אבחון וטיפול ב-ITP בילדים
חברי הוועדה: ד"ר שרגא אבינר, ד"ר שושנה רבל־וילק, ד"ר חגית מיסקין, פרופ' חנה תמרי
חברי הוועדה: ד"ר שרגא אבינר, ד"ר שושנה רבל־וילק, ד"ר חגית מיסקין, פרופ' חנה תמרי
Patients with b-thalassemia major (TM) and other refractory anemias requiring regular blood transfusions accumulate iron that damages the liver, endocrine system, and most
Light transmission aggregometry (LTA) is used worldwide for the investigation of
The periprocedural management of patients receiving long-term oral anticoagulant therapy remains
Patients with ?-thalassemia major (TM) and other refractory anemias requiring regular
The paradigm for managing primary immune thrombocytopenia (ITP) in adults has
Polycythemia vera (PV) is a clonal disorder characterized by unwarranted production
Survival in severe aplastic anemia (SAA) has markedly improved in the
wo novel oral anticoagulants, dabigatran and rivaroxaban, have recently been approved.
Heparin-induced thrombocytopenia is a prothrombotic adverse drug effect induced by platelet-activating antibodies against multimolecular complexes of platelet factor 4
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