Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Protein C Deficiency and PROS1[original query] |
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| A large deletion of the PROS1 gene in a deep vein thrombosis patient with protein S deficiency. Thrombosis and haemostasis 2007 Oct 98 (4): 783-9. Yin Tong, Takeshita Satoshi, Sato Yukiko, Sakata Toshiyuki, Shin Yongchol, Honda Shigenori, Kawasaki Tomio, Tsuji Hajime, Kojima Tetsuhito, Madoiwa Seiji, Sakata Yoichi, Murata Mitsuru, Ikeda Yasuo, Miyata Toshiyu |
| PROS1 analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotype-phenotype associations. Human mutation 2008 Jul 29 (7): 939-47. Ten Kate Min Ki, Platteel Mathieu, Mulder Rene, Terpstra Peter, Nicolaes Gerry A F, Reitsma Pieter H, van der Steege Gerrit, van der Meer J |
| Protein S levels and the risk of venous thrombosis: results from the MEGA case-control study. Blood 2013 Oct 122 (18): 3210-9. Pintao Maria Carolina, Ribeiro Daniel D, Bezemer Irene D, Garcia Andrea A, de Visser Marieke C H, Doggen Carine J M, Lijfering Willem M, Reitsma Pieter H, Rosendaal Frits |
| 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 genotype phenotype relationships in a large cohort of adults with suspicion of inherited quantitative protein S deficiency. Thrombosis and haemostasis 2015 Oct 115 (3): . Alhenc-Gelas M, Plu-Bureau G, Horellou M H, Rauch A, Suchon P, |
| Two Novel Variants in the Protein S Gene PROS1 Are Associated with Protein S Deficiency and Thrombophilia. Acta haematologica 2020 7 144 (2): 222-226. Juhl David, Kuta Piotr, Shneyder Maria, Wünsche Falko, Nowak-Göttl Ulri |
| Genetic Variants in the Protein S ( PROS1 ) Gene and Protein S Deficiency in a Danish Population. TH open : companion journal to thrombosis and haemostasis 2021 11 5 (4): e479-e488. Larsen Ole Halfdan, Kjaergaard Alisa D, Hvas Anne-Mette, Nissen Peter |
| Protein S Deficiency and the Risk of Venous Thromboembolism in the Han Chinese Population. Frontiers in cardiovascular medicine 2021 8 796755. Wu Yingying, Liu Jingdi, Zeng Wei, Hu Bei, Hu Yu, Tang Liang |
| 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 impact of PROS1 mutation position on thrombotic risk in protein S-deficient patients. Research and practice in thrombosis and haemostasis 2023 6 7 (4): 100194. Tereza Fenclova, Miloslava Matyskova, Dana Provaznikova, Frantisek Marecek, Vera Geierova, Zuzana Kovarova-Kudrnova, Ingrid Hrachovino |
| The risk profiles of pregnancy-related cerebral venous thrombosis: a retrospective study in a comprehensive hospital. BMC neurology 2024 5 24 (1): 182. Shaoying Wang, Ming Yao, Nan Hu, Juntao Liu, Bin Pe |
- Page last reviewed:Feb 1, 2024
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