Suzuki Sachiko

鈴木幸子 | Suzuki Sachiko

Affiliation and department：

Research field (1)： Lifelong developmental nursing

Research keywords (2)：助産学 , 母性看護学

Research theme for competitive and other funds (4)：

2021 - 2025 血友病保因者・家族における遺伝子検査受検のニーズ・課題の明確化と支援システム構築
2010 - 2013 二分脊椎女性のリプロダクティブヘルスケアプログラムの実践と評価
2009 - 2011 計画妊娠が母親の生活リズム、母親役割・育児行動及び夫婦関係に及ぼす好影響
2006 - 2008 Development of Comprehensive Care Program for Menstrual and Sexual Health of Female Patients with Spinal Bifida

Papers (13)：

Koya Odaira, Shogo Tamura, Nobuaki Suzuki, Misaki Kakihara, Yuna Hattori, Mahiru Tokoro, Sachiko Suzuki, Akira Takagi, Akira Katsumi, Fumihiko Hayakawa, et al. Apparent synonymous mutation F9 c.87A>G causes secretion failure by in-frame mutation with aberrant splicing. Thrombosis research. 2019. 179. 95-103
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
S. Tamura, Y. Suga, M. Tanamura, M. Murata-Kawakami, Y. Takagi, Y. Hottori, M. Kakihara, S. Suzuki, A. Takagi, T. Kojima. Optimisation of antithrombin resistance assay as a practical clinical laboratory test: Development of prothrombin activator using factors Xa/Va and automation of assay. International Journal of Laboratory Hematology. 2018. 40. 3. 312-319

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Lectures and oral presentations (9)：

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)
血液凝固第V因子欠乏症を合併する血友病A症例:第2報・凝血学的評価.
(第40回日本血栓止血学会学術集会 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)

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Work history (2)：

Association Membership(s) (2)：

JAPAN SOCIETY OF MATERNAL HEALTH , JAPAN ACADEMY OF MIDWIFERY

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