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Clinical Chemistry|August 12, 2025
Gene Therapy for Hemophilias: Opportunities and Challenges for the Clinical LaboratoryArmando Tripodi, Isabella Garagiola, Niccolò Bitto, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 27, 2022
The evolution of physiotherapy in the multidisciplinary management of persons with haemophilia (PWH): A scoping reviewElena A Boccalandro, Valentina Begnozzi, Sofia Garofalo, et al.
Blood Reviews|February 19, 2013
The emerging concept of residual ADAMTS13 activity in ADAMTS13-deficient thrombotic thrombocytopenic purpuraLuca A Lotta, Haifeng M Wu, Khaled M Musallam, et al.
Haematologica|April 3, 2025
Global estimation of the bleeding episodes treatable with desmopressin in von Willebrand disease and hemophilia AAlessandro Gringeri, Pier Mannuccio Mannucci, Michele Gringeri, et al.
Blood Advances|June 27, 2024
Global prevalence of hereditary thrombotic thrombocytopenic purpura determined by genetic analysisOmid Seidizadeh, Andrea Cairo, Ilaria Mancini, et al.
Fertility and Sterility|November 9, 2005
Hemostasis and menstruation: appropriate investigation for underlying disorders of hemostasis in women with excessive menstrual bleedingPeter A Kouides, Jacqueline Conard, Flora Peyvandi, et al.
Blood Transfusion = Trasfusione Del Sangue|June 1, 2021
Von Willebrand disease combined with coagulation defects in IranOmid Seidizadeh, Minoo Ahmadinejad, Sanaz Homayoun, et al.
Research and Practice in Thrombosis and Haemostasis|January 15, 2025
Gene therapy in hemophilia: the dawn of a new eraRoberta Gualtierotti, Andrea Giachi, Niccolò Bitto, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 21, 2006
Molecular characterization of an Italian patient with plasminogen deficiency and ligneous conjunctivitisSimona M Siboni, Marta Spreafico, Marzia Menegatti, et al.
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