Literature DB >> 13441010

[Phenylpyruvic oligophrenia & heart defects].

J H JONXIS.   

Abstract

Entities:  

Keywords:  CARDIOVASCULAR DEFECTS, CONGENITAL/physiology; MENTAL DEFICIENCY

Mesh：

Year:  1957        PMID： 13441010

Source DB:  PubMed          Journal:  Ned Tijdschr Geneeskd        ISSN： 0028-2162


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  6 in total

1.  [ON A FAMILIAL DISEASE WITH AN UNUSUAL NEUROLOGIC SYMPTOM COMBINATION, OLIGOPHRENIA, DEMENTIA, MULTIPLE SKIN ULCERATIONS, SPLENOMEGALY AND AMINO ACID METABOLIC DISORDERS].

Authors:  J BRUCK; F GERSTENBRAND; P PROSENZ; R SANTLER; B SCHOBEL; F WEWALKA
Journal:  Dtsch Z Nervenheilkd       Date:  1964-02-21

2.  DISORDERS OF AMINO-ACID TRANSPORT.

Authors:  M D MILNE
Journal:  Br Med J       Date:  1964-02-08

3.  [Photodermatosis with aminoaciduria, indolaceturia & cerebral manifestations (Hartnup syndrome)].

Authors:  H WEYERS; H BICKEL
Journal:  Klin Wochenschr       Date:  1958-10-01

4.  Hartnup disease in psychiatric practice: clinical and biochemical features of three cases.

Authors:  L A HERSOV; R RODNIGHT
Journal:  J Neurol Neurosurg Psychiatry       Date:  1960-02       Impact factor: 10.154

5.  A case of Hartnup disease.

Authors:  W HENDERSON
Journal:  Arch Dis Child       Date:  1958-04       Impact factor: 3.791

6.  Clinical and biochemical observations in two cases of hartnup disease.

Authors:  P W Wong; P M Pillai
Journal:  Arch Dis Child       Date:  1966-08       Impact factor: 3.791
  6 in total

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