(Q47971925)

English

Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life

scientific article published in June 1998

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

0 references

Miguel Reyes-Múgica

1 reference

ORCID Public Data File 2021

author name string

Boles RG

1

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

Buck EA

2

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

Blitzer MG

3

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

Platt MS

4

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

Cowan TM

5

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

Martin SK

6

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

Yoon H

7

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

Madsen JA

8

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

Reyes-Mugica M

9

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

Rinaldo P

10

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

language of work or name

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publication date

1 June 1998

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

The Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

132

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

6

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

924-933

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

Fatty acid oxidation disorders: A new class of metabolic diseases

1 reference

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7 January 2021

Mammalian mitochondrial beta-oxidation

1 reference

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7 January 2021

Metabolic disease and sudden, unexpected death in infancy

1 reference

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7 January 2021

Medium-chain acyl-coenzyme A dehydrogenase deficiency: clinical course in 120 affected children.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Evidence of duration and type of illness in children found unexpectedly dead

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7 January 2021

Mutations in the medium chain acyl-CoA dehydrogenase (MCAD) gene

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

The frequency of a disease-causing point mutation in the gene coding for medium-chain acyl-CoA dehydrogenase in sudden infant death syndrome

1 reference

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7 January 2021

Is the medium-chain acyl-CoA dehydrogenase G985 mutation involved in sudden infant death in Norway?

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7 January 2021

Comparison of post-mortem urinary and vitreous humour organic acids

1 reference

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7 January 2021

Biochemical diagnosis of fatty acid oxidation disorders by metabolite analysis of postmortem liver.

1 reference

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7 January 2021

Glutaric aciduria type II: autopsy study of a case with electron-transferring flavoprotein dehydrogenase deficiency

1 reference

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7 January 2021

Molecular basis of inherited medium-chain acyl-CoA dehydrogenase deficiency causing sudden child death

1 reference

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7 January 2021

Sudden neonatal death in carnitine transporter deficiency.

1 reference

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7 January 2021

Two alpha subunit donor splice site mutations cause human trifunctional protein deficiency

1 reference

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7 January 2021

A survey of the newborn populations in Belgium, Germany, Poland, Czech Republic, Hungary, Bulgaria, Spain, Turkey, and Japan for the G985 variant allele with haplotype analysis at the medium chain Acyl-CoA dehydrogenase gene locus: clinical and evol

1 reference

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7 January 2021

Medium Chain Acyl-CoA Dehydrogenase Deficiency in Pennsylvania: Neonatal Screening Shows High Incidence and Unexpected Mutation Frequencies

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970385-3

7 January 2021

Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970385-3

7 January 2021

Renal handling of carnitine in secondary carnitine deficiency disorders

1 reference

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7 January 2021

Deficiency of medium chain fatty acylcoenzyme A dehydrogenase presenting as the sudden infant death syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970385-3

7 January 2021

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Identifiers

10.1016/S0022-3476(98)70385-3

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9627580

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