نتایج جستجو برای: major ß thalassemia

تعداد نتایج: 639703  

Journal: :iranian journal of immunology 0
ali asghar vahidi department of pediatrics and neonatology majid varesvazirian department of pediatrics and neonatology ayeh shamsadini department of pediatrics and neonatology sadollah shamsadini department of dermatology, school of medicine, kerman university of medical sciences, kerman, iran

background: thalassemia patients are more susceptible to hepatitis than the normal population due to the frequent blood transfusions. objective: to determine the immune response of children with major ß-thalassemia, by measuring anti-hepatitis b surface antibody (anti-hbs ab) following the last hbv vaccine injection. methods: this study was carried out on 215 thalassemic children who received t...

Journal: :Annals of International medical and Dental Research 2017

2009
Sara Malik Serajuddaula Syed Nisar Ahmed

ßthalassemia is an inherited disorder of hemoglobin synthesis characterized by deficient synthesis of the ß-globin chain that causes severe anemia. Over the years, the combination of hypertransfusion and chelation therapy has significantly increased the survival of patients of ß-thalassemia. At the same time, there has been an increase in the frequency of complications, mainly caused by iron ov...

زینلی , سیروس, سواد کوهی , فریبا, عشقی , پیمان, میری مقدم , ابراهیم, نارویی نژاد , مهرناز,

Background and purpose : bata thlassemia is the most common monogenic disorders in Iran. The gene frequency varies the country. Sistan and Baluchistan province, located in the southeast of iran with more than 1200 affected individuals, represents one of the regions where thalassemia id not only an important public health problem but also a socioeconomic problem. As a matter of fact high frequ...

Journal: :iranian journal of blood and cancer 0
a mehrvar a azarkeivan j saberi nejad m faranoush n mehrvar p vossough

introduction: thalassemia is common in iran. appropriate therapy for this disease includes a regular blood transfusion and chelation therapy. however, patients will inevitably confront with side effects, particularly iron overloads in critical organ including heart, ductless glands and liver. this study tries to determine the prevalence of diabetes mellitus in transfusion dependent β thalassemi...

ساری سرخابی, روح انگیز, شیوا, سیامک,

S Shiva , MD R Sarisorkhabi , MD Received: 24 Oct, 2007 Accepted: 12 March, 2008 Abstract Background & Aims: Combination of chelating therapy regimens with regular blood transfusion has significantly improved the life expectancy of thalassemic patients. Despite progresses in treatment of these patients, growth failure, and short stature are found in significant number of them. Factors such...

Journal: :ژورنال پزشکی بین المللی الکترونیک 0
najmeh niroomand moradinejhad mahshid sarafraz majid sarneyzadeh pormehr-yabandeh asiyeh susan hamedi

background: iran is a country located on the thalassemic belt of the globe. investigating such issues is of a greater significance in southern provinces of the country where the high prevalence of thalassemia has imposed high costs and mental pressure on families and the healthcare system. methods: in this cross-sectional study conducted in 2011 as a census, the data related to patients or dise...

Journal: :Religions 2022

The four principles of Western medical bioethics, i.e., autonomy, nonmaleficence, beneficence and justice, published by Beauchamps Childress in their seminal ‘Principles Biomedical Ethics’, are understood as universal. However, Non-Western governments argue that they refer to cultural contexts, neglecting specifics Non-Western, for instance Islamic, civilizations. This paper addresses the claim...

Journal: :iranian journal of public health 0
mr salehi dd farhud tz tohidast m sahebjamee

background: major -thalassemia is the most common monogenic known disorder in iran and about 15000 persons are af fected. the purpose of this study was to evaluate the prevalence of orofacial complications. methods: in this cross-sectional study during 2003-2004, 300 patients with major -thalassemia referring to 8 hospitals for routine examinations, blood infusion and treatment in cities of teh...

Journal: :international journal of hematology-oncology and stem cell research 0
mohamad ali mashhadi genetic of non communicable disease research center, zahedan university of medical sciences, zahedan, iran.

introduction: there have been many reports and papers on deficient, normal and high levels of copper in patients with thalassemia major. the aim of this study is to evaluate copper status in a series of more than 300 patients with thalassemia major and determine the degree of copper deficiency or excess. methods: three hundred and seventy patients with thalassemia major over 5 years of age were...

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