Literature DB >> 13224247

A possible mechanism for disturbance in tyrosine metabolism in phenylpyruvic oligophrenia.

J DANCIS, M E BALIS.   

Abstract

Entities:  

Keywords:  MENTAL DEFICIENCY; TYROSINE/metabolism

Mesh：

Substances：

Year:  1955        PMID： 13224247

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  6 in total

1.  Diminished phenylketonuria in phenylpyruvic oligophrenia after administration of L-glutamine, L-glutamate or L-asparagine.

Authors:  A MEISTER; S UDENFRIEND; S P BESSMAN
Journal:  J Clin Invest       Date:  1956-06       Impact factor: 14.808

2.  Phenylketonuria with normal intelligence and Gowers' muscular dystrophy.

Authors:  S COATES; A P NORMAN; L I WOOLF
Journal:  Arch Dis Child       Date:  1957-08       Impact factor: 3.791

3.  Epinephrine metabolites and pigmentation in the central nervous system in a case of phenylpyruvic oligophrenia.

Authors:  J H FELLMAN
Journal:  J Neurol Neurosurg Psychiatry       Date:  1958-02       Impact factor: 10.154

4.  The dietary treatment of phenylketonuria.

Authors:  L I WOOLF; R GRIFFITHS; A MONCRIEFF; S COATES; F DILLISTONE
Journal:  Arch Dis Child       Date:  1958-02       Impact factor: 3.791

5.  Bibliography of human genetics.

Authors:  R P MERICLE
Journal:  Am J Hum Genet       Date:  1956-03       Impact factor: 11.025

Review 6.  Measurements of uridine diphosphate glucose and uridine diphosphate galactose--an appraisal.

Authors:  H N Kirkman
Journal:  Eur J Pediatr       Date:  1995       Impact factor: 3.183
  6 in total

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