Wolff JA - 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: wolff ja. 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. 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. Am J Med Genet. 1990 Feb;35(2):222-8. doi: 10.1002/ajmg.1320350216. Am J Med Genet. 1990. PMID: 2309761

4

Anabolic effect of human growth hormone: management of inherited disorders of catabolic pathways.

Marsden D, Barshop BA, Capistrano-Estrada S, Rice M, Prodanos C, Sartoris D, Wolff J, Jones KL, Spector S, Nyhan WL. Marsden D, et al. Biochem Med Metab Biol. 1994 Aug;52(2):145-54. doi: 10.1006/bmmb.1994.1047. Biochem Med Metab Biol. 1994. PMID: 7993663

5

Effects of ascorbic acid in alkaptonuria: alterations in benzoquinone acetic acid and an ontogenic effect in infancy.

Wolff JA, Barshop B, Nyhan WL, Leslie J, Seegmiller JE, Gruber H, Garst M, Winter S, Michals K, Matalon R. Wolff JA, et al. Pediatr Res. 1989 Aug;26(2):140-4. doi: 10.1203/00006450-198908000-00015. Pediatr Res. 1989. PMID: 2771520

6

Carnitine reduces fasting ketogenesis in patients with disorders of propionate metabolism.

Wolff JA, Carroll JE, Le Phuc Thuy, Prodanos C, Haas R, Nyhan WL. Wolff JA, et al. Lancet. 1986 Feb 8;1(8476):289-91. doi: 10.1016/s0140-6736(86)90826-3. Lancet. 1986. PMID: 2868163 Clinical Trial.

7

Myopathy in an infant with a fatal peroxisomal disorder.

Wolff J, Nyhan WL, Powell H, Takahashi D, Hutzler J, Hajra AK, Datta NS, Singh I, Moser HW. Wolff J, et al. Pediatr Neurol. 1986 May-Jun;2(3):141-6. doi: 10.1016/0887-8994(86)90004-4. Pediatr Neurol. 1986. PMID: 3508688 Free article.

8

Pharmacologic amino acid acylation in the acute hyperammonemia of propionic acidemia.

Petrowski S, Nyhan WL, Reznik V, Sweetman L, Kulovich S, Wolff J, Jones G. Petrowski S, et al. J Neurogenet. 1987 Apr;4(2-3):87-96. J Neurogenet. 1987. PMID: 3598771

9

Clinical and biochemical variation and family studies in the multiple acyl-CoA dehydrogenation disorders.

Rhead WJ, Wolff JA, Lipson M, Falace P, Desai N, Fritchman K, Moon A, Sweetman L. Rhead WJ, et al. Among authors: wolff ja. Pediatr Res. 1987 Apr;21(4):371-6. doi: 10.1203/00006450-198704000-00010. Pediatr Res. 1987. PMID: 3574988

10

The role of lipid in the management of methylmalonic acidaemia: administration of linoleic acid does not increase excretion of methylmalonic acid.

Wolff JA, Sweetman L, Nyhan WL. Wolff JA, et al. J Inherit Metab Dis. 1985;8(3):100. doi: 10.1007/BF01819288. J Inherit Metab Dis. 1985. PMID: 3939583 No abstract available.

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