Gibson KM - Search Results

1

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

2

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

3

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

4

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.

5

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.

6

4-Hydroxybutyric aciduria in a patient without ataxia or convulsions.

Gibson KM, Hoffmann G, Nyhan WL, Aramaki S, Thompson JA, Goodman SI, Johnson DA, Fife RR. Gibson KM, et al. Eur J Pediatr. 1988 Jun;147(5):529-31. doi: 10.1007/BF00441983. Eur J Pediatr. 1988. PMID: 3409929

7

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

8

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

9

Conservation of central nervous system glutaryl-coenzyme A dehydrogenase in fruit-eating bats with glutaric aciduria and deficient hepatic glutaryl-coenzyme A dehydrogenase.

McMillan TA, Gibson KM, Sweetman L, Meyers GS, Green R. McMillan TA, et al. Among authors: gibson km. J Biol Chem. 1988 Nov 25;263(33):17258-61. J Biol Chem. 1988. PMID: 3182847 Free article.

10

Defective succinic semialdehyde dehydrogenase activity in 4-hydroxybutyric aciduria.

Gibson KM, Sweetman L, Nyhan WL, Lenoir G, Divry P. Gibson KM, et al. Eur J Pediatr. 1984 Sep;142(4):257-9. doi: 10.1007/BF00540247. Eur J Pediatr. 1984. PMID: 6489377

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