Maruyama K - Search Results

1

A novel homozygous variant of the thrombomodulin gene causes a hereditary bleeding disorder.

Osada M, Maruyama K, Kokame K, Denda R, Yamazaki K, Kunieda H, Hirao M, Madoiwa S, Okumura N, Murata M, Ikeda Y, Watanabe K, Tsukada Y, Kikuchi T. Osada M, et al. Among authors: maruyama k. Blood Adv. 2021 Oct 12;5(19):3830-3838. doi: 10.1182/bloodadvances.2020003814. Blood Adv. 2021. PMID: 34474479 Free PMC article.

2

ELISA-Based Detection System for Protein S K196E Mutation, a Genetic Risk Factor for Venous Thromboembolism.

Maruyama K, Akiyama M, Kokame K, Sekiya A, Morishita E, Miyata T. Maruyama K, et al. PLoS One. 2015 Jul 17;10(7):e0133196. doi: 10.1371/journal.pone.0133196. eCollection 2015. PLoS One. 2015. PMID: 26186226 Free PMC article.

3

Protein S K196E mutation reduces its cofactor activity for APC but not for TFPI.

Maruyama K, Akiyama M, Miyata T, Kokame K. Maruyama K, et al. Res Pract Thromb Haemost. 2018 Sep 25;2(4):751-756. doi: 10.1002/rth2.12152. eCollection 2018 Oct. Res Pract Thromb Haemost. 2018. PMID: 30349894 Free PMC article.

4

Cerebral venous sinus thrombosis associated with protein S deficiency during pregnancy: a case report.

Usui M, Ozawa T, Kim Y, Mashiko T, Matsuzono K, Maruyama K, Kokame K, Usui R, Koide R, Fujimoto S. Usui M, et al. Among authors: maruyama k. J Obstet Gynaecol. 2020 Jan;40(1):135-136. doi: 10.1080/01443615.2019.1606789. Epub 2019 Sep 1. J Obstet Gynaecol. 2020. PMID: 31475594 No abstract available.

5

Predictive value of protein S-specific activity and ELISA testing in patients with the protein S K196E mutation.

Miyoshi T, Maruyama K, Oku H, Asahara S, Hanada H, Neki R, Yoshimatsu J, Kokame K, Miyata T. Miyoshi T, et al. Among authors: maruyama k. Thromb Res. 2020 Jan;185:1-4. doi: 10.1016/j.thromres.2019.10.026. Epub 2019 Oct 31. Thromb Res. 2020. PMID: 31731088 No abstract available.

6

Carrier frequencies of antithrombin, protein C, and protein S deficiency variants estimated using a public database and expression experiments.

Maruyama K, Kokame K. Maruyama K, et al. Res Pract Thromb Haemost. 2020 Nov 27;5(1):179-186. doi: 10.1002/rth2.12456. eCollection 2021 Jan. Res Pract Thromb Haemost. 2020. PMID: 33537542 Free PMC article.

7

First report of inherited protein S deficiency caused by paternal PROS1 mosaicism.

Nagaya S, Maruyama K, Watanabe A, Meguro-Horike M, Imai Y, Hiroshima Y, Horike SI, Kokame K, Morishita E. Nagaya S, et al. Among authors: maruyama k. Haematologica. 2022 Jan 1;107(1):330-333. doi: 10.3324/haematol.2021.278527. Haematologica. 2022. PMID: 34647440 Free PMC article. No abstract available.

8

Alpha-HIT assay: A new assay for heparin-induced thrombocytopenia antibody detection using FcγRIIa-coated beads and Alpha technology.

Maruyama K, Miyata S, Kokame K. Maruyama K, et al. Res Pract Thromb Haemost. 2022 Dec 27;6(7):e12818. doi: 10.1002/rth2.12818. eCollection 2022 Oct. Res Pract Thromb Haemost. 2022. PMID: 37602359 Free PMC article. No abstract available.

9

Antithrombin deficiency in three Japanese families: one novel and two reported point mutations in the antithrombin gene.

Maruyama K, Morishita E, Karato M, Kadono T, Sekiya A, Goto Y, Sato T, Nomoto H, Omi W, Tsuzura S, Imai H, Asakura H, Ohtake S, Nakao S. Maruyama K, et al. Thromb Res. 2013 Aug;132(2):e118-23. doi: 10.1016/j.thromres.2013.06.001. Epub 2013 Jun 25. Thromb Res. 2013. PMID: 23809926

10

[An elderly case of congenital prekallikrein deficiency].

Nagaya S, Morishita E, Takami A, Maruyama K, Sekiya A, Asakura H, Nakao S, Ohtake S. Nagaya S, et al. Among authors: maruyama k. Nihon Ronen Igakkai Zasshi. 2009 Jul;46(4):348-51. doi: 10.3143/geriatrics.46.348. Nihon Ronen Igakkai Zasshi. 2009. PMID: 19713668 Free article. Japanese.

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