Literature DB >> 13626378

Phenylketonuria treated from earliest infancy; report of three cases.

F A HORNER, C W STREAMER.   

Abstract

Entities:  

Keywords:  PHENYLALANINE/metabolism

Mesh：

Substances：

Year:  1959        PMID： 13626378     DOI： 10.1001/archpedi.1959.02070010347014

Source DB:  PubMed          Journal:  AMA J Dis Child        ISSN： 0096-6916


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  7 in total

1.  The detection and diagnosis of phenylketonuria.

Authors:  R J ALLEN
Journal:  Am J Public Health Nations Health       Date:  1960-11

2.  Further experiences in the treatment of phenylketonuria.

Authors:  A MONCRIEFF; R H WILKINSON
Journal:  Br Med J       Date:  1961-03-18

3.  Megaloblastic Anaemia Complicating Dietary Treatment of Phenylketonuria in Infancy.

Authors:  N J Royston; T E Parry
Journal:  Arch Dis Child       Date:  1962-08       Impact factor: 3.791

4.  Variations in intelligence in phenylktonuria.

Authors:  M W PARTINGTON
Journal:  Can Med Assoc J       Date:  1962-04-21       Impact factor: 8.262

5.  Phenylketonuria. Early detection, diagnosis and treatment.

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

6.  Long-term outcome of expanded newborn screening at Boston children's hospital: benefits and challenges in defining true disease.

Authors:  Yuval E Landau; Susan E Waisbren; Lawrence M A Chan; Harvey L Levy
Journal:  J Inherit Metab Dis       Date:  2017-01-04       Impact factor: 4.982

7.  Biochemical Genetics and Mental Retardation.

Authors:  W C McMurray
Journal:  Can Med Assoc J       Date:  1962-09-01       Impact factor: 8.262
  7 in total

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