Hematological manifestations of antiphospholipid syndrome: going beyond thrombosis

G El Hasbani, AN Saliba, I Uthman, AT Taher - Blood Reviews, 2023 - Elsevier
Thrombotic complications are a hallmark of antiphospholipid syndrome (APS). These
vascular–arterial, venous, and/or small vessel–complications are well described and known …

Clinical Complications and Their Management

R Bou-Fakhredin, I Motta… - Hematology …, 2023 - hemonc.theclinics.com
Thalassemia syndromes are complex systemic disorders. Clinical complications are related
to the underlying pathophysiological mechanisms, namely ineffective erythropoiesis, chronic …

Evidence for the Metabolic Activation of Deferasirox In Vitro and In Vivo

M Su, Y Zhao, M Li, C Jia, H Liu, Y Zhang… - Chemical Research …, 2023 - ACS Publications
Deferasirox (DFS) is used for the treatment of iron accumulation caused by the need for long-
term blood transfusions, such as thalassemia or other rare anemia. Liver injury due to …

[HTML][HTML] Metagenomic next-generation sequencing of bronchoalveolar lavage fluid assists in the diagnosis of pathogens associated with lower respiratory tract …

Y Xu, Y Jiang, Y Wang, F Meng, W Qin… - Frontiers in Cellular and …, 2023 - ncbi.nlm.nih.gov
Worldwide, lower respiratory tract infections (LRTI) are an important cause of hospitalization
in children. Due to the relative limitations of traditional pathogen detection methods, new …

[HTML][HTML] Application of the magnetic resonance 3D multiecho Dixon sequence for quantifying hepatic iron overload and steatosis in patients with thalassemia

F Zhao, Y Chen, T Zhou, C Tang, J Huang… - Magnetic Resonance …, 2024 - Elsevier
Objective To investigate the feasibility and diagnostic efficacy of a 3D multiecho Dixon
(qDixon) research application for simultaneously quantifying the liver iron concentration …

Ascertaining Genetics of β—Thalassemia and Sickle Cell Disease Using Machine Learning Heuristics

P Aswathi, SR Anjana, S Kumar, G Singh, S Kapoor… - 2024 - preprints.org
Hemoglobinopathies are a group of disorders in which the hemoglobin molecule has
abnormal production or structure. The hemoglobin molecules in red blood cells (RBC) are …

Global Trends on β-thalassemia Research over 10 Years: A Bibliometric Analysis

M Chen, W Wang, L Xu, H Huang - 2023 - researchsquare.com
Methods In this study, a bibliometric analysis will be conducted of thalassemia articles
published in the Web of Science Core Collection database between 2013 and 2023 to …

[PDF][PDF] Ascertaining Genetics of Beta-Thalassemia and Sickle Cell Disease using Molecular Techniques and Machine Learning Heuristics

P Aswathi, SR Anjana, R Somesh Kumar… - researchgate.net
A collection of blood illnesses affecting red blood cells are called hemoglobinopathies.
Hemoglobin, a protein found in blood cells, transports oxygen throughout the body and …