HuGE Literature Finder
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Records 1-28
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Global prevalence of prothrombin gene mutation G20210A and implications in women's health: a systematic review.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2016 Apr . Dziadosz Margaret, Baxi Laxmi |
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Association of folate metabolism gene polymorphisms and pulmonary embolism: A case-control study of West-Siberian population.
Thrombosis research 2015 May 135 (5): 788-95. Karmadonova N A, Shilova A N, Kozyreva V S, Subbotovskaya A I, Klevanets J E, Karpenko A |
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Associations of coagulation factor V Leiden and prothrombin G20210A mutations with Budd-Chiari syndrome and portal vein thrombosis: a systematic review and meta-analysis.
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 2014 Nov 12 (11): 1801-12.e7. Qi Xingshun, Ren Weirong, De Stefano Valerio, Fan Daimi |
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Prothrombin G20210A mutation is associated with young-onset stroke: the genetics of early-onset stroke study and meta-analysis.
Stroke; a journal of cerebral circulation 2014 Apr 45 (4): 961-7. Jiang Baijia, Ryan Kathleen A, Hamedani Ali, Cheng Yuching, Sparks Mary J, Koontz Deborah, Bean Christopher J, Gallagher Margaret, Hooper W Craig, McArdle Patrick F, O'Connell Jeffrey R, Stine O Colin, Wozniak Marcella A, Stern Barney J, Mitchell Braxton D, Kittner Steven J, Cole John |
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Risk of Budd-Chiari syndrome associated with factor V Leiden and G20210A prothrombin mutation: a meta-analysis.
PloS one 2014 9 (4): e95719. Zhang Peijin, Zhang Jing, Sun Guixiang, Gao Xiuyin, Wang Hui, Yan Wenjun, Xu Hao, Zu Maoheng, Ma He, Wang Wei, Lu Zhaoj |
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Who are at risk for thromboembolism after arthroplasty? A systematic review and meta-analysis.
Thrombosis research 2013 Nov 132 (5): 531-6. Zhou Xindie, Qian Wenkang, Li Jin, Zhang Pengli, Yang Zhigao, Chen Weiping, Wu Lido |
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Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls.
European journal of epidemiology 2013 Aug 28 (8): 621-47. Simone Benedetto, De Stefano Valerio, Leoncini Emanuele, Zacho Jeppe, Martinelli Ida, Emmerich Joseph, Rossi Elena, Folsom Aaron R, Almawi Wassim Y, Scarabin Pierre Y, den Heijer Martin, Cushman Mary, Penco Silvana, Vaya Amparo, Angchaisuksiri Pantep, Okumus Gulfer, Gemmati Donato, Cima Simona, Akar Nejat, Oguzulgen Kivilcim I, Ducros Véronique, Lichy Christoph, Fernandez-Miranda Consuelo, Szczeklik Andrzej, Nieto José A, Torres Jose Domingo, Le Cam-Duchez Véronique, Ivanov Petar, Cantu-Brito Carlos, Shmeleva Veronika M, Stegnar Mojka, Ogunyemi Dotun, Eid Suhair S, Nicolotti Nicola, De Feo Emma, Ricciardi Walter, Boccia Stefan |
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Genetic Polymorphisms Associated with Retinal Vein Occlusion: A Greek Case-control Study and Meta-analysis.
Ophthalmic genetics 2013 Jan . Yioti GG, Panagiotou OA, Vartholomatos GA, Kolaitis NI, Pappa CN, Evangelou E, Stefaniotou MI |
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Association of Allelic Variants of Factor V Leiden, Prothrombin And Methylenetetrahydrofolate Reductase with Thrombosis Or Ocular Involvement In Behçet's Disease: A Systematic Review And Meta-Analysis.
Autoimmunity reviews 2012 Nov . Chamorro AJ, Marcos M, Hernández-García I, Calvo A, Mejia JC, Cervera R, Espinosa G |
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Oral contraceptives and venous thromboembolism: a systematic review and meta-analysis.
Drug safety 2012 Mar 35 (3): 191-205. Manzoli Lamberto, De Vito Corrado, Marzuillo Carolina, Boccia Antonio, Villari Pao |
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Varied association of prothrombin G20210A polymorphism with coronary artery disease susceptibility in different ethnic groups: evidence from 15,041 cases and 21,507 controls.
Molecular biology reports 2011 Apr 38 (4): 2371-6. Jin Bo, Li Yong, Ge-Shang Qu-Zhen, Ni Huan-Chun, Shi Hai-Ming, Shen W |
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The association of factor V Leiden with myocardial infarction is replicated in 1880 patients with premature disease.
Journal of thrombosis and haemostasis : JTH 2010 Oct 8 (10): 2116-21. Mannucci P M, Asselta R, Duga S, Guella I, Spreafico M, Lotta L, Merlini P A, Peyvandi F, Kathiresan S, Ardissino |
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Factor V Leiden and prothrombin 20210G>A [corrected] mutation and paediatric ischaemic stroke: a case-control study and two meta-analyses.
