Heymans H - Search Results

1

Lethal hypoglycemia in a child with a deficiency of 3-hydroxy-3-methylglutarylcoenzyme A lyase.

Schutgens RB, Heymans H, Ketel A, Veder HA, Duran M, Ketting D, Wadman SK. Schutgens RB, et al. Among authors: heymans h. J Pediatr. 1979 Jan;94(1):89-91. doi: 10.1016/s0022-3476(79)80364-9. J Pediatr. 1979. PMID: 758433 No abstract available.

2

3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency: postnatal management following prenatal diagnosis by analysis of maternal urine.

Duran M, Schutgens RB, Ketel A, Heymans H, Bertssen MW, Ketting D, Wadman SK. Duran M, et al. Among authors: heymans h. J Pediatr. 1979 Dec;95(6):1004-7. doi: 10.1016/s0022-3476(79)80297-8. J Pediatr. 1979. PMID: 91680 No abstract available.

3

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

4

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

5

Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndrome.

Heymans HS, vd Bosch H, Schutgens RB, Tegelaers WH, Walther JU, Müller-Höcker J, Borst P. Heymans HS, et al. Eur J Pediatr. 1984 Apr;142(1):10-5. doi: 10.1007/BF00442582. Eur J Pediatr. 1984. PMID: 6714253

6

A milder variant of Zellweger syndrome.

Barth PG, Schutgens RB, Bakkeren JA, Dingemans KP, Heymans HS, Douwes AC, van der Klei-van Moorsel JM. Barth PG, et al. Among authors: heymans hs. Eur J Pediatr. 1985 Nov;144(4):338-42. doi: 10.1007/BF00441774. Eur J Pediatr. 1985. PMID: 4076250

7

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. Nature. 1983 Nov 3-9;306(5938):69-70. doi: 10.1038/306069a0. Nature. 1983. PMID: 6633659

8

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: heymans hs. J Lipid Res. 1985 Jul;26(7):867-73. J Lipid Res. 1985. PMID: 4031664 Free article.

9

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.

10

Deficient cholesterol side chain oxidation in patients without peroxisomes (Zellweger syndrome): evidence for the involvement of peroxisomes in bile acid synthesis in man.

Wanders RJ, Schutgens RB, Heymans HS. Wanders RJ, et al. Among authors: heymans hs. Clin Chim Acta. 1987 Feb 15;162(3):295-301. doi: 10.1016/0009-8981(87)90048-9. Clin Chim Acta. 1987. PMID: 3568406

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