An improved LC-MS/MS method for the detection of classic and low excretor glutaric acidemia type 1

Journal of Inherited Metabolic Disease

Volumn 35, Issue 3, 2012, Pages 431-435

  Moore, Tereza ^a   Le, Anthony ^a   Cowan, Tina M ^a  

^a STANFORD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYDECANOYLCARNITINE; ACYLCARNITINE; CARNITINE DERIVATIVE; GLUTARYLCARNITINE; UNCLASSIFIED DRUG;

ARTICLE; CLASSIC GLUTARIC ACIDEMIA TYPE 1; CLINICAL ARTICLE; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; DIAGNOSTIC PROCEDURE; FOLLOW UP; HUMAN; INBORN ERROR OF METABOLISM; LIPID BLOOD LEVEL; LIQUID CHROMATOGRAPHY; LOW EXCRETOR GLUTARIC ACIDEMIA TYPE 1; MASS SPECTROMETRY; SENSITIVITY AND SPECIFICITY;

AMINO ACID METABOLISM, INBORN ERRORS; BRAIN DISEASES, METABOLIC; CARNITINE; CASE-CONTROL STUDIES; CHROMATOGRAPHY, LIQUID; FOLLOW-UP STUDIES; GLUTARYL-COA DEHYDROGENASE; HUMANS; IONS; PREDICTIVE VALUE OF TESTS; REPRODUCIBILITY OF RESULTS; TANDEM MASS SPECTROMETRY;

EID: 84863327201     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-011-9405-6     Document Type: Article

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