Differential diagnosis of homocystinuria by urease treatment, isotope dilution and gas chromatography–mass spectrometry
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference15 articles.
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1. Present Status of Expanded Newborn Screening Project for Inborn Errors of Metabolism by Tandem Mass Spectrometry;Nippon Eiseigaku Zasshi (Japanese Journal of Hygiene);2014
2. Determination of plasma dibasic amino acids following trimethylsilyl–trifluoroacyl derivatization using gas chromatography–mass spectrometry;Archives of Pharmacal Research;2013-03
3. Methionine/galactose ratio on newborn blood spots useful for reduction of false positives for homocystinuria and galactosemia by high-performance anion-exchange chromatography with pulsed amperometric detection;Clinica Chimica Acta;2012-01
4. Five cases of β-ureidopropionase deficiency detected by GC/MS analysis of urine metabolome;Journal of Mass Spectrometry;2009-02
5. Noninvasive human metabolome analysis for differential diagnosis of inborn errors of metabolism;Journal of Chromatography B;2007-08
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