Van der Put NM - Search Results

1

The molecular basis of Dutch infantile nephropathic cystinosis.

Heil SG, Levtchenko E, Monnens LA, Trijbels FJ, Van der Put NM, Blom HJ. Heil SG, et al. Among authors: van der put nm. Nephron. 2001 Sep;89(1):50-5. doi: 10.1159/000046043. Nephron. 2001. PMID: 11528232

2

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: van der put nm. Eur J Hum Genet. 2002 Jul;10(7):433-8. doi: 10.1038/sj.ejhg.5200830. Eur J Hum Genet. 2002. PMID: 12107818

3

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: van den heuvel lp. J Mol Med (Berl). 1996 Nov;74(11):691-4. doi: 10.1007/s001090050073. J Mol Med (Berl). 1996. PMID: 8956155

4

Is the common 677C-->T mutation in the methylenetetrahydrofolate reductase gene a risk factor for neural tube defects? A meta-analysis.

van der Put NM, Eskes TK, Blom HJ. van der Put NM, et al. QJM. 1997 Feb;90(2):111-5. doi: 10.1093/qjmed/90.2.111. QJM. 1997. PMID: 9068801

5

Sequence analysis of the coding region of human methionine synthase: relevance to hyperhomocysteinaemia in neural-tube defects and vascular disease.

van der Put NM, van der Molen EF, Kluijtmans LA, Heil SG, Trijbels JM, Eskes TK, Van Oppenraaij-Emmerzaal D, Banerjee R, Blom HJ. van der Put NM, et al. Among authors: van oppenraaij emmerzaal d, van der molen ef. QJM. 1997 Aug;90(8):511-7. doi: 10.1093/qjmed/90.8.511. QJM. 1997. PMID: 9327029 Free article.

6

Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate-dehydrogenase, methenyltetrahydrofolate-cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defects.

Hol FA, van der Put NM, Geurds MP, Heil SG, Trijbels FJ, Hamel BC, Mariman EC, Blom HJ. Hol FA, et al. Among authors: van der put nm. Clin Genet. 1998 Feb;53(2):119-25. doi: 10.1111/j.1399-0004.1998.tb02658.x. Clin Genet. 1998. PMID: 9611072

7

Molecular genetic analysis of human folate receptors in neural tube defects.

Heil SG, van der Put NM, Trijbels FJ, Gabreëls FJ, Blom HJ. Heil SG, et al. Among authors: van der put nm. Eur J Hum Genet. 1999 Apr;7(3):393-6. doi: 10.1038/sj.ejhg.5200305. Eur J Hum Genet. 1999. PMID: 10234517

8

Neural tube defects and a disturbed folate dependent homocysteine metabolism.

van der Put NM, Blom HJ. van der Put NM, et al. Eur J Obstet Gynecol Reprod Biol. 2000 Sep;92(1):57-61. doi: 10.1016/s0301-2115(00)00426-7. Eur J Obstet Gynecol Reprod Biol. 2000. PMID: 10986435 Review.

9

Is mutated serine hydroxymethyltransferase (SHMT) involved in the etiology of neural tube defects?

Heil SG, Van der Put NM, Waas ET, den Heijer M, Trijbels FJ, Blom HJ. Heil SG, et al. Among authors: van der put nm. Mol Genet Metab. 2001 Jun;73(2):164-72. doi: 10.1006/mgme.2001.3175. Mol Genet Metab. 2001. PMID: 11386852

10

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: van der put nm. J Mol Med (Berl). 2001 Sep;79(9):522-8. doi: 10.1007/s001090100253. J Mol Med (Berl). 2001. PMID: 11692165

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