Shida Y - Search Results

1

Assessing the clinical severity of type 1 von Willebrand disease patients with a microchip flow-chamber system.

Nogami K, Ogiwara K, Yada K, Shida Y, Takeyama M, Yaoi H, Minami H, Furukawa S, Hosokawa K, Shima M. Nogami K, et al. Among authors: shida y. J Thromb Haemost. 2016 Apr;14(4):667-74. doi: 10.1111/jth.13273. Epub 2016 Mar 15. J Thromb Haemost. 2016. PMID: 27061057 Free article.

2

Antithrombotic properties of pravastatin reducing intra-thrombus fibrin deposition under high shear blood flow conditions.

Hamada M, Sugimoto M, Matsui H, Mizuno T, Shida Y, Doi M, Fukushima H, Nishio K, Yoshioka A, Shima M. Hamada M, et al. Among authors: shida y. Thromb Haemost. 2011 Feb;105(2):313-20. doi: 10.1160/TH10-09-0587. Epub 2010 Dec 6. Thromb Haemost. 2011. PMID: 21136018

3

The utility of VWF multimer analysis in response to the desmopressin administration for the diagnosis of severe type 1 von Willebrand disease.

Takeyama M, Nogami K, Onaka M, Yada K, Shida Y, Shima M. Takeyama M, et al. Among authors: shida y. Haemophilia. 2016 Mar;22(2):e106-e108. doi: 10.1111/hae.12874. Epub 2016 Jan 29. Haemophilia. 2016. PMID: 26823111 No abstract available.

4

Successful haemostatic management of replacement of the ascending aorta for type A acute aortic dissection in a patient with mild haemophilia B.

Takeyama M, Nogami K, Shida Y, Yada K, Hirose T, Hayata Y, Tabayashi N, Taniguchi S, Akasaki Y, Kawaraguchi Y, Kawaguchi M, Shima M. Takeyama M, et al. Among authors: shida y. Haemophilia. 2016 Mar;22(2):e109-e111. doi: 10.1111/hae.12879. Epub 2016 Jan 29. Haemophilia. 2016. PMID: 26823376 No abstract available.

5

Role of red blood cells in the anemia-associated bleeding under high shear conditions.

Yaoi H, Shida Y, Ogiwara K, Hosokawa K, Shima M, Nogami K. Yaoi H, et al. Among authors: shida y. Haemophilia. 2017 Sep;23(5):750-758. doi: 10.1111/hae.13252. Epub 2017 May 4. Haemophilia. 2017. PMID: 28470853

6

Highly elevated plasma level of von Willebrand factor accelerates the formation of platelet thrombus under high shear stress in plasma with deficient ADAMTS13 activity.

Yagi H, Yamaguchi N, Shida Y, Sugimoto M, Tubaki K, Fujimura Y, Matsumoto M. Yagi H, et al. Among authors: shida y. Thromb Res. 2017 Nov;159:91-95. doi: 10.1016/j.thromres.2017.10.007. Epub 2017 Oct 10. Thromb Res. 2017. PMID: 29040872

7

Factor (F)VIII/VIIa enhances global haemostatic function in the co-presence of bypassing agents and FVIII among patients with haemophilia A with inhibitor.

Nogami K, Matsumoto T, Yada K, Ogiwara K, Furukawa S, Shida Y, Takeyama M, Shima M. Nogami K, et al. Among authors: shida y. Br J Haematol. 2018 May;181(4):528-536. doi: 10.1111/bjh.15209. Epub 2018 Apr 2. Br J Haematol. 2018. PMID: 29611182 Free article.

8

A case of moderate haemophilia A with inhibitor, carrying the p.R1800H mutation, complicated with juvenile idiopathic arthritis.

Kondo Y, Shida Y, Ishikawa T, Yada K, Takeyama M, Shima M, Nogami K. Kondo Y, et al. Among authors: shida y. Haemophilia. 2019 Jan;25(1):e51-e54. doi: 10.1111/hae.13648. Epub 2018 Dec 3. Haemophilia. 2019. PMID: 30507053 No abstract available.

9

Global coagulation function assessed by rotational thromboelastometry predicts coagulation-steady state in individual hemophilia A patients receiving emicizumab prophylaxis.

Yada K, Nogami K, Ogiwara K, Shida Y, Furukawa S, Yaoi H, Takeyama M, Kasai R, Shima M. Yada K, et al. Among authors: shida y. Int J Hematol. 2019 Oct;110(4):419-430. doi: 10.1007/s12185-019-02698-8. Epub 2019 Jun 28. Int J Hematol. 2019. PMID: 31254165

10

Emicizumab Augments Thrombus Formation in Whole Blood from Patients with Hemophilia A under High Shear Flow Conditions.

Yaoi H, Shida Y, Kitazawa T, Shima M, Nogami K. Yaoi H, et al. Among authors: shida y. Thromb Haemost. 2021 Mar;121(3):279-286. doi: 10.1055/s-0040-1716542. Epub 2020 Sep 9. Thromb Haemost. 2021. PMID: 32906155

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