Wijburg FA - Search Results

1

Occurrence of subdural hematomas in Dutch glutaric aciduria type 1 patients.

Vester ME, Visser G, Wijburg FA, van Spronsen FJ, Williams M, van Rijn RR. Vester ME, et al. Among authors: wijburg fa. Eur J Pediatr. 2016 Jul;175(7):1001-6. doi: 10.1007/s00431-016-2734-6. Epub 2016 May 31. Eur J Pediatr. 2016. PMID: 27246831 Free PMC article.

2

Clinical and biochemical observations in a patient with combined Pompe disease and cblC mutation.

Wijburg FA, Rosenblatt DS, Vos GD, Oorthuys JW, van't Hek LG, Poorthuis BJ, Sanders MK, Schutgens RB. Wijburg FA, et al. Eur J Pediatr. 1992 Feb;151(2):127-31. doi: 10.1007/BF01958957. Eur J Pediatr. 1992. PMID: 1537354

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

5

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: wijburg fa. Pediatrics. 2002 Jan;109(1):99-104. doi: 10.1542/peds.109.1.99. Pediatrics. 2002. PMID: 11773547

6

Mitochondrial trifunctional protein deficiency: a severe fatty acid oxidation disorder with cardiac and neurologic involvement.

den Boer ME, Dionisi-Vici C, Chakrapani A, van Thuijl AO, Wanders RJ, Wijburg FA. den Boer ME, et al. Among authors: wijburg fa. J Pediatr. 2003 Jun;142(6):684-9. doi: 10.1067/mpd.2003.231. J Pediatr. 2003. PMID: 12838198

7

Hepatocellular carcinoma in hereditary tyrosinemia type I despite 2-(2 nitro-4-3 trifluoro- methylbenzoyl)-1, 3-cyclohexanedione treatment.

van Spronsen FJ, Bijleveld CM, van Maldegem BT, Wijburg FA. van Spronsen FJ, et al. Among authors: wijburg fa. J Pediatr Gastroenterol Nutr. 2005 Jan;40(1):90-3. doi: 10.1097/00005176-200501000-00017. J Pediatr Gastroenterol Nutr. 2005. PMID: 15625434 No abstract available.

8

Tyrosinemia type I treated by NTBC: how does AFP predict liver cancer?

Koelink CJ, van Hasselt P, van der Ploeg A, van den Heuvel-Eibrink MM, Wijburg FA, Bijleveld CM, van Spronsen FJ. Koelink CJ, et al. Among authors: wijburg fa. Mol Genet Metab. 2006 Dec;89(4):310-5. doi: 10.1016/j.ymgme.2006.07.009. Epub 2006 Sep 27. Mol Genet Metab. 2006. PMID: 17008115

9

The course of life and quality of life of early and continuously treated Dutch patients with phenylketonuria.

Bosch AM, Tybout W, van Spronsen FJ, de Valk HW, Wijburg FA, Grootenhuis MA. Bosch AM, et al. Among authors: wijburg fa. J Inherit Metab Dis. 2007 Feb;30(1):29-34. doi: 10.1007/s10545-006-0433-6. Epub 2006 Dec 11. J Inherit Metab Dis. 2007. PMID: 17160615

10

[Extensive neonatal heel injection screening for metabolic diseases in the Netherlands].

Visser G, van Spronsen FJ, de Sain-van der Velden MG, Blom HJ, Wijburg FA. Visser G, et al. Among authors: wijburg fa. Ned Tijdschr Geneeskd. 2009 May 2;153(18):848-53. Ned Tijdschr Geneeskd. 2009. PMID: 19475862 Dutch. No abstract available.

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