Long chain acyl-CoA dehydrogenase deficiency

Known as: Long-chain acyl-CoA dehydrogenase deficiency, Acyl-Coa Dehydrogenase, Long-Chain, Deficiency of, Acyl-CoA Dehydrogenase, Long-Chain Deficiency 
A genetic disorder characterized by deficiency of the enzyme long-chain acyl-coenzyme A dehydrogenase that metabolizes long-chain fatty acids. Signs… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1987-2017
024619872017

Papers overview

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2016
2016
Rhabdomyolysis is common in very long-chain acyl-CoA dehydrogenase deficiency (VLCADD) and other metabolic myopathies, but its… (More)
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Highly Cited
2010
Highly Cited
2010
Sirtuins are NAD(+)-dependent protein deacetylases. They mediate adaptive responses to a variety of stresses, including calorie… (More)
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2009
2009
Cardiac hypertrophy is a common finding in human patients with inborn errors of long-chain fatty acid oxidation. Mice with either… (More)
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Highly Cited
2007
Highly Cited
2007
Alterations in mitochondrial function have been implicated in the pathogenesis of insulin resistance and type 2 diabetes. However… (More)
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2004
2004
Long chain acyl-CoA dehydrogenase (LCAD) has recently been shown to be the mitochondrial enzyme responsible for the beta… (More)
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2001
2001
Although many patients have been found to have very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency, none have been… (More)
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Highly Cited
1998
Highly Cited
1998
Abnormalities of fatty acid metabolism are recognized to play a significant role in human disease, but the mechanisms remain… (More)
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1993
1993
ABSTRACT: Long-chain acyl-CoA dehydrogenase (LCAD) deficiency is a disorder of fatty acid β-oxidation. Its diagnosis has been… (More)
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1993
1993
Long-chain acyl-CoA dehydrogenase (LCAD) deficiency is an autosomal recessive disorder of fatty acid metabolism characterized by… (More)
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1991
1991
ABSTRACT: Long-chain acyl-CoA dehydrogenase (LCAD) deficiency is a disorder of mitochondrial fatty acid oxidation that is… (More)
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