Nyhan WL - Search Results

1

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: nyhan wl. J Clin Invest. 1986 Apr;77(4):1148-52. doi: 10.1172/JCI112415. J Clin Invest. 1986. PMID: 3082934 Free PMC article.

2

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. Among authors: nyhan wl. Eur J Pediatr. 1988 Oct;148(1):76-82. doi: 10.1007/BF00441821. Eur J Pediatr. 1988. PMID: 3197737

3

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: nyhan wl. Clin Chim Acta. 1989 Sep 15;184(1):57-64. doi: 10.1016/0009-8981(89)90256-8. Clin Chim Acta. 1989. PMID: 2480857

4

3-Hydroxy-3-methylglutaric aciduria.

Greene CL, Cann HM, Robinson BH, Gibson KM, Sweetman L, Holm J, Nyhan WL. Greene CL, et al. Among authors: nyhan wl. J Neurogenet. 1984 Apr;1(2):165-73. doi: 10.3109/01677068409107082. J Neurogenet. 1984. PMID: 6085636

5

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. Among authors: nyhan wl. Clin Chim Acta. 1982 Dec 9;126(2):171-81. doi: 10.1016/0009-8981(82)90033-x. Clin Chim Acta. 1982. PMID: 6185253

6

Succinic semialdehyde dehydrogenase deficiency.

Gibson KM, Sweetman L, Nyhan WL, Rating D. Gibson KM, et al. Among authors: nyhan wl. J Neurogenet. 1984 Sep;1(3):213-8. doi: 10.3109/01677068409107087. J Neurogenet. 1984. PMID: 6536727

7

Prenatal diagnosis of glutaric aciduria type II by direct chemical analysis of dicarboxylic acids in amniotic fluid.

Jakobs C, Sweetman L, Wadman SK, Duran M, Saudubray JM, Nyhan WL. Jakobs C, et al. Among authors: nyhan wl. Eur J Pediatr. 1984 Jan;141(3):153-7. doi: 10.1007/BF00443213. Eur J Pediatr. 1984. PMID: 6698061

8

Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency.

Burri BJ, Sweetman L, Nyhan WL. Burri BJ, et al. Among authors: nyhan wl. J Clin Invest. 1981 Dec;68(6):1491-5. doi: 10.1172/jci110402. J Clin Invest. 1981. PMID: 6798072 Free PMC article.

9

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. Among authors: nyhan wl. Enzyme. 1989;41(1):47-55. doi: 10.1159/000469050. Enzyme. 1989. PMID: 2543551

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: nyhan wl. J Inherit Metab Dis. 1988;11 Suppl 2:229-32. doi: 10.1007/BF01804243. J Inherit Metab Dis. 1988. PMID: 2846965 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

444 results

Search Page

Filters