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Journal of Inherited Metabolic Disease|January 1, 1978
Combined deficiency of xanthine oxidase and sulphite oxidase: a defect of molybdenum metabolism or transport?M Duran, F A Beemer, C van de Heiden, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 2, 1978
Nepsilon-(beta-Aspartyl)lysinuria in children with various pathological conditionsJ P Kamerling, G Aarsen, P K de Bree, et al.
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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 16, 1978
Lanthionine detected in human urineS K Wadman, P K De Bree, J P Kamerling
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1990
Rapid diagnosis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency via enzyme activity measurements in leukocytes or platelets using a simple spectrophotometric methodR J Wanders, P H Zoeters, R B Schutgens, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 20, 1976
D-Glyceric acidemia in a patient with chronic metabolic acidosisS K Wadman, M Duran, D Ketting, et al.
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