نتایج جستجو برای: viii
تعداد نتایج: 21094 فیلتر نتایج به سال:
New and expensive therapeutic products can place great pressure on health care purchasers. Often, evidence to support the inclusion of such products in the purchasing process is lacking or confusing, yet demand can be organized and forceful. In this paper we use the example of the introduction of recombinant factor VIII (rFVIII) in the management of haemophilia A, to highlight some problems pur...
Six recombinant factor VIII (rFVIII) products have been marketed worldwide. In 2013, the Research of Determinants of Inhibitor Development (RODIN) study group reported an unexpectedly high risk of inhibitor development with a second-generation full-length rFVIII (Product D) in previously untreated patients (PUPs) with severe hemophilia A (HA). In 1994, French public health authorities establish...
background: factor viii administration to hemophilia a patients results in an immune response (inhibitor formation) which significantly complicates the therapy. the present study was performed to determine the prevalence of inhibitor development in hemophilia a patients receiving recombinant factor viii therapy. materials and methods: this was an observational descriptive study. clotting factor...
چکیده سابقه و هدف فعالیت (fviii:c) fviii در بیماران هموفیلی a با روش های یک مرحله ای، دو مرحله ای مبتنی بر تشکیل لخته و کروموژنیک سنجش می شود. نتایج این سنجش ها در اغلب بیماران هموفیلی a خفیف و متوسط مشابه است ولی در برخی بیماران اختلاف بارزی دارد که می تواند باعث عدم تشخیص یا تشخیص نادرست شدت بیماری شود. هدف مطالعه حاضر تعیین مقادیر فاکتور هشت به دو روش و میزان مغایرت در بیماران هموفیلی a است....
چکید ه سابقه و هدف از آن جایی که خطر خون ریزی در مبتلایان به فقر فاکتور viii ، وابسته به فعالیت فاکتور viii تزریق شده است، انتخاب روش مناسب برای اندازه گیری فعالیت این فاکتور در کرایو، امری ضروری به نظر می رسد. در این مطالعه فعالیت فاکتور viii در کرایو به دو روش تشکیل لخته و رنگ زایی مقایسه شد. مواد و روش ها در یک مطالعه تحلیلی، میانگین فعالیت فاکتور viii در 48 نمونه کرایواز گروه های مخ...
In this issue of Blood, back-to-back (dos-à-dos) papers by Chiu et al and Yee et al present complementary findings of structural investigations into the interaction between factor VIII (FVIII) and von Willebrand factor (VWF). The binding of FVIII to VWF contributes in a major way to the regulation of hemostasis.
background: haemophilia a (ha) is an x-linked bleeding disorder caused by the absence or reduced activity of coagulation factor viii (fviii). coagulation factors are a group of related proteins that are essential for the formation of blood clots. the aim of this study was to genotype the coagulation factor viii gene mutations using inverse shifting pcr (is-pcr) in an iranian family with severe ...
we prepared a highly purified and relatively heat stable form of factor viii which contained 25 units per ml (u/ml) activity using peg-4000 and developed an effective and new manufacturing process. heat treatment was performed at 80°c for 72 hrs in the presence of different stabilizers. in our studies, we used different organic solvents as preservatives to maintain factor viii activity, since f...
patients with coagulation factor(s) deficiency who use coagulation therapy are susceptible to forming inhibitors against coagulation factor(s). in this survey we detected factor v and viii inhibitor in ten patients with combined deficiency of factors v and viii from north east of iran (khorassan province). it was revealed in our survey that eight patients had both factor v and factor viii inhib...
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