(Q48555647)

English

Neuropathology of ornithine carbamyl transferase deficiency

scientific article published in January 1985

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/3976361

Neuropathology of ornithine carbamyl transferase deficiency (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/3976361

author name string

M Kornfeld

1

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/3976361

B M Woodfin

2

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/3976361

L Papile

3

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/3976361

L E Davis

4

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/3976361

L R Bernard

5

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/3976361

publication date

1 January 1985

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/3976361

Acta Neuropathologica

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/3976361

65

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Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/3976361

3-4

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/3976361

261-264

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/3976361

Infantile neuroaxonal dystrophy. Early form with preferential cerebellar involvement

1 reference

https://pubmed.ncbi.nlm.nih.gov/3976361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Hyperammonemia due to ornithine transcarbamylase deficiency--a cause of lethal metabolic crisis during the newborn period and infancy (author's transl)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/3976361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distribution of cerebral lesions in acquired hepatocerebral degeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/3976361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3976361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3976361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary hyperammonaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/3976361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3976361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuropathology of citrullinaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/3976361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Focal cerebellar and cerebellar atrophy in a human subject due to organic mercury compounds

1 reference

https://pubmed.ncbi.nlm.nih.gov/3976361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperammonemia in pediatric diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/3976361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/3976361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00687006

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/3976361

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/3976361

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