Wanders RJ - Search Results

1

MRI as diagnostic tool in early-onset peroxisomal disorders.

van der Knaap MS, Wassmer E, Wolf NI, Ferreira P, Topçu M, Wanders RJ, Waterham HR, Ferdinandusse S. van der Knaap MS, et al. Among authors: wanders rj. Neurology. 2012 Apr 24;78(17):1304-8. doi: 10.1212/WNL.0b013e31825182dc. Epub 2012 Mar 28. Neurology. 2012. PMID: 22459681 Free article.

2

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

3

Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes.

Tager JM, Brul S, Wiemer EA, Strijland A, Van Driel R, Schutgens RB, Van den Bosch H, Wanders RJ, Westerveld A. Tager JM, et al. Among authors: wanders rj. Prog Clin Biol Res. 1990;321:545-58. Prog Clin Biol Res. 1990. PMID: 2183242

4

Peroxisomal disorders in neurology.

Wanders RJ, Heymans HS, Schutgens RB, Barth PG, van den Bosch H, Tager JM. Wanders RJ, et al. J Neurol Sci. 1988 Dec;88(1-3):1-39. doi: 10.1016/0022-510x(88)90203-1. J Neurol Sci. 1988. PMID: 3066850 Review.

5

Peroxisomal disorders: a review.

Wanders RJ, Schutgens RB, Barth PG. Wanders RJ, et al. J Neuropathol Exp Neurol. 1995 Sep;54(5):726-39. doi: 10.1097/00005072-199509000-00016. J Neuropathol Exp Neurol. 1995. PMID: 7545216 Review.

6

Postnatal diagnosis of peroxisomal disorders: a biochemical approach.

Wanders RJ, Schutgens RB, Barth PG, Tager JM, van den Bosch H. Wanders RJ, et al. Biochimie. 1993;75(3-4):269-79. doi: 10.1016/0300-9084(93)90087-9. Biochimie. 1993. PMID: 7685190 Review.

7

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.

8

Clinical and magnetic resonance imaging features of L-2-hydroxyglutaric acidemia: report of three cases in comparison with Canavan disease.

Topçu M, Erdem G, Saatçi I, Aktan G, Simşek A, Renda Y, Schutgens RB, Wanders RJ, Jacobs C. Topçu M, et al. Among authors: wanders rj. J Child Neurol. 1996 Sep;11(5):373-7. doi: 10.1177/088307389601100505. J Child Neurol. 1996. PMID: 8877604

9

Metabolic aspects of peroxisomal disorders.

Wanders RJ, Jansen G, van Roermund CW, Denis S, Schutgens RB, Jakobs BS. Wanders RJ, et al. Ann N Y Acad Sci. 1996 Dec 27;804:450-60. doi: 10.1111/j.1749-6632.1996.tb18636.x. Ann N Y Acad Sci. 1996. PMID: 8993564

10

Immunoblot analysis of peroxisomal proteins in liver and fibroblasts from patients.

Wanders RJ, Dekker C, Ofman R, Schutgens RB, Mooijer P. Wanders RJ, et al. J Inherit Metab Dis. 1995;18 Suppl 1:101-12. doi: 10.1007/BF00711433. J Inherit Metab Dis. 1995. PMID: 9053545

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