نتایج جستجو برای: thalassemic patient

تعداد نتایج: 710072  

انصاری, شهلا, باقرسلیمی, عادل, تشویقی, مریم ,

    Introduction: Beta thalassemia major is a severe hemolytic anemia due to inadequate synthesis of beta chain globin. Splenomegaly secondary to extramedullary hematopoiesis and iron overload is one of the most prominent findings and makes splenectomy inevitable in majority of these patients. For many reasons these patients are at risk of hypercoagulation. Portal vein thrombosis is a rare cons...

Journal: :medical journal of islamic republic of iran 0
h foroutan from the department of1nternal medicine.imom hospital. tehran university of medical sciences, h ghofrani sh . mirmomen s kazemi asl mj farahvash m nasiri tousi

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 - transfused ...

Journal: :Asian Pacific journal of tropical biomedicine 2014
Kanokwan Kulprachakarn Nittaya Chansiw Kanjana Pangjit Chada Phisalaphong Suthat Fucharoen Robert C Hider Sineenart Santitherakul Somdet Srichairatanakool

OBJECTIVE To evaluate the iron-chelating properties and free-radical scavenging activities of 1-(N-acetyl-6-aminohexyl)-3-hydroxy-2-methylpyridin-4-one (CM1) treatment in chronic iron-loaded β-thalassemic (BKO) mice. METHODS The BKO mice were fed with a ferrocene-rich diet and were orally administered with CM1 [50 mg/(kg.day)] for 6 months. Blood levels of non-transferrin bound iron, labile p...

Journal: :Journal of Nepal Medical Association 2023

Introduction: Raised serum ferritin levels often indicate iron overload, but they are not specific as the elevated in inflammatory disorders, liver diseases, alcohol excess, or malignancy. If regular transfusions required for patient with thalassemia, this doubles rate of accumulation leading to earlier massive overload and iron-related damage. The aim study aimed find out prevalence high among...

Journal: :iranian journal of child neurology 0
soroor inaloo md,pediatric neurologist, associate professor, shiraz neuroscience research center, shiraz university of medical sciences, shiraz, iran saeedeh haghbin md,pediatric intensivist, assistant professor, shiraz university of medical sciences, shiraz, iran samaneh karimi md,general physician, shiraz university of medical sciences shiraz, iran

objective febrile seizure is the most common seizure disorder in children. its pathophysiology is not fully understood yet; however, some risk factors have been cited for it. iron is one of these influential elements and is involved in the metabolism of some neurotransmitters which are reduced in irondeficiency anemia and also increases the sensitivity of neural cells during a febrile episode. ...

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: :Blood 1999
K Pattanapanyasat K Yongvanitchit P Tongtawe K Tachavanich W Wanachiwanawin S Fucharoen D S Walsh

Certain red blood cell (RBC) disorders, including thalassemia, have been associated with an innate protection against malaria infection. However, many in vitro correlative studies have been inconclusive. To better understand the relationship between human RBCs with thalassemia hemoglobinopathies and susceptibility to in vitro infection, we used an in vitro coculture system that involved biotin ...

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...

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