Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Death and F2[original query] |
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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 |
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 |
MERTK rs4374383 polymorphism affects the severity of fibrosis in non-alcoholic fatty liver disease. Journal of hepatology 2015 Oct . Petta Salvatore, Valenti Luca, Marra Fabio, Grimaudo Stefania, Tripodo Claudio, Bugianesi Elisabetta, Cammà Calogero, Cappon Andrea, Marco Vito Di, Maira Giovanni Di, Dongiovanni Paola, Rametta Raffaela, Gulino Alessandro, Mozzi Enrico, Orlando Emanuele, Maggioni Marco, Pipitone Rosaria Maria, Fargion Silvia, Craxì 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 |
The genetic basis for susceptibility to Rift Valley fever disease in MBT/Pas mice. Genes and immunity 2015 1 16 (3): 206-12. Tokuda S, Do Valle T Z, Batista L, Simon-Chazottes D, Guillemot L, Bouloy M, Flamand M, Montagutelli X, Panthier J |
Cardiac arrhythmia and neuroexcitability gene variants in resected brain tissue from patients with sudden unexpected death in epilepsy (SUDEP). NPJ genomic medicine 2018 4 3 9. Friedman Daniel, Kannan Kasthuri, Faustin Arline, Shroff Seema, Thomas Cheddhi, Heguy Adriana, Serrano Jonathan, Snuderl Matija, Devinsky Orr |
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 |
[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 |
Polymorphisms in Interleukin 13 Signaling and Interacting Genes Predict Advanced Fibrosis and Hepatocellular Carcinoma Development in Non-Alcoholic Steatohepatitis. Biology 2020 Apr 9 (4): . El-Derany Marwa |
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 |
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 |
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- Page last updated:Apr 16, 2024
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