Heymans HS - Search Results

1

Heterozygosity for the common LCHAD mutation (1528g>C) is not a major cause of HELLP syndrome and the prevalence of the mutation in the Dutch population is low.

den Boer ME, Ijlst L, Wijburg FA, Oostheim W, van Werkhoven MA, van Pampus MG, Heymans HS, Wanders RJ. den Boer ME, et al. Among authors: heymans hs. Pediatr Res. 2000 Aug;48(2):151-4. doi: 10.1203/00006450-200008000-00006. Pediatr Res. 2000. PMID: 10926288

2

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: clinical presentation and follow-up of 50 patients.

den Boer ME, Wanders RJ, Morris AA, IJlst L, Heymans HS, Wijburg FA. den Boer ME, et al. Among authors: heymans hs. Pediatrics. 2002 Jan;109(1):99-104. doi: 10.1542/peds.109.1.99. Pediatrics. 2002. PMID: 11773547

3

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: heymans hs. Biochim Biophys Acta. 1992 Oct 13;1180(1):28-32. doi: 10.1016/0925-4439(92)90023-g. Biochim Biophys Acta. 1992. PMID: 1390941

4

Caustic esophageal lesions in childhood: prevention of stricture formation.

Wijburg FA, Heymans HS, Urbanus NA. Wijburg FA, et al. Among authors: heymans hs. J Pediatr Surg. 1989 Feb;24(2):171-3. doi: 10.1016/s0022-3468(89)80241-6. J Pediatr Surg. 1989. PMID: 2724008

5

Measurement of short-chain acyl-CoA dehydrogenase (SCAD) in cultured skin fibroblasts with hexanoyl-CoA as a competitive inhibitor to eliminate the contribution of medium-chain acyl-CoA dehydrogenase.

Niezen-Koning KE, Wanders RJ, Nagel GT, Sewell AC, Heymans HS. Niezen-Koning KE, et al. Among authors: heymans hs. Clin Chim Acta. 1994 Sep;229(1-2):99-106. doi: 10.1016/0009-8981(94)90232-1. Clin Chim Acta. 1994. PMID: 7988059

6

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: heymans hs. J Inherit Metab Dis. 1989;12 Suppl 1:118-34. doi: 10.1007/BF01799291. J Inherit Metab Dis. 1989. PMID: 2509803 Review.

7

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: heymans hs. J Inherit Metab Dis. 1987;10 Suppl 1:33-45. doi: 10.1007/BF01812845. J Inherit Metab Dis. 1987. PMID: 3119940 Review.

8

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: heymans hs. Eur J Pediatr. 1992 Feb;151(2):117-20. doi: 10.1007/BF01958955. Eur J Pediatr. 1992. PMID: 1371465

9

Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studies.

Schutgens RB, Wanders RJ, Nijenhuis A, van den Hoek CM, Heymans HS, Schrakamp G, Bleeker-Wagemakers EM, Delleman JW, Schram AW, Tager JM, et al. Schutgens RB, et al. Among authors: heymans hs. Enzyme. 1987;38(1-4):161-76. doi: 10.1159/000469202. Enzyme. 1987. PMID: 3440444

10

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: heymans hs. J Clin Invest. 1990 Jul;86(1):126-30. doi: 10.1172/JCI114674. J Clin Invest. 1990. PMID: 2365812 Free PMC article.

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