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Journal of Inherited Metabolic Disease|January 1, 1985
Thiamine-responsive inborn errors of metabolismM Duran, S K WadmanEnzyme|January 1, 1987
Chemical diagnosis of inherited defects of fatty acid metabolism and ketogenesisM Duran, S K WadmanCiba Foundation Symposium|January 1, 1982
Organic acidurias: approach, results and clinical relevanceS K Wadman, M Duran, J P KamerlingJournal of Inherited Metabolic Disease|January 1, 1978
Deranged isoleucine metabolism during ketotic attacks in patients with methylmalonic acidaemiaM Duran, L Bruinvis, D Ketting, et al.European Journal of Pediatrics|January 1, 1994
Group tests for selective screening of inborn errors of metabolismM Duran, L Dorland, S K Wadman, et al.Biochemical Medicine|April 1, 1983
The urinary excretion of ethylmalonic acid: what level requires further attention?M Duran, F J Walther, L Bruinvis, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|January 2, 1978
The variability of metabolite excretion in propionicacidaemiaM Duran, D Gompertz, L Bruinvis, et al.Ophthalmic Paediatrics and Genetics|April 1, 1985
Absence of hepatic molybdenum cofactor. An inborn error of metabolism associated with lens dislocationF A Beemer, M Duran, S K Wadman, et al.Journal of Inherited Metabolic Disease|January 1, 1986
Direct identification of propionylcarnitine in propionic acidaemia: biochemical and clinical results of oral carnitine supplementationM Duran, D Ketting, T E Beckeringh, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1978
Methylmalonate excretion in a pregnancy at risk for methylmalonic acidaemiaH D Bakker, A H van Gennip, M Duran, et al.Pageof 56