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Thrombosis Research|August 7, 1998
The role of platelet von Willebrand factor in the binding of factor VIII to activated plateletsH Suzuki, M Shima, S Kamisue, et al.Gastroenterologia Japonica|October 1, 1982
Differential diagnosis of liver parenchymal diseases by likelihood method using 12 laboratory data and ageT Itoshima, K Kawaguchi, S Morichika, et al.Acta Medica Okayama|April 1, 1982
Percutaneous transhepatic portal catheterization-modification of Chiba method and portal vein pressure in liver diseasesT Ito, T Itoshima, S Kiyotoshi, et al.British Journal of Haematology|November 5, 1997
Factor VIII gene analysis in Japanese CRM-positive and CRM-reduced haemophilia A patients by single-strand conformation polymorphismS Morichika, M Shima, S Kamisue, et al.British Journal of Haematology|October 16, 1999
Identification of a factor VIII peptide, residues 2315-2330, which neutralizes human factor VIII C2 inhibitor alloantibodies: requirement of Cys2326 and Glu2327 for maximum effectK Nogami, M Shima, H Nakai, et al.Gastroenterologia Japonica|April 1, 1983
Ranking of liver tests for differential diagnosis of liver parenchymal diseasesT Itoshima, K Kawaguchi, S Morichika, et al.Thrombosis and Haemostasis|May 1, 1997
Factor VIII Ise (R2159C) in a patient with mild hemophilia A, an abnormal factor VIII with retention of function but modification of C2 epitopesH Suzuki, M Shima, M Arai, et al.Thrombosis and Haemostasis|October 6, 2000
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 sequenceM Shibata, M Shima, S Morichika, et al.Pageof 2