Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Venous Thrombosis and SERPINC1[original query] |
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| Gene variants associated with deep vein thrombosis. JAMA 2008 Mar 299 (11): 1306-14. Bezemer Irene D, Bare Lance A, Doggen Carine J M, Arellano Andre R, Tong Carmen, Rowland Charles M, Catanese Joseph, Young Bradford A, Reitsma Pieter H, Devlin James J, Rosendaal Frits |
| New gene variants associated with venous thrombosis: a replication study in White and Black Americans. Journal of thrombosis and haemostasis : JTH 2011 Mar 9 (3): 489-95. Austin H, De Staercke C, Lally C, Bezemer I D, Rosendaal F R, Hooper W |
| Type II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: clinical picture. Journal of thrombosis and haemostasis : JTH 2013 Aug . Puurunen M, Salo P, Engelbarth S, Javela K, Perola M |
| Association of F11 polymorphism rs2289252 with deep vein thrombosis and related phenotypes in population of Latvia. Thrombosis research 2014 Sep 134 (3): 659-63. Rovite Vita, Maurins Uidis, Megnis Kaspars, Vaivade Iveta, Pe?ulis Raitis, Rits Juris, Prave Sandra, Klovins Jan |
| Genetic analysis should be included in clinical practice when screening for antithrombin deficiency. Thrombosis and haemostasis 2015 Feb 113 (2): 262-71. Zeng Wei, Tang Liang, Jian Xiao-Rong, Li Yi-Qing, Guo Tao, Wang Qing-Yun, Liu Hui, Wu Ying-Ying, Cheng Zhi-Peng, Hu Bei, Lu Xuan, Yu Jian-Ming, Deng Jun, Wang Hua-Fang, Sun Chun-Yan, Yang Yan, Hu |
| Thrombotic risk according to SERPINC1 genotype in a large cohort of subjects with antithrombin inherited deficiency. Thrombosis and haemostasis 2017 Mar . Alhenc-Gelas Martine, Plu-Bureau Genevieve, Hugon-Rodin Justine, Picard Véronique, Horellou Marie-Helene, |
| Recurrent mutations in a SERPINC1 hotspot associate with venous thrombosis without apparent antithrombin deficiency. Oncotarget 2017 11 8 (48): 84417-84425. Zeng Wei, Hu Bei, Tang Liang, You Yan-Yan, Toderici Mara, de la Morena-Barrio Maria Eugenia, Corral Javier, Hu |
| The influence of specific mutations in the AT gene (SERPINC1) on the type of pregnancy related complications. Thrombosis research 2019 01 173 12-19. Kovac Mirjana, Mitic Gorana, Mikovic Zeljko, Mandic Vesna, Miljic Predrag, Mitrovic Mirjana, Tomic Branko, Bereczky Zsuzsan |
| Genotype phenotype correlation in a pediatric population with antithrombin deficiency. European journal of pediatrics 2019 7 178 (10): 1471-1478. Kovac Mirjana, Mitic Gorana, Djilas Iva, Kuzmanovic Milos, Serbic Olivera, Lekovic Danijela, Tomic Branko, Bereczky Zsuzsan |
| Congenital antithrombin deficiency in patients with splanchnic vein thrombosis. Liver international : official journal of the International Association for the Study of the Liver 2019 12 40 (5): 1168-1177. Baiges Anna, de la Morena-Barrio María Eugenia, Turon Fanny, Miñano Antonia, Alberto Ferrusquía Jose, Magaz Marta, Reverter Juan Carlos, Vicente Vicente, Hernández-Gea Virginia, Corral Javier, García-Pagán Juan Carl |
| Association of SERPINC1 Gene Polymorphism (rs2227589) With Pulmonary Embolism Risk in a Chinese Population. Frontiers in genetics 2019 10 10 844. Yue Yongjian, Sun Qing, Xiao Lu, Liu Shengguo, Huang Qijun, Wang Minlian, Huo Mei, Yang Mo, Fu Yingy |
| Utility of the SERPINC1 Gene Test in Ischemic Stroke Patients With Antithrombin Deficiency. Frontiers in neurology 2022 6 13 841934. Kim Seondeuk, Lee Woo-Jin, Moon Jangsup, Jung Keun-H |
| Patients with SERPINC1 rs2227589 polymorphism found to have multiple cerebral venous sinus thromboses despite a normal antithrombin level: A case report. World journal of clinical cases 2022 1 10 (2): 618-624. Liao Feng, Zeng Jun-Ling, Pan Jian-Gang, Ma Jing, Zhang Zhi-Jian, Lin Zhi-Jun, Lin Li-Feng, Chen Yu-Sen, Ma Xiao-Ta |
| The genetic risk factors for cerebral venous thrombosis: a case-control study in a Chinese national comprehensive hospital. Thrombosis journal 2024 6 22 (1): 50. Shaoying Wang, Ming Yao, Xinzhuang Yang, Yicheng Zhu, Bin Pe |
| Long-range and real-time PCR identification of a large SERPINC1 deletion in a patient with antithrombin deficiency. International journal of hematology 2024 5 . Shinya Matsumoto, Takeshi Uchiumi, Yasushi Ueyanagi, Nozomi Noda, Atsuhiko Sakai, Taeko Hotta, Kiyoko Kato, Shouichi Ohga, Yuya Kunisaki, Dongchon Ka |
- Page last reviewed:Feb 1, 2024
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