نتایج جستجو برای: factor v inhibitor

تعداد نتایج: 1288426  

Aliakbar Pourfathollah, Hassan Mansouri Torghabeh, Mahmoud Mahmoudian Shoushtari,

Background: Hemophilia B is a bleeding disorder with a recessive X-linked inheritance pattern, in which the infected individuals have low levels of factor IX in their plasma. Affected individuals may have bleeding episodes after trauma or spontaneously considering the plasma level of factor IX. In order to prevent these episodes and to control bleeding, they should use coagulation factor concen...

Journal: :iranian journal of medical sciences 0
hassan mansouritorghabeh

this review summarizes current data on the pathomechanisms and new genetic findings of combined factor v and viii deficiency (cf5f8d). congenital haemorrhagic disorders characterized by deficiency of two clotting factors comprise an interesting group. among dual coagulation disorders, cf5f8d is the most common type. for the first time combined factor v and viii deficiency (f5f8d) was reported b...

2011
Andrea Rubboli

BACKGROUND Triple therapy (TT) with vitamin K-antagonists (VKA), aspirin and clopidogrel is the recommended antithrombotic treatment following percutaneous coronary intervention with stent implantation (PCI-S) in patients with an indication for oral anticoagulation. TT is associated with an increased risk of bleeding, but available evidence is flawed by important limitations, including the limi...

Journal: :journal of research in medical sciences 0
mohammad saadatnia mansour salehi ahmad movahedian sz samsam shariat mehri salari marzieh tajmirriahi

background: factor v g1691a (fv leiden), fii ga20210, and methylenetetrahydrofolate reductase (mthfr) c677t mutations are the most common genetic risk factors for thromboembolism in the western countries. however, there is rare data in iran about cerebral venous and sinus thrombosis (cvst) patients. the aim of this study was to evaluate the frequency of common genetic thrombophilic factors in c...

Journal: :acta medica iranica 0
sharifian r hosseini m safai r tugeh gh ehsani ah lak m

development of inhibitor to factor viii is the most serious complication of hemophilia therapy. to determine the prevalence of inhibitors in iran hemophilia a patients exposed to blood products, 1280 hemophilia a patients (age range 9 months-84 years) were evaluated. all patients received several blood products such as fresh frozen plasma (ffp), cryoprecipitate, and factor viii. 635 of 1280 pat...

A Aaleyasin L Safdarian M Aghahossieni M Rashidi, S Asadollah Z Najmi,

a:4:{s:10:"Background";s:363:"The largest percentage of failed in vitro fertilization (IVF) cycles are due to lack of implantation. As hereditary thrombophilia can cause in placentation failure, it may have a role in recurrent IVF failure. The aim of this case-control study was to determine whether or not hereditary thrombophilia is more prevalent in women with recurrent IVF failures.";s:19:"Ma...

Journal: :Blood 1983
K Suzuki J Nishioka S Hashimoto T Kamiya H Saito

Protein-C inhibitor (PCI) is a newly described plasma inhibitor directed against a vitamin-K-dependent serine protease, activated protein-C, which is involved in the inactivation of factor V and factor VIII. Marlar and Griffin have reported that PCI activity is absent in the plasma of patients with congenital combined factor V/VIII deficiency. We have measured the levels of PCI in the plasma of...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه اصفهان - دانشکده علوم 1392

سلول های بنیادی جنینی انسانی قابلیت های شگرفی در حوزه ی پزشکی و سلول درمانی دارند. در این راستا، منفرد کردن سلول های بنیادی انسانی با هدف گسترش سریع این سلول ها و انجام دست ورزی های مختلف بر روی آن ها اجتناب ناپذیر است. اما در این فرایند مانعی وجود دارد، بدین معنا که آپوپتوز القا شده در اثر فعالیت مسیر سیگنالی rho/rock که در نتیجه ی منفرد شدن سلول های بنیادی انسانی فعال می شود، کشت و دست ورزی ا...

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