(Q52206544)

27 April 2018

title

Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathy. (English)

1 reference

27 April 2018

0 references

C L Pridmore

1

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27 April 2018

J T Clarke

series ordinal

2

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27 April 2018

S Blaser

series ordinal

3

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27 April 2018

publication date

1 September 1995

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27 April 2018

Journal of Child Neurology

published in

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27 April 2018

volume

10

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27 April 2018

issue

5

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27 April 2018

page(s)

369-374

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27 April 2018

Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies.

cites work

1 reference

https://api.crossref.org/works/10.1177%2F088307389501000506

Six New Mutations in the Ornithine Transcarbamylase Gene Detected by Single-Strand Conformational Polymorphism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389501000506

Natural history of symptomatic partial ornithine transcarbamylase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389501000506

Neurological features and computed tomography of the brain in children with ornithine carbamoyl transferase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389501000506

Acute hemiparesis as the presenting sign in a heterozygote for ornithine transcarbamylase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389501000506

Lysinuric protein intolerance

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389501000506

Orotic aciduria in lysinuric protein intolerance: dependence on the urea cycle intermediates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389501000506

10.1177/088307389501000506

21 January 2018

Identifiers

DOI

1 reference

27 April 2018

1 reference

27 April 2018