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Journal of Inherited Metabolic Disease|January 1, 1980
L-2-Hydroxyglutaric aciduria: an inborn error of metabolism?M Duran, J P Kamerling, H D Bakker, et al.
European Journal of Pediatrics|January 1, 1984
Prenatal diagnosis of glutaric aciduria type II by direct chemical analysis of dicarboxylic acids in amniotic fluidC Jakobs, L Sweetman, S K Wadman, et al.
European Journal of Pediatrics|June 28, 1979
Two sisters with isovaleric acidaemia, multiple attacks of ketoacidosis and normal developmentM Duran, F J van Sprang, J G Drewes, et al.
Acta Paediatrica Scandinavica|January 1, 1981
5-oxoprolinuria due to hereditary 5-oxoprolinase deficiency in two brothers--a new inborn error of the gamma-glutamyl cycleA Larsson, B Mattsson, E A Wauters, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Isovaleric acidaemia presenting with dwarfism, cataract and congenital abnormalitiesM Duran, L Bruinvis, D Ketting, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1980
Inborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactorJ L Johnson, W R Waud, K V Rajagopalan, et al.
European Journal of Pediatrics|July 1, 1982
Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency in two sibsF A Beemer, K Bartlett, M Duran, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 18, 1981
Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemiaR Berger, G P Smit, S A Stoker-de Vries, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 15, 1985
Octanoylglucuronide excretion in patients with a defective oxidation of medium-chain fatty acidsM Duran, D Ketting, R van Vossen, et al.
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