Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Protein C Deficiency and SERPINC1[original query] |
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Prevalence of hereditary antithrombin mutations is higher than estimated in patients with thrombotic events. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2013 Jun 24 (4): 444-8. Fischer Ronald, Sachs Ulrich J, Heidinger Kathrin S, Eisenburger Dominik, Kemkes-Matthes Betti |
Distinct frequencies and mutation spectrums of genetic thrombophilia in Korea in comparison with other Asian countries both in patients with thromboembolism and in the general population. Haematologica 2014 Mar 99 (3): 561-9. Kim Hee-Jin, Seo Ja-Young, Lee Ki-O, Bang Sung-Hwan, Lee Seung-Tae, Ki Chang-Seok, Kim Jong-Won, Jung Chul Won, Kim Duk-Kyung, Kim Sun-H |
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 |
Prevalence, Genetic Background, and Clinical Phenotype of Congenital Thrombophilia in Chronic Thromboembolic Pulmonary Hypertension. JACC. Asia 2022 11 2 (3): 247-255. Lian Tian-Yu, Liu Jian-Zhou, Guo Fan, Zhou Yu-Ping, Wu Tao, Wang Hui, Li Jing-Yi, Yan Xin-Xin, Peng Fu-Hua, Sun Kai, Xu Xi-Qi, Han Zhi-Yan, Jiang Xin, Wang Duo-Lao, Miao Qi, Jing Zhi-Che |
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 |
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