Gibson KM - Search Results

1

3-Methylglutaconyl-CoA hydratase, 3-methylcrotonyl-CoA carboxylase and 3-hydroxy-3-methylglutaryl-CoA lyase deficiencies: a coupled enzyme assay useful for their detection.

Narisawa K, Gibson KM, Sweetman L, Nyhan WL. Narisawa K, et al. Among authors: gibson km. Clin Chim Acta. 1989 Sep 15;184(1):57-64. doi: 10.1016/0009-8981(89)90256-8. Clin Chim Acta. 1989. PMID: 2480857

2

3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patients.

Gibson KM, Breuer J, Nyhan WL. Gibson KM, et al. Eur J Pediatr. 1988 Dec;148(3):180-6. doi: 10.1007/BF00441397. Eur J Pediatr. 1988. PMID: 3063529 Review.

3

3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normal.

Gibson KM, Nyhan WL, Sweetman L, Narisawa K, Lehnert W, Divry P, Robinson BH, Roth KS, Beemer FA, van Sprang FJ, et al. Gibson KM, et al. Eur J Pediatr. 1988 Oct;148(1):76-82. doi: 10.1007/BF00441821. Eur J Pediatr. 1988. PMID: 3197737

4

3-hydroxy-3-methylglutaric aciduria: a new assay of 3-hydroxy-3-methylglutaryl-coa lyase using high performance liquid chromatography.

Gibson KM, Sweetman L, Nyhan WL, Page TM, Greene C, Cann HM. Gibson KM, et al. Clin Chim Acta. 1982 Dec 9;126(2):171-81. doi: 10.1016/0009-8981(82)90033-x. Clin Chim Acta. 1982. PMID: 6185253

5

Mevalonate kinase in lysates of cultured human fibroblasts and lymphoblasts: kinetic properties, assay conditions, carrier detection and measurement of residual activity in a patient with mevalonic aciduria.

Gibson KM, Lohr JL, Broock RL, Hoffmann G, Nyhan WL, Sweetman L, Brandt IK, Wappner RS, Bader PI. Gibson KM, et al. Enzyme. 1989;41(1):47-55. doi: 10.1159/000469050. Enzyme. 1989. PMID: 2543551

6

Metabolism of [U-14C]-4-hydroxybutyric acid to intermediates of the tricarboxylic acid cycle in extracts of rat liver and kidney mitochondria.

Gibson KM, Nyhan WL. Gibson KM, et al. Eur J Drug Metab Pharmacokinet. 1989 Jan-Mar;14(1):61-70. doi: 10.1007/BF03190843. Eur J Drug Metab Pharmacokinet. 1989. PMID: 2759135

7

Mevalonate kinase deficiency in a child with cerebellar ataxia, hypotonia and mevalonic aciduria.

Gibson KM, Hoffmann G, Nyhan WL, Sweetman L, Berger R, le Coultre R, Smit GP. Gibson KM, et al. Eur J Pediatr. 1988 Dec;148(3):250-2. doi: 10.1007/BF00441413. Eur J Pediatr. 1988. PMID: 2850914

8

Deficiency of 3-methylglutaconyl-coenzyme A hydratase in two siblings with 3-methylglutaconic aciduria.

Narisawa K, Gibson KM, Sweetman L, Nyhan WL, Duran M, Wadman SK. Narisawa K, et al. Among authors: gibson km. J Clin Invest. 1986 Apr;77(4):1148-52. doi: 10.1172/JCI112415. J Clin Invest. 1986. PMID: 3082934 Free PMC article.

9

3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: report of five new patients.

Gibson KM, Breuer J, Kaiser K, Nyhan WL, McCoy EE, Ferreira P, Greene CL, Blitzer MG, Shapira E, Reverte F, et al. Gibson KM, et al. J Inherit Metab Dis. 1988;11(1):76-87. doi: 10.1007/BF01800058. J Inherit Metab Dis. 1988. PMID: 3128690

10

Oxidation of [U-14C]succinic semialdehyde in cultured human lymphoblasts: measurement of residual succinic semialdehyde dehydrogenase activity in 11 patients with 4-hydroxybutyric aciduria.

Pattarelli PP, Nyhan WL, Gibson KM. Pattarelli PP, et al. Among authors: gibson km. Pediatr Res. 1988 Oct;24(4):455-60. doi: 10.1203/00006450-198810000-00007. Pediatr Res. 1988. PMID: 3140205

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