نتایج جستجو برای: hemoglobin

تعداد نتایج: 57591  

Journal: :medical journal of islamic republic of iran 0
nasrin khalesi pediatrics department, faculty of medicine, iran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences) nastaran khosravi pediatrics department, faculty of medicine, iran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences) mohammad reza rezaee faculty of medicine, tehran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) leila amini midwifery department, faculty of nursing & midwifery, iran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences)

background :identification of α thalassemia (α thal) a common cause of microcytosis during neonatal periods is an important step prevent unnecessary interventions. thus, low the mean corpuscular volume (mcv) and the mean corpuscular hemoglobin (mch) may consider as α-thalassemia key detection points. the present study aimed to determine the prevalence of microcytosis among neonates who born in ...

Journal: :international journal of hematology-oncology and stem cell research 0
majid farshdousti hagh division of laboratory hematology and blood banking, faculty of medicine, tabriz university of medical sciences, tabrez, iran ali dehghani fard department of hematology and blood banking, faculty of medical sciences, tarbiat modares university,tehran, iran najmaldin saki research center of thalassemia and hemoglobinopathies, ahvaz jundishapur university of medical sciences, ahvaz, iran mohammad shahjahani department of hematology and blood banking, faculty of medical sciences, tarbiat modares university,tehran, iran saied kaviani department of hematology and blood banking, faculty of medical sciences, tarbiat modares university,tehran, iran

hemoglobin f (hbf, α 2 γ 2 ) is a major contributor to the clinical heterogeneity and ameliorating agent observed in patients with the β-globin disorders including β-thalassemia and sickle cell disease (scd). during fetal life, hbf is the major hemoglobin but is largely substituted by adult hemoglobin (hba, α 2 β 2 ) following a globin expression switch after birth. increased γ-globin expressio...

Journal: :مجله دانشگاه علوم پزشکی شهید صدوقی یزد 0
مصطفی آلبوکردی m albockordi . [email protected] احمد محمودیان a mahmoudian رضا اسحاقی r eshaghi زیبا فرج زادگان z farajzadegan

introduction: iron deficiency anemia (ida) is the most common form of anemia and one of the most important health problems. iron supplementation for high risk groups can prevent ida and its complications in the community. we need to have a holistic approach to control ida with minimum cost and complications. considering the high prevalence rate of ida in iran, assessment of the effects of micro...

Journal: :international journal of hematology-oncology and stem cell research 0
mohammad ali jalali far health research institute, research center of thalassemia & hemoglobinopathy, ahvaz jundishapur university of medical sciences, ahvaz, iran ali dehghani fard sarem cell research center-scrc, sarem women’s hospital, tehran, iran saiedeh hajizamani diagnosticlaboratory sciences and technology research center, school of paramedical sciences, shiraz university of medical sciences, shiraz, iran majid mossahebi-mohammadi department of hematology, faculty of medical sciences, tarbiat modares university, tehran, iran hamid yaghooti department of medical laboratory sciences, school of paramedicine, ahvaz jundishapur university of medical sciences, ahvaz, iran najmaldin saki health research institute, research center of thalassemia & hemoglobinopathy, ahvaz jundishapur university of medical sciences, ahvaz, iran

background: efficient induction of fetal hemoglobin (hbf) is considered as an effective therapeutic approach in beta thalassemia. hbf inducer agents can induce the expression of γ-globin gene and produce high levels of hbf via different epigenetic and molecular mechanisms. thalidomide and sodium butyrate are known as hbf inducer drugs. material and methods : cd133 + stem cells were isolated fro...

Journal: :caspian journal of internal medicine 0
azar aghamohammadi mandana zafari maryam tofighi

background: high maternal hemoglobin (hb) concentration was considered a risk factor for the developing of pregnancy hypertension. the purpose of this study was to determine whether high maternal hb concentration in first trimesters associated with pregnancy induced hypertension in iranian nulliparous women. methods: this study was carried out in teaching hospital in sari, iran. samples were ob...

Journal: :iranian journal of medical sciences 0
r. janghorban s. ziaei s. faghihzade

adverse outcomes of pregnancy increase among women with high density of hemoglobin. this study evaluates the effects of iron supplementation on serum copper level in pregnant women with hemoglobin higher than 13.2 g/dl. sixty two pregnant women with hemoglobin >13.2 g/dl and normal serum copper levels in their 13-18 weeks of gestation were randomized into case and control groups. from 20 th wee...

Journal: :The Journal of biological chemistry 1974
T Sasazuki H Tsunoo H Nakajima

The physicochemical and biochemical properties of hemoglobin associated with haptoglobin were compared with those of hemoglobin bour,d by antihemoglobin antibody. The mechanism of enhanced peroxidase activity of hemoglobin bound by haptoglobin was concluded not to be activation but stabilization of hemoglobin at acidic pH by haptoglobin. Haptoglobin protects hemoglobin from denaturation by acid...

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