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兀拉拉
Lv3
310 积分
2022-05-29 加入
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已完结
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Molecular mechanisms and clinical manifestations of hereditary hemorrhagic telangiectasia
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A novel GATA1 variant p.G229D causing the defect of procoagulant platelet formation
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Identification of non‐neutralizing anti‐factor X autoantibodies in three Japanese cases of autoimmune acquired factor X deficiency
5个月前
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Clinical and functional characterization of rare compound heterozygous mutations in the SERPINC1 gene causing severe thrombophilia
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Impact of Antithrombin Activity Levels Following Recombinant Antithrombin Gamma Therapy in Patients with Sepsis-Induced Disseminated Intravascular Coagulation
9个月前
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Antithrombin Therapy: Current State and Future Outlook
9个月前
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