Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Protein C Deficiency and PROC[original query] |
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Modification of the ProC Global assay using dilution of patient plasma in factor V-depleted plasma as a screening assay for factor V Leiden mutation. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2001 Oct 12 (7): 569-76. Quincampoix J C, Legarff M, Rittling C, Andiva S, Toulon |
R147W mutation of PROC gene is common in venous thrombotic patients in Taiwanese Chinese. American journal of hematology 2004 May 76 (1): 8-13. Tsay Woei, Shen Ming-Chi |
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 |
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