HuGE Literature Finder
Records
1
-
11
| PROS1 variant in sudden death case of pulmonary embolism caused by calcification in the inferior vena cava: The importance of postmortem genetic analysis. Legal medicine (Tokyo, Japan) 2022 2 55 102029. Miura Aya, Funayama Kazuhisa, Nyuzuki Hiromi, Takahashi Naoya, Yamamoto Takuma, Koyama Akihide, Ikeuchi Takeshi, Takatsuka Hisakazu, Nishio Haji |
| Polymorphisms of F2 (G20210A), F5 (G1691A), F 7 (G10976A), F 13(G13T), FGB, ITGA2, ITGB3, PAI-I genes and its association with thrombotic complications in patients suffering from Takayasu aortoarteritis of Urals population. Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir 2021 Sep 49 (6): 448-455. Borodina Irina, Salavatova Gezel, Shardina Lub |
| [Hemostatic Gene Polymorphisms in Acute Coronary Syndrome with Nonobstructive Coronary Atherosclerosis]. Kardiologiia 2019 Oct 59 (10): 14-22. Fedorova S B, Kulagina I V, Ryabov V |
| Increased incidence of cancer in the follow-up of obstetric antiphospholipid syndrome within the NOH-APS cohort. Haematologica 2019 5 105 (2): 490-497. Gris Jean-Christophe, Mousty Éve, Bouvier Sylvie, Ripart Sylvie, Cochery-Nouvellon Éva, Fabbro-Peray Pascale, Broner Jonathan, Letouzey Vincent, Pérez-Martin Anton |
| F11 is associated with recurrent VTE in women. A prospective cohort study. Thrombosis and haemostasis 2015 Oct 115 (2): . Bruzelius M, Ljungqvist M, Bottai M, Bergendal A, Strawbridge R J, Holmström M, Silveira A, Kieler H, Hamsten A, Lärfars G, Odeberg |
| Genetic variation in the coagulation factor V gene and risk of femoral head osteonecrosis. Molecular medicine reports 2015 Sep 12 (3): 4434-40. Kim Tae-Ho, Baek Seung-Hoon, Lim Jeong Ok, Lee Sang-Han, Kim Shin-Yo |
| Comparative incidence of pregnancy outcomes in thrombophilia-positive women from the NOH-APS observational study. Blood 2014 Jan 123 (3): 414-21. Bouvier Sylvie, Cochery-Nouvellon Eva, Lavigne-Lissalde Géraldine, Mercier Erick, Fabbro-Peray Pascale, Balducchi Jean-Pierre, Marès Pierre, Gris Jean-Christop |
| Identification of genetic contribution to ischemic stroke by screening of single nucleotide polymorphisms in stroke patients by using a case control study design. BMC neurology 2013 13 (1): 136. Kumar Amit, Sagar Ram, Kumar Pradeep, Sahu Jitendra K, Grover Ashoo, Srivastava Achal K, Vivekanandhan S, Prasad Kameshw |
| Candidate gene polymorphisms and the risk for pregnancy-related venous thrombosis. British journal of haematology 2012 Jun 157 (6): 753-61. Dahm Anders E A, Bezemer Irene D, Bergrem Astrid, Jacobsen Anne F, Jacobsen Eva M, Skretting Grethe, Rosendaal Frits R, Sandset Per Mort |
| Comparative incidence of a first thrombotic event in purely obstetric antiphospholipid syndrome with pregnancy loss: the NOH-APS observational study. Blood 2012 Mar 119 (11): 2624-32. Gris Jean-Christophe, Bouvier Sylvie, Molinari Nicolas, Galanaud Jean-Philippe, Cochery-Nouvellon Eva, Mercier Erik, Fabbro-Peray Pascale, Balducchi Jean-Pierre, Marès Pierre, Quéré Isabelle, Dauzat Mich |
| The association of inherited thrombophilia and intrauterine fetal death: a case-control study. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2011 Dec 22 (8): 8. Helgadottir LB, Skjeldestad FE, Jacobsen AF, Sandset PM, Jacobsen EM |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 20, 2023
- Content source: