Giddings JC - Search Results

1

Successful treatment of two brothers with congenital afibrinogenemia for splenic rupture using heat- and solvent detergent-treated fibrinogen concentrates.

Shima M, Tanaka I, Sawamoto Y, Kanehiro H, Matsuo N, Nishimura A, Giddings JC, Yoshioka A. Shima M, et al. Among authors: giddings jc. J Pediatr Hematol Oncol. 1997 Sep-Oct;19(5):462-5. doi: 10.1097/00043426-199709000-00011. J Pediatr Hematol Oncol. 1997. PMID: 9329471

2

Transient hypoplastic anemia caused by primary human parvovirus B19 infection in a previously untreated patient with hemophilia transfused with a plasma-derived, monoclonal antibody-purified factor VIII concentrate.

Matsui H, Sugimoto M, Tsuji S, Shima M, Giddings J, Yoshioka A. Matsui H, et al. J Pediatr Hematol Oncol. 1999 Jan-Feb;21(1):74-6. J Pediatr Hematol Oncol. 1999. PMID: 10029819

3

Relationship between the binding sites for von Willebrand factor, phospholipid, and human factor VIII C2 inhibitor alloantibodies within the factor VIII C2 domain.

Nogami K, Shima M, Giddings JC, Takeyama M, Tanaka I, Yoshioka A. Nogami K, et al. Among authors: giddings jc. Int J Hematol. 2007 May;85(4):317-22. doi: 10.1532/IJH97.06192. Int J Hematol. 2007. PMID: 17483075

4

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: giddings jc. Thromb Res. 1996 Aug 15;83(4):279-86. doi: 10.1016/0049-3848(96)00136-3. Thromb Res. 1996. PMID: 8870172

5

Management of haemophilia B inhibitor patients with anaphylactic reactions to FIX concentrates.

Shibata M, Shima M, Misu H, Okimoto Y, Giddings JC, Yoshioka A. Shibata M, et al. Among authors: giddings jc. Haemophilia. 2003 May;9(3):269-71. doi: 10.1046/j.1365-2516.2003.00772.x. Haemophilia. 2003. PMID: 12694516

6

Ecthyma gangrenosum combined with multiple perforations of the small intestine associated with Pseudomonas aeruginosa.

Hayashi Y, Shima M, Kanehiro H, Nakajima Y, Daikoku N, Higuchi M, Miyagawa S, Kamisue S, Fukuda K, Tanaka I, Giddings JC, Yoshioka A. Hayashi Y, et al. Among authors: giddings jc. Pediatr Int. 2004 Feb;46(1):104-8. doi: 10.1111/j.1328-0867.2004..x. Pediatr Int. 2004. PMID: 15043678 No abstract available.

7

Heparin-induced inhibitory effects of a prothrombin complex concentrate on global tests of haemostasis.

Takeyama M, Sakurai Y, Shima M, Matsumoto T, Nogami K, Tanaka I, Takeda T, Giddings JC, Yoshioka A. Takeyama M, et al. Among authors: giddings jc. Blood Coagul Fibrinolysis. 2007 Jan;18(1):1-7. doi: 10.1097/01.mbc.0000256021.16453.de. Blood Coagul Fibrinolysis. 2007. PMID: 17179819

8

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: giddings jc. Thromb Res. 1998 Jun 1;90(5):207-14. doi: 10.1016/s0049-3848(98)00034-6. Thromb Res. 1998. PMID: 9694242

9

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: giddings jc. Thromb Res. 2001 Dec 15;104(6):381-8. doi: 10.1016/s0049-3848(01)00385-1. Thromb Res. 2001. PMID: 11755947

10

Unresponsiveness to factor VIII inhibitor bypassing agents during haemostatic treatment for life-threatening massive bleeding in a patient with haemophilia A and a high responding inhibitor.

Hayashi T, Tanaka I, Shima M, Yoshida K, Fukuda K, Sakurai Y, Matsumoto T, Giddings JC, Yoshioka A. Hayashi T, et al. Among authors: giddings jc. Haemophilia. 2004 Jul;10(4):397-400. doi: 10.1111/j.1365-2516.2004.00924.x. Haemophilia. 2004. PMID: 15230956

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