A. Massa

发表

Fully Automated Regional Analysis of Myocardial T2* Values for Iron Quantification Using Deep Learning

Filippo Cademartiri, N. Martini, V. Positano, 2022, Electronics.

Quantitative T2* MRI for bone marrow iron overload: normal reference values and assessment in thalassemia major patients

Filippo Cademartiri, V. Positano, A. Meloni, 2022, La radiologia medica.

Frequency, pattern, and associations of renal iron accumulation in sickle/β-thalassemia patients

Filippo Cademartiri, V. Positano, A. Meloni, 2022, Annals of Hematology.

Italian patients with hemoglobinopathies exhibit a 5‐fold increase in age‐standardized lethality due to SARS‐CoV‐2 infection

S. Perrotta, M. Cappellini, L. De Franceschi, 2021, American journal of hematology.

Thalassaemia is paradoxically associated with a reduced risk of in‐hospital complications and mortality in COVID‐19: Data from an international registry

M. Cappellini, L. De Franceschi, I. Akin, 2022, Journal of cellular and molecular medicine.

Patients with myelodysplastic syndromes show reduced frequencies of CD4+ CD8+ double‐positive T cells

P. Virdis, C. Fozza, M. Longinotti, 2012, European journal of haematology.

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

V. Positano, A. Meloni, M. Putti, 2024, International journal of cardiology.

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

V. Positano, A. Meloni, M. Putti, 2024, The international journal of cardiovascular imaging.

Oxidative Stress and Antioxidant Status in Adult Patients with Transfusion-Dependent Thalassemia: Correlation with Demographic, Laboratory, and Clinical Biomarkers

A. Meloni, C. Vassalle, M. Putti, 2024, Antioxidants.