Shima M - Search Results

1

A prospective, multicenter, open-label phase III study of emicizumab prophylaxis in patients with acquired hemophilia A.

Shima M, Amano K, Ogawa Y, Yoneyama K, Ozaki R, Kobayashi R, Sakaida E, Saito M, Okamura T, Ito T, Hattori N, Higasa S, Suzuki N, Seki Y, Nogami K. Shima M, et al. J Thromb Haemost. 2023 Mar;21(3):534-545. doi: 10.1016/j.jtha.2022.10.004. Epub 2022 Dec 22. J Thromb Haemost. 2023. PMID: 36696195 Free article. Clinical Trial.

2

Factor VIII Ise (R2159C) in a patient with mild hemophilia A, an abnormal factor VIII with retention of function but modification of C2 epitopes.

Suzuki H, Shima M, Arai M, Kagawa K, Fukutake K, Kamisue S, Nakai H, Morichika S, Tanaka I, Inoue M, Gale K, Tuddenham EG, Yoshioka A. Suzuki H, et al. Among authors: shima m. Thromb Haemost. 1997 May;77(5):862-7. Thromb Haemost. 1997. PMID: 9184393

3

The role of platelet von Willebrand factor in the binding of factor VIII to activated platelets.

Suzuki H, Shima M, Kamisue S, Nakai H, Nogami K, Shibata M, Morichika S, Tanaka I, Giddings JC, Yoshioka A. Suzuki H, et al. Among authors: shima m. Thromb Res. 1998 Jun 1;90(5):207-14. doi: 10.1016/s0049-3848(98)00034-6. Thromb Res. 1998. PMID: 9694242

4

Factor VIII C2 domain contains the thrombin-binding site responsible for thrombin-catalyzed cleavage at Arg1689.

Nogami K, Shima M, Hosokawa K, Nagata M, Koide T, Saenko EL, Tanaka I, Shibata M, Yoshioka A. Nogami K, et al. Among authors: shima m. J Biol Chem. 2000 Aug 18;275(33):25774-80. doi: 10.1074/jbc.M002007200. J Biol Chem. 2000. PMID: 10831589 Free article.

5

An alloantibody recognizing the FVIII A1 domain in a patient with CRM reduced haemophilia A due to deletion of a large portion of the A1 domain DNA sequence.

Shibata M, Shima M, Morichika S, McVey J, Tuddenham EG, Tanaka I, Suzuki H, Nogami K, Minamoto Y, Hato T, Saenko EL, Scandella D, Yoshioka A. Shibata M, et al. Among authors: shima m. Thromb Haemost. 2000 Sep;84(3):442-8. Thromb Haemost. 2000. PMID: 11019969

6

Circulating factor VIII immune complexes in patients with type 2 acquired hemophilia A and protection from activated protein C-mediated proteolysis.

Nogami K, Shima M, Giddings JC, Hosokawa K, Nagata M, Kamisue S, Suzuki H, Shibata M, Saenko EL, Tanaka I, Yoshioka A. Nogami K, et al. Among authors: shima m. Blood. 2001 Feb 1;97(3):669-77. doi: 10.1182/blood.v97.3.669. Blood. 2001. PMID: 11157483 Free article.

7

Immunological characterization of factor VIII autoantibodies in patients with acquired hemophilia A in the presence or absence of underlying disease.

Matsumoto T, Shima M, Fukuda K, Nogami K, Giddings JC, Murakami T, Tanaka I, Yoshioka A. Matsumoto T, et al. Among authors: shima m. Thromb Res. 2001 Dec 15;104(6):381-8. doi: 10.1016/s0049-3848(01)00385-1. Thromb Res. 2001. PMID: 11755947

8

Anticoagulant effects of a synthetic peptide containing residues Thr-2253-Gln-2270 within factor VIII C2 domain that selectively inhibits factor Xa-catalysed factor VIII activation.

Nogami K, Shima M, Nishiya K, Hosokawa K, Saenko EL, Giddings JC, Tanaka I, Yoshioka A. Nogami K, et al. Among authors: shima m. Br J Haematol. 2002 Mar;116(4):868-74. doi: 10.1046/j.0007-1048.2002.03360.x. Br J Haematol. 2002. PMID: 11886394 Free article.

9

The utility of activated partial thromboplastin time (aPTT) clot waveform analysis in the investigation of hemophilia A patients with very low levels of factor VIII activity (FVIII:C).

Shima M, Matsumoto T, Fukuda K, Kubota Y, Tanaka I, Nishiya K, Giles AR, Yoshioka A. Shima M, et al. Thromb Haemost. 2002 Mar;87(3):436-41. Thromb Haemost. 2002. PMID: 11916076

10

Human factor VIII inhibitor alloantibodies with a C2 epitope inhibit factor Xa-catalyzed factor VIII activation: a new anti-factor VIII inhibitory mechanism.

Nogami K, Shima M, Nishiya K, Sakurai Y, Tanaka I, Giddings JC, Saenko EL, Yoshioka A. Nogami K, et al. Among authors: shima m. Thromb Haemost. 2002 Mar;87(3):459-65. Thromb Haemost. 2002. PMID: 11916079

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