Literature DB >> 14329976

ADVANCES IN THE MANAGEMENT OF PATIENT WITH PHENYLKETONURIA.

B UMBARGER, H K BERRY, B S SUTHERLAND.   

Abstract

Entities:  

Keywords:  BLOOD; CHILD; DEFICIENCY DISEASES; DIET THERAPY; INFANT; INFANT, NEWBORN; PHENYLALANINE; PHENYLKETONURIA; URINE

Mesh：

Substances：

Year:  1965        PMID： 14329976     DOI： 10.1001/jama.1965.03090100030007

Source DB:  PubMed          Journal:  JAMA        ISSN： 0098-7484            Impact factor:   56.272


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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.  [Phenylketonuria with normal IQ].

Authors:  J G Gostomzyk; F Dressler
Journal:  Klin Wochenschr       Date:  1967-08-01

3.  Phenylketonuria. Early detection, diagnosis and treatment.

Authors:  G C Cunningham
Journal:  Calif Med       Date:  1966-07

4.  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.  Survey of departments of health about PKU screening programs.

Authors:  K C Steiner; H A Smith
Journal:  Public Health Rep       Date:  1975 Jan-Feb       Impact factor: 2.792
  5 in total

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