Wanders RJ - Search Results

1

Delay in diagnosis of X-linked adrenoleukodystrophy.

van Geel BM, Assies J, Haverkort EB, Barth PG, Wanders RJ, Schutgens RB, Keyser A, Zwetsloot CP. van Geel BM, et al. Among authors: wanders rj. Clin Neurol Neurosurg. 1993 Jun;95(2):115-20. doi: 10.1016/0303-8467(93)90004-z. Clin Neurol Neurosurg. 1993. PMID: 8344008

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

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.

4

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.

5

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

6

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

7

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.

8

Zellweger-like phenotype in two siblings: a defect in peroxisomal beta-oxidation with elevated very long-chain fatty acids but normal bile acids.

Mandel H, Berant M, Aizin A, Gershony R, Hemmli S, Schutgens RB, Wanders RJ. Mandel H, et al. Among authors: wanders rj. J Inherit Metab Dis. 1992;15(3):381-4. doi: 10.1007/BF02435982. J Inherit Metab Dis. 1992. PMID: 1405475 No abstract available.

9

Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder.

Wanders RJ, Schumacher H, Heikoop J, Schutgens RB, Tager JM. Wanders RJ, et al. J Inherit Metab Dis. 1992;15(3):389-91. doi: 10.1007/BF02435984. J Inherit Metab Dis. 1992. PMID: 1405476 No abstract available.

10

Molecular analysis of disorders of peroxisomal beta-oxidation.

Wanders RJ, van Roermund CW, Denis S, Schutgens RB, Ijlst L, Tager JM. Wanders RJ, et al. Prog Clin Biol Res. 1992;375:507-19. Prog Clin Biol Res. 1992. PMID: 1438395 Review. No abstract available.

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