

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7 January 2021

Congenital hyperammonemic syndromes

1 reference

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7 January 2021

Familial Protein Intolerance with Deficient Transport of Basic Amino Acids: An Analysis of 10 Patients

1 reference

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7 January 2021

L-Lysine dehydrogenase deficiency in a patient with congenital lysine intolerance

1 reference

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7 January 2021

Ornithinemia, hyperammonemia, and homocitrullinuria. A disease associated with mental retardation and possibly caused by defective mitochondrial transport

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2881%2980121-9

7 January 2021

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

1 reference

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7 January 2021

Carbamylphosphate synthetase deficiency in an infant with severe cerebral damage

1 reference

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7 January 2021

Congenital hyperammonemia. Association with hyperglycinemia and decreased levels of carbamyl phosphate synthetase

1 reference

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7 January 2021

Lethal neonatal deficiency of carbamyl phosphate synthetase.

1 reference

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7 January 2021

Treatment of Carbamyl Phosphate Synthetase Deficiency with Keto Analogues of Essential Amino Acids

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7 January 2021

Massive pulmonary hemorrhage as a presenting feature in congenital hyperammonemia

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7 January 2021

Carbamyl-phosphate-synthetase deficiency with neonatal onset of symptoms

1 reference

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7 January 2021

Urea-Cycle Enzyme Deficiencies and an Increased Nitrogen Load Producing Hyperammonemia in Reye's Syndrome

1 reference

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7 January 2021

Proceedings: Hepatic ultrastructure in a child with carbamyl phosphate synthetase deficiency, hyperornithinaemia, hyperammonaemia, and homocitrullinuria

1 reference

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7 January 2021

Fine structure of the liver in human idiopathic diabetes mellitus. I. Parenchymal cell mitochondria

1 reference

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7 January 2021

A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study

1 reference

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7 January 2021

Crystalloid structures of hepatic mitochondria in children with heparitin sulphate mucopolysaccharidosis (sanfilippo type)

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2881%2980121-9

7 January 2021

Heritable urea cycle enzyme deficiency-liver disease in 16 patients

1 reference

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7 January 2021

Lysinuric protein intolerance

1 reference

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7 January 2021

Argininosuccinic aciduria: investigation of an affected family.

1 reference

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7 January 2021

Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase

1 reference

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7 January 2021

Ornitbine transcarbamylase deficiency in the newborn infant

1 reference

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7 January 2021

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

1 reference

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7 January 2021

https://api.crossref.org/works/10.1016%2FS0046-8177%2881%2980121-9

1 reference

7 January 2021

Metabolic and genetic studies of a family with ornithine transcarbamylase deficiency

1 reference

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7 January 2021

Hyperammonaemia due to ornithine transcarbamylase deficiency

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Hereditary hyperammonaemia

1 reference

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7 January 2021

Neuropathological observations in a patient with carbamylphosphate-synthetase deficiency and in two sibs

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2881%2980121-9

7 January 2021

3-Aminopiperid-2-one, an unusual metabolite in the urine of a patient with hyperammonaemia, hyperornithinaemia and homocitrullinuria

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2881%2980121-9

7 January 2021

A Case of Carbamyl Phosphate Synthetase Deficiency

1 reference

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7 January 2021

Neonatal argininosuccinic aciduria with normal brain and kidney but absent liver argininosuccinate lyase activity

40

1 reference

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The pathological findings in a case of argininosuccinic aciduria

13 March 2024

47

1 reference

https://api.crossref.org/works/10.1016/S0046-8177(81)80121-9

13 March 2024

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7228016%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference