Wanders RJ - Search Results

1

Primary hyperoxaluria type 1 in The Netherlands: prevalence and outcome.

van Woerden CS, Groothoff JW, Wanders RJ, Davin JC, Wijburg FA. van Woerden CS, et al. Among authors: wanders rj. Nephrol Dial Transplant. 2003 Feb;18(2):273-9. doi: 10.1093/ndt/18.2.273. Nephrol Dial Transplant. 2003. PMID: 12543880

2

Prenatal diagnosis of systemic disorders of the respiratory chain in cultured amniocytes and chorionic villus fibroblasts by studying the formation of lactate and pyruvate from glucose.

Wanders RJ, Wijburg FA, Ruiter J, Trijbels JM, Ruitenbeek W, Sengers RC, Bakkeren JA, Feller N. Wanders RJ, et al. J Inherit Metab Dis. 1992;15(1):84-91. doi: 10.1007/BF01800349. J Inherit Metab Dis. 1992. PMID: 1316525

3

Unusual clinical presentation in two boys with cytochrome c oxidase deficiency.

Hrebícek M, Zeman J, Petrák B, Kozich V, Hyánek J, Ruiter JP, Wanders RJ, Wijburg FA. Hrebícek M, et al. Among authors: wanders rj. J Inherit Metab Dis. 1992;15(3):320-2. doi: 10.1007/BF02435966. J Inherit Metab Dis. 1992. PMID: 1357227 No abstract available.

4

Restoration of NADH-oxidation in complex I and complex III deficient fibroblasts by menadione.

Wijburg FA, de Groot CJ, Feller N, Wanders RJ. Wijburg FA, et al. Among authors: wanders rj. J Inherit Metab Dis. 1991;14(3):293-6. doi: 10.1007/BF01811685. J Inherit Metab Dis. 1991. PMID: 1663191 No abstract available.

5

NADH:Q1 oxidoreductase deficiency without lactic acidosis in a patient with Leigh syndrome: implications for the diagnosis of inborn errors of the respiratory chain.

Wijburg FA, Wanders RJ, van Lie Peters EM, Vos GD, Loggers HG, Bolhuis PA, Herzberg NH, Ruitenbeek W, van Wilsem A, ten Houten R, et al. Wijburg FA, et al. Among authors: wanders rj. J Inherit Metab Dis. 1991;14(3):297-300. doi: 10.1007/BF01811686. J Inherit Metab Dis. 1991. PMID: 1770777 No abstract available.

6

Menadione partially restores NADH-oxidation and ATP-synthesis in complex I deficient fibroblasts.

Wijburg FA, Feller N, de Groot CJ, Wanders RJ. Wijburg FA, et al. Among authors: wanders rj. Biochem Int. 1990 Oct;22(2):303-9. Biochem Int. 1990. PMID: 2128595

7

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: wanders rj. J Inherit Metab Dis. 1990;13(3):355-8. doi: 10.1007/BF01799394. J Inherit Metab Dis. 1990. PMID: 2172645 No abstract available.

8

Familial NADH: Q1 oxidoreductase (complex I) deficiency: variable expression and possible treatment.

Wijburg FA, Barth PG, Ruitenbeek W, Wanders RJ, Vos GD, Ploos van Amstel SL, Schutgens RB. Wijburg FA, et al. Among authors: wanders rj. J Inherit Metab Dis. 1989;12 Suppl 2:349-51. doi: 10.1007/BF03335419. J Inherit Metab Dis. 1989. PMID: 2512441 No abstract available.

9

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: wanders rj. Biochem Int. 1989 Sep;19(3):563-70. Biochem Int. 1989. PMID: 2554914

10

Respiratory chain function in Leber's hereditary optic neuropathy: lack of correlation with clinical disease.

Cornelissen JC, Wanders RJ, Bolhuis PA, Bleeker-Wagemakers E, Oostra RJ, Wijburg FA. Cornelissen JC, et al. Among authors: wanders rj. J Inherit Metab Dis. 1993;16(3):531-3. doi: 10.1007/BF00711673. J Inherit Metab Dis. 1993. PMID: 7609444 Clinical Trial. No abstract available.

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