Kamisue S - Search Results

1

Anti-factor VIII inhibitor alloantibodies recognizing the A2 domain in the human factor VIII heavy chain poorly bind to porcine factor VIII.

Sawamoto Y, Shima M, Tanaka I, Nakai H, Kamisue S, Scandella D, Yoshioka A. Sawamoto Y, et al. Among authors: kamisue s. Int J Hematol. 1997 Feb;65(2):151-8. doi: 10.1016/s0925-5710(96)00555-5. Int J Hematol. 1997. PMID: 9071819

2

Epitope localization of monoclonal antibodies against factor VIII light chain which inhibit complex formation by factor VIII with von Willebrand factor.

Shima M, Yoshioka A, Nakai H, Tanaka I, Sawamoto Y, Kamisue S, Terada S, Fukui H. Shima M, et al. Among authors: kamisue s. Int J Hematol. 1991 Dec;54(6):515-22. Int J Hematol. 1991. PMID: 1724391

3

Changes in polypeptide-specific factor VIII antigen levels during whole blood clotting.

Tanaka I, Yoshioka A, Shima M, Fujiwara T, Terada S, Nakai H, Sawamoto Y, Kamisue S, Fukui H. Tanaka I, et al. Among authors: kamisue s. Int J Hematol. 1991 Dec;54(6):523-30. Int J Hematol. 1991. PMID: 1724392

4

Measurement of anti-factor VIII IgG, IgG4 and IgM alloantibodies in previously untreated hemophilia A patients treated with recombinant factor VIII. Kogenate Japanese Clinical Study Group.

Shima M, Sawamoto Y, Nakai H, Kamisue S, Murakami T, Morichika S, Tanaka I, Hayashi K, Yoshioka A. Shima M, et al. Among authors: kamisue s. Int J Hematol. 1995 Jul;62(1):35-43. doi: 10.1016/0925-5710(95)00378-6. Int J Hematol. 1995. PMID: 7670006 Clinical Trial.

5

A factor VIII neutralizing monoclonal antibody and a human inhibitor alloantibody recognizing epitopes in the C2 domain inhibit factor VIII binding to von Willebrand factor and to phosphatidylserine.

Shima M, Scandella D, Yoshioka A, Nakai H, Tanaka I, Kamisue S, Terada S, Fukui H. Shima M, et al. Among authors: kamisue s. Thromb Haemost. 1993 Mar 1;69(3):240-6. Thromb Haemost. 1993. PMID: 7682339

6

Abnormal factor VIII Hiroshima: defect in crucial proteolytic cleavage by thrombin at Arg1689 detected by a novel ELISA.

Kamisue S, Shima M, Nishimura T, Tanaka I, Nakai H, Morichika S, Takata N, Kuramoto A, Yoshioka A. Kamisue S, et al. Br J Haematol. 1994 Jan;86(1):106-11. doi: 10.1111/j.1365-2141.1994.tb03259.x. Br J Haematol. 1994. PMID: 8011517

7

Common inhibitory effects of human anti-C2 domain inhibitor alloantibodies on factor VIII binding to von Willebrand factor.

Shima M, Nakai H, Scandella D, Tanaka I, Sawamoto Y, Kamisue S, Morichika S, Murakami T, Yoshioka A. Shima M, et al. Among authors: kamisue s. Br J Haematol. 1995 Nov;91(3):714-21. doi: 10.1111/j.1365-2141.1995.tb05374.x. Br J Haematol. 1995. PMID: 8555081

8

Measurement of anti-factor IX IgG subclasses in haemophilia B patients who developed inhibitors with episodes of allergic reactions to factor IX concentrates.

Sawamoto Y, Shima M, Yamamoto M, Kamisue S, Nakai H, Tanaka I, Hayashi K, Giddings JC, Yoshioka A. Sawamoto Y, et al. Among authors: kamisue s. Thromb Res. 1996 Aug 15;83(4):279-86. doi: 10.1016/0049-3848(96)00136-3. Thromb Res. 1996. PMID: 8870172

9

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: kamisue s. Thromb Haemost. 1997 May;77(5):862-7. Thromb Haemost. 1997. PMID: 9184393

10

Factor VIII gene analysis in Japanese CRM-positive and CRM-reduced haemophilia A patients by single-strand conformation polymorphism.

Morichika S, Shima M, Kamisue S, Tanaka I, Imanaka Y, Suzuki H, Shibata H, Pemberton S, Gale K, McVey J, Tuddenham EG, Yoshioka A. Morichika S, et al. Among authors: kamisue s. Br J Haematol. 1997 Sep;98(4):901-6. doi: 10.1046/j.1365-2141.1997.2963113.x. Br J Haematol. 1997. PMID: 9326186 Free article.

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