Farruggia P, Puccio G, Sala A, Todesco A, Buffardi S, Garaventa A, Bottigliero G, Bianchi M, Zecca M, Locatelli F, Pession A, Pillon M, Favre C, D'Amico S, Provenzi M, Trizzino A, Zanazzo GAndrea, Sau A, Santoro N, Murgia G, Casini T, Mascarin M, Burnelli R. The prognostic value of biological markers in paediatric Hodgkin lymphoma. Eur J Cancer 2016;52:33-40.

Faraci M, Zecca M, Pillon M, Rovelli A, Menconi MCristina, Ripaldi M, Fagioli F, Rabusin M, Ziino O, Lanino E, Locatelli F, Daikeler T, Prete A. Autoimmune hematological diseases after allogeneic hematopoietic stem cell transplantation in children: an Italian multicenter experience. Biol Blood Marrow Transplant 2014;20(2):272-8.

Conter V, Valsecchi MGrazia, Parasole R, Putti MCaterina, Locatelli F, Barisone E, Nigro LLo, Santoro N, Aricò M, Ziino O, Pession A, Testi AMaria, Micalizzi C, Casale F, Zecca M, Casazza G, Tamaro P, La Barba G, Notarangelo LDora, Silvestri D, Colombini A, Rizzari C, Biondi A, Masera G, Basso G. Childhood high-risk acute lymphoblastic leukemia in first remission: results after chemotherapy or transplant from the AIEOP ALL 2000 study. Blood 2014;123(10):1470-8.

Fagioli F, Zecca M, Rognoni C, Lanino E, Balduzzi A, Berger M, Messina C, Favre C, Rabusin M, Nigro LLo, Masetti R, Prete A, Locatelli F. Allogeneic hematopoietic stem cell transplantation for Philadelphia-positive acute lymphoblastic leukemia in children and adolescents: a retrospective multicenter study of the Italian Association of Pediatric Hematology and Oncology (AIEOP). Biol Blood Marrow Transplant 2012;18(6):852-60.

Rondelli R, Dini G, De Rosa M, Quarello P, Bisogno G, Aricò M, Vasconcelos C, Tamaro P, Casazza G, Zecca M, De Laurentis C, Porta F, Pession A. Foreign children with cancer in Italy. Ital J Pediatr 2011;37:44.

Noris P, Perrotta S, Seri M, Pecci A, Gnan C, Loffredo G, Pujol-Moix N, Zecca M, Scognamiglio F, De Rocco D, Punzo F, Melazzini F, Scianguetta S, Casale M, Marconi C, Pippucci T, Amendola G, Notarangelo LD, Klersy C, Civaschi E, Balduini CL, Savoia A. Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families. Blood 2011;117(24):6673-80.