(Q40909099)

24 September 2017

title

Prevalence of medium-chain acyl-coenzyme A dehydrogenase deficiency in the sudden infant death syndrome (English)

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24 September 2017

Arens R

1

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24 September 2017

Gozal D

2

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24 September 2017

Jain K

3

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24 September 2017

Muscati S

4

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24 September 2017

Heuser ET

5

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24 September 2017

Williams JC

6

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24 September 2017

Keens TG

7

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24 September 2017

Ward SL

8

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24 September 2017

language of work or name

English

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publication date

1 May 1993

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The Journal of Pediatrics

24 September 2017

published in

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24 September 2017

volume

122

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24 September 2017

issue

5 Pt 1

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24 September 2017

page(s)

715-718

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Defining the sudden infant death syndrome (SIDS): deliberations of an expert panel convened by the National Institute of Child Health and Human Development

24 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

Symptoms and signs in organic acidurias

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

Sudden infant death syndrome and multiple acyl-coenzyme A dehydrogenase deficiency, ethylmalonic-adipic aciduria, or systemic carnitine deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

Sudden infant death syndrome and inherited disorders of fatty acid beta-oxidation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acids

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

Medium chain acyl-CoA dehydrogenase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

Molecular characterization of inherited medium-chain acyl-CoA dehydrogenase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

Molecular lesion in patients with medium-chain acyl-CoA dehydrogenase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

Molecular basis of medium chain acyl-coenzyme A dehydrogenase deficiency. An A to G transition at position 985 that causes a lysine-304 to glutamate substitution in the mature protein is the single prevalent mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

Medium-chain acyl-coenzyme A dehydrogenase deficiency and sudden infant death

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

Frequency of the G985 MCAD mutation in the general population

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

Frequency of medium-chain acyl-CoA dehydrogenase deficiency G-985 mutation in sudden infant death syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

Defects of metabolism of fatty acids in the sudden infant death syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980010-7

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-3476(06)80010-7

1 reference

24 September 2017

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