Literature DB >> 943900

Hyperprolinaemia: a disease which does not need treatment?

F Mollica, L Pavone.   

Abstract

The authors observed two cases of hyperprolinaemia (one of type I and the other of type II) which were asymptomatic. The anomalies described up to the present time in association with hyperprolinaemia are inconstant, nonspecific, and extremely heterogeneous. This suggests that the relationship between hyperprolinaemia and other anomalies is purely coincidental, and that a therapeutic approach by diet is unjustified.

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Year:  1976        PMID: 943900     DOI: 10.1111/j.1651-2227.1976.tb16538.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


  2 in total

1.  Diminished concentration of the NF-H subunit of neurofilaments in cerebral cortex of rats chronically treated with proline, methylmalonate and phenylalanine plus alpha-methylphenylalanine.

Authors:  M A Rubin; C M Wannmacher; G B Valente; M M Camargo; R P Pureur
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

2.  Type II hyperprolinaemia in a pedigree of Irish travellers (nomads).

Authors:  M P Flynn; M C Martin; P T Moore; J A Stafford; G A Fleming; J M Phang
Journal:  Arch Dis Child       Date:  1989-12       Impact factor: 3.791

  2 in total

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