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Thrombosis and Haemostasis|May 25, 2001
A standard nomenclature for von Willebrand factor gene mutations and polymorphisms. On behalf of the ISTH SSC Subcommittee on von Willebrand factorA C Goodeve, J C Eikenboom, D Ginsburg, et al.Haematologica|August 27, 1998
Outcome assessment of age group-specific (+/- 50 years) post-remission consolidation with high-dose cytarabine or bone marrow autograft for adult acute myelogenous leukemiaR Bassan, R Raimondi, T Lerede, et al.Hematological Oncology|January 1, 1985
Treatment of acute lymphoblastic leukemia in adultsT Barbui, R Bassan, T Chisesi, et al.Journal of Thrombosis and Haemostasis : JTH|July 2, 2009
Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD studyJ Eikenboom, L Hilbert, A S Ribba, et al.British Journal of Haematology|February 1, 1978
Subunits A and S inheritance in four families with congenital factor XIII deficiencyT Barbui, F Rodeghiero, E Dini, et al.Blood|April 15, 1996
Interleukin-15 promotes the growth of leukemic cells of patients with B-cell chronic lymphoproliferative disordersL Trentin, A Cerutti, R Zambello, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|October 12, 2013
The spectrum of factor XI deficiency in ItalyG Castaman, S H Giacomelli, S Caccia, et al.British Journal of Haematology|June 1, 1976
Immunoradiometric assay of factor VIII related antigen, with observations in 32 patients with von Willebrand's diseaseZ M Ruggeri, P M Mannucci, S L Jeffcoate, et al.The Journal of Biological Chemistry|April 12, 1996
Conformational changes in the A1 domain of von Willebrand factor modulating the interaction with platelet glycoprotein IbalphaS Miyata, S Goto, A B Federici, et al.The Journal of Biological Chemistry|February 5, 1993
Disulfide bond requirements for assembly of the platelet glycoprotein Ib-binding domain of von Willebrand factorH Azuma, T Hayashi, J A Dent, et al.Pageof 81