نتایج جستجو برای: thalassemic patients

تعداد نتایج: 2085514  

Journal: :گوارش 0
fatemeh mirershadi alireza jafari masoud ghane

background: generally, a number of people with î²-thalassemia are susceptible to hbv since they receive multiple blood transfusions. these people have high infection rates despite vaccination against hbv. in this study, we explore the seroprevalence and risk factors of hbv infection in thalassemic patients who reside in ardabil. materials and methods: hospital in ardabil. patients' demographic ...

Journal: :Thrombosis and haemostasis 2008
Boris Shenkman

Thromb Haemost 2008; 100: 735 Thalassemia is the most common form of congenital hemolytic anemia caused by partial or complete deficiency in one of the major α or β proteins of haemoglobin A (1). Improvement of the standard care of homozygous patients, with almost doubling of their life expectancy, unveiled a higher incidence of additional complications which have not been previously recognized...

2010
Dharam Vir N. K. Panda R. K. Marwaha

BACKGROUND Thalassemia is a hereditary disorder requiring regular blood transfusion. PURPOSE To determine hearing sensitivity in transfusion-dependent thalassemics who were receiving desferioximine and on oral iron chelation (desferioximine) therapy. METHODS 26 patients with B-thelassemia in the age range of 5-22 years were enrolled in the thalassemia transfusion unit in the Advanced Pediat...

Journal: :Haematologica 1997
P Giordano V Sabato F Schettini D De Mattia A Iolascon

It is well known that thalassemic patients exhibit an increased frequency of thrombotic events. Most individuals with resistance to activated protein C (APCR) are the result of a point mutation replacing Arg 506 with Gln in the factor V aminoacidic sequence (factor V Leiden). Recently APCR has been shown to account for up to 50% of cases of thrombophilia. In this report, we describe a 10 year o...

Journal: :Blood 2004
Pietro Sodani David Gaziev Paola Polchi Buket Erer Claudio Giardini Emanuele Angelucci Donatella Baronciani Marco Andreani Marisa Manna Sonia Nesci Barbarella Lucarelli Reginald A Clift Guido Lucarelli

When prepared for transplantation with busulfan (BU) 14 mg/kg and cyclophosphamide (CY) 120 to 160 mg/kg, patients with thalassemia in risk class 3, aged younger than 17 years, who receive transplants from HLA-identical donors, had a 30% incidence of transplant rejection with recurrence of thalassemia. This, relatively poor, outcome was ascribed to insufficient immune suppression or to inadequa...

Journal: :Egyptian Liver Journal 2021

Abstract Background Hepatitis C virus (HCV) infection is a major cause of liver-related morbidity and mortality among thalassemic patients. Direct-acting antiviral agents (DAAs) are highly effective well-tolerated by chronic HCV Results The mean age our patients was 29 years. Sustained virologic response (SVR) at 12 24 weeks achieved in all (100%). most common side effects were fatigue (18%), a...

امیرمسعودی , مجید, صانعی مقدم , اسماعیل, عشقی , پیمان,

Background and purpose: Ïncreasing transfusion need is one of the main problems in thalassemic pathients. Âlloimmunization is one of the most complicated causes of this problem which is an immunologic response to foreign antigens. Âccording to different studies, its frequency is 5% to 21% in major B-thalassemic patients. Âlloimmunization leads to decrease RBÇs life span, an so, demands for in...

Journal: :iranian journal of blood and cancer 0
seyed-moayed alavian hassan abolghasemi seyyed mohammad miri maryam keshvari pegah karimi elizee bita behnava

background: hepatitis c virus (hcv) infection is the most common transfusion transmitted disease in poly-transfused patients worldwide. in this study we aimed to evaluate the effects of pegylated interferon alfa-2a (peg-ifn a-2a) in reducing serum alt and eradicating serum hepatitis c virus (hcv) rna in hcv infected polytransfused thalassemic patients. materials and methods: a cohort of 51 hcv-...

Abstract Background and Objectives Hemagglutination has limitations in identifying the phenotype of patients who have been recently transfused due to the presence of donor red cells (RBCs) in the patient’s circulation. Kidd blood group is one of the most important blood groups in transfusion medicine and related antibodies are responsible for one third of delayed haemolytic transfusion reactio...

Journal: :Polish journal of pharmacology 2004
Nandita Das Tapasi Das Chowdhury Aindrila Chattopadhyay Asoke G Datta

The oxidative stress status of the transfusion-dependent Ebeta- and beta-thalassemia patients were studied before and after treatment with vitamin E for a period of four weeks. The level of cellular vitamin antioxidants viz. ascorbic acid and vitamin E in the thalassemia patients were found to be considerably lower compared to normal subjects. The activities of enzymatic antioxidants viz. catal...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید