Thalassemia major (TM) patients have altered ventricular volumes and ejection fraction compared to normals, although evidence for these findings stem from restricted patient groups and has never been reproduced. We sought to evaluate cardiac parameters by cardiovascular magnetic resonance (CMR) in a group of young TM patients not covered by previous studies that are more representative of the TM population in many countries. Seventy patients including 40 TM with normal myocardial iron concentrations, and 30 age- and gender-matched normal (NL) volunteers underwent a CMR study for assessment of left and right ventricle volumes and function using a 1.5-T scanner. Left and right ventricle ejection fraction, indexed systolic and diastolic volume...
Beta thalassemia major (β-TM) displays a great deal of phenotypic heterogeneity, not fully investiga...
Cardiac complications are the leading cause of death in β-thalassemia major (TM) patients. The aim o...
Background and objective: One of the chief causes of death in patients with beta-thalassemia major (...
Thalassemia major (TM) patients have altered ventricular volumes and ejection fraction compared to n...
Objectives. To evaluate a population of asymptomatic thalassemia major (TM) and t...
Abstract Aim We aimed to define reference ranges for right ventricular (RV) volumes, ejection fracti...
AIM: We aimed to define reference ranges for right ventricular (RV) volumes, ejection fraction (EF) ...
PubMed ID: 21647857PURPOSE: Cardiac involvement in thalassemia major (TM) is mainly characterized by...
Background Thalassemia major (TM) is a transfusion-depen- dent disease. Multiple transfusions cause ...
WOS: 000297602100009PubMed ID: 21647857PURPOSE Cardiac involvement in thalassemia major (TM) is main...
Patients with chronic anemia develop compensatory ventricular dilation, even when maintained on chro...
Background: Cardiac MRI plays a critical role in the management of thalassemic patients. No accurate...
ObjectivesWe sought to evaluate whether echocardiographic diastolic function indices correlate with ...
Background- Cardiac involvement which leads to congestive heart failure (CHF) is a major cause of de...
Aims Cardiovascular magnetic resonance (CMR) has dramatically changed the clinical practice in thala...
Beta thalassemia major (β-TM) displays a great deal of phenotypic heterogeneity, not fully investiga...
Cardiac complications are the leading cause of death in β-thalassemia major (TM) patients. The aim o...
Background and objective: One of the chief causes of death in patients with beta-thalassemia major (...
Thalassemia major (TM) patients have altered ventricular volumes and ejection fraction compared to n...
Objectives. To evaluate a population of asymptomatic thalassemia major (TM) and t...
Abstract Aim We aimed to define reference ranges for right ventricular (RV) volumes, ejection fracti...
AIM: We aimed to define reference ranges for right ventricular (RV) volumes, ejection fraction (EF) ...
PubMed ID: 21647857PURPOSE: Cardiac involvement in thalassemia major (TM) is mainly characterized by...
Background Thalassemia major (TM) is a transfusion-depen- dent disease. Multiple transfusions cause ...
WOS: 000297602100009PubMed ID: 21647857PURPOSE Cardiac involvement in thalassemia major (TM) is main...
Patients with chronic anemia develop compensatory ventricular dilation, even when maintained on chro...
Background: Cardiac MRI plays a critical role in the management of thalassemic patients. No accurate...
ObjectivesWe sought to evaluate whether echocardiographic diastolic function indices correlate with ...
Background- Cardiac involvement which leads to congestive heart failure (CHF) is a major cause of de...
Aims Cardiovascular magnetic resonance (CMR) has dramatically changed the clinical practice in thala...
Beta thalassemia major (β-TM) displays a great deal of phenotypic heterogeneity, not fully investiga...
Cardiac complications are the leading cause of death in β-thalassemia major (TM) patients. The aim o...
Background and objective: One of the chief causes of death in patients with beta-thalassemia major (...