Blom HJ - Search Results

1

The 2756A>G variant in the gene encoding methionine synthase: its relation with plasma homocysteine levels and risk of coronary heart disease in a Dutch case-control study.

Klerk M, Lievers KJ, Kluijtmans LA, Blom HJ, den Heijer M, Schouten EG, Kok FJ, Verhoef P. Klerk M, et al. Among authors: blom hj. Thromb Res. 2003 May 1;110(2-3):87-91. doi: 10.1016/s0049-3848(03)00341-4. Thromb Res. 2003. PMID: 12893022

2

Two novel missense mutations in the cystathionine beta-synthase gene in homocystinuric patients.

Kluijtmans LA, Blom HJ, Boers GH, van Oost BA, Trijbels FJ, van den Heuvel LP. Kluijtmans LA, et al. Among authors: blom hj. Hum Genet. 1995 Aug;96(2):249-50. doi: 10.1007/BF00207394. Hum Genet. 1995. PMID: 7635485

3

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase.

Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG, Boers GJ, den Heijer M, Kluijtmans LA, van den Heuvel LP, et al. Frosst P, et al. Among authors: blom hj. Nat Genet. 1995 May;10(1):111-3. doi: 10.1038/ng0595-111. Nat Genet. 1995. PMID: 7647779 Free article.

4

Is hyperhomocysteinaemia a risk factor for recurrent venous thrombosis?

den Heijer M, Blom HJ, Gerrits WB, Rosendaal FR, Haak HL, Wijermans PW, Bos GM. den Heijer M, et al. Among authors: blom hj. Lancet. 1995 Apr 8;345(8954):882-5. doi: 10.1016/s0140-6736(95)90008-x. Lancet. 1995. PMID: 7707810 Free article.

5

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: blom hj. Am J Hum Genet. 1996 Jan;58(1):35-41. Am J Hum Genet. 1996. PMID: 8554066 Free PMC article.

6

Hyperhomocysteinemia as a risk factor for deep-vein thrombosis.

den Heijer M, Koster T, Blom HJ, Bos GM, Briet E, Reitsma PH, Vandenbroucke JP, Rosendaal FR. den Heijer M, et al. Among authors: blom hj. N Engl J Med. 1996 Mar 21;334(12):759-62. doi: 10.1056/NEJM199603213341203. N Engl J Med. 1996. PMID: 8592549 Free article.

7

Defective cystathionine beta-synthase regulation by S-adenosylmethionine in a partially pyridoxine responsive homocystinuria patient.

Kluijtmans LA, Boers GH, Stevens EM, Renier WO, Kraus JP, Trijbels FJ, van den Heuvel LP, Blom HJ. Kluijtmans LA, et al. Among authors: blom hj. J Clin Invest. 1996 Jul 15;98(2):285-9. doi: 10.1172/JCI118791. J Clin Invest. 1996. PMID: 8755636 Free PMC article.

8

Variability of the methionine loading test: no effect of a low protein diet.

den Heijer M, Bos GM, Brouwer IA, Gerrits WB, Blom HJ. den Heijer M, et al. Among authors: blom hj. Ann Clin Biochem. 1996 Nov;33 ( Pt 6):551-4. doi: 10.1177/000456329603300611. Ann Clin Biochem. 1996. PMID: 8937588

9

The 677C-->T mutation in the methylenetetrahydrofolate reductase gene: associations with plasma total homocysteine levels and risk of coronary atherosclerotic disease.

Verhoef P, Kok FJ, Kluijtmans LA, Blom HJ, Refsum H, Ueland PM, Kruyssen DA. Verhoef P, et al. Among authors: blom hj. Atherosclerosis. 1997 Jul 11;132(1):105-13. doi: 10.1016/s0021-9150(97)00084-1. Atherosclerosis. 1997. PMID: 9247365 Free article.

10

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: blom hj. QJM. 1997 Aug;90(8):511-7. doi: 10.1093/qjmed/90.8.511. QJM. 1997. PMID: 9327029 Free article.

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