Wanders RJ - Search Results

1

Defective inactivation of leukotriene B4 in patients with Sjögren-Larsson syndrome.

Willemsen MA, de Jong JG, van Domburg PH, Rotteveel JJ, Wanders RJ, Mayatepek E. Willemsen MA, et al. Among authors: wanders rj. J Pediatr. 2000 Feb;136(2):258-60. doi: 10.1016/s0022-3476(00)70113-2. J Pediatr. 2000. PMID: 10657837

2

Sjögren-Larsson syndrome.

Willemsen MA, de Jong JG, van Domburg PH, Rotteveel JJ, Wanders RJ, Mayatepek E. Willemsen MA, et al. Among authors: wanders rj. J Pediatr. 2000 Feb;136(2):261. doi: 10.1016/s0022-3476(00)70114-4. J Pediatr. 2000. PMID: 10657838 No abstract available.

3

Defective metabolism of leukotriene B4 in the Sjögren-Larsson syndrome.

Willemsen MA, Rotteveel JJ, de Jong JG, Wanders RJ, IJlst L, Hoffmann GF, Mayatepek E. Willemsen MA, et al. Among authors: wanders rj. J Neurol Sci. 2001 Jan 15;183(1):61-7. doi: 10.1016/s0022-510x(00)00474-3. J Neurol Sci. 2001. PMID: 11166796

4

Clinical, biochemical and molecular genetic characteristics of 19 patients with the Sjögren-Larsson syndrome.

Willemsen MA, IJlst L, Steijlen PM, Rotteveel JJ, de Jong JG, van Domburg PH, Mayatepek E, Gabreëls FJ, Wanders RJ. Willemsen MA, et al. Among authors: wanders rj. Brain. 2001 Jul;124(Pt 7):1426-37. doi: 10.1093/brain/124.7.1426. Brain. 2001. PMID: 11408337 Review.

5

Sjögren-Larsson syndrome: clinical and MRI/MRS findings in FALDH-deficient patients.

van Domburg PH, Willemsen MA, Rotteveel JJ, de Jong JG, Thijssen HO, Heerschap A, Cruysberg JR, Wanders RJ, Gabreëls FJ, Steijlen PM. van Domburg PH, et al. Among authors: wanders rj. Neurology. 1999 Apr 22;52(7):1345-52. doi: 10.1212/wnl.52.7.1345. Neurology. 1999. PMID: 10227616

6

Sjögren-Larsson syndrome in clinical practice.

Fuijkschot J, Theelen T, Seyger MM, van der Graaf M, de Groot IJ, Wevers RA, Wanders RJ, Waterham HR, Willemsen MA. Fuijkschot J, et al. Among authors: wanders rj. J Inherit Metab Dis. 2012 Nov;35(6):955-62. doi: 10.1007/s10545-012-9518-6. Epub 2012 Jul 26. J Inherit Metab Dis. 2012. PMID: 22833178 Review.

7

A novel 4 bp deletion mutation in the FALDH gene segregating in a Turkish family with Sjögren-Larsson syndrome.

Willemsen MA, Steijlen PM, de Jong JG, Rotteveel JJ, IJlst L, van Werkhoven MA, Wanders RJ. Willemsen MA, et al. Among authors: wanders rj. J Invest Dermatol. 1999 May;112(5):827-8. doi: 10.1046/j.1523-1747.1999.00574.x. J Invest Dermatol. 1999. PMID: 10233781 Free article. No abstract available.

8

Molecular basis of Sjögren-Larsson syndrome: frequency of the 1297-1298 del GA and 943C-->T mutation in 29 patients.

Ijlst L, Oostheim W, van Werkhoven M, Willemsen MA, Wanders RJ. Ijlst L, et al. Among authors: wanders rj. J Inherit Metab Dis. 1999 May;22(3):319-21. doi: 10.1023/a:1005508205450. J Inherit Metab Dis. 1999. PMID: 10384396 No abstract available.

9

Incomplete Sjögren-Larsson syndrome in two Japanese siblings?

Willemsen MA, Rotteveel JJ, Steijlen PM, Wanders RJ. Willemsen MA, et al. Among authors: wanders rj. Dermatology. 1999;199(2):187-8. doi: 10.1159/000018237. Dermatology. 1999. PMID: 10559596 No abstract available.

10

Mevalonate kinase deficiency: enlarging the clinical and biochemical spectrum.

Prietsch V, Mayatepek E, Krastel H, Haas D, Zundel D, Waterham HR, Wanders RJ, Gibson KM, Hoffmann GF. Prietsch V, et al. Among authors: wanders rj. Pediatrics. 2003 Feb;111(2):258-61. doi: 10.1542/peds.111.2.258. Pediatrics. 2003. PMID: 12563048

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