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Items: 1 to 20 of 252

1.

The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation.

Margaglione M, D'Andrea G, d'Addedda M, Giuliani N, Cappucci G, Iannaccone L, Vecchione G, Grandone E, Brancaccio V, Di Minno G.

Thromb Haemost. 1998 May;79(5):907-11.

PMID:
9609218
2.

No evidence for an increased risk of venous thrombosis in patients with factor V Leiden by the homozygous 677 C to T mutation in the methylenetetrahydrofolate-reductase gene.

Rintelen C, Mannhalter C, Lechner K, Eichinger S, Kyrle PA, Papagiannopoulos M, Schneider B, Pabinger I.

Blood Coagul Fibrinolysis. 1999 Mar;10(2):101-5.

PMID:
10192659
3.
5.

Venous thromboembolic disease and the prothrombin, methylene tetrahydrofolate reductase and factor V genes.

Alhenc-Gelas M, Arnaud E, Nicaud V, Aubry ML, Fiessinger JN, Aiach M, Emmerich J.

Thromb Haemost. 1999 Apr;81(4):506-10.

PMID:
10235429
6.
7.

Inherited prothrombotic conditions and premature ischemic stroke: sex difference in the association with factor V Leiden.

Margaglione M, D'Andrea G, Giuliani N, Brancaccio V, De Lucia D, Grandone E, De Stefano V, Tonali PA, Di Minno G.

Arterioscler Thromb Vasc Biol. 1999 Jul;19(7):1751-6.

8.

Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease.

Toydemir PB, Elhan AH, Tükün A, Toydemir R, Gürler A, Tüzüner A, Bökesoy I.

J Rheumatol. 2000 Dec;27(12):2849-54.

PMID:
11128675
9.

Thermolabile methylenetetrahydrofolate reductase and factor V Leiden in the risk of deep-vein thrombosis.

Kluijtmans LA, den Heijer M, Reitsma PH, Heil SG, Blom HJ, Rosendaal FR.

Thromb Haemost. 1998 Feb;79(2):254-8.

PMID:
9493571
10.

Lipoprotein (a) and genetic polymorphisms of clotting factor V, prothrombin, and methylenetetrahydrofolate reductase are risk factors of spontaneous ischemic stroke in childhood.

Nowak-Göttl U, Sträter R, Heinecke A, Junker R, Koch HG, Schuierer G, von Eckardstein A.

Blood. 1999 Dec 1;94(11):3678-82.

11.

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
12.

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
13.

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.

14.

Relation of three genetic traits to venous thrombosis in an African-American population.

Dilley A, Austin H, Hooper WC, Lally C, Ribeiro MJ, Wenger NK, Silva V, Rawlins P, Evatt B.

Am J Epidemiol. 1998 Jan 1;147(1):30-5.

PMID:
9440395
15.

Prospective evaluation of the risk conferred by factor V Leiden and thermolabile methylenetetrahydrofolate reductase polymorphisms in pregnancy.

Murphy RP, Donoghue C, Nallen RJ, D'Mello M, Regan C, Whitehead AS, Fitzgerald DJ.

Arterioscler Thromb Vasc Biol. 2000 Jan;20(1):266-70.

16.

Risk of recurrent venous thrombosis in patients with G20210A mutation in the prothrombin gene or factor V Leiden mutation.

González-Porras JR, García-Sanz R, Alberca I, López ML, Balanzategui A, Gutierrez O, Lozano F, San Miguel J.

Blood Coagul Fibrinolysis. 2006 Jan;17(1):23-8.

PMID:
16607075
17.

Prevalence of factor V G1691A (Leiden), prothrombin G20210A, and methylene tetrahydrofolate reductase C677T thrombophilic mutations in children with inflammatory bowel disease.

Kader HA, Berman WF, Al-Seraihy AS, Ware RE, Ulshen MH, Treem WR.

J Pediatr Gastroenterol Nutr. 2002 Nov;35(5):629-35.

PMID:
12454577
18.
19.

Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism.

Margaglione M, D'Andrea G, Colaizzo D, Cappucci G, del Popolo A, Brancaccio V, Ciampa A, Grandone E, Di Minno G.

Thromb Haemost. 1999 Dec;82(6):1583-7.

PMID:
10613638
20.

Factor V leiden and prothrombin G20210A mutations, but not methylenetetrahydrofolate reductase C677T, are associated with recurrent miscarriages.

Foka ZJ, Lambropoulos AF, Saravelos H, Karas GB, Karavida A, Agorastos T, Zournatzi V, Makris PE, Bontis J, Kotsis A.

Hum Reprod. 2000 Feb;15(2):458-62.

PMID:
10655323

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