Hildgund Schmidt

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

Psychiatric Disorders in Adult Patients With Early-treated Phenylketonuria

Joachim Pietz, B. Fätkenheuer, Peter Burgard et al. · PEDIATRICS · 1997 · 119 citations

Effect of high-dose tyrosine supplementation on brain function in adults with phenylketonuria

Joachim Pietz, Ralf Landwehr, Ansgar Kutscha et al. · The Journal of Pediatrics · 1995 · 55 citations

Brain Function, Neurophysiology, Nutritional Neuroscience +6

Genotype-phenotype correlations in phenylketonuria

Friedrich K. Trefz, Peter Burgard, Thomas König et al. · Clinica Chimica Acta · 1993 · 36 citations

Biology, Genotype-phenotype Correlations, Genotype-phenotype Association +6

Acid-Base Status in Dietary Treatment of Phenylketonuria

Friedrich Manz, Hildgund Schmidt, KARL SCH RER et al. · Pediatric Research · 1977 · 25 citations

Nutrition, Medicine, Clinical Nutrition +4