Newborn Screening by Tandem Mass Spectrometry
Author:
Affiliation:
1. Institute of Metabolic Disease, Baylor University Medical Center, 3812 Elm Street, Dallas, TX 75226, Fax 214-820-4853
Publisher
Oxford University Press (OUP)
Subject
Biochemistry (medical),Clinical Biochemistry
Link
http://academic.oup.com/clinchem/article-pdf/47/11/1937/32727148/clinchem1937.pdf
Reference18 articles.
1. Tandem mass spectrometry: A new method for acylcarnitine profiling with potential for neonatal screening for inborn errors of metabolism
2. The analysis of diagnostic markers of genetic disorders in human blood and urine using tandem mass spectrometry with liquid secondary ion mass spectrometry
3. Rapid diagnosis of phenylketonuria by quantitative analysis for phenylalanine and tyrosine in neonatal blood spots by tandem mass spectrometry
4. Use of phenylalanine-to-tyrosine ratio determined by tandem mass spectrometry to improve newborn screening for phenylketonuria of early discharge specimens collected in the first 24 hours
5. Rapid diagnosis of maple syrup urine disease in blood spots from newborns by tandem mass spectrometry
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1. Harmonization of distributed multi‐center analysis based on dried blood spot reference materials supporting the screening of neonatal inherited metabolic disorders;Journal of Clinical Laboratory Analysis;2023-10
2. Stability of Plasma Protein Composition in Dried Blood Spot during Storage;Processes;2020-11-20
3. Inborn Errors of Metabolism in the Era of Untargeted Metabolomics and Lipidomics;Metabolites;2019-10-21
4. Newborn screening for 3-hydroxy-3-methylglutaric aciduria using direct analysis in real-time mass spectrometry;Journal of Mass Spectrometry;2019-01-31
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