Shogo Tamura, Erika Hashimoto, Nobuaki Suzuki, Misaki Kakihara, Koya Odaira, Yuna Hattori, Mahiru Tokoro, Sachiko Suzuki, Akira Takagi, Akira Katsumi, et al. Molecular basis of SERPINC1 mutations in Japanese patients with antithrombin deficiency. Thrombosis research. 2019. 178. 159-170
Sachiko Suzuki. Combined deficiency of factors V and VIII by chance coinheritance of parahaemophilia and haemophilia A, but not by mutations of either LMAN1 or MCFD2. Nagoya University. 2019
Suzuki S, Nakamura Y, Suzuki N, Yamazaki T, Takagi Y, Tamura S, Takagi A, Kanematsu T, Matsushita T, Kojima T. Combined deficiency of factors V and VIII by chance coinheritance of parahaemophilia and haemophilia A, but not by mutations of either LMAN1 or MCFD2, in a Japanese family. Haemophilia. 2018. 24. 1. e13-e16
Haploid origin of unusual Inv-22 X-chromosome carrying wild-type telomere region in severe hemophilia A patients
(The 10th Congress of the Asian-Pacific Society on Thrombosis and Hemostasis. 2018)
Combined deficiency of factors V and VIII caused by chance coinheritance of parahemophilia and hemophilia A (the second report); Evaluations on clotting assay parameters and clinical symptom.
(The 10th Congress of the Asian-Pacific Society on Thrombosis and Hemostasis. 2018)
Thrombin generation assay CANNOT identify antithrombin resistance during anticoagulant therapy.
(XXVI Congress of International Society on Thrombosis and Haemostasis, Berlin, Germany 2017)
活性化プロテインC抵抗性(Activated Protein C Resistance:APCR)と産科関連静脈血栓症.
(第39回日本血栓止血学会学術集会 2017)
