Volume 12, Issue 4
مرور بر اساس
ارسال های اخیر
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Factor 13 Activity in Children with Henoch-Schonlein Purpura in Iranian Children (Tehran, Iranian Blood and Cancer Society, 2020-12-01)
 
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Sirolimus: A Rapid Treatment for Coagulopathy Because of Vascular Malformations (Tehran, Iranian Blood and Cancer Society, 2020-12-01)
 
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Synchronous Gastrointestinal Stromal Tumor and Axillary Deep Fibromatosis: A Rare Association (Tehran, Iranian Blood and Cancer Society, 2020-12-01)Gastrointestinal Stromal Tumor (GIST) is the most common mesenchymal tumor of the gastrointestinal tract and most commonly affects the stomach, while fibromatosis is a rare locally aggressive fibrous tissue neoplasm. There ...
 
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Sub-acute Exposure to Benzene Accelerates the Aging Process of Red Blood Cells; an In vivo Study (Tehran, Iranian Blood and Cancer Society, 2020-12-01)Background: The well-known toxic effects of benzene toxicity are bone marrow depression, reduction in blood cell counts, and induction of leukemia and aplastic anemia. This study was designed to evaluate biomarkers of aging ...
 
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Evaluation of Normal Range of Bleeding Scores in Healthy Iranian Adults using the International Society on Thrombosis and Hemostasis Bleeding Assessment Tool (Tehran, Iranian Blood and Cancer Society, 2020-12-01)Background: Bleeding assessment tools are key components in the evaluation of patients suspicious for bleeding disorders. The exact determination of the normal ranges of ISTH-BAT (International Society on Thrombosis and ...
 
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Investigation of Paternal RhD Zygosity by Two Molecular Methods among Blood Donors in Kurdistan Province, Iran (Tehran, Iranian Blood and Cancer Society, 2020-12-01)Background: RhD antigen system is the leading cause of hemolytic disease of the fetus and newborn (HDFN). Paternal molecular RhD zygosity test is valuable to decide on the use of anti-D immunoglobulin prophylaxis in Rh ...
 
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Thrombotic Thrombocytopenic Purpura: Diagnosis and Treatment (Tehran, Iranian Blood and Cancer Society, 2020-12-01)Thrombotic Thrombocytopenic purpura (TTP) is a rare thrombotic microangiopathic disease, associated with thrombocytopenia and hemolytic anemia. It is caused by an enzymatic dysfunction responsible in cleavage of blood ...
 



