Literature DB >> 13815969

Argininosuccinic aciduria. A new form of mental deficiency due to metabolic causes.

C E DENT.   

Abstract

Entities:  

Keywords:  MENTAL DEFICIENCY/etiology; METABOLIC DISEASES/in infancy and childhood; SUCCINATES/pharmacology

Mesh：

Substances：

Year:  1959        PMID： 13815969      PMCID： PMC1869735     

Source DB:  PubMed          Journal:  Proc R Soc Med        ISSN： 0035-9157


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  1 in total

1.  A disease, probably hereditary characterised by severe mental deficiency and a constant gross abnormality of aminoacid metabolism.

Authors:  J D ALLAN; D C CUSWORTH; C E DENT; V K WILSON
Journal:  Lancet       Date:  1958-01-25       Impact factor: 79.321
  1 in total
  4 in total

1.  HOMOCYSTINURIA.

Authors:  R H JACKSON
Journal:  Br Med J       Date:  1963-12-14

2.  A survey of some hereditary metabolic diseases.

Authors:  R W WATTS
Journal:  Postgrad Med J       Date:  1960-08       Impact factor: 2.401

3.  Growing older: the adult metabolic clinic.

Authors:  P J Lee
Journal:  J Inherit Metab Dis       Date:  2002-05       Impact factor: 4.982

4.  A defect in pyruvate decarboxylase in a child with an intermittent movement disorder.

Authors:  J P Blass; J Avigan; B W Uhlendorf
Journal:  J Clin Invest       Date:  1970-03       Impact factor: 14.808
  4 in total

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