Rey F - Search Results

1

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

Labrune P, Melle D, Rey F, Berthelon M, Caillaud C, Rey J, Munnich A, Lyonnet S. Labrune P, et al. Among authors: rey j, rey f. Am J Hum Genet. 1991 Jun;48(6):1115-20. Am J Hum Genet. 1991. PMID: 2035532 Free PMC article.

2

[Hypercholesteremia and the prevention of atheroma].

Rey J, Rey F. Rey J, et al. Among authors: rey f. Arch Fr Pediatr. 1976 Oct;33(8):821-33. Arch Fr Pediatr. 1976. PMID: 185983 Review. French. No abstract available.

3

Kinetics of phenylalanine disappearance after intravenous load in phenylketonuria and its genetic variants.

Rey F, Blandin-Savoja F, Rey J. Rey F, et al. Among authors: rey j. Pediatr Res. 1979 Jan;13(1):21-5. doi: 10.1203/00006450-197901000-00005. Pediatr Res. 1979. PMID: 431997 No abstract available.

4

["Transitory" phenylketonuria. A permanent deficit].

Rey F, Leeming RJ, Curtius HC, Niederwieser A, Viscontini M, Rey J. Rey F, et al. Among authors: rey j. Arch Fr Pediatr. 1979 Nov;36(9 Suppl):XLVIII-LV. Arch Fr Pediatr. 1979. PMID: 539882 French.

5

[Results after 5 years of early treated phenyketonuria. Correlations with the quality of dietetic control].

Rey F, Rapoport D, du Fraysseix M, Briard ML, Rey J. Rey F, et al. Among authors: rey j. Arch Fr Pediatr. 1978 Dec;35(10 Suppl):11-22. Arch Fr Pediatr. 1978. PMID: 749750 French. No abstract available.

6

[Phenylketonuria and mental development: a badly stated problem].

Rey J, Rey F. Rey J, et al. Among authors: rey f. Arch Fr Pediatr. 1978 Dec;35(10 Suppl):3-10. Arch Fr Pediatr. 1978. PMID: 749751 French. No abstract available.

7

Atypical phenylketonuria with normal dihydropteridine reductase activity.

Rey F, Blandin-Savoja F, Rey J. Rey F, et al. Among authors: rey j. N Engl J Med. 1976 Nov 11;295(20):1138-9. doi: 10.1056/NEJM197611112952018. N Engl J Med. 1976. PMID: 980015 No abstract available.

8

[Phenotypic expression of 12 mutations of the phenylalanine hydroxylase gene].

Rey F, Abadie V, Lyonnet S, Berthelon M, Caillaud C, Melle D, Labrune P, Saudubray JM, Munnich A, Rey J. Rey F, et al. Among authors: rey j. Arch Fr Pediatr. 1992 Oct;49(8):705-10. Arch Fr Pediatr. 1992. PMID: 1288453 French.

9

[Intellectual development after relaxing the diet at the age of 5 years in typical phenylketonuria].

Abadie V, Rey F, Plainguet F, Rey J. Abadie V, et al. Among authors: rey j, rey f. Arch Fr Pediatr. 1992 Nov;49(9):773-8. Arch Fr Pediatr. 1992. PMID: 1300964 French.

10

Linkage disequilibrium between phenylketonuria and RFLP haplotype 1 at the phenylalanine hydroxylase locus in Portugal.

Caillaud C, Vilarinho L, Vilarinho A, Rey F, Berthelon M, Santos R, Lyonnet S, Briard ML, Osorio RV, Rey J, et al. Caillaud C, et al. Among authors: rey j, rey f. Hum Genet. 1992 Apr;89(1):69-72. doi: 10.1007/BF00207045. Hum Genet. 1992. PMID: 1349566

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