G. P. A. Smit

Impaired prenatal and postnatal growth in Dutch patients with phenylketonuria. The National PKU Steering Committee.

P.H. Verkerk, F. J. van Spronsen, G. P. A. Smit et al. · Archives of Disease in Childhood · 1994 · 84 citations · Full text

Mevalonic aciduria: an inborn error of cholesterol biosynthesis?

Rolf M.F. Berger, G. P. A. Smit, Henk H. Schierbeek et al. · Clinica Chimica Acta · 1985 · 81 citations

Oxysterol, Pathology, Mevalonic Aciduria +4

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

Type Iiib Glycogen Storage Disease Associated With End–Stage Cirrhosis and Hepatocellular Carcinoma

E. B. Haagsma, G. P. A. Smit, Klary E. Niezen‐Koning et al. · Hepatology · 1997 · 72 citations

Transplantation, Hepatology, Gsd Subtype Iiib +15

Identification and Characterization of Three Novel Missense Mutations in Mevalonate Kinase cDNA Causing Mevalonic Aciduria, a Disorder of Isoprene Biosynthesis

Sander M. Houten, G. J. Romeijn, Janet Koster et al. · Human Molecular Genetics · 1999 · 64 citations