نتایج جستجو برای: major ß thalassemia

تعداد نتایج: 639703  

Journal: :Türk Osteoporoz Dergisi 2012

Journal: :Journal of Evolution of Medical and Dental Sciences 2016

اکرمی پور, رضا, خالقی, سمیه, علی بخشی, رضا, بیدکی, سید کاظم ,

  Background: Alpha thalassemia is a single gene disorder, inherited in an autosomal recessive manner. The thalassemia occurs mostly in peoples from the Mediterranean to Southeast Asia. The present study was aimed to identify the prevalence of nondeletional Alpha thalassemia mutations in our samples in the Kermanshah province.   Methods : This study included Alpha thalassemia individuals who ha...

2017
Abdolreza Sotoodeh Jahromi Zhila Rahmanian

Background and aims: Thalassemia is one of the most prevalent hematologic disorders worldwide. Thalassemia is the most common inherited anemia and genetic disease. Diabetes mellitus and insulin resistance is one of the major endocrine problems in major thalassemia patients. This study was done to evaluate the association of serum γinterferon and IL-10 concentrations with insulin resistance in s...

Journal: :گوارش 0
farhad zamani ramin shakeri masoomeh islam hassan taheri mehdi mohamadnejad reza malekzadeh

background: major thalassemia is the most common form of anemia requiring blood transfusion in iran. since ribavirin provokes anemia in the treated patients, interferon monotherapy may be an appropriate treatment in major thalassemic patients. the aim of this study was to determine the safety and efficacy of interferon monotherapy in thalassemic patients with hepatitis c virus infection. materi...

Journal: :iranian journal of pediatric hematology and oncology 0
ali bazi faculty of allied medical sciences, zabol university of medical sciences, zabol, iran ebrahim miri-moghaddam genetics of non-communicable disease research center, dept. of genetics, faculty of medicine, zahedan university of mediسازمان اصلی تایید شده: دانشگاه علوم پزشکی زابل (zabol university of medical sciences)

abstract β-thalassemia major (β –tm) is the most common thalassemia severe phenotype among iranians. in recent years, molecular understanding of pathogenesis of β –tm has provided a great opportunity regarding diagnostic issues. creating comprehensive molecular databases provides highly sensitive diagnostic tools for β –tm and effective prenatal diagnosis (pnd) molecular screening tests. despit...

Journal: :International Journal of Research in Medical Sciences 2017

Background Beta thalassemiais a genetic blood abnormality identified through mutations, which reduce the synthesis of the ß-globin chain. Gene therapy through Lentiviral vectors have cured many of genetic disorders. The purpose of this study was to investigate the efficacy of lentiviral vectors in treatment of ß-thalassemia a...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید