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Pediatric Research|November 1, 1984
Identification of methyl-branched chain dicarboxylic acids in amniotic fluid and urine in propionic and methylmalonic acidemiaC Jakobs, L Dorland, L Sweetman, et al.Clinical Genetics|September 1, 1984
Occurrences of methylmalonic aciduria and Hartnup disorder in the same familyV E Shih, J T Coulombe, S K Wadman, et al.Clinical Biochemistry|December 1, 1979
Simultaneous occurrence of xanthine oxidase and sulfite oxidase deficiency. A molybdenum dependent inborn error of metabolism?C van der Heiden, F A Beemer, W Brink, et al.Acta Paediatrica Scandinavica|May 1, 1978
Effects of thiamine in a patient with a variant form of branched-chian ketoaciduriaM Duran, A G Tielens, S K Wadman, et al.European Journal of Pediatrics|December 1, 1988
Report on a new patient with combined deficiencies of sulphite oxidase and xanthine dehydrogenase due to molybdenum cofactor deficiencyW Endres, Y S Shin, R Günther, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|December 1, 1978
Organic acid excretion in a patient with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency: facts and artefactsM Duran, D Ketting, S K Wadman, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|December 31, 1991
Gas chromatography method for the separation of amino acids enantiomers in plasma and urine. Application in a case of short bowel syndromeD Ketting, S K Wadman, L J Spaapen, et al.The Journal of Clinical Investigation|April 1, 1986
Deficiency of 3-methylglutaconyl-coenzyme A hydratase in two siblings with 3-methylglutaconic aciduriaK Narisawa, K M Gibson, L Sweetman, et al.The Journal of Pediatrics|October 1, 1982
Inherited 3-methylglutaconic aciduria in two brothers--another defect of leucine metabolismM Duran, F A Beemer, A S Tibosch, et al.Journal of Inherited Metabolic Disease|January 1, 1980
Leigh's disease with decreased activities of pyruvate carboxylase and pyruvate decarboxylaseJ P Van Biervliet, M Duran, S K Wadman, et al.Pageof 56