Skip to search formSkip to main content

3-methylglutaric acid

 
National Institutes of Health

Related topics

Related topics

2 relations

Broader (1)

Meglutol
analogs & derivatives

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
Neurochemical evidence that 3-methylglutaric acid inhibits synaptic Na+,K+-ATPase activity probably through oxidative damage in brain cortex of young rats
3-Methylglutaconic aciduria (MGTA) comprehends a group of disorders biochemically characterized by accumulation of 3… Expand
  • table 1
  • figure 1
  • figure 2
  • figure 4
  • figure 5
Is this relevant?
2006
2006
3-Methylglutaric acid as a 13C solid-state NMR standard.
The calibration of a solid-state NMR spectrometer requires setting the magic angle, setting the reference and decoupler… Expand
Is this relevant?
Highly Cited
2004
Highly Cited
2004
OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract.
Hereditary optic atrophy is a generic term that refers to a heterogeneous group of genetic disorders for which several modes of… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 5
  • figure 6
Is this relevant?
2002
2002
3-Methylglutaconic aciduria type I is caused by mutations in AUH.
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
Is this relevant?
Highly Cited
2001
Highly Cited
2001
Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews.
Type III 3-methylglutaconic aciduria (MGA) (MIM 258501) is a neuro-ophthalmologic syndrome that consists of early-onset bilateral… Expand
  • figure 1
  • figure 2
Is this relevant?
2001
2001
3-Hydroxy-3-methylglutaric aciduria in an Italian patient is caused by a new nonsense mutation in the HMGCL gene.
3-Hydroxy-3-methylglutaric aciduria is a rare autosomal recessive inborn error of metabolism caused by deficiency of the… Expand
Is this relevant?
Review
1999
Review
1999
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)
X-linked cardioskeletal myopathy, neutropenia and abnormal mitochondria (MIM 302060) (synonyms: Barth syndrome, 3… Expand
  • figure 1
  • table 1
  • figure 2
  • figure 3
Is this relevant?
1996
1996
Combined 3-methylglutaconic and 3-hydroxy-3-methylglutaric aciduria with endocardial fibroelastosis and dilatative cardiomyopathy in male and female siblings with partial deficiency of complex II/III…
We report on 2 children, brother and sister, who presented with cardiomyopathy and muscular hypotonia at the age of B months… Expand
Is this relevant?
1976
1976
The urinary organic acid profile associated with 3-hydroxy-3-methylglutaric aciduria.
Abstract The urinary organic acid profile of 3-hydroxy-3-methylglutaric aciduria contains excessive amounts of 3-methylglutaconic… Expand
Is this relevant?
1976
1976
3-Hydroxy-3-methylglutaric aciduria, combined with 3-methylglutaconic aciduria.
1. A baby with severe metabolic acidosis was found to excrete abnormal amounts of 3-methylcrotonic acid, 3-methylglutaconic acid… Expand
Is this relevant?