Hildgund Schmidt
Universitätskinderklinik(DE)
Publications by Year
Research Areas
Metabolism and Genetic Disorders, Mitochondrial Function and Pathology, Diet and metabolism studies, Diabetes, Cardiovascular Risks, and Lipoproteins, Folate and B Vitamins Research
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
- → Psychiatric Disorders in Adult Patients With Early-treated Phenylketonuria(1997)119 cited
- → Effect of high-dose tyrosine supplementation on brain function in adults with phenylketonuria(1995)55 cited
- → Genotype-phenotype correlations in phenylketonuria(1993)36 cited
- → Acid-Base Status in Dietary Treatment of Phenylketonuria(1977)25 cited
- → Body growth in primary de Toni-Debré-Fanconi syndrome(1997)24 cited
- → Six-year follow up of phenylalanine intakes and plasma phenylalanine concentrations(1990)23 cited
- → Study design and description of patients(1990)22 cited
- → PHENYLKETONURIA VARIANTS(1979)20 cited
- → Microheterogeneity of urinary albumin and tubular proteinuria in juvenile diabetes mellitus(1991)8 cited