R. Berger

Hereditary Tyrosinemia Type I: A New Clinical Classification With Difference in Prognosis on Dietary Treatment

Francjan J. van Spronsen, Yolande Thomasse, Peter Smit et al. · Hepatology · 1994 · 192 citations

New Clinical Classification, Tyrosinemia Type, Disease Progression +23

A Novel Disorder of N-Glycosylation Due to Phosphomannose Isomerase Deficiency

Tom J. de Koning, L. Dorland, O. P. van Diggelen et al. · Biochemical and Biophysical Research Communications · 1998 · 119 citations

Glycoproteomics, Cellular Enzymology, Biochemistry +6

The natural history of liver glycogenosis due to phosphorylase kinase deficiency: A longitudinal study of 41 patients

Patrick J. Willems, Willem J.M. Gerver, R. Berger et al. · European Journal of Pediatrics · 1990 · 96 citations

Hepatology, Liver Physiology, Inherited Metabolic Disease +6

Absence of hepatic molybdenum cofactor: An inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenase

S.K. Wadman, M. Durán, F. A. Beemer et al. · Journal of Inherited Metabolic Disease · 1983 · 76 citations

Lactate as a Cerebral Metabolic Fuel for Glucose-6-Phosphatase Deficient Children

J. Fernandes, R. Berger, Gerrit Smit · Pediatric Research · 1984 · 66 citations · Full text

Metabolic Syndrome, Energy Homeostasis, Energy Metabolism +9