نتایج جستجو برای: family history of hemophilia

تعداد نتایج: 21212455  

Journal: :مجله تحقیقات سلامت 0
حسن سعادتی hassan saadati محمد حسین لطفی mohammad hassan lotfi محمد افخمی اردکانی mohammad afkhami ardakani

introduction: diabetes mellitus (dm) is one of the most common chronic diseases in the world and the most challenging health problems of the twenty first century. this disease is common in yazd and has a high prevalence in the province. due to not available analytic study, the aim of this study was to determine the risk factors of type 2 diabetes among the adult yazd population, iran. materials...

Journal: :journal of cellular and molecular anesthesia 0
taregh bamedi department of parasitology, iranshahr university of medical sciences, iranshahr, iran ghazaleh dadashizadeh department of hematology and blood transfusion, school of medicine, mashhad university of medical sciences, mashhad, iran afsaneh sarabandi department of nursing, faculty of medical sciences, islamic azad university, zahedan branch, zahedan, iran shadi tabibian department of hematology and blood transfusion, school of allied medicine, iran university of medical sciences, tehran, iran mahmood shams department of laboratory sciences, paramedical faculty, babol university of medical sciences, babol akbar dorgalaleh department of hematology and blood transfusion, school of allied medicine, iran university of medical sciences, tehran, iran

inhibitor development is a lifelong challenge for patients with bleeding disorders who received replacement therapy. most commonly, inhibitor formation was observed in hemophilia a patients but patients with rare bleeding disorders (rbd) especially patients with deficiency of factor xiii (fxiii) and factor v (fv) can develop an inhibitor against exogenous factors. several factors considered as ...

Journal: :Blood 2017
Stéphanie G I Polderdijk Ty E Adams Lacramioara Ivanciu Rodney M Camire Trevor P Baglin James A Huntington

Hemophilia is a bleeding disorder caused by deficiency in factors VIII or IX, the two components of the intrinsic Xase complex. Treatment with replacement factor can lead to the development of inhibitory antibodies, requiring the use of bypassing agents such as factor VIIa and factor concentrates. An alternative approach to bypass the Xase complex is to inhibit endogenous anticoagulant activiti...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه سمنان - دانشکده ادبیات و علوم انسانی 1393

this thesis is an evaluation of poetry of sylvia plath (1932- 1963) and forough farrokhzad (1935-1967) using feminist approach and finds the positive concepts of hope, reason and strength through feminine images in their poetry. plath and farrokhzad are from different cultures and different countries but they share the same concepts and themes in their poetry. by applying feminist theory to the...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه علامه طباطبایی - دانشکده ادبیات و زبانهای خارجی 1390

monumental changes occurring on a daily basis have altered the world into a global village of expanding technology and shrinking geography in which preparing language learners for intercultural communication seems to be a sine qua non for modern language education. employing a cross-sectional design in its first phase, this study investigated the intercultural sensitivity and language proficien...

Journal: :Blood 1994
B Furie S A Limentani C G Rosenfield

D ESPITE CONSIDERABLE advances in the treatment of hemophilia, clinical expertise in hemophilia care is often concentrated within hemophilia treatment centers. These centers directly and indirectly care for most patients with hemophilia, and provide sophisticated services to this patient population. Much as bone marrow transplantation (BMT) and transfusion medicine have earned a special niche i...

Journal: :iranian journal of medical sciences 0
a. zahedmehr department of biotechnology, pas-teur institute of iran, tehran, iran s. delmaghani department of biotechnology, pas-teur institute of iran, tehran, iran r. sharifian hemophilia centre, imam khomeini hospital, tehran university of medical sciences, tehran, iran m. lak hemophilia centre, imam khomeini hospital, tehran university of medical sciences, tehran, iran s. zeinali department of biotechnology, pas-teur institute of iran, tehran, iran

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 pol...

Journal: :Archives of general psychiatry 2000
M M Weissman P Wickramaratne P Adams S Wolk H Verdeli M Olfson

BACKGROUND Brief screens to collect lifetime family psychiatric history are useful in clinical practice and for identifying potential families for genetic studies. METHODS The Family History Screen (FHS) collects information on 15 psychiatric disorders and suicidal behavior in informants and their first-degree relatives. Since each question is posed only once about all family members as a gro...

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...

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