van den Bosch H - Search Results

1

Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome).

Heymans HS, Schutgens RB, Tan R, van den Bosch H, Borst P. Heymans HS, et al. Among authors: van den bosch h. Nature. 1983 Nov 3-9;306(5938):69-70. doi: 10.1038/306069a0. Nature. 1983. PMID: 6633659

2

Alkyl dihydroxyacetone phosphate synthase in human fibroblasts and its deficiency in Zellweger syndrome.

Schrakamp G, Roosenboom CF, Schutgens RB, Wanders RJ, Heymans HS, Tager JM, van den Bosch H. Schrakamp G, et al. Among authors: van den bosch h. J Lipid Res. 1985 Jul;26(7):867-73. J Lipid Res. 1985. PMID: 4031664

3

Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome.

Schutgens RB, Romeyn GJ, Wanders RJ, van den Bosch H, Schrakamp G, Heymans HS. Schutgens RB, et al. Among authors: van den bosch h. Biochem Biophys Res Commun. 1984 Apr 16;120(1):179-84. doi: 10.1016/0006-291x(84)91430-x. Biochem Biophys Res Commun. 1984. PMID: 6712687

4

[Diagnosis of Zellweger's cerebrohepatorenal syndrome].

Schutgens RB, Heymans HS, Purvis R, Wanders RJ, Schrakamp G, van den Bosch H. Schutgens RB, et al. Among authors: van den bosch h. Tijdschr Kindergeneeskd. 1984 Dec;52(6):231-8. Tijdschr Kindergeneeskd. 1984. PMID: 6528320 Dutch.

5

Peroxisomal beta-oxidation enzyme proteins in the Zellweger syndrome.

Tager JM, Van der Beek WA, Wanders RJ, Hashimoto T, Heymans HS, Van den Bosch H, Schutgens RB, Schram AW. Tager JM, et al. Among authors: van den bosch h, van der beek wa. Biochem Biophys Res Commun. 1985 Feb 15;126(3):1269-75. doi: 10.1016/0006-291x(85)90322-5. Biochem Biophys Res Commun. 1985. PMID: 3977916

6

Prenatal diagnosis of the cerebro-hepato-renal (Zellweger) syndrome by detection of an impaired plasmalogen biosynthesis.

Schutgens RB, Heymans HS, Wanders RJ, van den Bosch H, Schrakamp G. Schutgens RB, et al. Among authors: van den bosch h. J Inherit Metab Dis. 1985;8 Suppl 2:153-4. doi: 10.1007/BF01811505. J Inherit Metab Dis. 1985. PMID: 3930873 No abstract available.

7

Age-related differences in plasmalogen content of erythrocytes from patients with the cerebro-hepato-renal (Zellweger) syndrome: implications for postnatal detection of the disease.

Wanders RJ, Purvis YR, Heymans HS, Bakkeren JA, Parmentier GG, van Eldere J, Eyssen H, van den Bosch H, Tager JM, Schutgens RB. Wanders RJ, et al. Among authors: van eldere j, van den bosch h. J Inherit Metab Dis. 1986;9(4):335-42. doi: 10.1007/BF01800482. J Inherit Metab Dis. 1986. PMID: 3104670

8

Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatment.

Schutgens RB, Wanders RJ, Heymans HS, Schram AW, Tager JM, Schrakamp G, van den Bosch H. Schutgens RB, et al. Among authors: van den bosch h. J Inherit Metab Dis. 1987;10 Suppl 1:33-45. doi: 10.1007/BF01812845. J Inherit Metab Dis. 1987. PMID: 3119940 Review.

9

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

10

Peroxisomal beta-oxidation of palmitoyl-CoA in human liver homogenates and its deficiency in the cerebro-hepato-renal (Zellweger) syndrome.

Wanders RJ, van Roermund CW, de Vries CT, van den Bosch H, Schrakamp G, Tager JM, Schram AW, Schutgens RB. Wanders RJ, et al. Among authors: van roermund cw, van den bosch h. Clin Chim Acta. 1986 Aug 30;159(1):1-10. doi: 10.1016/0009-8981(86)90160-9. Clin Chim Acta. 1986. PMID: 2944672

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