3-Methylglutarate

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1989-2018
01219892018

Papers overview

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2018
2018
BACKGROUND Glycogen storage disease type I (GSDI) is an inborn error of carbohydrate metabolism caused by mutations of either the… (More)
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2018
2018
Single large-scale mitochondrial DNA deletions disorders are classified into three main phenotypes with frequent clinical overlap… (More)
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Review
2015
Review
2015
3-Hydroxy-3-methylglutaryl-CoA lyase (HL) deficiency is an inherited disorder of organic acid metabolism biochemically… (More)
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2013
2013
3-Hydroxy-3-methylglutaryl-CoA lyase (HL) deficiency is a disorder biochemically characterized by the predominant accumulation of… (More)
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2012
2012
The pathway for anaerobic degradation of 4-methylbenzoate was studied in the denitrifying alphaproteobacterium Magnetospirillum… (More)
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2009
2009
The present work investigated the in vitro effects of 3-hydroxy-3-methylglutarate, 3-methylglutarate, 3-methylglutaconate and 3… (More)
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2007
2007
The branched alkanoic acid, 3-methylvaleric acid (3-MVA), was used to test the effect of a β-methyl branch on short chain… (More)
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Highly Cited
1991
Highly Cited
1991
Seven boys with an apparently X-linked syndrome of dilated cardiomyopathy, growth retardation, neutropenia, and persistently… (More)
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1991
1991
A 13-month-old girl with dysphagia, severe psychomotor retardation, spasticity, hypertonicity and Kostmann type neutropenia was… (More)
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1989
1989
Glutaric aciduria type I (McKusick 23167), caused by deficiency of glutaryl-CoA dehydrogenase, is a severe autosomal recessively… (More)
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