Characterization of fatty acid oxidation in human muscle mitochondria and myoblasts. (Q44345949)

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1 November 2019

title

Characterization of fatty acid oxidation in human muscle mitochondria and myoblasts (English)

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1 November 2019

0 references

0 references

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1

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1 November 2019

Jean-Paul Bonnefont

series ordinal

2

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1 November 2019

Jean Bastin

series ordinal

4

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1 November 2019

author name string

Arnold Munnich

series ordinal

3

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1 November 2019

publication date

1 February 2003

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Molecular Genetics and Metabolism

1 November 2019

published in

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volume

78

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1 November 2019

issue

2

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1 November 2019

page(s)

112-118

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Recognition and management of fatty acid oxidation defects: a series of 107 patients.

1 November 2019

cites work

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Rapid diagnosis of long chain and medium chain fatty acid oxidation disorders using lymphocytes

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Carnitine palmitoyltransferase deficiencies

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Infantile form of carnitine palmitoyltransferase II deficiency with hepatomuscular symptoms and sudden death. Physiopathological approach to carnitine palmitoyltransferase II deficiencies

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7 January 2021

Biochemical and molecular investigations in respiratory chain deficiencies

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7 January 2021

Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotype.

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7 January 2021

The mitochondrial carnitine palmitoyltransferase system. From concept to molecular analysis

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7 January 2021

Requirement for the heart-type fatty acid binding protein in cardiac fatty acid utilization

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7 January 2021

Defective uptake and utilization of long chain fatty acids in muscle and adipose tissues of CD36 knockout mice

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7 January 2021

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Identifiers

DOI

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1 November 2019

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