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3-methylglutaric acid

 
National Institutes of Health

Papers overview

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2011
2011
3-Methylglutaconic aciduria (MGTA) comprehends a group of disorders biochemically characterized by accumulation of 3… Expand
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2006
2006
The calibration of a solid-state NMR spectrometer requires setting the magic angle, setting the reference and decoupler… Expand
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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
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2002
2002
3-Methylglutaconic aciduria type I is an autosomal recessive disorder clinically characterized by various symptoms ranging from… Expand
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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
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2001
2001
3-Hydroxy-3-methylglutaric aciduria is a rare autosomal recessive inborn error of metabolism caused by deficiency of the… Expand
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Review
1999
Review
1999
X-linked cardioskeletal myopathy, neutropenia and abnormal mitochondria (MIM 302060) (synonyms: Barth syndrome, 3… Expand
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1996
1996
We report on 2 children, brother and sister, who presented with cardiomyopathy and muscular hypotonia at the age of B months… Expand
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1976
1976
Abstract The urinary organic acid profile of 3-hydroxy-3-methylglutaric aciduria contains excessive amounts of 3-methylglutaconic… Expand
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1976
1976
1. A baby with severe metabolic acidosis was found to excrete abnormal amounts of 3-methylcrotonic acid, 3-methylglutaconic acid… Expand
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