(Q43753314)

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Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotype

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Europe PubMed Central

PubMed publication ID

26 November 2017

Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotype (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

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very long chain acyl-CoA dehydrogenase deficiency

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author name string

D S Roe

1

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

C Vianey-Saban

2

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

S Sharma

3

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

M T Zabot

4

1 reference

Europe PubMed Central

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26 November 2017

C R Roe

5

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Europe PubMed Central

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26 November 2017

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1 October 2001

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Europe PubMed Central

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26 November 2017

Clinica Chimica Acta

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26 November 2017

312

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Europe PubMed Central

PubMed publication ID

26 November 2017

1-2

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Europe PubMed Central

PubMed publication ID

26 November 2017

55-67

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Europe PubMed Central

PubMed publication ID

26 November 2017

Genomic DNA organization of human mitochondrial very-long-chain acyl-CoA dehydrogenase and mutation analysis

1 reference

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7 January 2021

Assignment of the human mitochondrial very-long-chain acyl-CoA dehydrogenase gene (LCACD) to 17p13 by in situ hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900594-0

7 January 2021

Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia.

1 reference

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7 January 2021

Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients

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7 January 2021

Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood

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7 January 2021

Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900594-0

7 January 2021

Recent developments in the investigation of inherited metabolic disorders using cultured human cells

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900594-0

7 January 2021

Mitochondrial very long chain acyl-CoA dehydrogenase deficiency--a new disorder of fatty acid oxidation

1 reference

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7 January 2021

Very long chain acyl-CoA dehydrogenase deficiency: successful treatment of acute cardiomyopathy

1 reference

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7 January 2021

Molecular heterogeneity in very-long-chain acyl-CoA dehydrogenase deficiency causing pediatric cardiomyopathy and sudden death

1 reference

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7 January 2021

Prenatal diagnosis of mitochondrial fatty acid oxidation defects

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900594-0

7 January 2021

Pristanic acid beta-oxidation in peroxisomal disorders: studies in cultured human fibroblasts

1 reference

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7 January 2021

Evidence for intermediate channeling in mitochondrial beta-oxidation

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900594-0

7 January 2021

Investigation of beta-oxidation intermediates in normal and MCAD-deficient human fibroblasts using tandem mass spectrometry

1 reference

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7 January 2021

Identifiers

10.1016/S0009-8981(01)00594-0

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

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