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Journal of Inherited Metabolic Disease|January 1, 1996
Late-onset holocarboxylase synthetase deficiencyK M Gibson, M J Bennett, W L Nyhan, et al.
European Journal of Drug Metabolism and Pharmacokinetics|January 1, 1989
Metabolism of [U-14C]-4-hydroxybutyric acid to intermediates of the tricarboxylic acid cycle in extracts of rat liver and kidney mitochondriaK M Gibson, W L Nyhan
European Journal of Pediatrics|December 1, 1988
3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patientsK M Gibson, J Breuer, W L Nyhan
Pediatric Research|October 1, 1988
Oxidation of [U-14C]succinic semialdehyde in cultured human lymphoblasts: measurement of residual succinic semialdehyde dehydrogenase activity in 11 patients with 4-hydroxybutyric aciduriaP P Pattarelli, W L Nyhan, K M Gibson
American Journal of Human Genetics|July 1, 1984
Genetic complementation analysis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency in cultured fibroblastsO Sovik, L Sweetman, K M Gibson, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1989
3-Methylglutaconyl-CoA hydratase, 3-methylcrotonyl-CoA carboxylase and 3-hydroxy-3-methylglutaryl-CoA lyase deficiencies: a coupled enzyme assay useful for their detectionK Narisawa, K M Gibson, L Sweetman, et al.
Journal of Neurogenetics|September 1, 1984
Succinic semialdehyde dehydrogenase deficiencyK M Gibson, L Sweetman, W L Nyhan, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Demonstration of 4-aminobutyric acid aminotransferase deficiency in lymphocytes and lymphoblastsK M Gibson, L Sweetman, W L Nyhan, et al.
The Journal of Pediatrics|December 1, 1992
3-Methylglutaconic aciduria associated with Pearson syndrome and respiratory chain defectsK M Gibson, M J Bennett, C E Mize, et al.
European Journal of Pediatrics|September 1, 1984
Defective succinic semialdehyde dehydrogenase activity in 4-hydroxybutyric aciduriaK M Gibson, L Sweetman, W L Nyhan, et al.
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