(Q39648699)

13 September 2017

1 reference

title

Inborn errors of metabolism and Reye syndrome: differential diagnosis (English)

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13 September 2017

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Greene CL

1

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13 September 2017

Blitzer MG

series ordinal

2

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13 September 2017

Shapira E

series ordinal

3

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13 September 2017

language of work or name

English

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publication date

1 July 1988

1 reference

The Journal of Pediatrics

13 September 2017

published in

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13 September 2017

volume

113

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13 September 2017

issue

1 Pt 1

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13 September 2017

page(s)

156-159

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Grade I Reye's syndrome. A frequent cause of vomiting and liver dysfunction after varicella and upper-respiratory-tract infection

13 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980551-1

How common is Reye's syndrome?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980551-1

Amino acid pattern in Reye syndrome: Comparison with clinically similar entities

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980551-1

Urinary dicarboxylic acids in Reye syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980551-1

Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980551-1

Carnitine deficiency, organic acidemias, and Reye's syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980551-1

Patient with Defect in Leucine Metabolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980551-1

beta-Hydroxy-beta-methyglutaricaciduria presenting as Reye's syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980551-1

beta-hydroxy-beta-methylglutaricaciduria, Reye's syndrome, and Echovirus 11

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980551-1

Hydroqnnethylglutaryl CoA lyase deficiency: Features resembling Reye syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980551-1

3-Hydroxy-3-Methylglutaric Aciduria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980551-1

A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980551-1

Atypical Clinical Course of Ornithine Transcarbamyiase Deficiency Due to a New Mutant (Comparison with Reye's Disease)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980551-1

Metabolic and biochemical studies in fructose 1,6-diphosphatase deficiency.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980551-1

The urinary organic acid profile associated with 3-hydroxy-3-methylglutaric aciduria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980551-1

Organic acid excretion in a patient with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency: facts and artefacts

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980551-1

10.1016/S0022-3476(88)80551-1

7 January 2021

Identifiers

DOI

1 reference

13 September 2017

1 reference