Introduction: β-thalassemia major due to ineffective erythrocyte life span leads to severe anemiarequiring regular transfusion, which it can lead to major organs damage. Renal damage can beattributed to chronic anemia, iron over load and or defferoxamin toxicity. The object of this study wasto analyze renal tubular and glomerular function in pediatric patients with beta-thalassemia major.Materials and Methods: 39 patients with β -thalassemia major whose mean ages were 11.8 yr and22 sex and age matched healthy children as control group were studied. Blood rine samplesand uwereobtained for measuring biochemical markers. Urinary N-Acetyl-β.D.glucosaminidase (NAG) andurine NAG to creatine ratio (U Cr /NAGratio) were measuredResults: No signific...
WOS: 000173955100005PubMed ID: 11863122Background: Patients with sickle cell anemia have various for...
Background: Limited data are available about renal involvement in thalassemia patients. Renal dysfun...
Increased survival in patients with \u3b2 thalassaemia major (TM) allowed for several morbidities to...
34th Annual Meeting of the European-Paediatric-Nephrology-Congress -- JUN 18-20, 2000 -- HELSINKI, F...
PubMedID: 11095025In patients with ß-thalassemia major, the most important cause of mortality and mo...
BACKGROUND: Although there are many available data about renal involvement in patients with beta tha...
Thalassemia syndromes are the most prevalent hereditary hemoglobinopathy in the world. Reduction or ...
BACKGROUND: Thalassemia is a disorder of inherited blood and inticated by the abnormal hemoglobin. T...
ResearchRenal functions in pediatric patients with beta-thalassemia major: relation to chelation the...
AbstractBackgroundLimited data are available about renal involvement in thalassemia patients. Renal ...
Background & objective: β-Thalassemia minor is an asymptomatic hereditary disease. The first study o...
Abstract- To find if some indices have predictive value for renal complications. We conducted a cros...
Background: Although there are many available data about renal involvement in patients with beta tha...
Background: Thalassemia is the commonest hemoglobinopathy in Southeast Asia. Kidney dysfunction is a...
Copyright: © 2014 Gokce M, et al. This is an open-access article distributed under the terms of the...
WOS: 000173955100005PubMed ID: 11863122Background: Patients with sickle cell anemia have various for...
Background: Limited data are available about renal involvement in thalassemia patients. Renal dysfun...
Increased survival in patients with \u3b2 thalassaemia major (TM) allowed for several morbidities to...
34th Annual Meeting of the European-Paediatric-Nephrology-Congress -- JUN 18-20, 2000 -- HELSINKI, F...
PubMedID: 11095025In patients with ß-thalassemia major, the most important cause of mortality and mo...
BACKGROUND: Although there are many available data about renal involvement in patients with beta tha...
Thalassemia syndromes are the most prevalent hereditary hemoglobinopathy in the world. Reduction or ...
BACKGROUND: Thalassemia is a disorder of inherited blood and inticated by the abnormal hemoglobin. T...
ResearchRenal functions in pediatric patients with beta-thalassemia major: relation to chelation the...
AbstractBackgroundLimited data are available about renal involvement in thalassemia patients. Renal ...
Background & objective: β-Thalassemia minor is an asymptomatic hereditary disease. The first study o...
Abstract- To find if some indices have predictive value for renal complications. We conducted a cros...
Background: Although there are many available data about renal involvement in patients with beta tha...
Background: Thalassemia is the commonest hemoglobinopathy in Southeast Asia. Kidney dysfunction is a...
Copyright: © 2014 Gokce M, et al. This is an open-access article distributed under the terms of the...
WOS: 000173955100005PubMed ID: 11863122Background: Patients with sickle cell anemia have various for...
Background: Limited data are available about renal involvement in thalassemia patients. Renal dysfun...
Increased survival in patients with \u3b2 thalassaemia major (TM) allowed for several morbidities to...