F. Blandin-Savoja

Atypical phenylketonuria with normal dihydropteridine reductase activity.

J. Rey, F. Rey, F. Blandin-Savoja, 1976, The New England journal of medicine.

Kinetics of Phenylalanine Disappearance after Intravenous Load in Phenylketonuria and Its Genetic Variants

J. Rey, F. Rey, F. Blandin-Savoja, 1979, Pediatric Research.

The mutant genotype is the main determinant of the metabolic phenotype in phenylalanine hydroxylase deficiency.

P. Bénit, A. Munnich, V. Abadie, 1999, Molecular genetics and metabolism.

Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in France.

A. Munnich, S. Lyonnet, J. Frézal, 1988, American journal of human genetics.

Phenylalanine hydroxylase. Evidence that the enzyme from human liver might not be a phosphoprotein.

J. Abita, F. Rey, F. Blandin-Savoja, 1983, Biochemistry international.

Phenylalanine 4-monooxygenase from human liver.

J. Abita, F. Rey, F. Blandin-Savoja, 1987, Methods in enzymology.

Influence of Age on ortho-Hydroxyphenylacetic Acid Excretion in Phenylketonuria and Its Genetic Variants

J. Frézal, C. Pellié, J. Rey, 1974, Pediatric Research.