نتایج جستجو برای: factor viii

تعداد نتایج: 859518  

ژورنال: پژوهش در پزشکی 2006
دکتر امیر هوشنگ محمد علیزاده, , دکتر سید محسن موسوی, , دکتر فرحناز فلاحیان, , دکتر محمد رضا زالی, , دکتر محمد عباسی, , دکتر مهرداد حاجیلویی, , دکتر میترا رنجبر, , دکترمهدی رضازاده, ,

Abstract: Background: Hemophilia is a x-linked deficiency of factor VIII. The aim of the present study was to determine the frequencies of hepatitis B and C infections, markers of inflammation and liver function tests and also to assess the possible association between factor VIII inhibitor and hepatitis B and C infections in hemophiliacs of Hamedan Province of Iran. Materials and methods: Si...

Journal: :medical journal of islamic republic of iran 0
t zandieh from the iranian blood fractionation and research company, tehran m farhadi the iranian blood transfusion service, tehran m shahr-abadi the virology lab, rasool akram hospital, tehran, i.r. iran. h lotfi from the iranian blood fractionation and research company, tehran

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...

Journal: :acta medica iranica 0
fereydoun ala irandokht shoa'i

0

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: :مجله دانشگاه علوم پزشکی کرمانشاه 0
farzad company dept. of haematology & oncology, school of medicine, kurdistan university of medical science. sanandaj nazila rezaei dept. of haematology & oncology, school of medicine, kurdistan university of medical science. sanandaj mariam aliasgharpoor dept. of haematology & oncology, school of medicine, kurdistan university of medical science. sanandaj

background: factor viii inhibitor is one of the most problems in the treatment of hemophilia. patients with hemophilia who have inhibitors are capable of severe hemorrhage and treatments of these patients are more expensive and more difficult than those patients without inhibitor. the aim of present study was to determine the prevalence of inhibitor and to assess the necessity of screening of t...

B Habibpanah, E Fatohlahzadeh, F Gorji, P Eshghi, Y Panahi, F Malek , H Abolghasemi , M Naderi ,

Background: Considering the increasing number of patients with hemophilia and infrastructure requirements for a comprehensive approach, development of a recombinant factor has become a milestone. The objective of this study was to assess the safety, efficacy and non inferiority of Safacto (Recombinant factor VIII) compared with plasma-derived factor in the treatment of hemophilia A. Methods: 10 ...

Journal: :The Journal of clinical investigation 1967
S S Shapiro

Investigations were undertaken of the chemical nature and kinetics of interaction of three acquired inhibitors of Factor VIII. The inhibition was stoichiometric, one molecule of inhibitor (or one site on a molecule) being required to inactivate one molecule of Factor VIII. All three inhibitors were found to be monotypic antibodies of class IgG, Type K (gamma(2) kappa(2)). This appears to be the...

Journal: :The Journal of clinical investigation 1963
E ADELSON J J RHEINGOLD O PARKER M STEINER J C KIRBY

Journal: :Journal of public health medicine 1998
C Green R Akehurst

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...

Journal: :Blood 2014
Thierry Calvez Hervé Chambost Ségolène Claeyssens-Donadel Roseline d'Oiron Véronique Goulet Benoît Guillet Virginie Héritier Vanessa Milien Chantal Rothschild Valérie Roussel-Robert Christine Vinciguerra Jenny Goudemand

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...

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