Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

3-methylglutaric acid

 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2006
Highly Cited
2006
The calibration of a solid-state NMR spectrometer requires setting the magic angle, setting the reference and decoupler… Expand
Review
2004
Review
2004
X-linked cardioskeletal myopathy, neutropenia and abnormal mitochondria (MIM 302060) (synonyms: Barth syndrome, 3… Expand
Highly Cited
2004
Highly Cited
2004
Hereditary optic atrophy is a generic term that refers to a heterogeneous group of genetic disorders for which several modes of… Expand
Highly Cited
2002
Highly Cited
2002
3-Methylglutaconic aciduria type I is an autosomal recessive disorder clinically characterized by various symptoms ranging from… Expand
  • figure 1
  • figure 2
  • figure 3
  • table 1
Highly Cited
2001
Highly Cited
2001
Type III 3-methylglutaconic aciduria (MGA) (MIM 258501) is a neuro-ophthalmologic syndrome that consists of early-onset bilateral… Expand
  • figure 1
  • figure 2
2001
2001
3-Hydroxy-3-methylglutaric aciduria is a rare autosomal recessive inborn error of metabolism caused by deficiency of the… Expand
Highly Cited
1998
Highly Cited
1998
We examined the inhibitory activity against bacterial peptidoglycan biosynthesis, mammalian glycoprotein biosynthesis and growth… Expand
Highly Cited
1982
Highly Cited
1982
Two brothers, aged 7 and 5 years, who excreted large amounts of the leucine metabolites 3-methylglutaconic acid, 3-methylglutaric… Expand
Highly Cited
1976
Highly Cited
1976
Abstract The urinary organic acid profile of 3-hydroxy-3-methylglutaric aciduria contains excessive amounts of 3-methylglutaconic… Expand
1976
1976
1. A baby with severe metabolic acidosis was found to excrete abnormal amounts of 3-methylcrotonic acid, 3-methylglutaconic acid… Expand