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Items: 9

1.

Role of methylenetetrahydrofolate reductase gene (MTHFR) 677C>T polymorphism in pediatric cerebrovascular disorders.

Alsayouf H, Zamel KM, Heyer GL, Khuhro AL, Kahwash SB, de los Reyes EC.

J Child Neurol. 2011 Mar;26(3):318-21. doi: 10.1177/0883073810381446. Epub 2011 Jan 26.

PMID:
21270470
2.

The MTHFR 677C->T polymorphism and the risk of congenital heart defects: a literature review and meta-analysis.

van Beynum IM, den Heijer M, Blom HJ, Kapusta L.

QJM. 2007 Dec;100(12):743-53. Epub 2007 Oct 26. Review.

PMID:
17965089
3.

Homocysteine, methylenetetrahydrofolate reductase and risk of schizophrenia: a meta-analysis.

Muntjewerff JW, Kahn RS, Blom HJ, den Heijer M.

Mol Psychiatry. 2006 Feb;11(2):143-9. Review.

PMID:
16172608
4.

MTHFR 677C>T and ACE D/I polymorphisms in migraine: a systematic review and meta-analysis.

Sch├╝rks M, Rist PM, Kurth T.

Headache. 2010 Apr;50(4):588-99. doi: 10.1111/j.1526-4610.2009.01570.x. Epub 2009 Nov 17. Review.

5.

The role of the MTHFR gene in migraine.

Stuart S, Cox HC, Lea RA, Griffiths LR.

Headache. 2012 Mar;52(3):515-20. doi: 10.1111/j.1526-4610.2012.02106.x. Epub 2012 Feb 29. Review.

PMID:
22375693
6.

Survival and psychomotor development with early betaine treatment in patients with severe methylenetetrahydrofolate reductase deficiency.

Diekman EF, de Koning TJ, Verhoeven-Duif NM, Rovers MM, van Hasselt PM.

JAMA Neurol. 2014 Feb;71(2):188-94. doi: 10.1001/jamaneurol.2013.4915. Review.

PMID:
24323041
7.

MTHFR genetic testing: Controversy and clinical implications.

Long S, Goldblatt J.

Aust Fam Physician. 2016 Apr;45(4):237-40. Review.

8.

Advances in stroke 2009: update on the genetics of stroke and cerebrovascular disease 2009.

Hegele RA, Dichgans M.

Stroke. 2010 Feb;41(2):e63-6. doi: 10.1161/STROKEAHA.109.571034. Epub 2010 Jan 14. Review. No abstract available.

9.

[Gene and cerebrovascular pathology (association studies)].

Torshin IIu, Gromova OA, Nikonov AA.

Zh Nevrol Psikhiatr Im S S Korsakova. 2009;109(3):56-9. Review. Russian. No abstract available.

PMID:
19469043

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