Amber E. ten Hoedt

Recessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy

Thomas Cullup, Ay Lin Kho, Carlo Dionisi‐Vici et al. · Nature Genetics · 2012 · 272 citations · Full text

Cell Autophagy, Mendelian Disorder, Autoimmune Disease +9

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

Parenting a child with phenylketonuria or galactosemia: implications for health‐related quality of life

Amber E. ten Hoedt, Heleen Maurice‐Stam, C Boelen et al. · Journal of Inherited Metabolic Disease · 2011 · 80 citations · Full text

Metabolic Disorder, Parental Mental Hrqol, Health Psychology +18

"MY PKU": increasing self-management in patients with phenylketonuria. A randomized controlled trial

Amber E. ten Hoedt, Carla E. M. Hollak, C Boelen et al. · Orphanet Journal of Rare Diseases · 2011 · 17 citations · Full text

High incidence of hypermethioninaemia in a single neonatal intensive care unit detected by a newly introduced neonatal screening programme

Amber E. ten Hoedt, Anne Van Kempen, Anita Boelen et al. · Journal of Inherited Metabolic Disease · 2007 · 15 citations