نتایج جستجو برای: human coagulation factor viii
تعداد نتایج: 2336393 فیلتر نتایج به سال:
BACKGROUND Elevations of coagulation factor VIII have recently been described in significant numbers of patients with venous thromboembolism (VTE) previously thought to have had an "idiopathic" event. Three patients from a family practice are presented with recurrent VTE and increased factor VIII levels. METHOD The case histories and results of laboratory tests were reviewed. RESULTS The 3 ...
Background Hemophilia A and B are disorders resulting from a deficiency in factor VIII (FVIII), and factor IX (FIX), respectively. Tissue Factor (TF) is a key component of the extrinsic pathway and plays a role in the coagulation defect of hemophilic blood. Neutralizing the activity of TFPI represents a promising treatment concept in patients with hereditary or acquired hemophilia. ARC19499 is ...
Systemic thromboembolism is a major complication of mitral stenosis (MS), especially in those patients having atrial fibrillation (AF). Recent evidence has suggested that regional left atrial coagulation activity may be increased in MS and may contribute to the pathophysiology of left atrial thrombus. However, the relation of left atrial coagulation activity to factors that predispose to left a...
Hemophilia A is a X-linked hereditary condition that lead to decreased factor VIII activity, occurs mainly in males. Decreased factor VIII activity leads to increased risk of bleeding events. During neonatal period, diagnosis is made after post-partum bleeding complication or unexpected bleeding after medical procedures. Subgaleal hemorrhage during neonatal period is a rare, severe extracranial...
چکیده : مقدمه وهدف : درمان دندانهای نکروتیک نابالغ از موارد پیچیده ای است که دردرمانهای اندودنتیک با آن مواجه میشویم. مطالعات اخیرنشان داده است که امکان رژنریشن پالپ در فضای کانال وادامه تشکیل ریشه در دندان های نکروتیک با اپکس باز وجود دارد. هدف از این مطالعه برسی بیان فاکتور های vegf و viii دررژنریشن پالپ دندان های نکروزه با اپکس بالغ ونا بالغ با استفاده از prp به روش ایمونوهیستوشیمی بوده اس...
Hemophilia A is a worldwide disorder of coagulation system. It is a male disorder, yet females with hemophilia are rarely seen in communities with high rate of consanguineous marriages. The abnormalities in factor VIII gene transfer as an X-linked pattern in the family, affects as many as one-third of patients who had no family history of abnormality and thus the occurrence of a sporadic mutati...
Blood coagulation in vivo is a spatially nonuniform, multistage process: coagulation factors from plasma bind to tissue factor (TF)-expressing cells, become activated, dissociate, and diffuse into plasma to form enzymatic complexes on the membranes of activated platelets. We studied spatial regulation of coagulation using two approaches: 1), an in vitro experimental model of clot formation in a...
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