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S K Wadman

Showing results (1-10 of 157) with videos related to

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Acta Universitatis Carolinae. Medica. Monographia|January 1, 1977
Chemical diagnosis of amino acid abnormalities. Possibilities and desirabilitiesS K Wadman
Journal of Inherited Metabolic Disease|January 1, 1985
Thiamine-responsive inborn errors of metabolismM Duran, S K Wadman
Enzyme|January 1, 1987
Chemical diagnosis of inherited defects of fatty acid metabolism and ketogenesisM Duran, S K Wadman
Journal of Chromatography|September 5, 1986
Quantitative gas chromatographic determination of urinary hydantoin-5-propionic acid in patients with disorders of folate/vitamin B12 metabolismM Duran, L Bruinvis, S K Wadman
Acta Paediatrica Scandinavica|September 1, 1971
A variant form of branched-chain keto aciduriaJ L van der Horst, S K Wadman
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 1, 1978
Excretion of cis- and trans-4-hydroxycyclohexylacetic acid in addition to hawkinsin in a family with a postulated defect of 4-hydroxyphenylpyruvate dioxygenaseA Niederwieser, S K Wadman, D M Danks
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 1, 1972
Densitometric determination of catecholamine metabolites and 5-hydroxy-indoleacetic acid after two-dimensional thin-layer chromatography on celluloseK Breebaart, A M Haan, S K Wadman
Ciba Foundation Symposium|January 1, 1982
Organic acidurias: approach, results and clinical relevanceS K Wadman, M Duran, J P Kamerling
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 1, 1976
Gas chromatographic determination of urinary vanilglycolic acid, vanilglycol, vanilacetic acid and vanillactic acid-chemical parameters for the diagnosis of neurogenic tumours and the evaluation of their treatmentS K Wadman, D Ketting, P A Voûte
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 28, 1985
The occurrence of lactyl lactate and succinyl lactate in the urine of patients screened for inherited metabolic diseaseD Ketting, S K Wadman, L Bruinvis, et al.
Pageof 16

Showing results (1-10 of 157) with videos related to

Sort By:
Pageof 16
Acta Universitatis Carolinae. Medica. Monographia|January 1, 1977
Chemical diagnosis of amino acid abnormalities. Possibilities and desirabilitiesS K Wadman
Journal of Inherited Metabolic Disease|January 1, 1985
Thiamine-responsive inborn errors of metabolismM Duran, S K Wadman
Enzyme|January 1, 1987
Chemical diagnosis of inherited defects of fatty acid metabolism and ketogenesisM Duran, S K Wadman
Journal of Chromatography|September 5, 1986
Quantitative gas chromatographic determination of urinary hydantoin-5-propionic acid in patients with disorders of folate/vitamin B12 metabolismM Duran, L Bruinvis, S K Wadman
Acta Paediatrica Scandinavica|September 1, 1971
A variant form of branched-chain keto aciduriaJ L van der Horst, S K Wadman
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 1, 1978
Excretion of cis- and trans-4-hydroxycyclohexylacetic acid in addition to hawkinsin in a family with a postulated defect of 4-hydroxyphenylpyruvate dioxygenaseA Niederwieser, S K Wadman, D M Danks
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 1, 1972
Densitometric determination of catecholamine metabolites and 5-hydroxy-indoleacetic acid after two-dimensional thin-layer chromatography on celluloseK Breebaart, A M Haan, S K Wadman
Ciba Foundation Symposium|January 1, 1982
Organic acidurias: approach, results and clinical relevanceS K Wadman, M Duran, J P Kamerling
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 1, 1976
Gas chromatographic determination of urinary vanilglycolic acid, vanilglycol, vanilacetic acid and vanillactic acid-chemical parameters for the diagnosis of neurogenic tumours and the evaluation of their treatmentS K Wadman, D Ketting, P A Voûte
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 28, 1985
The occurrence of lactyl lactate and succinyl lactate in the urine of patients screened for inherited metabolic diseaseD Ketting, S K Wadman, L Bruinvis, et al.
Pageof 16