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Items: 1 to 20 of 685

1.

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
2.

Hyperhomocyst(e)inemia and MTHFR C677T genotypes in patients with central retinal vein occlusion.

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

Graefes Arch Clin Exp Ophthalmol. 2002 Apr;240(4):286-90. Epub 2002 Feb 21.

PMID:
11981642
3.

Hyperhomocyst(e)inemia, but not methylenetetrahydrofolate reductase C677T mutation, as a risk factor in branch retinal vein occlusion.

Weger M, Stanger O, Deutschmann H, Temmel W, Renner W, Schmut O, Quehenberger F, Semmelrock J, Haas A.

Ophthalmology. 2002 Jun;109(6):1105-9.

PMID:
12045051
5.

The C677T mutation in methylenetetrahydrofolate reductase gene, plasma homocysteine concentration and the risk of coronary artery disease.

Kadziela J, Janas J, Dzielińska Z, Szperl M, Gaździk D, Chotkowska E, Piotrowski W, Ruzyłło W.

Kardiol Pol. 2003 Jul;59(7):17-26; discussion 26.

PMID:
14560345
6.

Hyperhomocyst(e)inaemia, but not MTHFR C677T mutation, as a risk factor for non-arteritic ischaemic optic neuropathy.

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

Br J Ophthalmol. 2001 Jul;85(7):803-6.

7.
8.

Hyperhomocysteinemia and the MTHFR C677T mutation in Budd-Chiari syndrome.

Li XM, Wei YF, Hao HL, Hao YB, He LS, Li JD, Mei B, Wang SY, Wang C, Wang JX, Zhu JZ, Liang JQ.

Am J Hematol. 2002 Sep;71(1):11-4.

9.

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.

10.

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
11.

Plasma homocysteine, methylenetetrahydrofolate reductase genotypes, and age at onset of symptoms of myocardial ischemia.

Mager A, Battler A, Birnbaum Y, Magal N, Shohat M.

Am J Cardiol. 2002 Apr 15;89(8):919-23.

PMID:
11950428
12.

The 677T genotype of the common MTHFR thermolabile variant and fasting homocysteine in childhood venous thrombosis.

Koch HG, Nabel P, Junker R, Auberger K, Schobess R, Homberger A, Linnebank M, Nowak-Göttl U.

Eur J Pediatr. 1999 Dec;158 Suppl 3:S113-6.

PMID:
10650848
13.

The effect of methylenetetrahydrofolate reductase C677T common variant on hypertensive risk is not solely explained by increased plasma homocysteine values.

Rodríguez-Esparragón F, Hernández-Perera O, Rodríguez-Pérez JC, Anábitarte A, Díaz-Cremades JM, Losada A, Fiuza D, Hernández E, Yunis C, Ferrario CM.

Clin Exp Hypertens. 2003 May;25(4):209-20.

PMID:
12797595
14.
15.

Thermolabile MTHFR genotype and retinal vascular occlusive disease.

Cahill M, Karabatzaki M, Donoghue C, Meleady R, Mynett-Johnson LA, Mooney D, Graham IM, Whitehead AS, Shields DC.

Br J Ophthalmol. 2001 Jan;85(1):88-90.

16.
17.

The relation between erythrocyte volume and folate levels is influenced by a common mutation in the methylenetetrahydrofolate reductase (MTHFR) gene (C677T).

Lalouschek W, Aull S, Serles W, Wolfsberger M, Deecke L, Pabinger-Fasching I, Mannhalter C.

J Investig Med. 2000 Jan;48(1):14-20.

PMID:
10695265
19.

Genetic and nongenetic factors influencing plasma homocysteine levels in patients with ischemic cerebrovascular disease and in healthy control subjects.

Lalouschek W, Aull S, Serles W, Schnider P, Mannhalter C, Lang T, Deecke L, Zeiler K.

J Lab Clin Med. 1999 Jun;133(6):575-82.

PMID:
10360632
20.

Hyperhomocysteinemia increases the risk of venous thrombosis independent of the C677T mutation of the methylenetetrahydrofolate reductase gene in selected Brazilian patients.

Morelli VM, Lourenço DM, D'Almeida V, Franco RF, Miranda F, Zago MA, Noguti MA, Cruz E, Kerbauy J.

Blood Coagul Fibrinolysis. 2002 Apr;13(3):271-5.

PMID:
11943942

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