Literature DB >> 13434618

A case of phenylketonuria with borderline intelligence.

D Y HSIA, W E KNOX, R S PAINE.   

Abstract

Entities:  

Keywords:  MENTAL DEFICIENCY/case reports

Mesh：

Year:  1957        PMID： 13434618     DOI： 10.1001/archpedi.1957.04030020035008

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


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  6 in total

1.  Studies on linkage between phenylketonuria and the blood groups.

Authors:  D Y HSIA; A G STEINBERG
Journal:  Am J Hum Genet       Date:  1960-09       Impact factor: 11.025

2.  The detection in the heterozygote of the metabolic effect of the recessive gene for phenylketonuria.

Authors:  W E KNOX; E C MESSINGER
Journal:  Am J Hum Genet       Date:  1958-03       Impact factor: 11.025

3.  Studies on intestinal absorption of amino acids and a dipeptide in a case of Hartnup disease.

Authors:  F Navab; A M Asatoor
Journal:  Gut       Date:  1970-05       Impact factor: 23.059

Review 4.  Phenylketonuria and its variations. A review of recent developments.

Authors:  M E Blaskovics; T L Nelson
Journal:  Calif Med       Date:  1971-07

5.  [A case of "classical" phenylketonuria with average intelligence].

Authors:  W Schwenke; A Anke; A Knapp
Journal:  Klin Wochenschr       Date:  1969-10-01

6.  Intestinal absorption of two dipeptides in Hartnup disease.

Authors:  A M Asatoor; B Cheng; K D Edwards; A F Lant; D M Matthews; M D Milne; F Navab; A J Richards
Journal:  Gut       Date:  1970-05       Impact factor: 23.059
  6 in total

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