Wanders RJ - Search Results

1

Excessive urinary oxalate excretion after combined renal and hepatic transplantation for correction of hyperoxaluria type 1.

Ruder H, Otto G, Schutgens RB, Querfeld U, Wanders RJ, Herzog KH, Wölfel P, Pomer S, Schärer K, Rose GA. Ruder H, et al. Among authors: wanders rj. Eur J Pediatr. 1990 Nov;150(1):56-8. doi: 10.1007/BF01959482. Eur J Pediatr. 1990. PMID: 2079078

2

Isolated defect of peroxisomal beta-oxidation in a 16-year-old patient.

Santer R, Claviez A, Oldigs HD, Schaub J, Schutgens RB, Wanders RJ. Santer R, et al. Among authors: wanders rj. Eur J Pediatr. 1993 Apr;152(4):339-42. doi: 10.1007/BF01956749. Eur J Pediatr. 1993. PMID: 8482286

3

Clinical recognition of patients affected by a peroxisomal disorder: a retrospective study in 40 patients.

Theil AC, Schutgens RB, Wanders RJ, Heymans HS. Theil AC, et al. Among authors: wanders rj. Eur J Pediatr. 1992 Feb;151(2):117-20. doi: 10.1007/BF01958955. Eur J Pediatr. 1992. PMID: 1371465

4

Peroxisomal beta-oxidation defect with detectable peroxisomes: a case with neonatal onset and progressive course.

Barth PG, Wanders RJ, Schutgens RB, Bleeker-Wagemakers EM, van Heemstra D. Barth PG, et al. Among authors: wanders rj. Eur J Pediatr. 1990 Jul;149(10):722-6. doi: 10.1007/BF01959531. Eur J Pediatr. 1990. PMID: 2209666

5

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. 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

6

A prenatal test for the cerebro-hepato-renal (Zellweger) syndrome by demonstration of the absence of catalase-containing particles (peroxisomes) in cultured amniotic fluid cells.

Wanders RJ, Schrakamp G, van den Bosch H, Tager JM, Schutgens RB. Wanders RJ, et al. Eur J Pediatr. 1986 Apr;145(1-2):136-8. doi: 10.1007/BF00441876. Eur J Pediatr. 1986. PMID: 3732317

7

Isolated dihydroxyacetonephosphate-acyl-transferase deficiency in rhizomelic chondrodysplasia punctata: clinical presentation, metabolic and histological findings.

Hebestreit H, Wanders RJ, Schutgens RB, Espeel M, Kerckaert I, Roels F, Schmausser B, Schrod L, Marx A. Hebestreit H, et al. Among authors: wanders rj. Eur J Pediatr. 1996 Dec;155(12):1035-9. doi: 10.1007/BF02532526. Eur J Pediatr. 1996. PMID: 8956940

8

Very long fatty acids in amniotic fluid from a fetus affected with Zellweger syndrome.

Jakobs C, ten Brink H, Kok RM, Stellaard F, Kleijer WJ, Wanders RJ, Schutgens RB. Jakobs C, et al. Among authors: wanders rj. Eur J Pediatr. 1989 Apr;148(6):581. doi: 10.1007/BF00441567. Eur J Pediatr. 1989. PMID: 2744027 No abstract available.

9

Peroxisomal disorders: a newly recognised group of genetic diseases.

Schutgens RB, Heymans HS, Wanders RJ, van den Bosch H, Tager JM. Schutgens RB, et al. Among authors: wanders rj. Eur J Pediatr. 1986 Feb;144(5):430-40. doi: 10.1007/BF00441734. Eur J Pediatr. 1986. PMID: 3514227 Review. No abstract available.

10

Clinical and biochemical characteristics of peroxisomal disorders: an update.

Wanders RJ, Barth PG, Schutgens RB, Tager JM. Wanders RJ, et al. Eur J Pediatr. 1994;153(7 Suppl 1):S44-8. doi: 10.1007/BF02138777. Eur J Pediatr. 1994. PMID: 7957386 Review.

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