Search Results - "ARJMAND, A. R."

Evaluation of rFVIIa (NovoSeven) in Glanzmann patients with thromboelastogram by LAK, M., SCHARLING, B., BLEMINGS, A., SHARIFIAN, R., MALEKI, Z., DARAEE, A., ARJMAND, A. R., HEDNER, U.

“…Glanzmann thrombasthenia (GT) is a rare platelet function disorder characterized by a defect in fibrinogen binding to platelet membrane glycoprotein (GP)…”
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Evalution of HbA2 In Minor β Thalassemia Carriers Reffered to Kerman Special Disease Center by M Atapour, AR Zohoor, A Zolala, AR Arjmand

“…Increased HbA2 is a characteristic finding in minor beta thalassemia. Minor β-thalassemia is a heterozygote form of β-thalassemia that carries thalassemia…”
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