Trijbels FJ - Search Results

1

Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia.

Engbersen AM, Franken DG, Boers GH, Stevens EM, Trijbels FJ, Blom HJ. Engbersen AM, et al. Among authors: trijbels fj. Am J Hum Genet. 1995 Jan;56(1):142-50. Am J Hum Genet. 1995. PMID: 7825569 Free PMC article.

2

Gene-gene interaction between the cystathionine beta-synthase 31 base pair variable number of tandem repeats and the methylenetetrahydrofolate reductase 677C > T polymorphism on homocysteine levels and risk for neural tube defects.

Afman LA, Lievers KJ, Kluijtmans LA, Trijbels FJ, Blom HJ. Afman LA, et al. Among authors: trijbels fj. Mol Genet Metab. 2003 Mar;78(3):211-5. doi: 10.1016/s1096-7192(03)00021-0. Mol Genet Metab. 2003. PMID: 12649066

3

Effect of the methylenetetrahydrofolate reductase 677C-->T mutation on the relations among folate intake and plasma folate and homocysteine concentrations in a general population sample.

de Bree A, Verschuren WM, Bjørke-Monsen AL, van der Put NM, Heil SG, Trijbels FJ, Blom HJ. de Bree A, et al. Among authors: trijbels fj. Am J Clin Nutr. 2003 Mar;77(3):687-93. doi: 10.1093/ajcn/77.3.687. Am J Clin Nutr. 2003. PMID: 12600862

4

Cystathionine beta-synthase polymorphisms and hyperhomocysteinaemia: an association study.

Lievers KJ, Kluijtmans LA, Heil SG, Boers GH, Verhoef P, Den Heijer M, Trijbels FJ, Blom HJ. Lievers KJ, et al. Among authors: trijbels fj. Eur J Hum Genet. 2003 Jan;11(1):23-9. doi: 10.1038/sj.ejhg.5200899. Eur J Hum Genet. 2003. PMID: 12529702

5

Influence of a glutamate carboxypeptidase II (GCPII) polymorphism (1561C-->T) on plasma homocysteine, folate and vitamin B(12) levels and its relationship to cardiovascular disease risk.

Lievers KJ, Kluijtmans LA, Boers GH, Verhoef P, den Heijer M, Trijbels FJ, Blom HJ. Lievers KJ, et al. Among authors: trijbels fj. Atherosclerosis. 2002 Oct;164(2):269-73. doi: 10.1016/s0021-9150(02)00065-5. Atherosclerosis. 2002. PMID: 12204797

6

Single nucleotide polymorphisms in the transcobalamin gene: relationship with transcobalamin concentrations and risk for neural tube defects.

Afman LA, Lievers KJ, van der Put NM, Trijbels FJ, Blom HJ. Afman LA, et al. Among authors: trijbels fj. Eur J Hum Genet. 2002 Jul;10(7):433-8. doi: 10.1038/sj.ejhg.5200830. Eur J Hum Genet. 2002. PMID: 12107818

7

Polymorphisms in the transcobalamin gene: association with plasma homocysteine in healthy individuals and vascular disease patients.

Lievers KJ, Afman LA, Kluijtmans LA, Boers GH, Verhoef P, den Heijer M, Trijbels FJ, Blom HJ. Lievers KJ, et al. Among authors: trijbels fj. Clin Chem. 2002 Sep;48(9):1383-9. Clin Chem. 2002. PMID: 12194912

8

Spectrophotometric assay for complex I of the respiratory chain in tissue samples and cultured fibroblasts.

Janssen AJ, Trijbels FJ, Sengers RC, Smeitink JA, van den Heuvel LP, Wintjes LT, Stoltenborg-Hogenkamp BJ, Rodenburg RJ. Janssen AJ, et al. Among authors: trijbels fj. Clin Chem. 2007 Apr;53(4):729-34. doi: 10.1373/clinchem.2006.078873. Epub 2007 Mar 1. Clin Chem. 2007. PMID: 17332151 Free article.

9

The molecular basis of cystathionine beta-synthase deficiency in Dutch patients with homocystinuria: effect of CBS genotype on biochemical and clinical phenotype and on response to treatment.

Kluijtmans LA, Boers GH, Kraus JP, van den Heuvel LP, Cruysberg JR, Trijbels FJ, Blom HJ. Kluijtmans LA, et al. Among authors: trijbels fj. Am J Hum Genet. 1999 Jul;65(1):59-67. doi: 10.1086/302439. Am J Hum Genet. 1999. PMID: 10364517 Free PMC article.

10

Thiamine (vitamin B1) supplementation does not reduce fasting blood homocysteine concentration in most homozygotes for homocystinuria.

Franken DG, Blom HJ, Boers GH, Tangerman A, Thomas CM, Trijbels FJ. Franken DG, et al. Among authors: trijbels fj. Biochim Biophys Acta. 1996 Nov 15;1317(2):101-4. doi: 10.1016/s0925-4439(96)00033-6. Biochim Biophys Acta. 1996. PMID: 8950194 Free article. Clinical Trial.

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