(Q46206813)

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Post-mortem recognition of inherited metabolic disorders from specific acylcarnitines in tissue in cases of sudden infant death

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/2881073

Post-mortem recognition of inherited metabolic disorders from specific acylcarnitines in tissue in cases of sudden infant death (English)

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/2881073

author name string

C R Roe

1

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/2881073

D S Millington

2

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/2881073

D A Maltby

3

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/2881073

R B Wellman

4

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/2881073

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1 February 1987

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/2881073

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/2881073

1

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/2881073

8531

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/2881073

512

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/2881073

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2887%2992126-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Diagnostic and therapeutic implications of medium-chain acylcarnitines in the medium-chain acyl-coA dehydrogenase deficiency.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2887%2992126-X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2887%2992126-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0140-6736(87)92126-X

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/2881073

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/2881073

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