Aim To investigate the humeral immune markers in patients with ß-thalassemia major (TM). Methods In this historical – cohort study (August to December 2007), the case group consisted of 34 TM patients and the control group included the same number of their gender and age matched healthy siblings. Serum levels of CH50, C3, C4, IgE, IgG,IgA,IgM and also ASO & Isohemaglutinin titers were determined and compared between the case and control groups (P3000ng/ml had lower C4 and CH50 levels. C4-level in male patients was significantly lower. Conclusion This study indicated that there were no significant changes in humeral immune markers in the patients with ß-thalassemia major compared to the controls, except in the case of IgA which was higher in...
In the β-thalassemia's, oxidative stress, resulting from chronic hemolysis, globin chain imbalance, ...
OBJECTIVE: The aim of this study was to determine the frequency of cryoglobulinemia and associated s...
Background: Thalassemia remains to be the procured hemoglobinopathy due to the quantitative defect i...
PubMed ID: 10771839Serum IgG, IgM, IgA, IgG subclasses (IgG1, G2, G3, G4), isohemagglutinins and com...
Background: Beta-thalassemia major is one of the major health problems in our country. Many studies ...
Objective: Thalassemia is a common disease in many countries, in which several complications such as...
Background; Thalassemia is one of the most prevalent genetic disorders in world , and infections are...
Objective: Thalassemia is a common disease in many countries, in which several complications such a...
Plasma levels of ILr3 and IL-7 were studied in 23 patients with homozygous beta-thalassemia in order...
Background: Thalassemia and abnormal hemoglobin are the most common genetic disorders and are consid...
Abnormalities in the immune system and zi nc homeostasis in patients with P-thalassemia major (TM) h...
Thalassemia is a term that refers to a group of genetic disorders characterized by a de...
Abstract Introduction: Thalassemia is the most common hereditary anemia in Iran. The aim of this stu...
We evaluated phagocytic and lytic activities of peripheral blood monocytes (PBMo) from patients with...
everal immunological defects have been found in patients affected by b-tha-lassemia.1 They are mainl...
In the β-thalassemia's, oxidative stress, resulting from chronic hemolysis, globin chain imbalance, ...
OBJECTIVE: The aim of this study was to determine the frequency of cryoglobulinemia and associated s...
Background: Thalassemia remains to be the procured hemoglobinopathy due to the quantitative defect i...
PubMed ID: 10771839Serum IgG, IgM, IgA, IgG subclasses (IgG1, G2, G3, G4), isohemagglutinins and com...
Background: Beta-thalassemia major is one of the major health problems in our country. Many studies ...
Objective: Thalassemia is a common disease in many countries, in which several complications such as...
Background; Thalassemia is one of the most prevalent genetic disorders in world , and infections are...
Objective: Thalassemia is a common disease in many countries, in which several complications such a...
Plasma levels of ILr3 and IL-7 were studied in 23 patients with homozygous beta-thalassemia in order...
Background: Thalassemia and abnormal hemoglobin are the most common genetic disorders and are consid...
Abnormalities in the immune system and zi nc homeostasis in patients with P-thalassemia major (TM) h...
Thalassemia is a term that refers to a group of genetic disorders characterized by a de...
Abstract Introduction: Thalassemia is the most common hereditary anemia in Iran. The aim of this stu...
We evaluated phagocytic and lytic activities of peripheral blood monocytes (PBMo) from patients with...
everal immunological defects have been found in patients affected by b-tha-lassemia.1 They are mainl...
In the β-thalassemia's, oxidative stress, resulting from chronic hemolysis, globin chain imbalance, ...
OBJECTIVE: The aim of this study was to determine the frequency of cryoglobulinemia and associated s...
Background: Thalassemia remains to be the procured hemoglobinopathy due to the quantitative defect i...