Sweetman L - Search Results

1

Metabolism of 1-13C-propionate in vivo in patients with disorders of propionate metabolism.

Barshop BA, Yoshida I, Ajami A, Sweetman L, Wolff JA, Sweetman FR, Prodanos C, Smith M, Nyhan WL. Barshop BA, et al. Among authors: sweetman fr, sweetman l. Pediatr Res. 1991 Jul;30(1):15-22. doi: 10.1203/00006450-199107000-00004. Pediatr Res. 1991. PMID: 1909779

2

3-Hydroxyisobutyric aciduria: an inborn error of valine metabolism.

Ko FJ, Nyhan WL, Wolff J, Barshop B, Sweetman L. Ko FJ, et al. Among authors: sweetman l. Pediatr Res. 1991 Oct;30(4):322-6. doi: 10.1203/00006450-199110000-00006. Pediatr Res. 1991. PMID: 1956714

3

Transcobalamin II deficiency presenting with methylmalonic aciduria and homocystinuria and abnormal absorption of cobalamin.

Barshop BA, Wolff J, Nyhan WL, Yu A, Prodanos C, Jones G, Sweetman L, Leslie J, Holm J, Green R, et al. Barshop BA, et al. Among authors: sweetman l. Am J Med Genet. 1990 Feb;35(2):222-8. doi: 10.1002/ajmg.1320350216. Am J Med Genet. 1990. PMID: 2309761

4

Propionyl-CoA carboxylase deficiency in a patient with biotin-responsive 3-methylcrotonylglycinuria.

Sweetman L, Bates SP, Hull D, Nyhan WL. Sweetman L, et al. Pediatr Res. 1977 Nov;11(11):1144-7. doi: 10.1203/00006450-197711000-00006. Pediatr Res. 1977. PMID: 917614

5

An unusual presentation of medium-chain acyl coenzyme A dehydrogenase deficiency.

Marsden D, Sege-Petersen K, Nyhan WL, Roschinger W, Sweetman L. Marsden D, et al. Among authors: sweetman l. Am J Dis Child. 1992 Dec;146(12):1459-62. doi: 10.1001/archpedi.1992.02160240069023. Am J Dis Child. 1992. PMID: 1456259

6

Effect of lipoic acid in a patient with defective activity of pyruvate dehydrogenase, 2-oxoglutarate dehydrogenase, and branched-chain keto acid dehydrogenase.

Yoshida I, Sweetman L, Kulovich S, Nyhan WL, Robinson BH. Yoshida I, et al. Among authors: sweetman l. Pediatr Res. 1990 Jan;27(1):75-9. doi: 10.1203/00006450-199001000-00020. Pediatr Res. 1990. PMID: 2104971

7

Methylcitrate in maternal urine during a pregnancy with a fetus affected with propionic acidaemia.

Aramaki S, Lehotay D, Nyhan WL, MacLeod PM, Sweetman L. Aramaki S, et al. Among authors: sweetman l. J Inherit Metab Dis. 1989;12(1):86-8. doi: 10.1007/BF01805535. J Inherit Metab Dis. 1989. PMID: 2501588

8

Metabolism of branched-chain amino acids in fibroblasts from patients with maple syrup urine disease and other abnormalities of branched-chain ketoacid dehydrogenase activity.

Yoshida I, Sweetman L, Nyhan WL. Yoshida I, et al. Among authors: sweetman l. Pediatr Res. 1986 Feb;20(2):169-74. doi: 10.1203/00006450-198602000-00016. Pediatr Res. 1986. PMID: 3080729

9

Identification of methyl-branched chain dicarboxylic acids in amniotic fluid and urine in propionic and methylmalonic acidemia.

Jakobs C, Dorland L, Sweetman L, Duran M, Nyhan WL, Wadman SK. Jakobs C, et al. Among authors: sweetman l. Pediatr Res. 1984 Nov;18(11):1185-91. doi: 10.1203/00006450-198411000-00027. Pediatr Res. 1984. PMID: 6514446

10

A new immunochemical assay for biotin.

Thuy LP, Sweetman L, Nyhan WL. Thuy LP, et al. Among authors: sweetman l. Clin Chim Acta. 1991 Oct 31;202(3):191-7. doi: 10.1016/0009-8981(91)90049-i. Clin Chim Acta. 1991. PMID: 1814646

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