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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.
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
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.
Hepatic artery embolisation; successful treatment of multinodular haemangiomatosis of the liver.
Vomberg PP, Büller HA, Marsman JW, Lam J, van Zaane DJ, Heymans HS. Vomberg PP, et al. Among authors: heymans hs. Eur J Pediatr. 1986 Feb;144(5):472-4. doi: 10.1007/BF00441741. Eur J Pediatr. 1986. PMID: 3956535
Vitamin-K status beyond the neonatal period. A prospective study in normal breast-fed and formula-fed infants.
Büller H, Peters M, Burger B, Nagelkerke N, Ten Cate JW, Breederveld C, Heymans H. Büller H, et al. Among authors: heymans h. Eur J Pediatr. 1986 Dec;145(6):496-9. doi: 10.1007/BF02429050. Eur J Pediatr. 1986. PMID: 3816851
[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: heymans hs. Tijdschr Kindergeneeskd. 1989 Oct;57(5):186-97. Tijdschr Kindergeneeskd. 1989. PMID: 2683204 Review. Dutch.
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
Inspiratory stridor and dysphagia because of prolonged oesophageal foreign body.
Vos GD, Heymans HS, Urbanus NA. Vos GD, et al. Among authors: heymans hs. Eur J Pediatr. 1987 Jan;146(1):86-7. doi: 10.1007/BF00647297. Eur J Pediatr. 1987. PMID: 3582413
Cor pulmonale and acute liver necrosis, due to upper airway obstruction as part of pycnodysostosis.
Aronson DC, Heymans HS, Bijlmer RP. Aronson DC, et al. Among authors: heymans hs. Eur J Pediatr. 1984 Feb;141(4):251-3. doi: 10.1007/BF00572773. Eur J Pediatr. 1984. PMID: 6734678
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.
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