[HTML][HTML] Cardiovascular magnetic resonance native T2 and T2* quantitative values for cardiomyopathies and heart transplantations: a systematic review and meta …

GJH Snel, M van den Boomen, LM Hernandez… - Journal of …, 2020 - Elsevier
Background The clinical application of cardiovascular magnetic resonance (CMR) T 2 and T
2* mapping is currently limited as ranges for healthy and cardiac diseases are poorly …

[HTML][HTML] Early detection of cardiac involvement in thalassemia: From bench to bedside perspective

N Koonrungsesomboon, SC Chattipakorn… - World journal of …, 2013 - ncbi.nlm.nih.gov
Myocardial siderosis is known as the major cause of death in thalassemia major (TM)
patients since it can lead to iron overload cardiomyopathy. Although this condition can be …

[PDF][PDF] Health-related quality of life, depression, anxiety, and self-image in acute lymphocytic leukemia survivors

B Baytan, Ç Aşut, AÇ Kantarcıoğlu… - Turkish Journal of …, 2016 - jag.journalagent.com
Objective: With increasing survival rates in childhood acute lymphocytic leukemia (ALL), the
long-term side effects of treatment have become important. Our aim was to investigate health …

[HTML][HTML] The association between serum ferritin level, tissue Doppler echocardiography, cardiac T2* MRI, and heart rate recovery in patients with beta thalassemia …

IO Yuksel, E Koklu, E Kurtoglu, S Arslan… - Acta Cardiologica …, 2016 - ncbi.nlm.nih.gov
Background It is generally well-understood that iron-mediated cardiomyopathy is the major
complication that can arise from beta thalassemia major (TM). Therefore, early diagnosis …

[PDF][PDF] Optimal method for early detection of cardiac disorders in thalassemia major patients: magnetic resonance imaging or echocardiography?

F Moussavi, MA Ghasabeh, S Roodpeyma… - Blood …, 2014 - synapse.koreamed.org
Background Heart failure resulting from myocardial iron deposition is the most important
cause of death in β-thalassemia major (TM) patients. Cardiac T2* magnetic resonance …

Diagnosis and treatment of cardiac iron overload in transfusion-dependent thalassemia patients

N Siri-Angkul, SC Chattipakorn… - Expert review of …, 2018 - Taylor & Francis
Introduction: Thalassemia is among the most common genetic diseases. Patients with
severe forms of the disease are transfusion-dependent, leading to iron overload. A condition …

Myocardial and liver iron overload, assessed using T2* magnetic resonance imaging with an excel spreadsheet for post processing in Tunisian thalassemia major …

M Ouederni, M Ben Khaled, F Mellouli, E Ben Fraj… - Annals of …, 2017 - Springer
Thalassemia is a common genetic disorder in Tunisia. Early iron concentration assessment
is a crucial and challenging issue. Most of annual deaths due to iron overload occurred in …

Insulin-like growth factor-I and factors affecting it in thalassemia major

AT Soliman, V De Sanctis, R Elalaily… - Indian Journal of …, 2015 - journals.lww.com
Despite improvement of blood transfusion regimens and iron chelation therapy growth and
maturational delay, cardiomyopathy, endocrinopathies and osteoporosis still occur in good …

Effective method of evaluating myocardial iron concentration in pediatric patients with thalassemia major

A Khaled, DA Ezzat, HA Salem, HM Seif… - Journal of Blood …, 2019 - Taylor & Francis
Background The use of T2* magnetic resonance imaging (MRI) has been promoted by
recent studies as a noninvasive method for the detection of iron overload in thalassemia …

Assessment of cardiac parameters in evaluation of cardiac functions in patients with thalassemia major

K Oztarhan, Y Delibas, Z Salcioglu, G Kaya… - Pediatric hematology …, 2012 - Taylor & Francis
The aim of the study was to evaluate cardiac function and early cardiac dysfunction of
patients followed as thalassemia major. In this study, the authors compared 100 patients …