Similar articles for PMID: 11683544

Year	Number of Results
1996	7
1997	6
1998	10
1999	17
2000	11
2001	26
2002	19
2003	10
2004	3
2005	4
2006	3
2007	7
2008	7
2009	4
2010	5
2011	3
2012	6
2013	1
2016	1
2017	2
2018	2
2019	5
2020	2
2021	5
2022	8
2024	0

1

MTHFR gene polymorphism, homocysteine and cardiovascular disease.

Cortese C, Motti C. Cortese C, et al. Public Health Nutr. 2001 Apr;4(2B):493-7. doi: 10.1079/phn2001159. Public Health Nutr. 2001. PMID: 11683544 Review.

2

Effects of serum B vitamins on elevated plasma homocysteine levels associated with the mutation of methylenetetrahydrofolate reductase gene in Japanese.

Moriyama Y, Okamura T, Kajinami K, Iso H, Inazu A, Kawashiri M, Mizuno M, Takeda Y, Sakamoto Y, Kimura H, Suzuki H, Mabuchi H. Moriyama Y, et al. Atherosclerosis. 2002 Oct;164(2):321-8. doi: 10.1016/s0021-9150(02)00105-3. Atherosclerosis. 2002. PMID: 12204804

3

Effect of MTHFR 677C>T on plasma total homocysteine levels in renal graft recipients.

Födinger M, Wölfl G, Fischer G, Rasoul-Rockenschaub S, Schmid R, Hörl WH, Sunder-Plassmann G. Födinger M, et al. Kidney Int. 1999 Mar;55(3):1072-80. doi: 10.1046/j.1523-1755.1999.0550031072.x. Kidney Int. 1999. PMID: 10027946 Free article.

4

Determinants of fasting and post-methionine homocysteine levels in families predisposed to hyperhomocysteinemia and premature vascular disease.

de Jong SC, Stehouwer CD, van den Berg M, Kostense PJ, Alders D, Jakobs C, Pals G, Rauwerda JA. de Jong SC, et al. Arterioscler Thromb Vasc Biol. 1999 May;19(5):1316-24. doi: 10.1161/01.atv.19.5.1316. Arterioscler Thromb Vasc Biol. 1999. PMID: 10323785 Free article.

5

The effect of a common methylenetetrahydrofolate reductase mutation on levels of homocysteine, folate, vitamin B12 and on the risk of premature atherosclerosis.

Verhoeff BJ, Trip MD, Prins MH, Kastelein JJ, Reitsma PH. Verhoeff BJ, et al. Atherosclerosis. 1998 Nov;141(1):161-6. doi: 10.1016/s0021-9150(98)00156-7. Atherosclerosis. 1998. PMID: 9863549

6

The role of vitamin B12 in fasting hyperhomocysteinemia and its interaction with the homozygous C677T mutation of the methylenetetrahydrofolate reductase (MTHFR) gene. A case-control study of patients with early-onset thrombotic events.

D'Angelo A, Coppola A, Madonna P, Fermo I, Pagano A, Mazzola G, Galli L, Cerbone AM. D'Angelo A, et al. Thromb Haemost. 2000 Apr;83(4):563-70. Thromb Haemost. 2000. PMID: 10780318

7

Methylenetetrahydrofolate reductase genotype, vitamin B12, and folate influence plasma homocysteine in hemodialysis patients.

Nakamura T, Saionji K, Hiejima Y, Hirayama H, Tago K, Takano H, Tajiri M, Hayashi K, Kawabata M, Funamizu M, Makita Y, Hata A. Nakamura T, et al. Am J Kidney Dis. 2002 May;39(5):1032-9. doi: 10.1053/ajkd.2002.32779. Am J Kidney Dis. 2002. PMID: 11979347

8

Homocysteine and atheromatous renal artery stenosis.

Olivieri O, Friso S, Trabetti E, Girelli D, Pizzolo F, Faccini G, Stranieri C, Pignatti PF, Corrocher R. Olivieri O, et al. Clin Exp Med. 2001 Dec;1(4):211-8. doi: 10.1007/s102380100005. Clin Exp Med. 2001. PMID: 11918280

9

Folate status is the major determinant of fasting total plasma homocysteine levels in maintenance dialysis patients.

Bostom AG, Shemin D, Lapane KL, Nadeau MR, Sutherland P, Chan J, Rozen R, Yoburn D, Jacques PF, Selhub J, Rosenberg IH. Bostom AG, et al. Atherosclerosis. 1996 Jun;123(1-2):193-202. doi: 10.1016/0021-9150(96)05809-1. Atherosclerosis. 1996. PMID: 8782850

10

Methylenetetrahydrofolate reductase C677T mutation, plasma homocysteine, and folate in subjects from northern Italy with or without angiographically documented severe coronary atherosclerotic disease: evidence for an important genetic-environmental interaction.

Girelli D, Friso S, Trabetti E, Olivieri O, Russo C, Pessotto R, Faccini G, Pignatti PF, Mazzucco A, Corrocher R. Girelli D, et al. Blood. 1998 Jun 1;91(11):4158-63. Blood. 1998. PMID: 9596662 Free article.

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