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Thrombosis and Haemostasis
|
May 6, 2006
Impaired dimerization of von Willebrand factor subunit due to mutation A2801D in the CK domain results in a recessive type 2A subtype IID von Willebrand disease
Antoine Hommais, Alain Stépanian, Edith Fressinaud, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
October 4, 2022
Reinvestigation of unidentified causative variants in FXI-deficient patients: Focus on gene segment deletions
Philippe De Mazancourt, Annie Harroche, Katia Pouymayou, et al.
Transfusion
|
June 24, 2022
Screening platelet function in blood donors
Pascal Pedini, Jean-Baptiste Baudey, Katia Pouymayou, et al.
British Journal of Haematology
|
March 29, 2002
Inherited factor VII deficiency and surgery: clinical data are the best criteria to predict the risk of bleeding
Muriel Giansily-Blaizot, Christine Biron-Andreani, Patricia Aguilar-Martinez, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 1
Thrombosis and Haemostasis
|
May 6, 2006
Impaired dimerization of von Willebrand factor subunit due to mutation A2801D in the CK domain results in a recessive type 2A subtype IID von Willebrand disease
Antoine Hommais, Alain Stépanian, Edith Fressinaud, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
October 4, 2022
Reinvestigation of unidentified causative variants in FXI-deficient patients: Focus on gene segment deletions
Philippe De Mazancourt, Annie Harroche, Katia Pouymayou, et al.
Transfusion
|
June 24, 2022
Screening platelet function in blood donors
Pascal Pedini, Jean-Baptiste Baudey, Katia Pouymayou, et al.
British Journal of Haematology
|
March 29, 2002
Inherited factor VII deficiency and surgery: clinical data are the best criteria to predict the risk of bleeding
Muriel Giansily-Blaizot, Christine Biron-Andreani, Patricia Aguilar-Martinez, et al.
Page
of 1