Follow-up study of 16 years neonatal screening for inborn errors of metabolism in West Germany-Reference-Cited by-同舟云学术

Follow-up study of 16 years neonatal screening for inborn errors of metabolism in West Germany

Published:1986-09 Issue:4 Volume:145 Page:310-312
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Mathias D.,Bickel H.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/BF00439408.pdf

Reference8 articles.

1. Alm L, Larsen A (1981) Evaluation of a nation-wide neonatal metabolic screening programme in Sweden 1965?1979. Acta Paediatr Scand 70:601?607

2. Beutler E, Baluda MC (1966) A simple spot screening test for galactosemia J Lab Clin Med 68:137?141

3. Guthrie R, Susi A (1963) A simple phenylalanine method for detecting PKU in large populations of newborn infants. Pediatrics 32:338?343

4. Kirkman HN, Carroll CL, Moore EG, Matheson MS (1982) Fifteen-year experience with screening for phenylketonuria with an automated fluorometric method. Am J Hum Genet 34:743?752

5. Paigen K, Pacholec F, Levy HL (1982) A new method of screening for inherited disorders of galactose metabolism. J Lab Clin Med 99:895?907

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