Smit GP - Search Results

1

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: smit gp. 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.

2

[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: smit gp. Ned Tijdschr Geneeskd. 1992 Mar 21;136(12):565-9. Ned Tijdschr Geneeskd. 1992. PMID: 1552967 Review. Dutch. 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: smit gp. J Inherit Metab Dis. 1995;18(2):111-4. doi: 10.1007/BF00711742. J Inherit Metab Dis. 1995. PMID: 7564222 No abstract available.

4

Liver transplantation in tyrosinaemia type I: the Groningen experience.

Wijburg FA, Reitsma WC, Slooff MJ, van Spronsen FJ, Koetse HA, Reijngoud DJ, Smit GP, Berger R, Bijleveld CM. Wijburg FA, et al. Among authors: smit gp. J Inherit Metab Dis. 1995;18(2):115-8. doi: 10.1007/BF00711743. J Inherit Metab Dis. 1995. PMID: 7564223 No abstract available.

5

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: smit gp. J Inherit Metab Dis. 1995;18(2):230-2. doi: 10.1007/BF00711775. J Inherit Metab Dis. 1995. PMID: 7564255 No abstract available.

6

Hereditary tyrosinaemia type I: a long-term study of the relationship between the urinary excretions of succinylacetone and delta-aminolevulinic acid.

Schierbeek H, Beukeveld GJ, van Faassen H, van Spronsen FJ, Bijsterveld K, Venekamp-Hoolsema EE, Wolthers BG, Smit GP. Schierbeek H, et al. Among authors: smit gp. J Inherit Metab Dis. 1993;16(6):1034-40. doi: 10.1007/BF00711521. J Inherit Metab Dis. 1993. PMID: 8127053

7

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: smit gp. Hepatology. 1994 Nov;20(5):1187-91. Hepatology. 1994. PMID: 7927251

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: smit gp. Pediatrics. 1993 Oct;92(4):570-3. Pediatrics. 1993. PMID: 8414829

9

Large daily fluctuations in plasma tyrosine in treated patients with phenylketonuria.

van Spronsen FJ, van Dijk T, Smit GP, van Rijn M, Reijngoud DJ, Berger R, Heymans HS. van Spronsen FJ, et al. Among authors: smit gp. Am J Clin Nutr. 1996 Dec;64(6):916-21. doi: 10.1093/ajcn/64.6.916. Am J Clin Nutr. 1996. PMID: 8942417

10

Type IIIb glycogen storage disease associated with end-stage cirrhosis and hepatocellular carcinoma. The Liver Transplant Group.

Haagsma EB, Smit GP, Niezen-Koning KE, Gouw AS, Meerman L, Slooff MJ. Haagsma EB, et al. Among authors: smit gp. Hepatology. 1997 Mar;25(3):537-40. doi: 10.1002/hep.510250307. Hepatology. 1997. PMID: 9049194

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