Kok RM - Search Results

1

Phytanic acid alpha-oxidation: accumulation of 2-hydroxyphytanic acid and absence of 2-oxophytanic acid in plasma from patients with peroxisomal disorders.

ten Brink HJ, Schor DS, Kok RM, Poll-The BT, Wanders RJ, Jakobs C. ten Brink HJ, et al. Among authors: kok rm. J Lipid Res. 1992 Oct;33(10):1449-57. J Lipid Res. 1992. PMID: 1385561 Free article.

2

In vivo study of phytanic acid alpha-oxidation in classic Refsum's disease and chondrodysplasia punctata.

ten Brink HJ, Schor DS, Kok RM, Stellaard F, Kneer J, Poll-The BT, Saudubray JM, Jakobs C. ten Brink HJ, et al. Among authors: kok rm. Pediatr Res. 1992 Nov;32(5):566-70. doi: 10.1203/00006450-199211000-00016. Pediatr Res. 1992. PMID: 1282700

3

Pristanic acid and phytanic acid in plasma from patients with peroxisomal disorders: stable isotope dilution analysis with electron capture negative ion mass fragmentography.

ten Brink HJ, Stellaard F, van den Heuvel CM, Kok RM, Schor DS, Wanders RJ, Jakobs C. ten Brink HJ, et al. Among authors: kok rm. J Lipid Res. 1992 Jan;33(1):41-7. J Lipid Res. 1992. PMID: 1372637 Free article.

4

Stable isotope dilution analysis of very long chain fatty acids in plasma, urine and amniotic fluid by electron capture negative ion mass fragmentography.

Stellaard F, ten Brink HJ, Kok RM, van den Heuvel L, Jakobs C. Stellaard F, et al. Among authors: kok rm. Clin Chim Acta. 1990 Nov 30;192(2):133-44. doi: 10.1016/0009-8981(90)90077-6. Clin Chim Acta. 1990. PMID: 1705871

5

Determination of plasma bile acids by capillary gas-liquid chromatography-electron capture negative chemical ionization mass fragmentography.

Stellaard F, Langelaar SA, Kok RM, Jakobs C. Stellaard F, et al. Among authors: kok rm. J Lipid Res. 1989 Oct;30(10):1647-52. J Lipid Res. 1989. PMID: 2614267 Free article.

6

Very long fatty acids in amniotic fluid from a fetus affected with Zellweger syndrome.

Jakobs C, ten Brink H, Kok RM, Stellaard F, Kleijer WJ, Wanders RJ, Schutgens RB. Jakobs C, et al. Among authors: kok rm. Eur J Pediatr. 1989 Apr;148(6):581. doi: 10.1007/BF00441567. Eur J Pediatr. 1989. PMID: 2744027 No abstract available.

7

Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6-C14 hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation?

Poll-The BT, Bonnefont JP, Ogier H, Charpentier C, Pelet A, Le Fur JM, Jakobs C, Kok RM, Duran M, Divry P, et al. Poll-The BT, et al. Among authors: kok rm. J Inherit Metab Dis. 1988;11 Suppl 2:183-5. doi: 10.1007/BF01804230. J Inherit Metab Dis. 1988. PMID: 2846959 No abstract available.

8

Stable isotope dilution analysis of succinylacetone using electron capture negative ion mass fragmentography: an accurate approach to the pre- and neonatal diagnosis of hereditary tyrosinemia type I.

Jakobs C, Dorland L, Wikkerink B, Kok RM, de Jong AP, Wadman SK. Jakobs C, et al. Among authors: kok rm. Clin Chim Acta. 1988 Feb 15;171(2-3):223-31. doi: 10.1016/0009-8981(88)90147-7. Clin Chim Acta. 1988. PMID: 3286060

9

Stable isotope dilution analysis of pipecolic acid in cerebrospinal fluid, plasma, urine and amniotic fluid using electron capture negative ion mass fragmentography.

Kok RM, Kaster L, de Jong AP, Poll-Thé B, Saudubray JM, Jakobs C. Kok RM, et al. Clin Chim Acta. 1987 Sep 30;168(2):143-52. doi: 10.1016/0009-8981(87)90283-x. Clin Chim Acta. 1987. PMID: 3315316

10

Elevated plasma galactitol levels in patients with congenital cataracts without apparent enzyme defect.

Jakobs C, Douwes AC, Kok R, de Jong A, Endres W, Shin YS. Jakobs C, et al. Eur J Pediatr. 1988 May;147(4):446. doi: 10.1007/BF00496438. Eur J Pediatr. 1988. PMID: 3396605 No abstract available.

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