3-Hydroxyglutarate

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1984-2013
012319842013

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2011
2011
CONTEXT AND OBJECTIVE Recessive mutations in the hydroxyacyl-CoA dehydrogenase (HADH) gene encoding the enzyme 3-hydroxyacyl-CoA… (More)
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2011
2011
Striatal degeneration from glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type 1, GA1) is associated with cerebral… (More)
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2010
2010
Concentrations of glutarate (GA) and its derivatives such as 3-hydroxyglutarate (3OHGA), D- (D-2OHGA) and L-2-hydroxyglutarate (L… (More)
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2009
2009
BACKGROUND HADH encodes for the enzyme 3-hydroxyacyl-coenzyme A dehydrogenase (HADH) and catalyses the penultimate reaction in… (More)
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2006
2006
The blood–brain barrier (BBB) metabolically isolates the central nervous system (CNS) from the circulation and protects it… (More)
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2003
2003
The pathogenesis of neurological sequelae in glutaric aciduria I (GA I) is still unclear. Some evidence exists for compromised… (More)
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2002
2002
Glutaryl-CoA dehydrogenase deficiency (also known as glutaric aciduria type I) is an autosomal, recessively inherited… (More)
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2002
2002
Three patients with ketosis had increased excretion of 3-hydroxyglutarate (21.8–37.9 μmol/mmol creatinine; controls 2.3 ± 1.6… (More)
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2001
2001
Neuronal damage in glutaryl-CoA dehydrogenase deficiency (GDD) has previously been addressed to N-methyl-D-aspartate (NMDA… (More)
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2000
2000
Glutaryl-CoA dehydrogenase (GCDH) deficiency causes glutaric aciduria type I (GA I), an inborn error of metabolism that is… (More)
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