van Spronsen FJ - Search Results

1

Dietary treatment of glycogen storage disease type Ia: uncooked cornstarch and/or continuous nocturnal gastric drip-feeding?

Derks TG, Martens DH, Sentner CP, van Rijn M, de Boer F, Smit GP, van Spronsen FJ. Derks TG, et al. Among authors: van rijn m, van spronsen fj. Mol Genet Metab. 2013 May;109(1):1-2. doi: 10.1016/j.ymgme.2013.02.005. Epub 2013 Feb 15. Mol Genet Metab. 2013. PMID: 23480859 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. Ned Tijdschr Geneeskd. 1992 Mar 21;136(12):565-9. Ned Tijdschr Geneeskd. 1992. PMID: 1552967 Review. Dutch. No abstract available.

3

Prevalence of congenital heart disease in patients with phenylketonuria.

Verkerk PH, van Spronsen FJ, Smit GP, Cornel MC, Kuipers JR, Verloove-Vanhorick SP. Verkerk PH, et al. Among authors: van spronsen fj. J Pediatr. 1991 Aug;119(2):282-3. doi: 10.1016/s0022-3476(05)80743-7. J Pediatr. 1991. PMID: 1861217 No abstract available.

4

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: van faassen h. 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.

5

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. J Inherit Metab Dis. 1995;18(2):111-4. doi: 10.1007/BF00711742. J Inherit Metab Dis. 1995. PMID: 7564222 No abstract available.

6

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: van spronsen fj. J Inherit Metab Dis. 1995;18(2):115-8. doi: 10.1007/BF00711743. J Inherit Metab Dis. 1995. PMID: 7564223 No abstract available.

7

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

8

Predictors of mean phenylalanine levels during the first five years of life in patients with phenylketonuria who were treated early. Dutch National PKU Steering Committee.

Verkerk PH, van Spronsen FJ, van Houten M, Smit GP, Sengers RC. Verkerk PH, et al. Among authors: van houten m, van spronsen fj. Acta Paediatr Suppl. 1994 Dec;407:70-2. doi: 10.1111/j.1651-2227.1994.tb13456.x. Acta Paediatr Suppl. 1994. PMID: 7766963

9

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

10

Impaired prenatal and postnatal growth in Dutch patients with phenylketonuria. The National PKU Steering Committee.

Verkerk PH, van Spronsen FJ, Smit GP, Sengers RC. Verkerk PH, et al. Among authors: van spronsen fj. Arch Dis Child. 1994 Aug;71(2):114-8. doi: 10.1136/adc.71.2.114. Arch Dis Child. 1994. PMID: 7944529 Free PMC article.

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