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Acylglycines

 
National Institutes of Health

Papers overview

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2011
2011
The analysis of organic acids in urine is commonly included in routine procedures for detecting many inborn errors of metabolism… Expand
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2010
2010
Acylglycines are an important class of metabolites that have been used in the diagnosis of several inborn errors of metabolism… Expand
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Review
2008
Review
2008
Inherited defects in mitochondrial fatty-acid beta-oxidation comprise a group of at least 12 diseases characterized by distinct… Expand
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Highly Cited
2006
Highly Cited
2006
The fatty acid oxidation disorder most commonly identified by tandem mass spectrometry newborn screening is the potentially fatal… Expand
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2000
2000
We analyzed the urinary acylglycine excretion in 26 patients with mitochondrial energy metabolism disorders and in 55 patients… Expand
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2000
2000
The analysis of acylglycines is an important biochemical tool for the diagnosis of inherited disorders of mitochondrial fatty… Expand
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1995
1995
OBJECTIVE We identified two additional patients with short-chain acyl-coenzyme A (CoA), further characterized the clinical and… Expand
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1991
1991
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is an inherited disorder of fatty acid oxidation associated with sudden… Expand
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1991
1991
To clarify the roles of butyrate and acylglycine formation in hypoxic proximal tubule cell injury and protection by glycine and… Expand
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1988
1988
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency, one of the most common inherited metabolic disorders, is often mistaken… Expand
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