NS 23876/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

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Year	Number of Results
1988	1
1989	1
2008	1
2025	0

Page 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. 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-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

'Succinic semialdehyde dehydrogenase deficiency: phenotype evolution in an adolescent patient at 20-year follow-up'.

Crutchfield SR, Haas RH, Nyhan WL, Gibson KM. Crutchfield SR, et al. Dev Med Child Neurol. 2008 Nov;50(11):880-1. doi: 10.1111/j.1469-8749.2008.03116.x. Epub 2008 Sep 20. Dev Med Child Neurol. 2008. PMID: 18811705 Free PMC article. No abstract available.

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