WOS: 000242386100002PubMed ID: 16924653Cardiac complications are considered to be the primary cause of death in patients with 0 thalassaemia major. QT dispersion is a marker variability of ventricular repolarization and is elevated in various high risk groups of patients. This study was carried out in patients with beta thalassaemia major to evaluate QT dispersion and to investigate the relationship between QT dispersion and body iron load. Sixty-two beta thalassaemia major patients were enrolled into the study. The average serum ferritin levels and liver iron concentration was assessed. For each patient, QT-QTc intervals and QT-QTc dispersions were calculated and V1S and V5R were measured. All the subjects underwent two-dimensional M mode ...
Beta-thalassemias are a group of inherited, autosomal recessive diseases, characterized by reduced o...
Background. Patients with beta-thalassemia major present with severe anemia and need continuous tran...
Objective: Beta-thalassemia major (TM) is a genetic hemoglobin disorder causing chronic hemolytic an...
PubMed ID: 16924653Cardiac complications are considered to be the primary cause of death in patients...
Thalassemia major patients require repeated transfusions of packed cell and their lysis lead to iron...
Background: Despite recent progress in iron chelation therapy, sudden cardiac death due to malignant...
Thalassemia major is inherited disease, which affect hemoglobin sintesis resulting in chronic anemia...
Background: Cardiac complications are the primary cause of death in patients with b thalassemia majo...
Background Doppler echocardiographic studies in patients with β-Thalassemia Major (β-TM) had shown d...
Beta thalassemia major (TM) is a common hereditary disease in Indonesia. Iron overload due to regula...
Iron overload is associated with an increased risk of atrial and ventricular arrhythmias. Data regar...
Purpose: The most important complication encountered in patients with b-thalassaemia major is degene...
Background: Cardiac complications, heart failure, and arrhythmias remain as the major causes of deat...
Background: To evaluate the use of electrocardiography (ECG) in thalassemia major patients, for the ...
Cardiac complications are the leading cause of death in β-thalassemia major (TM) patients. The aim o...
Beta-thalassemias are a group of inherited, autosomal recessive diseases, characterized by reduced o...
Background. Patients with beta-thalassemia major present with severe anemia and need continuous tran...
Objective: Beta-thalassemia major (TM) is a genetic hemoglobin disorder causing chronic hemolytic an...
PubMed ID: 16924653Cardiac complications are considered to be the primary cause of death in patients...
Thalassemia major patients require repeated transfusions of packed cell and their lysis lead to iron...
Background: Despite recent progress in iron chelation therapy, sudden cardiac death due to malignant...
Thalassemia major is inherited disease, which affect hemoglobin sintesis resulting in chronic anemia...
Background: Cardiac complications are the primary cause of death in patients with b thalassemia majo...
Background Doppler echocardiographic studies in patients with β-Thalassemia Major (β-TM) had shown d...
Beta thalassemia major (TM) is a common hereditary disease in Indonesia. Iron overload due to regula...
Iron overload is associated with an increased risk of atrial and ventricular arrhythmias. Data regar...
Purpose: The most important complication encountered in patients with b-thalassaemia major is degene...
Background: Cardiac complications, heart failure, and arrhythmias remain as the major causes of deat...
Background: To evaluate the use of electrocardiography (ECG) in thalassemia major patients, for the ...
Cardiac complications are the leading cause of death in β-thalassemia major (TM) patients. The aim o...
Beta-thalassemias are a group of inherited, autosomal recessive diseases, characterized by reduced o...
Background. Patients with beta-thalassemia major present with severe anemia and need continuous tran...
Objective: Beta-thalassemia major (TM) is a genetic hemoglobin disorder causing chronic hemolytic an...