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Results: 1 to 20 of 849

1.

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
[PubMed - indexed for MEDLINE]
3.

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
[PubMed - indexed for MEDLINE]
4.

Primary thrombophilia in Mexico. II. Factor V G1691A (Leiden), prothrombin G20210A, and methylenetetrahydrofolate reductase C677T polymorphism in thrombophilic Mexican mestizos.

Ruiz-Argüelles GJ, Garcés-Eisele J, Reyes-Núñez V, Ramírez-Cisneros FJ.

Am J Hematol. 2001 Jan;66(1):28-31.

PMID:
11426488
[PubMed - indexed for MEDLINE]
5.

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
[PubMed - indexed for MEDLINE]
6.

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
[PubMed - indexed for MEDLINE]
7.

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
[PubMed - indexed for MEDLINE]
8.

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
[PubMed - indexed for MEDLINE]
9.

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
[PubMed - indexed for MEDLINE]
10.

Interaction between hyperhomocysteinemia, mutated methylenetetrahydrofolatereductase (MTHFR) and inherited thrombophilic factors in recurrent venous thrombosis.

Keijzer MB, den Heijer M, Blom HJ, Bos GM, Willems HP, Gerrits WB, Rosendaal FR.

Thromb Haemost. 2002 Nov;88(5):723-8.

PMID:
12428084
[PubMed - indexed for MEDLINE]
11.

Inherited thrombophilia as a risk factor for the development of ischemic stroke in young adults.

Voetsch B, Damasceno BP, Camargo EC, Massaro A, Bacheschi LA, Scaff M, Annichino-Bizzacchi JM, Arruda VR.

Thromb Haemost. 2000 Feb;83(2):229-33.

PMID:
10739378
[PubMed - indexed for MEDLINE]
12.

Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis.

Amitrano L, Brancaccio V, Guardascione MA, Margaglione M, Iannaccone L, D'Andrea G, Marmo R, Ames PR, Balzano A.

Hepatology. 2000 Feb;31(2):345-8.

PMID:
10655256
[PubMed - indexed for MEDLINE]
13.

Prospective evaluation of the thrombotic risk in children with acute lymphoblastic leukemia carrying the MTHFR TT 677 genotype, the prothrombin G20210A variant, and further prothrombotic risk factors.

Nowak-Göttl U, Wermes C, Junker R, Koch HG, Schobess R, Fleischhack G, Schwabe D, Ehrenforth S.

Blood. 1999 Mar 1;93(5):1595-9.

PMID:
10029588
[PubMed - indexed for MEDLINE]
Free Article
14.

Mutations C677T and A1298C of the 5,10-methylenetetrahydrofolate reductase gene and fasting plasma homocysteine levels are not associated with the increased risk of venous thromboembolic disease.

Domagala TB, Adamek L, Nizankowska E, Sanak M, Szczeklik A.

Blood Coagul Fibrinolysis. 2002 Jul;13(5):423-31.

PMID:
12138370
[PubMed - indexed for MEDLINE]
15.

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
[PubMed - indexed for MEDLINE]
Free Article
16.

Homozygous cystathionine beta-synthase deficiency, combined with factor V Leiden or thermolabile methylenetetrahydrofolate reductase in the risk of venous thrombosis.

Kluijtmans LA, Boers GH, Verbruggen B, Trijbels FJ, Novakova IR, Blom HJ.

Blood. 1998 Mar 15;91(6):2015-8.

PMID:
9490685
[PubMed - indexed for MEDLINE]
Free Article
17.

Risk of venous thrombosis in carriers of the prothrombin G20210A variant and factor V Leiden and their interaction with oral contraceptives.

Aznar J, Vayá A, Estellés A, Mira Y, Seguí R, Villa P, Ferrando F, Falcó C, Corella D, España F.

Haematologica. 2000 Dec;85(12):1271-6.

PMID:
11114134
[PubMed - indexed for MEDLINE]
Free Article
18.

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.

Thromb Haemost. 2000 Apr;83(4):563-70.

PMID:
10780318
[PubMed - indexed for MEDLINE]
19.

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
[PubMed - indexed for MEDLINE]
20.

The mutation Ala677-->Val in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis.

Arruda VR, von Zuben PM, Chiaparini LC, Annichino-Bizzacchi JM, Costa FF.

Thromb Haemost. 1997 May;77(5):818-21.

PMID:
9184384
[PubMed - indexed for MEDLINE]

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