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Acta Universitatis Carolinae. Medica. Monographia
|
January 1, 1977
Chemical diagnosis of amino acid abnormalities. Possibilities and desirabilities
S K Wadman
Journal of Inherited Metabolic Disease
|
January 1, 1985
Thiamine-responsive inborn errors of metabolism
M Duran, S K Wadman
Enzyme
|
January 1, 1987
Chemical diagnosis of inherited defects of fatty acid metabolism and ketogenesis
M 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 metabolism
M Duran, L Bruinvis, S K Wadman
Acta Paediatrica Scandinavica
|
September 1, 1971
A variant form of branched-chain keto aciduria
J 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 dioxygenase
A 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 cellulose
K Breebaart, A M Haan, S K Wadman
Ciba Foundation Symposium
|
January 1, 1982
Organic acidurias: approach, results and clinical relevance
S 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 treatment
S 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 disease
D Ketting, S K Wadman, L Bruinvis, et al.
Page
of 16
Search research articles
Search
Showing results (1-10 of 157) with videos related to
Sort By:
Page
of 16
Acta Universitatis Carolinae. Medica. Monographia
|
January 1, 1977
Chemical diagnosis of amino acid abnormalities. Possibilities and desirabilities
S K Wadman
Journal of Inherited Metabolic Disease
|
January 1, 1985
Thiamine-responsive inborn errors of metabolism
M Duran, S K Wadman
Enzyme
|
January 1, 1987
Chemical diagnosis of inherited defects of fatty acid metabolism and ketogenesis
M 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 metabolism
M Duran, L Bruinvis, S K Wadman
Acta Paediatrica Scandinavica
|
September 1, 1971
A variant form of branched-chain keto aciduria
J 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 dioxygenase
A 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 cellulose
K Breebaart, A M Haan, S K Wadman
Ciba Foundation Symposium
|
January 1, 1982
Organic acidurias: approach, results and clinical relevance
S 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 treatment
S 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 disease
D Ketting, S K Wadman, L Bruinvis, et al.
Page
of 16