Baudouin François

A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype

Per Guldberg, Françoise Rey, Johannes Zschocke et al. · The American Journal of Human Genetics · 1998 · 357 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

High phenylalanine levels directly affect mood and sustained attention in adults with phenylketonuria: a randomised, double‐blind, placebo‐controlled, crossover trial

Amber E. ten Hoedt, Leo de Sonneville, Baudouin François et al. · Journal of Inherited Metabolic Disease · 2010 · 159 citations · Full text

Agriculture, Pharmacology, Pharmacotherapy +13

Ornithine trascarbamylase deficiencies in human males Kinetic and immunochemical classification

Pascale Briano, Baudouin François, Daniel Rabier et al. · Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology · 1982 · 67 citations

Life Sciences, Biochemistry, Immunology +12

Effects of selenium supplementation on thyroid hormone metabolism in phenylketonuria subjects on a phenylalanine restricted diet

M. Calomme, Jean Vanderpas, Baudouin François et al. · Biological Trace Element Research · 1995 · 27 citations

Medicine, Endocrinology, Nutritional Sciences +14

Polymerase gamma deficiency (POLG): Clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh’s encephalopathy

Emmanuel Scalais, Baudouin François, Patrick Schlesser et al. · European Journal of Paediatric Neurology · 2012 · 26 citations

Medicine, Neurology, Pediatrics +11