Diagnostic and therapeutic implications of persistent hyperphenylalaninemia in an infant heterozygous for the gene of phenylketonuria-Reference-Cited by-同舟云学术

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Diagnostic and therapeutic implications of persistent hyperphenylalaninemia in an infant heterozygous for the gene of phenylketonuria

Published:1966-05 Issue:5 Volume:68 Page:704-712
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Schneider A.J.,Garrard Sterling D.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference9 articles.

1. A modified procedure for the automatic analysis of amino acids;Piez;Anal. Biochem.,1960

2. Phenylalanine tolerance test on relatives of phenylketonuric children;Berry;Am. J. Human Genet.,1957

3. Phenylketonuria detection in the newborn infant as a routine hospital procedure;Guthrie;Children's Bureau Publication N. 419,1964

4. Phenylalanine hydroxylase activity in newborn infants;Allen;Pediatrics,1964

5. Serum phenylalanine and tyrosine levels in the newborn infant;Hsia;New England J. Med.,1962

Cited by 32 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. HYPERPHENYLALANINEMIA WITHOUT PHENYLKETONURIA;Developmental Medicine & Child Neurology;2008-11-12

2. Phenylketonuria 1967;Developmental Medicine & Child Neurology;2008-11-12

3. The Measurement of Phenylalanine and Tyrosine in Blood;Methods of Biochemical Analysis;2006-10-31

4. Prognosis after hyperphenylalaninemia;The Journal of Pediatrics;1983-10

5. Homocystinuria;Public Health Ophthalmology;1975

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