نتایج جستجو برای: coagulation factor concentrates

تعداد نتایج: 887776  

Journal: :international journal of hematology-oncology and stem cell research 0
maryam al-e-rasul dehkordi department of gynecology and obstetrics, shahrekord university of medical sciences, shahrekord, iran. akbar soleimani department of internal medicine, shahrekord university of medical sciences, shahrekord, iran. ali haji-gholami division of hematology, department of internal medicine, shahrekord university of medical sciences, shahrekord, iran. abdolrahim kazemi vardanjani deputy of research and technology, shahrekord university of medical sciences, shahrekord, iran. saeid al-e-rasul dehkordi general practitioner, isfahan university of medical sciences, isfahan, iran.

thrombophilia is a pathological state of increased blood coagulability. it causes problems during pregnancy including preeclampsia, stillbirth, repeated abortions, and detached pair. out of the most prevalent factors causing inherited thrombophilia, protein s (prs), protein c (prc), and antithrombin iii (atiii) deficiency, and factor v leiden (fvl) mutation could be mentioned. this study aimed ...

Journal: :Polskie Archiwum Medycyny Wewnetrznej 2007
Anna Buczma Jerzy Windyga

Acquired haemophilia (AH) is a severe bleeding diathesis that affects both males and females. It is caused by suddenly appearing autoantibodies that interfere with coagulation factor VIII (FVIII) activity. Although some conditions such as autoimmune diseases, cancer and puerperium seem likely to induce AH, in more than half of the observed cases autoantibodies to FVIII are idiopathic. The clini...

Abstract Background and Objectives Vitamin K-dependent clotting factor deficiency (VKCFD) is usually an acquired problem due to liver disease, malabsorption, and overdose of warfarin.  In the present paper the significance and role of vitamin K-dependent coagulation factors in menorrhagia were evaluated.   Case We present a rare case of 43 year woman with acquired vitamin K deficiency and se...

Journal: :Blood 1997
F De Filippi M Colombo M G Rumi F Tradati D Prati A Zanella P M Mannucci

The parallel measurement of serum antibodies to the hepatitis G virus (anti-HGV) and of viremia (HGV-RNA) should improve our understanding of HGV transmission by coagulation factor concentrates. The aim of this study was to assess the relationship between HGV, the type of concentrate infused, and liver disease in multitransfused hemophiliacs. To this end, anti-HGV and HGV-RNA were evaluated by ...

Journal: :Blood 1986
E A Thompson M A Howard

In vivo fragmentation of the von Willebrand factor antigen (vWF:Ag) molecule has been demonstrated on radiocrossed immunoelectrophoresis (CIE) in the plasma from patients with disseminated intravascular coagulation, in factor VIII concentrates, and in normal serum. Experiments reported here show that polymorphonuclear (PMN) cells contain a non-calcium-dependent protease(s) that when released an...

2014
Sébastien Lobet Cedric Hermans Catherine Lambert

Hemophilia is a hematological disorder characterized by a partial or complete deficiency of clotting factor VIII or IX. Its bleeding complications primarily affect the musculoskeletal system. Hemarthrosis is a major hemophilia-related complication, responsible for a particularly debilitating chronic arthropathy, in the long term. In addition to clotting factor concentrates, usually prescribed b...

2015
Bernhard Ziegler Cristina Solomon Janne Cadamuro Neil Jones

Prophylactic platelet concentrates transfusion represents a therapeutic choice in patients with chemotherapy-induced thrombocytopenia. This prospective, non-interventional study evaluated the effects of platelet concentrates transfusion on thromboelastometric parameters of platelet function in 36 transfusion occasions for 11 thrombocytopenic children undergoing chemotherapy. Pre- and posttransf...

2015
Kamran Mousavi Hosseini Saleh Nasiri

BACKGROUND Factor VII concentrates are used in patients with congenital or acquired factor VII deficiency or treatment of hemophilia patients with inhibitors. In this research, immunoaffinity chromatography was used to purify factor VII from prothrombin complex (Prothrombin- Proconvertin-Stuart Factor-Antihemophilic Factor B or PPSB) which contains coagulation factors II, VII, IX and X. The aim...

2017
Kamran Mousavi Hosseini Saleh Nasiri

Background: Factor VII concentrates are used in patients with congenital or acquired factor VII deficiency or treatment of hemophilia patients with inhibitors. In this research, immunoaffinity chromatography was used to purify factor VII from prothrombin complex (ProthrombinProconvertin-Stuart Factor-Antihemophilic Factor B or PPSB) which contains coagulation factors II, VII, IX and X. The aim ...

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