TOMMASINI, ALBERTO

TOMMASINI, ALBERTO  

Dipartimento Universitario Clinico di Scienze mediche, chirurgiche e della salute  

Docenti di ruolo di IIa fascia  

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Titolo Data di pubblicazione Autori File
"Hyper-IgD syndrome" or "mevalonate kinase deficiency": an old syndrome needing a new name? 1-gen-2014 CELSI, FulvioTOMMASINI, ALBERTOCROVELLA, SERGIO
A "SURFin' Leukemia": Acute Lymphoblastic Leukemia Masquerading as a Syndrome of Undifferentiated Recurrent Fever 1-gen-2023 De Nardi, LauraD'Agostin, MartinaNaviglio, SamueleTrombetta, AndreaDe Martino, EleonoraTommasini, AlbertoRabusin, Marco
A case of familial neurosensorial impairment with vasculitis: a new phenotype of CIAS1pathies? 1-gen-2008 De Cunto ATornese GGortani GTommasini A. +
A Case of Uveitis in a Patient with Juvenile Myelomonocytic Leukemia Successfully Treated with Adalimumab 1-gen-2020 Cortellazzo Wiel L.Pastore S.Taddio A.Tommasini A.
A common genetic background could explain early-onset Crohn's disease. 1-gen-2012 GIRARDELLI, MARTINAA. TommasiniMARCUZZI, ANNALISACROVELLA, SERGIO +
A diagnostic score for molecular analysis of hereditary autoinflammatory syndromes with periodic fever in children. 1-gen-2008 A. Tommasini +
A Next Generation Sequencing approach to the mutational screening of patients affected with systemic autoinflammatory disorders: Diagnosis improvement and interpretation of complex clinical phenotypes 1-gen-2015 Tommasini A. +
A Novel ELISA-Based Peptide Biosensor Assay for Screening ABL1 Activity in vitro: A Challenge for Precision Therapy in BCR-ABL1 and BCR-ABL1 Like Leukemias 1-gen-2021 Montecchini O.Braidotti S.Franca R.Zudeh G.Rabusin M.Tommasini A.Decorti G.Stocco G. +
A reliable screening procedure for coeliac disease in clinical practice. 1-gen-2002 VENTURA, ALESSANDROA. TommasiniCROVELLA, SERGIOSBLATTERO, DANIELEMARZARI, ROBERTONOT, TARCISIO +
A toddler with an unusually severe polyarticular arthritis and a lung involvement: a case report 1-gen-2022 Gortani, GiuliaTaddio, AndreaPastore, SerenaCorona, FedericaTesser, AlessandraBarbi, EgidioTommasini, Alberto +
A very rare cause of pre-capillary pulmonary hypertension: The PAMI syndrome 1-gen-2023 Savonitto, GiulioTommasini, AlbertoPin, AlessiaSinagra, GianfrancoStolfo, Davide +
A zonulin-occludens toxin synthetic esapeptide modifies the intestinal permeabilità in in-vivo animal model 1-gen-2005 NOT, TARCISIOTommasini ASBLATTERO, DANIELEMARZARI, ROBERTOVENTURA, ALESSANDRO +
Action of methotrexate and tofacitinib on directly stimulated and bystander-activated lymphocytes 1-gen-2016 PISCIANZ, ELISACANDILERA, VANESSALOGANES, CLAUDIADECORTI, GIULIANATommasini, Alberto +
Activated phosphoinositde 3-kinase (PI3Kδ) syndrome: an Italian point of view on diagnosis and new advances in treatment 1-gen-2024 Tommasini, AlbertoBadolato, Raffaele +
Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity 1-gen-2023 Chinello, MatteoKondratenko, IrinaTommasini, Alberto +
Acute rheumatic fever prophylaxis in high-income countries: clinical observations from an Italian multicentre, retrospective study 1-gen-2020 Taddio, AndreaPillon, RobertoPastore, SerenaTommasini, AlbertoMascheroni, ElisabettaVentura, Alessandro +
ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: A multicentre national study 1-gen-2017 Tommasini A. +
Ages of celiac disease: from changing environment to improved diagnostics 1-gen-2011 TOMMASINI, ALBERTONOT, TARCISIOVENTURA, ALESSANDRO
Alterations in zonulin secretion accompany the increase in permeability in BB/Wor rats 1-gen-2000 NOT, TARCISIOTommasini A +
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 1-gen-2015 FALETRA, FLAVIOVOZZI, DiegoMARCUZZI, ANNALISAVALENCIC, ERICAPISCIANZ, ELISABIANCO, ANNA MONICA ROSARIAGIRARDELLI, MARTINALOGANES, CLAUDIATOMMASINI, ALBERTO +