G. Calvaruso

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Long‐term use of deferiprone significantly enhances left‐ventricular ejection function in thalassemia major patients

P. Cianciulli, L. Cuccia, G. D'Ascola, 2012, American journal of hematology.

Long-term treatment with deferiprone enhances left ventricular ejection function when compared to deferoxamine in patients with thalassemia major.

P. Cianciulli, R. Barone, L. Cuccia, 2013, Blood cells, molecules & diseases.

Assessment of the frequency of additional cancers in patients with splenic marginal zone lymphoma

E. Iannitto, V. Callea, C. Tripodo, 2006, European journal of haematology.

Antimicrobial prophylaxis in patients with immune thrombocytopenia treated with rituximab: a retrospective multicenter analysis

U. Consoli, M. Napolitano, S. Raso, 2021, Annals of Hematology.

Cerebrovascular events in sickle cell‐beta thalassemia treated with hydroxyurea: A single center prospective survey in adult Italians

M. Steinberg, A. Maggio, A. Pecoraro, 2013, American journal of hematology.

Glutathione S transferase polymorphisms influence on iron overload in β-thalassemia patients

A. Maggio, S. Sclafani, V. Agrigento, 2013 .

Coheredity of a new silent mutation: c.‐29G>T, with a severe β‐thal mutation in a patient with β‐thalassemia intermediate

A. Maggio, A. Giambona, C. Passarello, 2018, International journal of laboratory hematology.

Phenotypic evaluations of HBB:c.93-23T>C, a nucleotide substitution in the IVS I nt 108 of β-globin gene

A. Maggio, A. Giambona, C. Passarello, 2017, Journal of Clinical Pathology.

HBB: c.316-125A>G and HBB: c.316-42delC: Phenotypic Evaluations of Two Rare Changes in the Second Intron of the HBB Gene

A. Maggio, A. Giambona, C. Passarello, 2017, Hemoglobin.

Chronic Administration of Hydroxyurea (HU) Benefits Caucasian Patients with Sickle-Beta Thalassemia

J. Tisdale, M. Hsieh, A. Maggio, 2018, International journal of molecular sciences.

Role of iron metabolism genetic determinants in response to chelation therapy in a cohort of β-thalassemia and sickle cell syndromes Italian patients

A. Maggio, D. Renda, G. Calvaruso, 2014 .

Co‐heredity of silent CAP + 1570 T>C (HBB:c*96T>C) defect and severe β‐thal mutation: a cause of mild β‐thalassemia intermedia

A. Maggio, R. Di Maggio, A. Giambona, 2016, International journal of laboratory hematology.

Second-line administration of thrombopoietin receptor agonists in immune thrombocytopenia: Italian Delphi-based consensus recommendations

F. Buccisano, E. Baldacci, F. Chiurazzi, 2021, Therapeutic advances in hematology.

Influence of genetic polymorphisms and mutations in the cardiac pathology of iron overload in thalassemia and sickle cell anemia patients: a retrospective study

A. Maggio, S. Sclafani, V. Agrigento, 2012 .

A Patient with Sickle Cell Disease and Recurrent Venous Thromboembolism after Renal Transplantation

S. Raso, L. Pitrolo, A. Maggio, 2022, Thalassemia Reports.

Co-inheritance of HBB:c.−106G > C, a rare single nucleotide variation at position −56 relative to transcription initiation site, with other known mutations in the globin clusters

A. Maggio, E. Ferro, A. Giambona, 2018, Hematology.

Hepatitis B virus reactivation and alemtuzumab therapy

E. Iannitto, A. Craxì, V. Abbadessa, 2005, European journal of haematology.

The era of comparable life expectancy between thalassaemia major and intermedia: Is it time to revisit the major‐intermedia dichotomy?

L. Cuccia, V. Caruso, A. Filosa, 2017, British journal of haematology.

Real‐life experience with liver iron concentration R2 MRI measurement in patients with hemoglobinopathies: baseline data from LICNET

B. Giorgi, G. Abbate, V. Caruso, 2016, European journal of haematology.

Nonsense-mediated decay mechanism is a possible modifying factor of clinical outcome in nonsense cd39 beta thalassemia genotype

M. Attanasio, A. Maggio, A. Giambona, 2012 .

Splenic marginal zone lymphoma with or without villous lymphocytes

E. Iannitto, C. Tripodo, F. Menestrina, 2004, Cancer.

Long-lasting remission of primary hepatic lymphoma and hepatitis C virus infection achieved by the alpha-interferon treatment.

E. Iannitto, C. Tripodo, A. Florena, 2004, The hematology journal : the official journal of the European Haematology Association.

Deoxycoformycin (pentostatin) in the treatment of splenic marginal zone lymphoma (SMZL) with or without villous lymphocytes

E. Iannitto, C. Tripodo, A. Florena, 2005, European journal of haematology.

The First Case of Haemophagocytic Lymphohistiocytosis Triggered by the Booster Dose of Anti-SARS-CoV-2 Vaccine in a Patient with β-Thalassemia

F. Dieli, M. Gentile, S. Raso, 2022, Thalassemia Reports.

Deferiprone versus deferoxamine in thalassemia intermedia: Results from a 5‐year long‐term Italian multicenter randomized clinical trial

L. Pitrolo, A. Maggio, R. Di Maggio, 2015, American journal of hematology.

Longitudinal changes in LIC and other parameters in patients receiving different chelation regimens: Data from LICNET

D. Fiorino, A. Filosa, L. Pitrolo, 2018, European journal of haematology.

Response-guided ABVD chemotherapy plus involved-field radiation therapy for intermediate-stage Hodgkin lymphoma in the pre-positron emission tomography era: a Gruppo Italiano Studio Linfomi (GISL) prospective trial.

F. Angrilli, P. Gobbi, E. Iannitto, 2009, Clinical lymphoma & myeloma.

Serial echocardiographic left ventricular ejection fraction measurements: a tool for detecting thalassemia major patients at risk of cardiac death.

N. Chattipakorn, A. Phrommintikul, P. Cianciulli, 2013, Blood cells, molecules & diseases.

Mesenchymal Fetal Stem Cells (FMSC) from Amniotic Fluid (AF): Expansion and Phenotypic Characterization

R. Maggio, A. Maggio, M. Sacco, 2015 .

New Codanin-1 Gene Mutations in a Italian Patient with Congenital Dyserythropoietic Anemia Type I and Heterozygous Beta-Thalassemia

R. Barone, L. Pitrolo, A. Maggio, 2016, Indian Journal of Hematology and Blood Transfusion.

Successful treatment of steroid resistant autoimmune thrombocytopenia associated with chronic lymphocytic leukemia with alemtuzumab

E. Iannitto, E. Ammatuna, C. Marino, 2004, European journal of haematology.

AIsolated Aspergillosis of Biliary Tract in a Patient with Both Solid Organ Transplantation and Haematological Malignancy? A Case Report

A. Rizzo, R. Maggio, A. Maggio, 2021 .