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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.
Assay of 3-hydroxy-3-methylglutaryl-CoA lyase.
Gibson KM. Gibson KM. Methods Enzymol. 1988;166:219-25. doi: 10.1016/s0076-6879(88)66028-9. Methods Enzymol. 1988. PMID: 3071704 No abstract available.
A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.
Wilson WG, Cass MB, Søvik O, Gibson KM, Sweetman L. Wilson WG, et al. Among authors: gibson km. Eur J Pediatr. 1984 Sep;142(4):289-91. doi: 10.1007/BF00540255. Eur J Pediatr. 1984. PMID: 6489380
Genetic complementation analysis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency in cultured fibroblasts.
Sovik O, Sweetman L, Gibson KM, Nyhan WL. Sovik O, et al. Among authors: gibson km. Am J Hum Genet. 1984 Jul;36(4):791-801. Am J Hum Genet. 1984. PMID: 6475954 Free PMC article.
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
Atypical presentation and neuropathological studies in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.
Zoghbi HY, Spence JE, Beaudet AL, O'Brien WE, Goodman CJ, Gibson KM. Zoghbi HY, et al. Among authors: gibson km. Ann Neurol. 1986 Sep;20(3):367-9. doi: 10.1002/ana.410200318. Ann Neurol. 1986. PMID: 3767322
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-hydroxy-3-methylglutaraturia. Clinical aspects, follow-up and therapy in a young child].
Plöchl E, Bachmann C, Colombo JP, Gibson KM. Plöchl E, et al. Among authors: gibson km. Klin Padiatr. 1990 Mar-Apr;202(2):76-80. doi: 10.1055/s-2007-1025492. Klin Padiatr. 1990. PMID: 1691326 German.
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
HMG CoA lyase deficiency: identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41Q.
Mitchell GA, Ozand PT, Robert MF, Ashmarina L, Roberts J, Gibson KM, Wanders RJ, Wang S, Chevalier I, Plöchl E, Miziorko H. Mitchell GA, et al. Among authors: gibson km. Am J Hum Genet. 1998 Feb;62(2):295-300. doi: 10.1086/301730. Am J Hum Genet. 1998. PMID: 9463337 Free PMC article.
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