van Spronsen FJ - Search Results

1

Biomarkers of Micronutrients in Regular Follow-Up for Tyrosinemia Type 1 and Phenylketonuria Patients.

van Vliet K, Rodenburg IL, van Ginkel WG, Lubout CMA, Wolffenbuttel BHR, van der Klauw MM, Heiner-Fokkema MR, van Spronsen FJ. van Vliet K, et al. Among authors: van der klauw mm, van spronsen fj, van ginkel wg. Nutrients. 2019 Aug 27;11(9):2011. doi: 10.3390/nu11092011. Nutrients. 2019. PMID: 31461828 Free PMC article.

2

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: van rijn m, van dijk t. Pediatrics. 1996 Jun;97(6 Pt 1):839-44. Pediatrics. 1996. PMID: 8657524 Clinical Trial.

3

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: van rijn m, van dijk t. Am J Clin Nutr. 1996 Dec;64(6):916-21. doi: 10.1093/ajcn/64.6.916. Am J Clin Nutr. 1996. PMID: 8942417

4

Phenylketonuria: tyrosine supplementation in phenylalanine-restricted diets.

van Spronsen FJ, van Rijn M, Bekhof J, Koch R, Smit PG. van Spronsen FJ, et al. Among authors: van rijn m. Am J Clin Nutr. 2001 Feb;73(2):153-7. doi: 10.1093/ajcn/73.2.153. Am J Clin Nutr. 2001. PMID: 11157309 Review.

5

Phenylketonuria: tyrosine beyond the phenylalanine-restricted diet.

van Spronsen FJ, Smit PG, Koch R. van Spronsen FJ, et al. J Inherit Metab Dis. 2001 Feb;24(1):1-4. doi: 10.1023/a:1005689232358. J Inherit Metab Dis. 2001. PMID: 11286377 Review.

6

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: van den heuvel eibrink mm, van hasselt p, van der ploeg a, van spronsen fj. 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

7

Protein metabolism in adult patients with phenylketonuria.

van Rijn M, Hoeksma M, Sauer P, Szczerbak B, Gross M, Reijngoud DJ, van Spronsen F. van Rijn M, et al. Nutrition. 2007 Jun;23(6):445-53. doi: 10.1016/j.nut.2007.03.009. Epub 2007 May 15. Nutrition. 2007. PMID: 17507200

8

The truth of treating patients with phenylketonuria after childhood: the need for a new guideline.

van Spronsen FJ, Burgard P. van Spronsen FJ, et al. J Inherit Metab Dis. 2008 Dec;31(6):673-9. doi: 10.1007/s10545-008-0918-6. Epub 2008 Aug 12. J Inherit Metab Dis. 2008. PMID: 18690552 Review.

9

A survey of natural protein intake in Dutch phenylketonuria patients: insight into estimation or measurement of dietary intake.

van Rijn M, Jansma J, Brinksma A, Bakker HD, Boers GH, Carbasius-Weber E, Douwes AC, van den Herberg A, Ter Horst NM, de Klerk JB, de Koning TJ, van den Ploeg L, Rubio-Gozalbo ME, Sels JP, Sengers RC, de Valk HW, Termeulen H, Zweers H, van Spronsen FJ. van Rijn M, et al. Among authors: van den ploeg l, van spronsen fj, van den herberg a. J Am Diet Assoc. 2008 Oct;108(10):1704-7. doi: 10.1016/j.jada.2008.07.008. J Am Diet Assoc. 2008. PMID: 18926138

10

Brain dysfunction in phenylketonuria: is phenylalanine toxicity the only possible cause?

van Spronsen FJ, Hoeksma M, Reijngoud DJ. van Spronsen FJ, et al. J Inherit Metab Dis. 2009 Feb;32(1):46-51. doi: 10.1007/s10545-008-0946-2. Epub 2009 Jan 13. J Inherit Metab Dis. 2009. PMID: 19191004 Review.

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