Heymans HS - Search Results

1

[The role of orthotopic liver transplantation in the treatment of metabolic diseases].

van Spronsen FJ, Smit GP, Slooff MJ, Bijleveld CM, Klompmaker IJ, Heymans HS. van Spronsen FJ, et al. Among authors: heymans hs. Ned Tijdschr Geneeskd. 1992 Mar 21;136(12):565-9. Ned Tijdschr Geneeskd. 1992. PMID: 1552967 Review. Dutch. No abstract available.

2

Tyrosinaemia type I: orthotopic liver transplantation as the only definitive answer to a metabolic as well as an oncological problem.

van Spronsen FJ, Berger R, Smit GP, de Klerk JB, Duran M, Bijleveld CM, van Faassen H, Slooff MJ, Heymans HS. van Spronsen FJ, et al. Among authors: heymans hs. J Inherit Metab Dis. 1989;12 Suppl 2:339-42. doi: 10.1007/BF03335416. J Inherit Metab Dis. 1989. PMID: 2556611 Review. No abstract available.

3

Tyrosinaemia type I: considerations of treatment strategy and experiences with risk assessment, diet and transplantation.

van Spronsen FJ, Smit GP, Wijburg FA, Thomasse Y, Visser G, Heymans HS. van Spronsen FJ, et al. Among authors: heymans hs. J Inherit Metab Dis. 1995;18(2):111-4. doi: 10.1007/BF00711742. J Inherit Metab Dis. 1995. PMID: 7564222 No abstract available.

4

A patient with lethal cardiomyopathy and a carnitine-acylcarnitine translocase deficiency.

Niezen-Koning KE, van Spronsen FJ, Ijlst L, Wanders RJ, Brivet M, Duran M, Reijngoud DJ, Heymans HS, Smit GP. Niezen-Koning KE, et al. Among authors: heymans hs. J Inherit Metab Dis. 1995;18(2):230-2. doi: 10.1007/BF00711775. J Inherit Metab Dis. 1995. PMID: 7564255 No abstract available.

5

Hereditary tyrosinemia type I: a new clinical classification with difference in prognosis on dietary treatment.

van Spronsen FJ, Thomasse Y, Smit GP, Leonard JV, Clayton PT, Fidler V, Berger R, Heymans HS. van Spronsen FJ, et al. Among authors: heymans hs. Hepatology. 1994 Nov;20(5):1187-91. Hepatology. 1994. PMID: 7927251

6

Succinyl-CoA:acetoacetate transferase deficiency: identification of a new patient with a neonatal onset and review of the literature.

Niezen-Koning KE, Wanders RJ, Ruiter JP, Ijlst L, Visser G, Reitsma-Bierens WC, Heymans HS, Reijngoud DJ, Smit GP. Niezen-Koning KE, et al. Among authors: heymans hs. Eur J Pediatr. 1997 Nov;156(11):870-3. doi: 10.1007/s004310050733. Eur J Pediatr. 1997. PMID: 9392403 Review.

7

Prognosis of extrahepatic biliary atresia.

Houwen RH, Zwierstra RP, Severijnen RS, Bouquet J, Madern G, Vos A, Bax NM, Heymans HS, Bijleveld CM. Houwen RH, et al. Among authors: heymans hs. Arch Dis Child. 1989 Feb;64(2):214-8. doi: 10.1136/adc.64.2.214. Arch Dis Child. 1989. PMID: 2930227 Free PMC article.

8

Plasma phenylalanine and tyrosine responses to different nutritional conditions (fasting/postprandial) in patients with phenylketonuria: effect of sample timing.

van Spronsen FJ, van Rijn M, van Dijk T, Smit GP, Reijngoud DJ, Berger R, Heymans HS. van Spronsen FJ, et al. Among authors: heymans hs. Pediatrics. 1993 Oct;92(4):570-3. Pediatrics. 1993. PMID: 8414829

9

Phenylketonuria: plasma phenylalanine responses to different distributions of the daily phenylalanine allowance over the day.

van Spronsen FJ, van Dijk T, Smit GP, van Rijn M, Reijngoud DJ, Berger R, Heymans HS. van Spronsen FJ, et al. Among authors: heymans hs. Pediatrics. 1996 Jun;97(6 Pt 1):839-44. Pediatrics. 1996. PMID: 8657524 Clinical Trial.

10

Adenosine triphosphate-dependent copper transport in human liver.

Dijkstra M, van den Berg GJ, Wolters H, In't Veld G, Slooff MJ, Heymans HS, Kuipers F, Vonk RJ. Dijkstra M, et al. Among authors: heymans hs. J Hepatol. 1996 Jul;25(1):37-42. doi: 10.1016/s0168-8278(96)80325-4. J Hepatol. 1996. PMID: 8836899

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