Jean Rey
Hôpital Necker-Enfants Malades(FR)Université Paris Cité(FR)
Publications by Year
Research Areas
Metabolism and Genetic Disorders, Folate and B Vitamins Research, Infant Nutrition and Health, Digestive system and related health, Amino Acid Enzymes and Metabolism
Most-Cited Works
- → A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype(1998)353 cited
- → Neuropsychologic Functions of Early Treated Patients with Phenylketonuria, on and off Diet: Results of a Cross-National and Cross-Sectional Study(1997)92 cited
- → CpG dinucleotides are mutation hot spots in phenylketonuria(1989)86 cited
- Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency.(1989)
- → Breastfeeding and cognitive development(2003)62 cited
- → Histochemical Localization of Intestinal Disaccharidases: Application to Peroral Biopsy Specimens(1967)42 cited
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