Wanders RJ - Search Results

1

Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme.

Heikoop JC, van Roermund CW, Just WW, Ofman R, Schutgens RB, Heymans HS, Wanders RJ, Tager JM. Heikoop JC, et al. Among authors: wanders rj. J Clin Invest. 1990 Jul;86(1):126-30. doi: 10.1172/JCI114674. J Clin Invest. 1990. PMID: 2365812 Free PMC article.

2

Rhizomelic chondrodysplasia punctata--a new clinical variant.

Gray RG, Green A, Chapman S, McKeown C, Schutgens RB, Wanders RJ. Gray RG, et al. Among authors: wanders rj. J Inherit Metab Dis. 1992;15(6):931-2. doi: 10.1007/BF01800236. J Inherit Metab Dis. 1992. PMID: 1293391 No abstract available.

3

Subcellular localization of squalene synthase in human hepatoma cell line Hep G2.

Cohen LH, Griffioen M, van Roermund CW, Wanders RJ. Cohen LH, et al. Among authors: wanders rj. Biochim Biophys Acta. 1992 Jun 5;1126(1):114-8. doi: 10.1016/0005-2760(92)90224-j. Biochim Biophys Acta. 1992. PMID: 1318747

4

Subcellular localisation and processing of non-specific lipid transfer protein are not aberrant in Rhizomelic Chondrodysplasia Punctata fibroblasts.

Heikoop JC, Ossendorp BC, Wanders RJ, Wirtz KW, Tager JM. Heikoop JC, et al. Among authors: wanders rj. FEBS Lett. 1992 Mar 9;299(2):201-4. doi: 10.1016/0014-5793(92)80247-e. FEBS Lett. 1992. PMID: 1347505 Free article.

5

Biochemistry of peroxisomes.

van den Bosch H, Schutgens RB, Wanders RJ, Tager JM. van den Bosch H, et al. Among authors: wanders rj. Annu Rev Biochem. 1992;61:157-97. doi: 10.1146/annurev.bi.61.070192.001105. Annu Rev Biochem. 1992. PMID: 1353950 Review. No abstract available.

6

Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis.

Wanders RJ, van Roermund CW, Brul S, Schutgens RB, Tager JM. Wanders RJ, et al. J Inherit Metab Dis. 1992;15(3):385-8. doi: 10.1007/BF02435983. J Inherit Metab Dis. 1992. PMID: 1357231 No abstract available.

7

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

8

Infantile refsum disease: gastrointestinal presentation of a peroxisomal disorder.

Mandel H, Meiron D, Schutgens RB, Wanders RJ, Berant M. Mandel H, et al. Among authors: wanders rj. J Pediatr Gastroenterol Nutr. 1992 Jan;14(1):83-5. J Pediatr Gastroenterol Nutr. 1992. PMID: 1374125

9

A new, simple assay for long-chain acyl-CoA dehydrogenase in cultured skin fibroblasts using stable isotopes and GC-MS.

Niezen-Koning KE, Wanders RJ, Nagel GT, IJlst L, Heymans HS. Niezen-Koning KE, et al. Among authors: wanders rj. Biochim Biophys Acta. 1992 Oct 13;1180(1):28-32. doi: 10.1016/0925-4439(92)90023-g. Biochim Biophys Acta. 1992. PMID: 1390941

10

Bone dysplasia associated with phytanic acid accumulation and deficient plasmalogen synthesis: a peroxisomal entity amenable to plasmapheresis.

Smeitink JA, Beemer FA, Espeel M, Donckerwolcke RA, Jakobs C, Wanders RJ, Schutgens RB, Roels F, Duran M, Dorland L, et al. Smeitink JA, et al. Among authors: wanders rj. J Inherit Metab Dis. 1992;15(3):377-80. doi: 10.1007/BF02435981. J Inherit Metab Dis. 1992. PMID: 1405474 No abstract available.

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