Acta paediatrica (Oslo, Norway : 1992) 2010 Aug 99 (8): 1168-74. Laugesaar R, Kahre T, Kolk A, Uustalu U, Kool P, Talvik |
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MTHFR C677T, FII G20210A, FV Leiden G1691A, NOS3 intron 4 VNTR, and APOE epsilon4 gene polymorphisms are not associated with spontaneous cervical artery dissection.
International journal of stroke : official journal of the International Stroke Society 2010 Apr 5 (2): 80-5. Jara-Prado A, Alonso M E, Martínez Ruano L, Guerrero Camacho J, Leyva A, López M, Gutierrez-Castrellon P, Arauz |
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Causal relationship of susceptibility genes to ischemic stroke: comparison to ischemic heart disease and biochemical determinants.
PloS one 2010 5 (2): e9136. Bentley Paul, Peck George, Smeeth Liam, Whittaker John, Sharma Pank |
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Replication of findings on the association of genetic variation in 24 hemostasis genes and risk of incident venous thrombosis.
Journal of thrombosis and haemostasis : JTH 2009 Oct 7 (10): 1743-6. Smith N L, Wiggins K L, Reiner A P, Lange L A, Cushman M, Heckbert S R, Lumley T, Rice K M, Folsom A R, Psaty B |
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A field synopsis and meta-analysis of genetic association studies in peripheral arterial disease: The CUMAGAS-PAD database.
American journal of epidemiology 2009 Jul 170 (1): 1-11. Zintzaras Elias, Zdoukopoulos Nik |
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Do common prothrombotic mutations influence the risk of cerebral ischaemia in patients with patent foramen ovale? Systematic review and meta-analysis.
Thrombosis and haemostasis 2009 May 101 (5): 813-7. Pezzini Alessandro, Grassi Mario, Zotto Elisabetta Del, Giossi Alessia, Volonghi Irene, Costa Paolo, Grau Armin, Magoni Mauro, Padovani Alessandro, Lichy Christo |
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A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.
Stroke; a journal of cerebral circulation 2009 Mar 40 (3): 683-95. Wang Xingyu, Cheng Suzanne, Brophy Victoria H, Erlich Henry A, Mannhalter Christine, Berger Klaus, Lalouschek Wolfgang, Browner Warren S, Shi Yu, Ringelstein E Bernd, Kessler Christof, Luedemann Jan, Lindpaintner Klaus, Liu Lisheng, Ridker Paul M, Zee Robert Y L, Cook Nancy R, |
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Inherited thrombophilic abnormalities and risk of portal vein thrombosis. a meta-analysis.
Thrombosis and haemostasis 2008 Apr 99 (4): 675-82. Dentali Francesco, Galli Matteo, Gianni Monica, Ageno Walt |
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The risk of recurrent venous thromboembolism among heterozygous carriers of factor V Leiden or prothrombin G20210A mutation. A systematic review of prospective studies.
Haematologica 2007 Aug 92 (8): 1107-14. Marchiori Antonio, Mosena Laura, Prins Martin H, Prandoni Pao |
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Thrombophilic abnormalities, oral contraceptives, and risk of cerebral vein thrombosis: a meta-analysis.
Blood 2006 Apr 107 (7): 2766-73. Dentali Francesco, Crowther Mark, Ageno Walt |
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Thrombophilic risk factors and homocysteine levels in Behçet's disease in eastern Spain and their association with thrombotic events.
Thrombosis and haemostasis 2006 Apr 95 (4): 618-24. Ricart José Ma, Vayá Amparo, Todolí José, Calvo Javier, Villa Piedad, Estellés Amparo, España Francisco, Santaolaria Marisa, Corella Dolores, Aznar Jus |
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Retinal vein occlusion: a form of venous thrombosis or a complication of atherosclerosis? A meta-analysis of thrombophilic factors.
Thrombosis and haemostasis 2005 Jun 93 (6): 1021-6. Janssen Mirian C H, den Heijer Martin, Cruysberg Johannes R M, Wollersheim Hub, Bredie Sebastian J |
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Meta-analysis of genetic studies in ischemic stroke: thirty-two genes involving approximately 18,000 cases and 58,000 controls.
Archives of neurology 2004 Nov 61 (11): 1652-61. Casas Juan P, Hingorani Aroon D, Bautista Leonelo E, Sharma Pank |
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G20210A prothrombin gene polymorphism and coronary ischaemic syndromes: a phenotype-specific meta-analysis of 12 034 subjects.
Heart (British Cardiac Society) 2004 Jan 90 (1): 82-6. Burzotta F, Paciaroni K, De Stefano V, Crea F, Maseri A, Leone G, Andreotti |
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Genetic variation in coagulation and fibrinolytic proteins and their relation with acute myocardial infarction: a systematic review.
Circulation 2001 Dec 104 (25): 3063-8. Boekholdt S M, Bijsterveld N R, Moons A H, Levi M, Büller H R, Peters R |
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Correlation of polymorphisms to coagulation and biochemical risk factors for cardiovascular diseases.
The American journal of cardiology 2001 Jun 87 (12): 1361-6. Wu A H, Tsongalis G |
- Page last reviewed:Mar 1, 2018
- Page last updated:Jun 13, 2019
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