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Items: 1 to 20 of 97

2.

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
4.

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.

Methionine synthase A2756G and methylenetetrahydrofolate reductase A1298C polymorphisms are not risk factors for idiopathic venous thromboembolism.

Salomon O, Rosenberg N, Zivelin A, Steinberg DM, Kornbrot N, Dardik R, Inbal A, Seligsohn U.

Hematol J. 2001;2(1):38-41.

PMID:
11920232
7.
8.

[C677T mutation in methylentetrahydrofolatereductase gene in patients with venous thromboses from the central region of Russia correlates with a high risk of pulmonary artery thromboembolism].

Avdonin PV, Kirienko AI, Kozhevnikova LM, Shostak NA, Babadaeva NM, Leont'ev SG, Petukhov EB, Kubatiev AA, Savel'ev VS.

Ter Arkh. 2006;78(6):70-6. Russian.

PMID:
16881367
9.
10.

Prevalence of genetic mutations that predispose to thrombophilia in a Greek Cypriot population.

Angelopoulou K, Nicolaides A, Constantinou Deltas C.

Clin Appl Thromb Hemost. 2000 Apr;6(2):104-7.

PMID:
10775032
11.

Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors.

Antoniadi T, Hatzis T, Kroupis C, Economou-Petersen E, Petersen MB.

Am J Hematol. 1999 Aug;61(4):265-7.

12.

Methylenetetrahydrofolate reductase C677T genotype and venous thromboembolic disease.

Couturaud F, Oger E, Abalain JH, Chenu E, Guias B, Floch HH, Mercier B, Mottier D, Leroyer C.

Respiration. 2000;67(6):657-61.

PMID:
11124649
13.

Lack of association between the C677T mutation in the 5,10-methylenetetrahydrofolate reductase gene and venous thromboembolism in Northwestern Greece.

Zalavras ChG, Giotopoulou S, Dokou E, Mitsis M, Ioannou HV, Tzolou A, Kolaitis N, Vartholomatos G.

Int Angiol. 2002 Sep;21(3):268-71.

PMID:
12384649
14.

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
15.

Increased Factor V Leiden frequency is associated with venous thrombotic events among young Brazilian patients.

de Paula Sabino A, Guimarães DA, Ribeiro DD, Paiva SG, Sant'Ana Dusse LM, das Graças Carvalho M, Fernandes AP.

J Thromb Thrombolysis. 2007 Dec;24(3):261-6. Epub 2007 Mar 31.

PMID:
17401546
16.

A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis.

Almawi WY, Tamim H, Kreidy R, Timson G, Rahal E, Nabulsi M, Finan RR, Irani-Hakime N.

J Thromb Thrombolysis. 2005 Jun;19(3):189-96.

PMID:
16082606
17.

Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A.

Rady PL, Szucs S, Grady J, Hudnall SD, Kellner LH, Nitowsky H, Tyring SK, Matalon RK.

Am J Med Genet. 2002 Jan 15;107(2):162-8.

PMID:
11807892
18.

Methylenetetrahydrofolate reductase (MTHFR): the incidence of mutations C677T and A1298C in the Ashkenazi Jewish population.

Rady PL, Tyring SK, Hudnall SD, Vargas T, Kellner LH, Nitowsky H, Matalon RK.

Am J Med Genet. 1999 Oct 8;86(4):380-4.

PMID:
10494095
19.

Abdominal venous thrombosis in neonates and infants: role of prothrombotic risk factors - a multicentre case-control study. For the Childhood Thrombophilia Study Group.

Heller C, Schobess R, Kurnik K, Junker R, Günther G, Kreuz W, Nowak-Göttl U.

Br J Haematol. 2000 Nov;111(2):534-9.

PMID:
11122096
20.

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