(Q41016966)

English

Analysis of carnitine esters by radio-high performance liquid chromatography in cultured skin fibroblasts from patients with mitochondrial fatty acid oxidation disorders

scientific article published on August 1998

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scholarly article

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Europe PubMed Central

PubMed publication ID

25 September 2017

Analysis of carnitine esters by radio-high performance liquid chromatography in cultured skin fibroblasts from patients with mitochondrial fatty acid oxidation disorders (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

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author name string

Schmidt-Sommerfeld E

1

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Europe PubMed Central

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25 September 2017

Bobrowski PJ

2

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Europe PubMed Central

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25 September 2017

Penn D

3

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Europe PubMed Central

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25 September 2017

Rhead WJ

4

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Europe PubMed Central

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25 September 2017

Wanders RJ

5

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Europe PubMed Central

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25 September 2017

Bennett MJ

6

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25 September 2017

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publication date

1 August 1998

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25 September 2017

Pediatric Research

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25 September 2017

44

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25 September 2017

2

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Europe PubMed Central

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25 September 2017

210-214

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Europe PubMed Central

PubMed publication ID

25 September 2017

The changing face of disorders of fatty acid oxidation

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199808000-00012

21 January 2018

Quantitation of urinary carnitine esters in a patient with medium-chain acyl-coenzyme A dehydrogenase deficiency: effect of metabolic state and L-carnitine therapy

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199808000-00012

21 January 2018

Evidence for intermediate channeling in mitochondrial beta-oxidation

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199808000-00012

21 January 2018

Fatty acid oxidation in peripheral blood cells: characterization and use for the diagnosis of defects of fatty acid oxidation.

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199808000-00012

21 January 2018

Identification of two variant short chain acyl-coenzyme A dehydrogenase alleles, each containing a different point mutation in a patient with short chain acyl-coenzyme A dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199808000-00012

21 January 2018

A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblasts

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199808000-00012

21 January 2018

Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199808000-00012

21 January 2018

Glutaric acidemia type II: heterogeneity of clinical and biochemical phenotypes

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199808000-00012

21 January 2018

Oxidation of fatty acids in cultured fibroblasts: a model system for the detection and study of defects in oxidation

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199808000-00012

21 January 2018

Quantitation of Short- and Medium-Chain Acylcarnitines in Plasma by Radioisotopic Exchange/High-Performance Liquid Chromatography

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199808000-00012

21 January 2018

Identifiers

10.1203/00006450-199808000-00012

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

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