Literature DB >> 14001384

Sjogren-Larsson syndrome and histidinemia: hereditary biochemical diseases with defects of speech and oral functions.

C J WITKOP, F V HENRY.   

Abstract

Entities:  

Keywords:  ICHTHYOSIS; MENTAL DEFICIENCY; PROTEIN METABOLISM DISORDERS; SPEECH DISORDERS

Mesh：

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Year:  1963        PMID： 14001384     DOI： 10.1044/jshd.2802.109

Source DB:  PubMed          Journal:  J Speech Hear Disord        ISSN： 0022-4677


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  3 in total

1.  The Sjögren-Larsson syndrome. A case report.

Authors:  U Beringer; M Mumenthaler; L Zala
Journal:  J Neurol       Date:  1977-02-17       Impact factor: 4.849

2.  Fanconi syndrome, ichthyosis, dysmorphism, jaundice and diarrhoea--a new syndrome.

Authors:  J E Deal; T M Barratt; M J Dillon
Journal:  Pediatr Nephrol       Date:  1990-07       Impact factor: 3.714

Review 3.  Sjögren-Larsson syndrome. Oligophrenia--ichthyosis--di-tetraplegia.

Authors:  U Theile
Journal:  Humangenetik       Date:  1974-05-17
  3 in total

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