S. K. Wadman

Adenylosuccinase deficiency: an inborn error of purine nucleotide synthesis

Jaak Jaeken, S. K. Wadman, M. Durán et al. · European Journal of Pediatrics · 1988 · 125 citations

Biosynthesis, Biochemistry, Genetic Disorder +7

Combined deficiency of xanthine oxidase and sulphite oxidase: A defect of molybdenum metabolism or transport?

M. Durán, F. A. Beemer, Colin van der Heiden et al. · Journal of Inherited Metabolic Disease · 1978 · 124 citations

Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemia

R. Berger, Orla Smit, S.A. Stoker-de Vries et al. · Clinica Chimica Acta · 1981 · 58 citations

Hereditary Tyrosinemia, Mendelian Disorder, Genetic Disorder +4

Cis-4-decenoic acid in plasma: a characteristic metabolite in medium-chain acyl-CoA dehydrogenase deficiency.

M. Durán, L. Bruinvis, D. Ketting et al. · Clinical Chemistry · 1988 · 55 citations · Full text

Metabolic Syndrome, Medium-chain Fatty Acids, Aldehyde Dehydrogenase +15

Gas chromatographic analysis of urinary tyrosine and phenylalanine metabolites in patients with gastrointestinal disorders

Colin van der Heiden, E.A.K. Wauteks, D. Ketting et al. · Clinica Chimica Acta · 1971 · 50 citations

Urinary Tyrosine, Urology, Functional Gastrointestinal Disorder +9