Przyrembel H - Search Results

1

Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndrome.

Wanders RJ, van Roermund CW, Westra R, Schutgens RB, van der Ende MA, Tager JM, Monnens LA, Baadenhuysen H, Govaerts L, Przyrembel H, et al. Wanders RJ, et al. Among authors: przyrembel h. Clin Chim Acta. 1987 Jun 15;165(2-3):311-9. doi: 10.1016/0009-8981(87)90176-8. Clin Chim Acta. 1987. PMID: 3652453

2

Diversity in residual alanine glyoxylate aminotransferase activity in hyperoxaluria type I: correlation with pyridoxine responsiveness.

Wanders RJ, van Roermund CW, Jurriaans S, Schutgens RB, Tager JM, van den Bosch H, Wolff ED, Przyrembel H, Berger R, Schaaphok FG, et al. Wanders RJ, et al. Among authors: przyrembel h. J Inherit Metab Dis. 1988;11 Suppl 2:208-11. doi: 10.1007/BF01804237. J Inherit Metab Dis. 1988. PMID: 3141704 No abstract available.

3

Wanders RJ, Smit W, Heymans HS, Schutgens RB, Barth PG, Schierbeek H, Smit GP, Berger R, Przyrembel H, Eggelte TA, et al. Wanders RJ, et al. Among authors: przyrembel h. Clin Chim Acta. 1987 Jun 30;166(1):45-56. doi: 10.1016/0009-8981(87)90193-8. Clin Chim Acta. 1987. PMID: 2440622

4

Di- and trihydroxycholestanoic acidaemia with hepatic failure.

Przyrembel H, Wanders RJ, van Roermund CW, Schutgens RB, Mannaerts GP, Casteels M. Przyrembel H, et al. J Inherit Metab Dis. 1990;13(3):367-70. doi: 10.1007/BF01799397. J Inherit Metab Dis. 1990. PMID: 2122102 No abstract available.

5

[X-linked adrenoleukodystrophy and other peroxisomal diseases caused by a failing peroxisomal beta-oxidation system: clinical expression, diagnosis and treatment].

Wanders RJ, Barth PG, Schutgens RB, Van den Bosch H, Tager JM, Stroink H, Przyrembel H, Heymans HS. Wanders RJ, et al. Among authors: przyrembel h. Tijdschr Kindergeneeskd. 1989 Oct;57(5):186-97. Tijdschr Kindergeneeskd. 1989. PMID: 2683204 Review. Dutch.

6

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: different clinical expression in three unrelated patients.

Wanders RJ, Ijlst L, Duran M, Jakobs C, de Klerk JB, Przyrembel H, Rocchiccioli F, Aubourg P. Wanders RJ, et al. Among authors: przyrembel h. J Inherit Metab Dis. 1991;14(3):325-8. doi: 10.1007/BF01811694. J Inherit Metab Dis. 1991. PMID: 1770784 No abstract available.

7

Studies on the formation of lactate and pyruvate from glucose in cultured skin fibroblasts: implications for detection of respiratory chain defects.

Wijburg FA, Feller N, Scholte HR, Przyrembel H, Wanders RJ. Wijburg FA, et al. Among authors: przyrembel h. Biochem Int. 1989 Sep;19(3):563-70. Biochem Int. 1989. PMID: 2554914

8

Octanoate and palmitate beta-oxidation in human leukocytes: implications for the rapid diagnosis of fatty acid beta-oxidation disorders.

Wanders RJ, Ijlst L, van Elk E, de Klerk JB, Przyrembel H. Wanders RJ, et al. Among authors: przyrembel h. J Inherit Metab Dis. 1991;14(3):317-20. doi: 10.1007/BF01811692. J Inherit Metab Dis. 1991. PMID: 1770782 No abstract available.

9

Detection of respiratory chain dysfunction by measuring lactate and pyruvate production in cultured fibroblasts.

Wijburg FA, Feller N, Ruitenbeek W, Trijbels JM, Sengers RC, Scholte HR, Przyrembel H, Wanders RJ. Wijburg FA, et al. Among authors: przyrembel h. J Inherit Metab Dis. 1990;13(3):355-8. doi: 10.1007/BF01799394. J Inherit Metab Dis. 1990. PMID: 2172645 No abstract available.

10

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Przyrembel H, Jakobs C, IJlst L, de Klerk JB, Wanders RJ. Przyrembel H, et al. J Inherit Metab Dis. 1991;14(5):674-80. doi: 10.1007/BF01799932. J Inherit Metab Dis. 1991. PMID: 1779613 No abstract available.

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