Advances in Newborn Screening for Metabolic Disorders: What the Pediatrician Needs to Know

Author:

Korson Mark S

Publisher

SLACK, Inc.

Subject

Pediatrics, Perinatology and Child Health

Reference12 articles.

1. 1. Guthrie R Susi A. A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants. Pediatrics. 1963;32:338-343.

2. 2. American Academy of Pediatrics Committee on Genetics. Newborn screening fact sheets. Pediatrics. 1996;98:473-501.

3. 3. Millington DM Chase DH Hillman SL et al Diagnosis of metabolic disease. In: Matsuo T Caprioli RM Gross ML Seyama Y eds. Biological Mass Spectrometry: Present and Future. New York: John Wiley & Sons; 1994:559-579.

4. 4. de Sousa C Piesowicz AT Brett EM et al. Focal changes in the globi pallidi associated with neurological dysfunction in methylmalonic acidemia. Neuropediatrics. 1989;20: 199-201.

5. 5. Korson MS Irons M Levy HL. The neonatal phenotype of galactosemia. Am J Hum Genet. 1987;41(suppl):A10.

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