Publication
Magnitude of cumulative iron overload correlates with the severity of anemia in untreated non-transfusion-dependent β-thalassemia
Musallam, Khaled M., Maria Domenica Cappellini, Shahina Daar, Amal El-Beshlawy and Ali T. Taher. 2023. Magnitude of cumulative iron overload...
Publication
Morbidity-free survival and hemoglobin level in non-transfusion-dependent β-thalassemia: a 10-year cohort study
Musallam, Khaled M., Maria Domenica Cappellini, Shahina Daar, Ali T. Taher. 2022. Morbidity-free survival and hemoglobin level in non-transf...
Publication
Survival and causes of death in 2,033 patients with non-transfusion-dependent β-thalassemia
Musallam, Khaled M., Angela Vitrano, Antonella Meloni, Walter Addario Pollina, Mehran Karimi, Amal El-Beshlawy, Mahmoud Hajipour, Vito Di Ma...
Publication
Risk of mortality from anemia and iron overload in nontransfusion‐dependent β‐thalassemia
Musallam, Khaled M., Angela Vitrano, Antonella Meloni, Sebastiano Addario Pollina, Mehran Karimi, Amal El‐Beshlawy, Mahmoud Hajipour, Vito D...
Publication
Random Forest Clustering Identifies Three Subgroups of β-Thalassemia with Distinct Clinical Severity
Vitrano, Angela, Khaled M. Musallam, Antonella Meloni., Sebastiano Addario Pollina, Mehran Karimi , Amal El-Beshlawy, Mahmoud Hajipour, Vito...
Project
Psychosocial evaluation of patients with beta thalassemia major in Oman
Homozygous Beta thalassaemia is a lifelong condition requiring regular blood transfusions from infancy.
Publication
A concise review on the frequency, major risk factors and surveillance of hepatocellular carcinoma (hcc) in β-thalassemias: past, present and future perspectives
De Sanctis, Vincenzo, Ashraf T. Soliman, Shahina Daar, Niveen Alansary, Antonis Kattamis, Myrto Skafida, Maria Concetta Galati, Soteroula Ch...
Project
Developing an International Prognostic Scoring System for Thalassemia: A New Tool for Revisiting Classification of Thalassemia
Β-thalassemia is classified into three phenotypes, depending on the severity of symptoms: 1) thalassemia major (TM); 2) thalassemia Intermedia (TI); 3) β trait or thalassemia minor (Tm).
Project
The use of shear wave elastography in patients with homozygous beta thalassemia
Patients with homozygous beta thalassemia have complex clinical complications due to the need for blood transfusions and iron overload.