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Results: 1 to 20 of 95

Similar articles for PubMed (Select 22021457)

1.

Prothrombin 20210G>A genotype and C-reactive protein level.

Hoppe B, Burmester GR, Häupl T.

Blood. 2011 Oct 20;118(16):4495-6. doi: 10.1182/blood-2011-08-373928. No abstract available.

2.

A knockout for knockin.

Mosnier LO.

Blood. 2011 Jun 9;117(23):6058-60. doi: 10.1182/blood-2011-04-345553. No abstract available.

3.

The development of inflammatory joint disease is attenuated in mice expressing the anticoagulant prothrombin mutant W215A/E217A.

Flick MJ, Chauhan AK, Frederick M, Talmage KE, Kombrinck KW, Miller W, Mullins ES, Palumbo JS, Zheng X, Esmon NL, Esmon CT, Thornton S, Becker A, Pelc LA, Di Cera E, Wagner DD, Degen JL.

Blood. 2011 Jun 9;117(23):6326-37. doi: 10.1182/blood-2010-08-304915. Epub 2011 Mar 24.

4.

Coagulation factors II, V, VII, and X, prothrombin gene 20210G-->A transition, and factor V Leiden in coronary artery disease: high factor V clotting activity is an independent risk factor for myocardial infarction.

Redondo M, Watzke HH, Stucki B, Sulzer I, Biasiutti FD, Binder BR, Furlan M, Lämmle B, Wuillemin WA.

Arterioscler Thromb Vasc Biol. 1999 Apr;19(4):1020-5.

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Prothrombin Saint-Denis: a natural variant with a point mutation resulting in Asp to Glu substitution at position 552 in prothrombin.

Rouy S, Vidaud D, Alessandri JL, Dautzenberg MD, Venisse L, Guillin MC, Bezeaud A.

Br J Haematol. 2006 Mar;132(6):770-3.

PMID:
16487178
8.

Factor V Leiden, prothrombin 20210G --> A, methylenetetrahydrofolate reductase 677C --> T and plasminogen activator inhibitor 4G/5G polymorphism in women with pregnancy-related venous thromboembolism.

Meglic L, Stegnar M, Milanez T, Bozic M, Peterlin B, Peternel P, Novak-Antolic Z.

Eur J Obstet Gynecol Reprod Biol. 2003 Dec 10;111(2):157-63.

PMID:
14597244
9.

Prothrombin A19911G and G20210A polymorphisms' role in thrombosis.

Pérez-Ceballos E, Corral J, Alberca I, Vayá A, Llamas P, Montes R, González-Conejero R, Vicente V.

Br J Haematol. 2002 Aug;118(2):610-4.

PMID:
12139755
10.

Factor V Leiden and prothrombin 20210G>A [corrected] mutation and paediatric ischaemic stroke: a case-control study and two meta-analyses.

Laugesaar R, Kahre T, Kolk A, Uustalu U, Kool P, Talvik T.

Acta Paediatr. 2010 Aug;99(8):1168-74. doi: 10.1111/j.1651-2227.2010.01784.x. Epub 2010 Mar 2. Erratum in: Acta Paediatr. 2010 Jul;99(7):1112.

PMID:
20337781
11.

Prothrombin 20210G>A is an ancestral prothrombotic mutation that occurred in whites approximately 24,000 years ago.

Zivelin A, Mor-Cohen R, Kovalsky V, Kornbrot N, Conard J, Peyvandi F, Kyrle PA, Bertina R, Peyvandi F, Emmerich J, Seligsohn U.

Blood. 2006 Jun 15;107(12):4666-8. Epub 2006 Feb 21.

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Prothrombin 20210G/A mutation in two patients with mesenteric ischemia.

Balian A, Veyradier A, Naveau S, Wolf M, Montembault S, Giraud V, Borotto E, Henry C, Meyer D, Chaput JC.

Dig Dis Sci. 1999 Sep;44(9):1910-3.

PMID:
10505734
15.

Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation.

Jayandharan G, Viswabandya A, Baidya S, Nair SC, Shaji RV, Chandy M, Srivastava A.

J Thromb Haemost. 2005 Jul;3(7):1446-53.

PMID:
15892853
16.

Severe prothrombin deficiency caused by prothrombin-Edmonton (R-4Q) combined with a previously undetected deletion.

Wong AY, Hewitt J, Clarke BJ, Hudson DM, Krisinger MJ, Dower NA, MacGillivray RT.

J Thromb Haemost. 2006 Dec;4(12):2623-8. Epub 2006 Sep 26.

PMID:
17002658
17.

Central retinal vein thrombosis associated with prothrombin 20210G/A gene variant.

Vayá A, López JM, Mira Y, Ricart JM, Villa P, España-Gregori E, Estellés A, Aznar J.

Clin Appl Thromb Hemost. 1999 Jul;5(3):190-1.

PMID:
10726008
18.

Differential effects of high prothrombin levels on thrombin generation depending on the cause of the hyperprothrombinemia.

Castoldi E, Simioni P, Tormene D, Thomassen MC, Spiezia L, Gavasso S, Rosing J.

J Thromb Haemost. 2007 May;5(5):971-9.

PMID:
17461930
19.

[20210G/A mutation of prothrombin gene in a patient with deep venous thrombosis ad pulmonary embolism without other risk factors of thrombosis].

de la Cuadra P, Nauffal MD, Vayá Montaña A, Martínez MA, Perpiñá M.

Arch Bronconeumol. 1999 Dec;35(11):567-70. Spanish.

PMID:
10687043
20.

Factor V Leiden, prothrombin 20210G-->A and the MTHFR C677T mutations in childhood stroke.

McColl MD, Chalmers EA, Thomas A, Sproul A, Healey C, Rafferty I, McWilliam R, Eunson P.

Thromb Haemost. 1999 May;81(5):690-4.

PMID:
10365738
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