van den Bosch H - Search Results

1

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: van den bosch h. Eur J Pediatr. 1986 Feb;144(5):430-40. doi: 10.1007/BF00441734. Eur J Pediatr. 1986. PMID: 3514227 Review. No abstract available.

2

Aberration in de novo ether lipid biosynthesis in peroxisomal disorders.

van den Bosch H, Schalkwijk CG, Schrakamp G, Wanders RJ, Schutgens RB, Schram AW, Tager JM. van den Bosch H, et al. Prog Clin Biol Res. 1988;282:139-50. Prog Clin Biol Res. 1988. PMID: 3071794 Review.

3

Plasmalogen biosynthesis in peroxisomal disorders: fatty alcohol versus alkylglycerol precursors.

Schrakamp G, Schalkwijk CG, Schutgens RB, Wanders RJ, Tager JM, van den Bosch H. Schrakamp G, et al. Among authors: van den bosch h. J Lipid Res. 1988 Mar;29(3):325-34. J Lipid Res. 1988. PMID: 3379344 Free article.

4

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. Among authors: van den bosch h. Eur J Pediatr. 1986 Apr;145(1-2):136-8. doi: 10.1007/BF00441876. Eur J Pediatr. 1986. PMID: 3732317

5

Ether lipid synthesis and its deficiency in peroxisomal disorders.

van den Bosch H, Schrakamp G, Hardeman D, Zomer AW, Wanders RJ, Schutgens RB. van den Bosch H, et al. Biochimie. 1993;75(3-4):183-9. doi: 10.1016/0300-9084(93)90076-5. Biochimie. 1993. PMID: 8507680 Review.

6

Impaired plasmalogen metabolism in infantile Refsum's disease.

Poll-Thé BT, Ogier H, Saudubray JM, Schutgens RB, Wanders RJ, van den Bosch H, Schrakamp G. Poll-Thé BT, et al. Among authors: van den bosch h. Eur J Pediatr. 1986 Feb;144(5):513-4. doi: 10.1007/BF00441753. Eur J Pediatr. 1986. PMID: 2420599 No abstract available.

7

Infantile Refsum disease: deficiency of catalase-containing particles (peroxisomes), alkyldihydroxyacetone phosphate synthase and peroxisomal beta-oxidation enzyme proteins.

Wanders RJ, Schutgens RB, Schrakamp G, van den Bosch H, Tager JM, Schram AW, Hashimoto T, Poll-Thé BT, Saudubrau JM. Wanders RJ, et al. Among authors: van den bosch h. Eur J Pediatr. 1986 Aug;145(3):172-5. doi: 10.1007/BF00446057. Eur J Pediatr. 1986. PMID: 2429839

8

Prenatal and perinatal diagnosis of peroxisomal disorders.

Schutgens RB, Schrakamp G, Wanders RJ, Heymans HS, Tager JM, van den Bosch H. Schutgens RB, et al. Among authors: van den bosch h. J Inherit Metab Dis. 1989;12 Suppl 1:118-34. doi: 10.1007/BF01799291. J Inherit Metab Dis. 1989. PMID: 2509803 Review.

9

[X-linked adrenoleukodystrophy and other peroxisomal diseases caused by a failing peroxisomal beta-oxidation system: clinical expression, diagnosis and treatment].

Wanders RJ, Barth PG, Schutgens RB, Van den Bosch H, Tager JM, Stroink H, Przyrembel H, Heymans HS. Wanders RJ, et al. Among authors: van den bosch h. Tijdschr Kindergeneeskd. 1989 Oct;57(5):186-97. Tijdschr Kindergeneeskd. 1989. PMID: 2683204 Review. Dutch.

10

Peroxisomal disorders in neurology.

Wanders RJ, Heymans HS, Schutgens RB, Barth PG, van den Bosch H, Tager JM. Wanders RJ, et al. Among authors: van den bosch h. 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.

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