PReS-FINAL-2338: Fate of lymphocytes after withdrawal of Tofacitinib treatment

por Tommasini, A, Piscianz, E, Valencic, E, Cuzzoni, E, Decorti, G, Taddio, A
Publicado 2013

Clinical evaluation of seven tumour markers in lung cancer diagnosis: can any combination improve the results?

por Plebani, M., Basso, D., Navaglia, F., De Paoli, M., Tommasini, A., Cipriani, A.
Publicado 1995

Pulmonary arterial hypertension in interferonophaties: a case report and a review of the literature

por Trombetta, A., Ghirardo, S., Pastore, S., Tesser, A., Piscianz, E., Tommasini, A., Bobbo, M., Taddio, A.
Publicado 2019

Elective bone marrow transplantation in a child with X-linked hyper-IgM syndrome presenting with acute respiratory distress syndrome

por Leone, V, Tommasini, A, Andolina, M, Runti, G, De Vonderweid, U, Campello, C, Notarangelo, LD, Ventura, A
Publicado 2002

PReS-FINAL-2196: The clinical significance of the Q703K mutation of NLRP3 gene. A multicentric national study

por Naselli, A, Cantarini, L, Insalaco, A, Alessio, M, Tommasini, A, Gallizzi, R, Signa, S, Lucherini, OM, Caroli, F, Ceccherini, I, Martini, A, Gattorno, M
Publicado 2013

Combined Analysis of Methylation and Gene Expression Profiles in Separate Compartments of Small Bowel Mucosa Identified Celiac Disease Patients’ Signatures

por Cielo, D., Galatola, M., Fernandez-Jimenez, N., De Leo, L., Garcia-Etxebarria, K., Loganes, C., Tommasini, A., Not, T., Auricchio, R., Greco, L., Bilbao, J. R.
Publicado 2019

Evidences for the need of new Diagnostic Criteria for PFAPA syndrome

por Caorsi, R, Meini, A, Sormani, MP, Cattalini, M, Pelagatti, MA, Zulian, F, Cortis, E, Calcagno, G, Tommasini, A, Traverso, F, Federici, S, Frenkel, J, Plebani, S, Martini, A, Gattorno, M
Publicado 2008

PReS-FINAL-2232: Long-term follow-up in a national cohort of MKD patients: search for clinical predictors of a spontaneous improvement

por Doglio, M, Federici, S, Tommasini, A, Meini, A, Cattalini, M, Obici, L, Cantarini, L, Zulian, F, Breda, L, Consolini, R, Corona, F, Insalaco, A, Rigante, D, Martini, A, Gattorno, M
Publicado 2013

Long-Term Clinical Profile of Children With the Low-Penetrance R92Q Mutation of the TNFRSF1A Gene

por Pelagatti, M A, Meini, A, Caorsi, R, Cattalini, M, Federici, S, Zulian, F, Calcagno, G, Tommasini, A, Bossi, G, Sormani, M P, Caroli, F, Plebani, A, Ceccherini, I, Martini, A, Gattorno, M
Publicado 2011

A Next Generation Sequencing approach to the mutational screening of patients affected with systemic autoinflammatory disorders: diagnosis improvement and interpretation of complex...

por Rusmini, M, Federici, S, Caroli, F, Grossi, A, Baldi, M, Obici, L, Insalaco, A, Tommasini, A, Caorsi, R, Gallo, E, Olivieri, AN, Marzano, AV, Coviello, D, Ravazzolo, R, Martini, A, Gattorno, M, Ceccherini, I
Publicado 2015