Literature DB >> 3329492

[Classification and heterogeneity of hyperphenylalaninemias linked to a phenylalanine hydroxylase deficiency].

F Rey1, A Munnich, S Lyonnet, J Rey.   

Abstract

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Year:  1987        PMID： 3329492

Source DB:  PubMed          Journal:  Arch Fr Pediatr        ISSN： 0003-9764


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  4 in total

1.  Single-strand conformation polymorphism for detection of mutations and base substitutions in phenylketonuria.

Authors:  P Labrune; D Melle; F Rey; M Berthelon; C Caillaud; J Rey; A Munnich; S Lyonnet
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

2.  Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in France.

Authors:  F Rey; M Berthelon; C Caillaud; S Lyonnet; V Abadie; F Blandin-Savoja; J Feingold; J M Saudubray; J Frézal; A Munnich
Journal:  Am J Hum Genet       Date:  1988-12       Impact factor: 11.025

3.  PKU-related dysgammaglobulinaemia: the effect of diet therapy on IgE and allergic sensitization.

Authors:  E Riva; A Fiocchi; C Agostoni; G Biasucci; M Sala; G Banderali; D Luotti; M Giovannini
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

4.  Significant phenylalanine hydroxylation in vivo in patients with classical phenylketonuria.

Authors:  G N Thompson; D Halliday
Journal:  J Clin Invest       Date:  1990-07       Impact factor: 14.808
  4 in total

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