Trijbels FJ - Search Results

1

Decreased methylene tetrahydrofolate reductase activity due to the 677C-->T mutation in families with spina bifida offspring.

van der Put NM, van den Heuvel LP, Steegers-Theunissen RP, Trijbels FJ, Eskes TK, Mariman EC, den Heyer M, Blom HJ. van der Put NM, et al. Among authors: trijbels fj. J Mol Med (Berl). 1996 Nov;74(11):691-4. doi: 10.1007/s001090050073. J Mol Med (Berl). 1996. PMID: 8956155

2

Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease.

Kluijtmans LA, van den Heuvel LP, Boers GH, Frosst P, Stevens EM, van Oost BA, den Heijer M, Trijbels FJ, Rozen R, Blom HJ. Kluijtmans LA, et al. Among authors: trijbels fj. Am J Hum Genet. 1996 Jan;58(1):35-41. Am J Hum Genet. 1996. PMID: 8554066 Free PMC article.

3

Altered folate and vitamin B12 metabolism in families with spina bifida offspring.

van der Put NM, Thomas CM, Eskes TK, Trijbels FJ, Steegers-Theunissen RP, Mariman EC, De Graaf-Hess A, Smeitink JA, Blom HJ. van der Put NM, et al. Among authors: trijbels fj. QJM. 1997 Aug;90(8):505-10. doi: 10.1093/qjmed/90.8.505. QJM. 1997. PMID: 9327028 Free article.

4

Thermolabile methylenetetrahydrofolate reductase in coronary artery disease.

Kluijtmans LA, Kastelein JJ, Lindemans J, Boers GH, Heil SG, Bruschke AV, Jukema JW, van den Heuvel LP, Trijbels FJ, Boerma GJ, Verheugt FW, Willems F, Blom HJ. Kluijtmans LA, et al. Among authors: trijbels fj. Circulation. 1997 Oct 21;96(8):2573-7. doi: 10.1161/01.cir.96.8.2573. Circulation. 1997. PMID: 9355896

5

A common 844INS68 insertion variant in the cystathionine beta-synthase gene.

Kluijtmans LA, Boers GH, Trijbels FJ, van Lith-Zanders HM, van den Heuvel LP, Blom HJ. Kluijtmans LA, et al. Among authors: trijbels fj. Biochem Mol Med. 1997 Oct;62(1):23-5. doi: 10.1006/bmme.1997.2623. Biochem Mol Med. 1997. PMID: 9367794

6

A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

van der Put NM, Gabreëls F, Stevens EM, Smeitink JA, Trijbels FJ, Eskes TK, van den Heuvel LP, Blom HJ. van der Put NM, et al. Among authors: trijbels fj. Am J Hum Genet. 1998 May;62(5):1044-51. doi: 10.1086/301825. Am J Hum Genet. 1998. PMID: 9545395 Free PMC article.

7

Folate, homocysteine and neural tube defects: an overview.

van der Put NM, van Straaten HW, Trijbels FJ, Blom HJ. van der Put NM, et al. Among authors: trijbels fj. Exp Biol Med (Maywood). 2001 Apr;226(4):243-70. doi: 10.1177/153537020122600402. Exp Biol Med (Maywood). 2001. PMID: 11368417 Review.

8

A second common variant in the methylenetetrahydrofolate reductase (MTHFR) gene and its relationship to MTHFR enzyme activity, homocysteine, and cardiovascular disease risk.

Lievers KJ, Boers GH, Verhoef P, den Heijer M, Kluijtmans LA, van der Put NM, Trijbels FJ, Blom HJ. Lievers KJ, et al. Among authors: trijbels fj. J Mol Med (Berl). 2001 Sep;79(9):522-8. doi: 10.1007/s001090100253. J Mol Med (Berl). 2001. PMID: 11692165

9

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida.

van der Put NM, Steegers-Theunissen RP, Frosst P, Trijbels FJ, Eskes TK, van den Heuvel LP, Mariman EC, den Heyer M, Rozen R, Blom HJ. van der Put NM, et al. Among authors: trijbels fj. Lancet. 1995 Oct 21;346(8982):1070-1. doi: 10.1016/s0140-6736(95)91743-8. Lancet. 1995. PMID: 7564788 Free article.

10

Identification of four novel mutations in severe methylenetetrahydrofolate reductase deficiency.

Kluijtmans LA, Wendel U, Stevens EM, van den Heuvel LP, Trijbels FJ, Blom HJ. Kluijtmans LA, et al. Among authors: trijbels fj. Eur J Hum Genet. 1998 May-Jun;6(3):257-65. doi: 10.1038/sj.ejhg.5200182. Eur J Hum Genet. 1998. PMID: 9781030

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