Literature DB >> 5910762

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

A J Schneider, S D Garrard.   

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Year:  1966        PMID： 5910762     DOI： 10.1016/s0022-3476(66)80442-0

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  5 in total

1.  Treatment of classical phenylketonuria.

Authors:  M S MCBean; J B Stephenson
Journal:  Arch Dis Child       Date:  1968-02       Impact factor: 3.791

2.  Screening for inherited metabolic disease by plasma chromatography (Scriver) in a large city.

Authors:  D N Raine; J R Cooke; W A Andrews; D F Mahon
Journal:  Br Med J       Date:  1972-07-01

3.  Phenylketonuria. Mass screening of newborns in Ireland.

Authors:  S F Cahalane
Journal:  Arch Dis Child       Date:  1968-04       Impact factor: 3.791

4.  The newborn phenylketonuria screening program in Ontario.

Authors: 
Journal:  Can Med Assoc J       Date:  1969-08-23       Impact factor: 8.262

5.  Diagnosis of phenylketonuria (phenylalanine hydroxylase deficiency, temporary and permanent).

Authors:  J B Stephenson; M S McBean
Journal:  Br Med J       Date:  1967-09-02
  5 in total

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