E. Mönch

Urinary excretion of gamma-hydroxybutyric acid in a patient with neurological abnormalities. The probability of a new inborn error of metabolism

Cornelis Jakobs, Monika Bojasch, E. Mönch et al. · Clinica Chimica Acta · 1981 · 174 citations

Life Sciences, Neurology, Neuroscience +6

Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997

H. J. Bremer, P Bührdel, P. Clemens et al. · European Journal of Pediatrics · 1999 · 144 citations

Medicine, Endocrinology, Pediatrics +6

Long-term treatment with tetrahydrobiopterin increases phenylalanine tolerance in children with severe phenotype of phenylketonuria

Julia B. Hennermann, Christoph Bührer, Nenad Blau et al. · Molecular Genetics and Metabolism · 2005 · 107 citations

Pharmacy, Pediatrics, Pharmacotherapy +10

Features and outcome of galactokinase deficiency in children diagnosed by newborn screening

Julia B. Hennermann, Peter Schadewaldt, Barbara Vetter et al. · Journal of Inherited Metabolic Disease · 2011 · 71 citations

Medicine, Child Health, Pediatrics +13

Inherited metabolic disorders in Turkey

İ Özalp, Turgay Coşkun, S. Tokol et al. · Journal of Inherited Metabolic Disease · 1989 · 59 citations

Life Sciences, Endocrinology, Genetics +10