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Items: 1 to 20 of 62

1.

Prothrombotic genetic variants and atherosclerosis in patients with cerebral ischemia of arterial origin.

Pruissen DM, Kappelle LJ, Rosendaal FR, Algra A; SMART Study Group.

Atherosclerosis. 2009 May;204(1):191-5. doi: 10.1016/j.atherosclerosis.2008.08.033. Epub 2008 Sep 4.

PMID:
18848323
2.

Prothrombotic gene variants and mortality after cerebral ischemia of arterial origin.

Pruissen DM, Rosendaal FR, Frijns CJ, Kappelle LJ, Vos HL, Algra A; SMART Study Group.

Neuroepidemiology. 2011;37(2):109-13. doi: 10.1159/000330353. Epub 2011 Oct 7.

3.

Prothrombotic gene variation and new vascular events after cerebral ischemia of arterial origin.

Pruissen DM, Rosendaal FR, Frijns CJ, Kappelle LJ, Vos HL, Algra A; Smart Study Group.

J Thromb Haemost. 2008 Oct;6(10):1639-44. doi: 10.1111/j.1538-7836.2008.03097.x. Epub 2008 Jul 25. Review.

4.

No association of nineteen COX-2 gene variants to preclinical markers of atherosclerosis The Cardiovascular Risk in Young Finns Study.

Lähteelä K, Kunnas T, Lyytikäinen LP, Mononen N, Taittonen L, Laitinen T, Kettunen J, Juonala M, Hutri-Kähönen N, Kähönen M, Viikari JS, Raitakari OT, Lehtimäki T, Nikkari ST.

BMC Med Genet. 2012 Jul 2;13:32. doi: 10.1186/1471-2350-13-32.

5.

Factor V Leiden, prothrombin gene mutation, and thrombosis risk in patients with antiphospholipid antibodies.

Chopra N, Koren S, Greer WL, Fortin PR, Rauch J, Fortin I, Senécal JL, Docherty P, Hanly JG.

J Rheumatol. 2002 Aug;29(8):1683-8.

PMID:
12180730
6.

Variants in COX-2, PTGIS, and TBXAS1 Are Associated with Carotid Artery or Intracranial Arterial Stenosis and Neurologic Deterioration in Ischemic Stroke Patients.

Yi X, Ming B, Wang C, Chen H, Ma C.

J Stroke Cerebrovasc Dis. 2017 May;26(5):1128-1135. doi: 10.1016/j.jstrokecerebrovasdis.2016.12.032. Epub 2017 Jan 17.

PMID:
28108096
7.

Prothrombotic gene variation in patients with large and small vessel disease.

Pruissen DM, Kappelle LJ, Rosendaal FR, Algra A; SMART Study Group.

Neuroepidemiology. 2008;31(2):89-92. doi: 10.1159/000144089. Epub 2008 Jul 12.

PMID:
18622144
8.

Genes influencing coagulation and the risk of aneurysmal subarachnoid hemorrhage, and subsequent complications of secondary cerebral ischemia and rebleeding.

Ruigrok YM, Slooter AJ, Rinkel GJ, Wijmenga C, Rosendaal FR.

Acta Neurochir (Wien). 2010 Feb;152(2):257-62. doi: 10.1007/s00701-009-0505-0. Epub 2009 Oct 14.

9.

Prothrombotic genetic risk factors in young survivors of myocardial infarction.

Ardissino D, Mannucci PM, Merlini PA, Duca F, Fetiveau R, Tagliabue L, Tubaro M, Galvani M, Ottani F, Ferrario M, Corral J, Margaglione M.

Blood. 1999 Jul 1;94(1):46-51.

10.

Are prothrombotic variants of platelet glycoprotein receptor polymorphisms involved in the pathogenesis of thrombotic microangiopathies?

Sucker C, Schmitz M, Hetzel GR, Grabensee B, Maruhn-Debowski B, Ostojic L, Scharf RE, Zotz RB.

Clin Appl Thromb Hemost. 2009 Jul-Aug;15(4):402-7. doi: 10.1177/1076029608316015. Epub 2008 May 22.

PMID:
18502778
11.

Inherited prothrombotic risk factors in children with stroke, transient ischemic attack, or migraine.

Herak DC, Antolic MR, Krleza JL, Pavic M, Dodig S, Duranovic V, Brkic AB, Zadro R.

Pediatrics. 2009 Apr;123(4):e653-60. doi: 10.1542/peds.2007-3737.

PMID:
19336355
12.

Ischaemic stroke patients with heterozygous factor V Leiden present with multiple brain infarctions and widespread atherothrombotic disease.

Haapaniemi E, Helenius J, Jakovljević D, Soinne L, Syrjälä M, Kaste M, Lassila R, Tatlisumak T.

Thromb Haemost. 2009 Jan;101(1):145-50.

PMID:
19132201
13.

Genetic risk factor characterizes abdominal aortic aneurysm from arterial occlusive disease in human beings: CCR5 Delta 32 deletion.

Ghilardi G, Biondi ML, Battaglioli L, Zambon A, Guagnellini E, Scorza R.

J Vasc Surg. 2004 Nov;40(5):995-1000.

14.

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
15.

Genetic and acquired prothrombotic risk factors and sudden hearing loss.

Capaccio P, Ottaviani F, Cuccarini V, Bottero A, Schindler A, Cesana BM, Censuales S, Pignataro L.

Laryngoscope. 2007 Mar;117(3):547-51.

PMID:
17334320
16.

AB0 blood group and risk of venous or arterial thrombosis in carriers of factor V Leiden or prothrombin G20210A polymorphisms.

Miñano A, Ordóñez A, España F, González-Porras JR, Lecumberri R, Fontcuberta J, Llamas P, Marín F, Estellés A, Alberca I, Vicente V, Corral J.

Haematologica. 2008 May;93(5):729-34. doi: 10.3324/haematol.12271. Epub 2008 Apr 2.

17.

The sex-specific association of Met62Ile gene polymorphism in P-selectin glycoprotein ligand (PSGL-1) with carotid plaque presence: preliminary study.

Zivković M, Kolaković A, Radak D, Dinčić D, Radak S, Djurić T, Stanković A.

Mol Biol Rep. 2012 Jun;39(6):6479-85. doi: 10.1007/s11033-012-1475-5. Epub 2012 Feb 4.

PMID:
22307784
18.

The role of classic risk factors and prothrombotic factor gene mutations in ischemic stroke risk development in young and middle-aged individuals.

Supanc V, Sonicki Z, Vukasovic I, Solter VV, Zavoreo I, Kes VB.

J Stroke Cerebrovasc Dis. 2014 Mar;23(3):e171-6. doi: 10.1016/j.jstrokecerebrovasdis.2013.09.025. Epub 2013 Nov 1.

PMID:
24189452
19.

The E-selectin gene polymorphism and carotid atherosclerosis in end-stage renal disease.

Testa A, Benedetto FA, Spoto B, Pisano A, Tripepi G, Mallamaci F, Malatino LS, Zoccali C.

Nephrol Dial Transplant. 2006 Jul;21(7):1921-6. Epub 2006 Mar 22.

PMID:
16554320
20.

Serum adipocyte fatty acid-binding protein levels were independently associated with carotid atherosclerosis.

Yeung DC, Xu A, Cheung CW, Wat NM, Yau MH, Fong CH, Chau MT, Lam KS.

Arterioscler Thromb Vasc Biol. 2007 Aug;27(8):1796-802. Epub 2007 May 17.

PMID:
17510463

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