نتایج جستجو برای: thalassemic patients

تعداد نتایج: 2085514  

Journal: :iranian journal of pediatric hematology and oncology 0
azam sadat hashemi department of pediatric, hematology, oncology and genetic research center, shahid sadoughi university of medical science shahin banaei-boroujeni general practitioner, shahid sadoughi university of medical sciences, yazd, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید صدوقی یزد (shahid sadooghi university of medical sciences) n kokab general practitioner, shahid sadoughi university of medical sciences, yazd, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید صدوقی یزد (shahid sadooghi university of medical sciences)

abstract background the purpose of this study was to assess the prevalence of major depressive and anxiety disorders in hemophilic and major beta thalassemic patients related to education of their mothers as a family’s agent. materials and methods a case-control study was performed on 34 major beta thalassemic patients. for each patient the control group was selected and matched (with age and s...

H FOROUTAN, H GHOFRANI, M NASIRI TOUSI, MJ FARAHVASH, S KAZEMI ASL, SH . MIRMOMEN,

Hepatitis C virus (HCV) infection is highly prevalent in thalassemic patients, and this may decrease the serum antibody response to hepatitis B virus (HBV) vaccine. There is also some alteration of the immune system in multi-transfused thalassemic patients, as a consequence of iron overload. We investigated whether HCY infection may reduce the effectiveness of HBY vaccine in multi - transf...

Journal: :Journal of the Medical Association of Thailand = Chotmaihet thangphaet 2009
Werasak Sutipornpalangkul Supeenun Unchern Yupin Sanvarinda Udom Chantharaksri Suthat Fucharoen

BACKGROUND Beta-thalassemia/Hemoglobin E (beta-thal/Hb E) is a congenital hemolytic anemia that is prevalent in Thailand Pulmonary arterial occlusion is the cause of morbidity and mortality in these patients. Abnormality of platelets has been implicated as pathogenesis of this condition. However the blood-borne factors that induce platelet activation are not identified Recently, oxidized low-de...

2012
Z Hashemian A Hashemi M Fateminasab

BACKGROUND β-Thalassemic children have oxidative stress and antioxidant deficiency even without iron overload status. In these patients, tissue damage due to oxidative stress may be occurred. Also, it seems that thalassemic patients have higher levels of ALT, AST therefore, the main aim of the present study was to determine the benefits of vitamin E as an antioxidant supplements in β-Thalassemi...

2017
Nadia A. Sadek Khaled S. Salem

Objective: to study the impact of haptoglobin gene polymorphism on iron overload, oxidative stress and antimullerian hormone in BTM women in Egypt. Methods: case-control study. 47 BTM women, aged between 16-26 years and 47 age-matched regularly menstruating women as control. Haptoglobin Hp1/2 gene polymorphism by PCR, Hemoglobin electrophoresis, serum haptoglobin, ferritin, malondialdehyde MDA,...

2013
Mohammad Abbasinazari Bita Behnava Yunes Panahi Azita Hajhossein Talasaz Shima Salimi Maryam Keshvari Leila Mehrnoush Pegah Karimi Elizee Mohammad Gholami Fesharaki Mansour Asgharinia Seyed Moayed Alavian

BACKGROUND Zinc deficiency has been reported frequently in hepatitis C patients in the literature. Furthermore, a decrease in zinc level has been shown in beta thalassemia major as well. Iranians consume a large amount of phytate in their regimens which can bind with zinc and decrease its gastrointestinal absorption. OBJECTIVES This study was designed to determine plasma zinc level in an Iran...

2011
Mohammadreza Rashidi Maryam Aboomardani Maryam Rafraf Seyed-Rafie Arefhosseini Abbasali Keshtkar Hamidreza Joshaghani

OBJECTIVE In beta thalassemic patients, tissue damage occurs due to oxidative stress and it happens because of the accumulation of iron in the body. This study was conducted to determine the effect of zinc and vitamin E supplementation on antioxidant status in beta-thalassemic major patients. METHODS This double blind randomized clinical trial was carried out on 120 beta thalassemic patients ...

2016
Sasima Srisukh Boonsong Ongphiphadhanakul Pongamorn Bunnag

Despite recent advances in iron chelation therapy, excess iron deposition in pituitary gonadotropic cells remains one of the major problems in thalassemic patients. Hypogonadism, mostly hypogonadotropic hypogonadism, is usually detected during puberty. Early diagnosis and treatment are crucial for normal pubertal development and to reduce the complications of hypogonadism. The risks and benefit...

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