| 主要論文・著書 | 論文
- Miyoshi T, Maruyama K, Oku H, Asahara S, Hanada H, Neki R, Yoshimatsu J, Kokame K, Miyata T. Predictive value of protein S-specific activity and ELISA testing in patients with the protein S K196E mutation. Thromb Res, 185: 1-4, 2020.
- Usui M, Ozawa T, Kim Y, Mashiko T, Matsuzono K, Maruyama K, Kokame K, Usui R, Koide R, Fujimoto S. Cerebral venous sinus thrombosis associated with protein S deficiency during pregnancy: a case report. J Obstet Gynaecol, 40: 135-6, 2020.
- Maruyama K, Akiyama M, Miyata T, Kokame K. Protein S K196E mutation reduces its cofactor activity for APC but not for TFPI. Res Pract Thromb Haemost, 2: 751-6, 2018.
- Miyata T, Maruyama K, Banno F, Neki R. Thrombophilia in East Asian countries: are there any genetic differences in these countries? Thromb J, 14: 123-8, 2016.
- Maruyama K, Akiyama M, Kokame K, Sekiya A, Morishita E, Miyata T. ELISA-based detection system for protein S K196E mutation, a genetic risk factor for venous thromboembolism. PLOS ONE, 10: e0133196, 2015.
- 丸山慶子, 小亀浩市. PS Tokushima（K196E）変異の検査. 臨床に直結する血栓止血学 改訂2版, 中外医学社, p.85-7, 2018.
- 丸山慶子, 宮田敏行.【動脈・静脈の疾患(上)-最新の診断・治療動向-】血栓性素因の遺伝要因．日本臨床, p.277-80, 2017.
- 丸山慶子, 宮田敏行. 日本人の血栓性素因. 止血・血栓ハンドブック, p.24-9，2015.
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