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Results: 1 to 20 of 92

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1.

Coexistence of Neurofibromatosis Type-1 and MTHFR C677T Gene Mutation in a Young Stroke Patient: A Case Report.

Yilmaz H, Erkin G, Gumus H, Nalbant L.

Case Rep Neurol Med. 2013;2013:735419. doi: 10.1155/2013/735419. Epub 2013 Feb 27.

3.

A common mutation in the methylenetetrahydrofolate reductase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (factor V:Q506).

Cattaneo M, Tsai MY, Bucciarelli P, Taioli E, Zighetti ML, Bignell M, Mannucci PM.

Arterioscler Thromb Vasc Biol. 1997 Sep;17(9):1662-6.

4.

[Prevalence of methylenetetrahydrofolate reductase C677T mutation among patients with acute ischemic cerebrovascular disease in Aragon].

Sánchez-Marín B, Grasa JM, Torres M, Calvo MT, Martínez-Jarreta B, García-Erce JA, Giralt M.

An Med Interna. 2006 Apr;23(4):153-5. Spanish.

PMID:
16796406
5.

Methylenetetrahydrofolate reductase gene polymorphisms are associated with ischemic and hemorrhagic stroke: Dual effect of MTHFR polymorphisms C677T and A1298C.

Sazci A, Ergul E, Tuncer N, Akpinar G, Kara I.

Brain Res Bull. 2006 Dec 11;71(1-3):45-50. Epub 2006 Aug 15.

PMID:
17113927
6.

MTHFR C677T gene mutation as a risk factor for arterial stroke: a hospital based study.

Alluri RV, Mohan V, Komandur S, Chawda K, Chaudhuri JR, Hasan Q.

Eur J Neurol. 2005 Jan;12(1):40-4.

PMID:
15613145
7.
8.

Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke.

Barbagallo M, Pavone P, Incorpora G, Domenico Praticò A, Romantshik O, Friso S, Spalice A, Nicita F, Polizzi A, Ruggieri M, Iannetti P.

Childs Nerv Syst. 2009 Mar;25(3):361-5. doi: 10.1007/s00381-008-0724-3. Epub 2008 Oct 29.

PMID:
18958479
9.

Case-control Study of methylenetetrahydrofolate reductase mutations and hyperhomocysteinemia and risk of stroke.

Almawi WY, Khan A, Al-Othman SS, Bakhiet M.

J Stroke Cerebrovasc Dis. 2009 Sep-Oct;18(5):407-8. doi: 10.1016/j.jstrokecerebrovasdis.2008.12.003.

PMID:
19717029
10.

Genetic analysis of the thermolabile variant of 5, 10-methylenetetrahydrofolate reductase as a risk factor for ischemic stroke.

Harmon DL, Doyle RM, Meleady R, Doyle M, Shields DC, Barry R, Coakley D, Graham IM, Whitehead AS.

Arterioscler Thromb Vasc Biol. 1999 Feb;19(2):208-11.

11.

Hyperhomocysteinemia and the MTHFR C677T mutation in central retinal vein occlusion.

Larsson J, Hultberg B, Hillarp A.

Acta Ophthalmol Scand. 2000 Jun;78(3):340-3.

PMID:
10893069
12.

Methylenetetrahydrofolate reductase C677T polymorphism in Iraqi patients with ischemic stroke.

Al-Allawi NA, Avo AS, Jubrael JM.

Neurol India. 2009 Sep-Oct;57(5):631-5. doi: 10.4103/0028-3886.57821.

13.

Role of a common mutation in the homocysteine regulatory enzyme methylenetetrahydrofolate reductase in ischemic stroke.

Press RD, Beamer N, Evans A, DeLoughery TG, Coull BM.

Diagn Mol Pathol. 1999 Mar;8(1):54-8.

PMID:
10408794
14.
15.

Peripheral arterial disease and methylenetetrahydrofolate reductase (MTHFR) C677T mutations: A case-control study and meta-analysis.

Khandanpour N, Willis G, Meyer FJ, Armon MP, Loke YK, Wright AJ, Finglas PM, Jennings BA.

J Vasc Surg. 2009 Mar;49(3):711-8. doi: 10.1016/j.jvs.2008.10.004. Epub 2009 Jan 21. Review.

16.
17.

Acute stroke in relation to homocysteine and methylenetetrahydrofolate reductase gene polymorphisms.

Dikmen M, Ozbabalik D, Gunes HV, Degirmenci I, Bal C, Ozdemir G, Basaran A.

Acta Neurol Scand. 2006 May;113(5):307-14.

PMID:
16629766
18.

The role of hyperhomocysteinemia and methylenetetrahydrofolate reductase (MTHFR) C677T mutation in patients with retinal artery occlusion.

Weger M, Stanger O, Deutschmann H, Leitner FJ, Renner W, Schmut O, Semmelrock J, Haas A.

Am J Ophthalmol. 2002 Jul;134(1):57-61.

PMID:
12095808
19.

Methyltetrahydrofolate reductase C677T gene mutation and hyperhomocysteinemia as a novel risk factor for diabetic nephropathy.

Ukinc K, Ersoz HO, Karahan C, Erem C, Eminagaoglu S, Hacihasanoglu AB, Yilmaz M, Kocak M.

Endocrine. 2009 Oct;36(2):255-61. doi: 10.1007/s12020-009-9218-7. Epub 2009 Jul 14.

PMID:
19598005
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