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 · 352 citations · Full text

Metabolic Syndrome, Mendelian Disorder, Biochemistry +11

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 · 156 citations · Full text

Neuropsychology, Psychopharmacology, Neuropsychiatry +16

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

Immunology, Pathology, Ornithine Trascarbamylase Deficiencies +2

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

Nutrition, Urology, Selenium Deficiency +12

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

Mendelian Disorder, Genetic Disorder, Alpers Syndrome +8