[HTML][HTML] Non-vitamin K antagonist oral anticoagulants in patients with β-thalassemia

M Malagu, F Longo, F Marchini, P Sirugo, A Capanni… - Biology, 2023 - mdpi.com
Simple Summary β-thalassemia is an inherited disorder characterized by the absent or
reduced production of the β-chains of the hemoglobin. The natural history of the disease is …

Left atrial strain in patients with β-thalassemia major: a cross-sectional CMR study

A Meloni, L Saba, V Positano, L Pistoia, M Porcu… - European …, 2024 - Springer
Objectives The aim of this cross-sectional study was to investigate the association of left
atrial (LA) strain parameters with demographics, clinical data, cardiovascular magnetic …

[HTML][HTML] Predicting Thalassemia Using Feature Selection Techniques: A Comparative Analysis

M Saleem, W Aslam, MIU Lali, HT Rauf, EA Nasr - Diagnostics, 2023 - mdpi.com
Thalassemia represents one of the most common genetic disorders worldwide,
characterized by defects in hemoglobin synthesis. The affected individuals suffer from …

Left and right atrioventricular coupling index in patients with beta-thalassemia major

A Meloni, L Saba, V Positano, L Pistoia… - … International Journal of …, 2024 - Springer
The aim of this cross-sectional study was to investigate the relationship of left atrioventricular
coupling index (LACI) and right atrioventricular coupling index (RACI) with demographics …

Global longitudinal strain by cardiac magnetic resonance is associated with cardiac iron and complications in beta-thalassemia major patients

A Meloni, L Saba, V Positano, L Pistoia… - International Journal of …, 2024 - Elsevier
Background The aim of this cross-sectional study was to investigate the association of left
ventricular (LV) strain parameters with demographics, clinical data, cardiovascular magnetic …

HSCT in Patients with Hemoglobinopathies

T Rostami, A Kiumarsi, M Mohseni - Cardiovascular Considerations in …, 2024 - Springer
Hemoglobinopathies, are a group of monogenic inherited disorders that affect the structure
or production of the globin chains. Improvements in red blood cell transfusion management …

[HTML][HTML] The Exploring of Growth Differentiation Factor-15 and H63D Gene Polymorphisms in β-thalassemia Major: Implications for Cardiovascular Risk and Iron …

HY Hamza, AG Al-Ziaydi… - Journal of Applied …, 2024 - journals.lww.com
BACKGROUND: β-thalassemia major (βTM) is a genetic disorder characterized by a
deficiency in hemoglobin production, ineffective erythropoiesis, chronic hemolysis, lifelong …

Anemias por hemoglobinopatías: Hallazgos clínicos, epidemiológicos y de laboratorio.

EJA Pino, EAD Ayala, KNP Rodríguez… - … Científica Higía de la …, 2023 - revistas.itsup.edu.ec
Las hemoglobinopatías son enfermedades genéticas que afectan la producción o estructura
de la hemoglobina, la proteína que transporta el oxígeno en los glóbulos rojos. Las …

Towards thalassemia detection using optoelectronic measurements assisted with machine-learning algorithms: a non-invasive, pain-free and blood-free approach …

B Nair, C Mysorekar, R Srivastava… - 2024 IEEE Applied …, 2024 - ieeexplore.ieee.org
In recent years, the convergence of electronic technology and machine learning has
revolutionized healthcare sector which is poised to transform the field of clinical diagnostics …

Anemia Heart Disease in a Patient with Suspected Non-Transfusion Dependent Thalassemia, a Case Report

AA Gunawan, RF Effendy - Eduvest-Journal of Universal …, 2024 - eduvest.greenvest.co.id
Case Report. A female, 22 years old, came to the emergency room at Waikabubak General
Hospital with complaints of weakness and pallor that had worsened since 1 week ago …