(Q82960853)

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Commentary on a Delphi clinical practice protocol for the diagnosis and management of very long chain acyl-CoA dehydrogenase deficiency by Arnold et al

scientific article published on 09 December 2008

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19081279%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

Commentary on a Delphi clinical practice protocol for the diagnosis and management of very long chain acyl-CoA dehydrogenase deficiency by Arnold et al (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19081279%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

very long chain acyl-CoA dehydrogenase deficiency

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author name string

Deborah Louise Marsden

1

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Europe PubMed Central

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18 January 2020

publication date

9 December 2008

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18 January 2020

Molecular Genetics and Metabolism

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19081279%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

96

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18 January 2020

3

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18 January 2020

81-82

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18 January 2020

A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.10.010

7 January 2021

Screening newborns for inborn errors of metabolism by tandem mass spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.10.010

7 January 2021

Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.10.010

7 January 2021

A Delphi-based consensus clinical practice protocol for the diagnosis and management of 3-methylcrotonyl CoA carboxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.10.010

7 January 2021

National Institutes of Health Consensus Development Conference Statement: phenylketonuria: screening and management, October 16-18, 2000.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.10.010

7 January 2021

Long-term follow-up study of patients with phenylketonuria detected by the newborn screening programme in Japan

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.10.010

7 January 2021

Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.10.010

7 January 2021

Carnitine supplementation induces acylcarnitine production in tissues of very long-chain acyl-CoA dehydrogenase-deficient mice, without replenishing low free carnitine

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2008.10.010

7 January 2021

Identifiers

10.1016/J.YMGME.2008.10.010

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19081279%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19081279%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

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