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European Heart Journal. Cardiovascular Imaging|February 16, 2017
Prediction of cardiac complications for thalassemia major in the widespread cardiac magnetic resonance era: a prospective multicentre study by a multi-parametric approachAlessia Pepe, Antonella Meloni, Giuseppe Rossi, et al.
Circulation. Cardiovascular Imaging|August 9, 2015
Multiparametric Cardiac Magnetic Resonance Survey in Children With Thalassemia Major: A Multicenter StudyMaddalena Casale, Antonella Meloni, Aldo Filosa, et al.
Blood Cells, Molecules & Diseases|January 23, 2013
Serial echocardiographic left ventricular ejection fraction measurements: a tool for detecting thalassemia major patients at risk of cardiac deathAurelio Maggio, Angela Vitrano, Giuseppina Calvaruso, et al.
Hemoglobin|February 16, 2008
Standardized T2* map of a normal human heart to correct T2* segmental artefacts; myocardial iron overload and fibrosis in thalassemia intermedia versus thalassemia major patients and electrocardiogram changes in thalassemia major patientsAnna Ramazzotti, Alessia Pepe, Vincenzo Positano, et al.
British Journal of Haematology|November 20, 2020
A complication risk score to evaluate clinical severity of thalassaemia syndromesAngela Vitrano, Antonella Meloni, Walter Addario Pollina, et al.
Orphanet Journal of Rare Diseases|June 1, 2019
Current challenges in the management of patients with sickle cell disease - A report of the Italian experienceGiovanna Russo, Lucia De Franceschi, Raffaella Colombatti, et al.
Cancer|November 2, 2022
Incidence of cancer and related deaths in hemoglobinopathies: A follow-up of 4631 patients between 1970 and 2021Raffaella Origa, Barbara Gianesin, Filomena Longo, et al.
Scientific Reports|November 23, 2019
Genetic disorder prenatal diagnosis and pregnancy termination practices among high consanguinity population, Saudi ArabiaSayed AbdulAzeez, Nourah H Al Qahtani, Noor B Almandil, et al.
Medicina (Kaunas, Lithuania)|February 24, 2024
<i>RP1</i> Dominant p.Ser740* Pathogenic Variant in 20 Knowingly Unrelated Families Affected by Rod-Cone Dystrophy: Potential Founder Effect in Western SicilyFabiana D'Esposito, Viviana Randazzo, Maria Igea Vega, et al.
British Journal of Haematology|February 25, 2009
Long-term sequential deferiprone-deferoxamine versus deferiprone alone for thalassaemia major patients: a randomized clinical trialAurelio Maggio, Angela Vitrano, Marcello Capra, et al.
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