Gibson KM - Search Results

1

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

2

3-Methylglutaconyl-coenzyme-A hydratase deficiency: a new case.

Gibson KM, Lee CF, Wappner RS. Gibson KM, et al. J Inherit Metab Dis. 1992;15(3):363-6. doi: 10.1007/BF02435977. J Inherit Metab Dis. 1992. PMID: 1383605 No abstract available.

3

3-Hydroxy-3-methylglutaryl coenzyme A reductase activity in cultured fibroblasts from patients with mevalonate kinase deficiency: differential response to lipid supplied by fetal bovine serum in tissue culture medium.

Gibson KM, Hoffmann G, Schwall A, Broock RL, Aramaki S, Sweetman L, Nyhan WL, Brandt IK, Wappner RS, Lehnert W, et al. Gibson KM, et al. J Lipid Res. 1990 Mar;31(3):515-21. J Lipid Res. 1990. PMID: 2160511 Free article.

4

Stable isotope dilution analysis of 4-hydroxybutyric acid: an accurate method for quantification in physiological fluids and the prenatal diagnosis of 4-hydroxybutyric aciduria.

Gibson KM, Aramaki S, Sweetman L, Nyhan WL, DeVivo DC, Hodson AK, Jakobs C. Gibson KM, et al. Biomed Environ Mass Spectrom. 1990 Feb;19(2):89-93. doi: 10.1002/bms.1200190207. Biomed Environ Mass Spectrom. 1990. PMID: 2407302

5

3-Hydroxy-3-methylglutaric aciduria: response to carnitine therapy and fat and leucine restriction.

Dasouki M, Buchanan D, Mercer N, Gibson KM, Thoene J. Dasouki M, et al. Among authors: gibson km. J Inherit Metab Dis. 1987;10(2):142-6. doi: 10.1007/BF01800039. J Inherit Metab Dis. 1987. PMID: 2443756 Free article.

6

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

7

3-Hydroxy-3-methylglutaryl-CoA-lyase deficiency.

Ploechl E, Bachmann C, Colombo JP, Gibson KM. Ploechl E, et al. Among authors: gibson km. J Inherit Metab Dis. 1989;12(3):343. doi: 10.1007/BF01799236. J Inherit Metab Dis. 1989. PMID: 2515385 No abstract available.

8

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

9

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

10

Mevalonic aciduria: pathobiochemical effects of mevalonate kinase deficiency on cholesterol metabolism in intact fibroblasts.

Hoffmann G, Gibson KM, Nyhan WL, Sweetman L. Hoffmann G, et al. Among authors: gibson km. J Inherit Metab Dis. 1988;11 Suppl 2:229-32. doi: 10.1007/BF01804243. J Inherit Metab Dis. 1988. PMID: 2846965 No abstract available.

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