نتایج جستجو برای: thalassemia carrier rate

تعداد نتایج: 1042539  

Journal: :Journal of pediatric hematology/oncology 2006
Ahmad Ghanizadeh Sirin Khajavian Hamid Ashkani

PURPOSE To study the rate of psychiatric disorder and suicidal behavior in children with thalassemia major. METHOD One hundred ten subjects with thalassemia major were interviewed according to the K-SADS Farsi version by face-to-face interview. RESULT The most common psychiatric disorders were major depressive disorder and separation anxiety disorder. The rate of oppositional defiant disord...

2015
Maliheh NAJAF POUR Majid FARSHDOUSTI HAGH Ali Akbar MOVASAGPOOR AKBARI Abbas Ali HOSEIN POOR FEYZI Majid MALAKI

Thalassemia is the most common single gene disorder around the world (1, 2). This disease is a type of chronic, microcytic and inherited anemia associated with defect in hemoglobin synthesis and reduction in life span of red blood cells (3). Thalassemia is distributed in Mediterranean, Middle East, Arabian Peninsula, Turkey, Iran, India, Burma and Southeast Asia (1). There are two types of thal...

2010
Suphan Soogarun Jamsai Suwansaksri Viroj Wiwanitkit

Thalassemia poses an important public health problem in Thailand. The Ministry of Public Health of Thailand has conducted many programs for the control of thalassemia. These programs are useless if there is no effective, affordable method of screening for carriers. We report on the possibility of using an automated reticulocyte analyzer in order to identify α-thalassemia. Thirty-one control sub...

2015
Jiraporn Kuesap W. Chaijaroenkul K. Rungsihirunrat K. Pongjantharasatien Kesara Na-Bangchang

Hemoglobinopathy and malaria are commonly found worldwide particularly in malaria endemic areas. Thalassemia, the alteration of globin chain synthesis, has been reported to confer resistance against malaria. The prevalence of thalassemia was investigated in 101 malaria patients with Plasmodium falciparum and Plasmodium vivax along the Thai-Myanmar border to examine protective effect of thalasse...

Journal: :Thalassemia Reports 2022

The recent transfer of Thalassemia Reports, the only journal fully dedicated on Thalassemia, from PagePress to MDPI was great news for those who contributed spread [...]

Journal: :Haematologica 2008
Wei Li Shuyang Xie Xinbing Guo Xiuli Gong Shu Wang Dan Lin Jingzhi Zhang Zhaorui Ren Shuzhen Huang Fanyi Zeng Yitao Zeng

BACKGROUND beta-thalassemia is one of the most common genetic diseases in the world and requires extensive therapy. Lentiviral-mediated gene therapy has been successfully exploited in the treatment of beta-thalassemia and showed promise in clinical application. Using a human beta-globin transgenic mouse line in a beta-thalassemia diseased model generated with a lentiviral-mediated approach, we ...

ژورنال: پژوهش در پزشکی 2015

Background: Beta thalassemia is one of the autosomal recessive diseases that related to synthesis disorder of beta globin chain. It is caused by any of the more than 200 mutations in the β-globin gene. DNA sequencing and genotyping of numerous mutations at beta globin gene is timely and expensive. Therefore, the best method for screening is linkage using polymorph markers at beta globin region ...

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