نتایج جستجو برای: factor ix

تعداد نتایج: 859517  

Journal: :iranian journal of allergy, asthma and immunology 0
hassan mansouri torghabeh aliakbar pourfathollah mahmood mahmoodian shooshtari zahra rezaie yazdi

many investigations have proved relations between abo blood groups with some diseases and factor viii and von willebrand level in plasma. in this study we investigated a relation between abo blood groups and factor viii and ix inhibitors in 102 patients with haemophilia a and 48 patients with haemophilia b. the assay of inhibitor was done by bethesda method. there were no relation between abo b...

Journal: :medical journal of islamic republic of iran 0
s nasiri from the department of research and development, blood research and fractionation co., tehran, and the *department of virology, tarbiat modarres university, tehran, i.r. iran. h rezvan k mousavi mh roostaei

in this study, anion-exchange chromatography was used to purify factor vii and factor ix from prothrombin complex (ppsb), which contains coagulation factors ii, vii, ix and x. for this purpose, deae-sepharose cl-6b gel , pharmacia column xk-26 , high flow rate and two stepwise gradients with phosphate citrate buffer were used. the yield of the two lyophylized products, factor vii and factor ix ...

Fatemeh Amiri, Hassan Abolghasemi, Mahyar Habibi Roudkenar, Mohammad Ali Jalili, Mostafa Paridar, Naser Amirizadeh,

Background: Hemophilia B is an X-linked hereditary disorder of blood coagulation system which is caused by factor IX (FIX) deficiency. Factor IX is a plasma glycoprotein that participates in the coagulation process leading to the generation of fibrin. Replacement of factor IX with plasma-derived or recombinant factor IX is the conventional treatment for hemophilia B to raise the factor IX le...

Journal: :iranian journal of blood and cancer 0
morteza karimipour sirous zeinali edward graham tuddenham nafiseh nafissi manijeh lak peter green

background: heterogeneous mutations in the human coagulation factor ix gene lead to an x-linked recessive bleeding disorder known as hemophilia b. the disease is distributed worldwide with no ethnic or geographical priority. materials and methods: the aim of this study was to characterize the factor ix gene mutations in 28 unrelated iranian hemophilia b patients. polymerase chain reaction (pcr)...

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...

H REZVAN, K MOUSAVI, MH ROOSTAEI, S NASIRI,

In this study, anion-exchange chromatography was used to purify factor VII and factor IX from prothrombin complex (PPSB), which contains coagulation factors II, VII, IX and X. For this purpose, DEAE-Sepharose CL-6B gel , Pharmacia column XK-26 , high flow rate and two stepwise gradients with phosphate citrate buffer were used. The yield of the two lyophylized products, factor VII and factor...

Journal: :medical journal of islamic republic of iran 0
hassan mansouri torghabeh experimental hematology group. medical sciencesschool. tarbiat modares university (t.m. u.). tehran, iran. allakbar pourfathollah experimental hematology group. medical sciencesschool. tarbiat modares university (t.m. u.). tehran, iran. mahmood mahmood ian shooshtari the iranian ~blood transfusion organization research center, tehran. zahra rezaie-yazd the internal ward, ghaem hospital. mashhad, iran. habffiollahe smaili mashhad medical sciences university, mashhad, iran.

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Journal: :iranian journal of blood and cancer 0
hassan mansouri torghabeh aliakbar pourfathollah 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 blood and cancer 0
mostafa paridar naser amirizadeh mahyar habibi roudkenar fatemeh amiri hassan abolghasemi mohammad ali jalili

background: hemophilia b is an x-linked hereditary disorder of blood coagulation system which is caused by factor ix (fix) deficiency. factor ix is a plasma glycoprotein that participates in the coagulation process leading to the generation of fibrin. replacement of factor ix with plasma-derived or recombinant factor ix is the conventional treatment for hemophilia b to raise the factor ix level...

A. Zahedmehr, M. Lak R. Sharifian S. Delmaghani S. Zeinali

Background: Hemophilia B is an X-linked recessive coagulation disorder caused by factor IX deficiency.  Analysis of factor IX gene polymorphisms is considered the best approach for prenatal diagnosis and carrier detection of hemophilia B where the identification of gene mutation is not easily possible. Objective: To study the frequency of three factor IX-linked restriction fragment length polym...

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