Present Status of Expanded Newborn Screening Project for Inborn Errors of Metabolism by Tandem Mass Spectrometry
Author:
Affiliation:
1. Japan Clinical Metabolomics Institute
Publisher
Japanese Society for Hygiene
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/jjh/69/1/69_60/_pdf
Reference48 articles.
1. (3) Chace DH, Millington DS, Terada N, Koehler SG, Roe CR, Hoffman LF. Rapid diagnosis of phenylketonuria by quantitative analysis for phenylalanine and tyrosine in neonatal blood spots by tandem mass spectrometry. Clin Chem 1993;39:66–71.
2. (4) Millington DS, Kodo N, Norwood DL, Roe CR. Tandem mass spectrometry: a new method for acylcarnitine profiling with potential for neonatal screening for inborn errors of metabolism. J Inherit Metab Dis 1990;13:321–324.
3. (5) Cipriano LE, Rupar CA, Zaric GS. The cost-effectiveness of expanding newborn screening for up to 21 inherited metabolic disorders using tandem mass spectrometry: results from a decision-analytic model. Value Health 2007;10:83–97.
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