(Q52229458)

27 April 2018

title

Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: neurologic, ophthalmologic, and neuropsychologic examination of six patients. (English)

1 reference

27 April 2018

author name string

Lemay JF

1

1 reference

27 April 2018

Lambert MA

2

1 reference

27 April 2018

Mitchell GA

3

1 reference

27 April 2018

Vanasse M

4

1 reference

27 April 2018

Valle D

5

1 reference

27 April 2018

Arbour JF

6

1 reference

27 April 2018

Dubé J

7

1 reference

27 April 2018

Flessas J

8

1 reference

27 April 2018

Laberge M

9

1 reference

27 April 2018

Lafleur L

10

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27 April 2018

language of work or name

English

0 references

publication date

1 November 1992

1 reference

27 April 2018

The Journal of Pediatrics

published in

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27 April 2018

volume

121

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27 April 2018

issue

5 Pt 1

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27 April 2018

page(s)

725-730

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27 April 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981900-6

Hyperornithinemia, hyperammonemia, and homocitrullinuria: case report and biochemical study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981900-6

A new family affected by the syndrome of hyperornithinaemia, hyperammonaemia and homocitrullinuria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981900-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981900-6

Ornithine loading did not prevent induced hyperammonemia in a patient with hyperornithinemia-hyperammonemia-homocitrullinuria syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981900-6

Somatosensory evoked potentials and auditory brain-stem responses in congenital hypothyroidism. II. A cross-sectional study in childhood. Correlations with hormonal levels and developmental quotients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981900-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981900-6

A COLORIMETRIC DETERMINATION OF OROTIC ACID

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981900-6

Metabolic and genetic studies of a family with ornithine transcarbamylase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981900-6

Neurologic syndromes in hyperammonemic disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981900-6

Hyperargininemia: intellectual and motor improvement related to changes in biochemical data

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981900-6

Gaucher disease: new molecular approaches to diagnosis and treatment

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981900-6

Clinical, biochemical and ultrastructural study on the pathogenesis of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2805%2981900-6

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-3476(05)81900-6

1 reference

27 April 2018

release_mvq65dff3nfvnm5p25ubcg7cnu

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/mvq65dff3nfvnm5p25ubcg7cnu

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

27 April 2018