Blom HJ - Search Results

1

Thioredoxin interacting protein in Dutch families with familial combined hyperlipidemia.

van der Vleuten GM, Hijmans A, Kluijtmans LA, Blom HJ, Stalenhoef AF, de Graaf J. van der Vleuten GM, et al. Among authors: blom hj. Am J Med Genet A. 2004 Sep 15;130A(1):73-5. doi: 10.1002/ajmg.a.30036. Am J Med Genet A. 2004. PMID: 15368498

2

Can we exclude the TXNIP gene as a candidate gene for familial combined hyperlipidemia?

van der Vleuten GM, Hijmans A, Heil S, Blom HJ, Stalenhoef AF, de Graaf J. van der Vleuten GM, et al. Among authors: blom hj. Am J Med Genet A. 2006 May 1;140(9):1010-2. doi: 10.1002/ajmg.a.31181. Am J Med Genet A. 2006. PMID: 16575890 No abstract available.

3

Plasma homocysteine in subjects with familial combined hyperlipidemia.

Veerkamp MJ, de Graaf J, den Heijer M, Blom HJ, Stalenhoef AF. Veerkamp MJ, et al. Among authors: blom hj. Atherosclerosis. 2003 Jan;166(1):111-7. doi: 10.1016/s0021-9150(02)00312-x. Atherosclerosis. 2003. PMID: 12482557

4

The Gln223Arg polymorphism in the leptin receptor is associated with familial combined hyperlipidemia.

van der Vleuten GM, Kluijtmans LA, Hijmans A, Blom HJ, Stalenhoef AF, de Graaf J. van der Vleuten GM, et al. Among authors: blom hj. Int J Obes (Lond). 2006 Jun;30(6):892-8. doi: 10.1038/sj.ijo.0803234. Int J Obes (Lond). 2006. PMID: 16432543

5

Effect of genetic variation in the human S-adenosylhomocysteine hydrolase gene on total homocysteine concentrations and risk of recurrent venous thrombosis.

Gellekink H, den Heijer M, Kluijtmans LA, Blom HJ. Gellekink H, et al. Among authors: blom hj. Eur J Hum Genet. 2004 Nov;12(11):942-8. doi: 10.1038/sj.ejhg.5201237. Eur J Hum Genet. 2004. PMID: 15241484

6

Hyperhomocysteinemia, methylenetetrahydrofolate reductase 677TT genotype, and the risk for schizophrenia: a Dutch population based case-control study.

Muntjewerff JW, Hoogendoorn ML, Kahn RS, Sinke RJ, Den Heijer M, Kluijtmans LA, Blom HJ. Muntjewerff JW, et al. Among authors: blom hj. Am J Med Genet B Neuropsychiatr Genet. 2005 May 5;135B(1):69-72. doi: 10.1002/ajmg.b.30179. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15806605

7

Homocysteine levels--before and after methionine loading--in 51 Dutch families.

den Heijer M, Graafsma S, Lee SY, van Landeghem B, Kluijtmans L, Verhoef P, Beaty TH, Blom H. den Heijer M, et al. Eur J Hum Genet. 2005 Jun;13(6):753-62. doi: 10.1038/sj.ejhg.5201389. Eur J Hum Genet. 2005. PMID: 15756298

8

Marfanoid features in a child with combined methylmalonic aciduria and homocystinuria (CblC type).

Heil SG, Hogeveen M, Kluijtmans LA, van Dijken PJ, van de Berg GB, Blom HJ, Morava E. Heil SG, et al. Among authors: blom hj. J Inherit Metab Dis. 2007 Oct;30(5):811. doi: 10.1007/s10545-007-0546-6. Epub 2007 Sep 4. J Inherit Metab Dis. 2007. PMID: 17768669

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: blom hj. 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

A genome-wide linkage scan for homocysteine levels suggests three regions of interest.

Vermeulen SH, van der Vleuten GM, de Graaf J, Hermus AR, Blom HJ, Stalenhoef AF, den Heijer M. Vermeulen SH, et al. Among authors: blom hj. J Thromb Haemost. 2006 Jun;4(6):1303-7. doi: 10.1111/j.1538-7836.2006.01977.x. J Thromb Haemost. 2006. PMID: 16706975 Free article.

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