Hoeksma M - Search Results

1

Pathogenesis of cognitive dysfunction in phenylketonuria: review of hypotheses.

de Groot MJ, Hoeksma M, Blau N, Reijngoud DJ, van Spronsen FJ. de Groot MJ, et al. Among authors: hoeksma m. Mol Genet Metab. 2010;99 Suppl 1:S86-9. doi: 10.1016/j.ymgme.2009.10.016. Mol Genet Metab. 2010. PMID: 20123477 Review.

2

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

van Spronsen FJ, Hoeksma M, Reijngoud DJ. van Spronsen FJ, et al. Among authors: hoeksma m. 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.

3

Phenylketonuria: High plasma phenylalanine decreases cerebral protein synthesis.

Hoeksma M, Reijngoud DJ, Pruim J, de Valk HW, Paans AM, van Spronsen FJ. Hoeksma M, et al. Mol Genet Metab. 2009 Apr;96(4):177-82. doi: 10.1016/j.ymgme.2008.12.019. Epub 2009 Feb 6. Mol Genet Metab. 2009. PMID: 19201235

4

Large neutral amino acids in the treatment of PKU: from theory to practice.

van Spronsen FJ, de Groot MJ, Hoeksma M, Reijngoud DJ, van Rijn M. van Spronsen FJ, et al. Among authors: hoeksma m. J Inherit Metab Dis. 2010 Dec;33(6):671-6. doi: 10.1007/s10545-010-9216-1. Epub 2010 Oct 26. J Inherit Metab Dis. 2010. PMID: 20976625 Free PMC article. Review.

5

Serum vitamin B12 concentrations within reference values do not exclude functional vitamin B12 deficiency in PKU patients of various ages.

Vugteveen I, Hoeksma M, Monsen AL, Fokkema MR, Reijngoud DJ, van Rijn M, van Spronsen FJ. Vugteveen I, et al. Among authors: hoeksma m. Mol Genet Metab. 2011 Jan;102(1):13-7. doi: 10.1016/j.ymgme.2010.07.004. Epub 2010 Oct 27. Mol Genet Metab. 2011. PMID: 21030277

6

Adult patients with well-controlled phenylketonuria tolerate incidental additional intake of phenylalanine.

van Rijn M, Hoeksma M, Sauer PJ, Modderman P, Reijngoud DJ, van Spronsen FJ. van Rijn M, et al. Among authors: hoeksma m. Ann Nutr Metab. 2011;58(2):94-100. doi: 10.1159/000324924. Epub 2011 Apr 8. Ann Nutr Metab. 2011. PMID: 21474926

7

Diurnal variations in blood phenylalanine of PKU infants under different feeding regimes.

van Rijn M, Hoeksma M, Sauer PJ, Modderman P, Reijngoud DJ, van Spronsen FJ. van Rijn M, et al. Among authors: hoeksma m. Mol Genet Metab. 2011;104 Suppl:S68-72. doi: 10.1016/j.ymgme.2011.08.010. Epub 2011 Aug 16. Mol Genet Metab. 2011. PMID: 21982628 Clinical Trial.

8

Relationships between lumbar bone mineral density and biochemical parameters in phenylketonuria patients.

de Groot MJ, Hoeksma M, van Rijn M, Slart RH, van Spronsen FJ. de Groot MJ, et al. Among authors: hoeksma m. Mol Genet Metab. 2012 Apr;105(4):566-70. doi: 10.1016/j.ymgme.2012.01.006. Epub 2012 Jan 16. Mol Genet Metab. 2012. PMID: 22300845

9

Phenylketonuria: reduced tyrosine brain influx relates to reduced cerebral protein synthesis.

de Groot MJ, Hoeksma M, Reijngoud DJ, de Valk HW, Paans AM, Sauer PJ, van Spronsen FJ. de Groot MJ, et al. Among authors: hoeksma m. Orphanet J Rare Dis. 2013 Sep 4;8:133. doi: 10.1186/1750-1172-8-133. Orphanet J Rare Dis. 2013. PMID: 24007597 Free PMC article.

10

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. Among authors: hoeksma m. Nutrition. 2007 Jun;23(6):445-53. doi: 10.1016/j.nut.2007.03.009. Epub 2007 May 15. Nutrition. 2007. PMID: 17507200

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