نتایج جستجو برای: factor viii inhibitor

تعداد نتایج: 1028472  

Journal: :international journal of hematology-oncology and stem cell research 0
ali naderi pediatric hematology- oncology department, kerman university of medical sciences, kerman, iran mohmmadreza ebadzadeh urology department, kerman university of medical sciences, kerman, iran jalal azmandyan nephrology, kerman university of medical sciences, kerman, iran razieh fayazfar hemophilia center of afzalipour hospital, kerman university of medical sciences, kerman, iran elham ahmadi pediatric ward, kerman university of medical sciences, kerman, iran ali rikhtehgaran tehrani researcher, kerman university of medical sciences, kerman, iran

introduction: the prevalence of rare bleeding disorders, including combined factor v+viii deficiency are higher in iran than in developed countries. there are only a few reports which have been written concerning kidney transplantation in the patients suffering from these disorders. case report: a 22-year old girl, with a known case of combined factor v+viii deficiency, a history of bladder sto...

Journal: :Blood 1984
A R Giles S Tinlin H Hoogendoorn P Greenwood R Greenwood

Classic hemophilia A (factor VIII:C deficiency) was diagnosed in a miniature Schnauzer dog and a breeding program established. Inbreeding and crossbreeding produced 16 hemophilic animals. All were initially treated with canine cryoprecipitate, as required, for sporadic hemorrhagic events. Five animals developed potent antibodies to canine factor VIII:C. All were the offspring of obligate carrie...

Journal: :Blood 1993
A E Morrison C A Ludlam C Kessler

Data have been collected from 47 centers in Europe and North America on the treatment with porcine factor VIII concentrate of 74 acute bleeding episodes in 65 patients with acquired hemophilia. The median initial anti-human factor VIII auto-antibody inhibitor level was 38 Bethesda unit (BU)/mL (range 1.2 to 1,024) whereas that against porcine was 1 BU/mL (range 0 to 15). The mean initial dose o...

Journal: :iranian journal of biotechnology 2013
parichehr darabi hamid galehdari saeed reza khatami nahid shahbazian mohammad shafeei

background: leukemia inhibitor factor (lif) is a very important pleiotropic cytokine which belongs to interleukin-6 (il-6) family. lif exerts multiple effects on different types of cells and tissues with numerous regulatory effects in vivo and in vitro. it is a lymphoid factor, which performs a number of activities including cholinergic neuron differentia­tion, control of stem cell pluripotency...

2005
Deborah Whitehurst Leon W. Hoyer A. Vijaya Rao Jack Lazerson

During a 4-year multicenter cooperative study of acquired factor VIII inhibitors in persons with hemophilia A. new inhibitors were detected in 31 of 1 .306 patients who entered the study without an inhibitor or the history of an inhibitor. The incidence of new inhibitors was eight per 1 .000 patient-years of observation. The factor Vlll:C level before inhibitor development was 0.03 U/mi in 29 m...

2005
Deborah Whitehurst Leon W. Hoyer A. Vijaya Rao Jack Lazerson

During a 4-year multicenter cooperative study of acquired factor VIII inhibitors in persons with hemophilia A. new inhibitors were detected in 31 of 1 .306 patients who entered the study without an inhibitor or the history of an inhibitor. The incidence of new inhibitors was eight per 1 .000 patient-years of observation. The factor Vlll:C level before inhibitor development was 0.03 U/mi in 29 m...

2005
Deborah Whitehurst Leon W. Hoyer A. Vijaya Rao Jack Lazerson

During a 4-year multicenter cooperative study of acquired factor VIII inhibitors in persons with hemophilia A. new inhibitors were detected in 31 of 1 .306 patients who entered the study without an inhibitor or the history of an inhibitor. The incidence of new inhibitors was eight per 1 .000 patient-years of observation. The factor Vlll:C level before inhibitor development was 0.03 U/mi in 29 m...

Journal: :Blood 1970
P A Castaldi R Penny

H EMOSTATIC DISORDERS with a varying incidence of bleeding, are common in the dysproteinemias, and are characteristic of the macroglobulinemia of \\Taldenstr#{246}m These abnormalities are most frequently attributed to abnormal platelet function,1 and depression of specific clotting factors appears to be a rare occurrence. Nilehn2 includes four instances of antihemophilic globulin ( factor VIII...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید