Aldo Filosa

Ospedale Antonio Cardarelli — Italy

Medicine · Health Sciences

30h-index2.7kcitations144works0.02yr avg
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Research Topics

Hemoglobinopathies and Related Disorders(125), Iron Metabolism and Disorders(77), Blood groups and transfusion(18), Pharmacological Effects and Toxicity Studies(12), Myeloproliferative Neoplasms: Diagnosis and Treatment(11)

Publications143 total

Development of a Thalassemia International Prognostic Scoring System (TIPSS)
Blood Cells Molecules and Diseases·2022· 8 cited
Luspatercept for the treatment of anaemia in non-transfusion-dependent β-thalassaemia (BEYOND): a phase 2, randomised, double-blind, multicentre, placebo-controlled trial
The Lancet Haematology·2022· 54 cited
The use of hydroxyurea in the real life of MIOT network: an observational study
Expert Opinion on Drug Safety·2022· 3 cited
Transfusional Approach in Multi-Ethnic Sickle Cell Patients: Real-World Practice Data From a Multicenter Survey in Italy
Frontiers in Medicine·2022· 6 citedOpen Access
Random Forest Clustering Identifies Three Subgroups of β-Thalassemia with Distinct Clinical Severity
Thalassemia Reports·2022· 3 citedOpen Access
National networking in rare diseases and reduction of cardiac burden in thalassemia major
European Heart Journal·2021· 53 cited
Risk of mortality from anemia and iron overload in nontransfusion‐dependent β‐thalassemia
American Journal of Hematology·2021· 33 citedOpen Access
Italian patients with hemoglobinopathies exhibit a 5‐fold increase in age‐standardized lethality due to SARS‐CoV‐2 infection
American Journal of Hematology·2021· 16 citedOpen Access
Primary <i>HBB</i> gene mutation severity and long‐term outcomes in a global cohort of β‐thalassaemia
British Journal of Haematology·2021· 14 citedOpen Access
A case of ischemic colitis in a patient with non transfusion dependent thalassemia (NTDT) infected by SARS-COV-2
Pediatric Hematology and Oncology·2021
Survival and causes of death in 2,033 patients with non-transfusion-dependent β-thalassemia
Haematologica·2021· 45 citedOpen Access
Hepatocellular carcinoma in patients with thalassemia in the post-DAA era: not a disappearing entity
Annals of Hematology·2021· 10 cited
Retinal and Choriocapillaris Vascular Changes in Patients Affected by Different Clinical Phenotypes of β-Thalassemia: An Optical Coherence Tomography Angiography Study
Biology·2021· 9 citedOpen Access
A complication risk score to evaluate clinical severity of thalassaemia syndromes
British Journal of Haematology·2020· 11 citedOpen Access
Three Distinct Groups of Phenotype Severity in Beta-Thalassemia
Blood·2020
Evaluation of the efficacy and safety of deferiprone compared with deferasirox in paediatric patients with transfusion-dependent haemoglobinopathies (DEEP-2): a multicentre, randomised, open-label, non-inferiority, phase 3 trial
The Lancet Haematology·2020· 68 cited
Longitudinal follow‐up of patients with thalassaemia intermedia who started transfusion therapy in adulthood: a cohort study
British Journal of Haematology·2020· 24 citedOpen Access
Red blood cell consumption in a large cohort of patients with thalassaemia: a retrospective analysis of main predictors
Annals of Hematology·2020· 3 cited
Myocardial iron is strongly associated with reproductive function in beta-thalassemic women under chelation therapy
Clinical and Experimental Obstetrics & Gynecology·2020Open Access
Prospective CMR Survey in Children With Thalassemia Major
JACC. Cardiovascular imaging·2020· 7 cited
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Frequent Co-authors

Aurelio Maggio(22), Alessia Pepe(20), Liana Cuccia(15), Antonella Meloni(13), Paolo Ricchi(13), Paolo Cianciulli(12), Vincenzo Caruso(12), Domenico Giuseppe D’Ascola(12), Angela Vitrano(12), Saveria Campisi(11), Anna Spasiano(11), Luciano Prossomariti(11), Lorella Pitrolo(10), Marcello Capra(10), Vincenzo Positano(9), Francesco Gagliardotto(8), Calogera Gerardi(8), Paolo Rigano(8), Maria Caterina Putti(7), Massimo Midiri(7)