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Titolo Data di pubblicazione Autori File
Defective and excessive immunities in pediatric diseases 1-gen-2012 Tommasini A +
Patient-centred screening for primary immunodeficiency, a multi-stage diagnostic protocol designed for non-immunologists: 2011 update 1-gen-2012 Tommasini A +
Phylloid pattern of hypomelanosis closely related to chromosomal abnormalities in the 13q detected by SNP array analysis 1-gen-2012 Faletra, FlavioTommasini, A.Cleva, L.Gasparini, P. +
Clinical impact of MEFV mutations in children with periodic fever in a prevalent western European Caucasian population 1-gen-2012 Tommasini A +
Immunomodulatory drugs in autoimmune lymphoproliferative syndrome (ALPS) 1-gen-2012 Tommasini A +
The MDM2 inhibitor Nutlin-3 modulates dendritic cell-induced T cell proliferation 1-gen-2012 Tommasini A +
A common genetic background could explain early-onset Crohn's disease. 1-gen-2012 GIRARDELLI, MARTINAA. TommasiniMARCUZZI, ANNALISACROVELLA, SERGIO +
Evolutionary hypothesis of the Mevalonate Kinase Deficiency. 1-gen-2013 VUCH, JOSEFMARCUZZI, ANNALISATommasini ACROVELLA, SERGIO +
Clinical Genetic Testing of Periodic Fever Syndromes 1-gen-2013 MARCUZZI, ANNALISAPISCIANZ, ELISACROVELLA, SERGIOTOMMASINI, ALBERTO +
Human IL2RA null mutation mediates immunodeficiency with lymphoproliferation and autoimmunity 1-gen-2013 Tommasini A +
Difetto di mevalonato-chinasi: molte facce di una stessa malattia 1-gen-2013 Taddio, AndreaBarbi, EgidioLepore, LoredanaTommasini, AlbertoVentura, Alessandro +
Selective IgA deficiency: ruling out coeliac disease and selective antibody deficiency to polysaccharides 1-gen-2013 Tommasini A +
TNF-α SNP rs1800629 and risk of relapse in childhood acute lymphoblastic leukemia: relation to immunophenotype 1-gen-2014 FRANCA, RAFFAELLAATHANASAKIS, EMMANOUILAlberto TommasiniDECORTI, GIULIANA +
Severe inflammatory bowel disease associated with congenital alteration of transforming growth factor beta signaling. 1-gen-2014 NAVIGLIO, SAMUELEMARTELOSSI, STEFANOTOMMASINI, ALBERTOLOGANES, CLAUDIAFABRETTO, ANTONELLAVENTURA, ALESSANDRO +
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome. 1-gen-2014 TAMARO, PAOLOTommasini A +
Fate of Lymphocytes after Withdrawal of Tofacitinib Treatment 1-gen-2014 PISCIANZ, ELISACUZZONI, EVADECORTI, GIULIANATOMMASINI, ALBERTO +
"Hyper-IgD syndrome" or "mevalonate kinase deficiency": an old syndrome needing a new name? 1-gen-2014 CELSI, FulvioTOMMASINI, ALBERTOCROVELLA, SERGIO
F402L variant in NLRP12 in subjects with undiagnosed periodic fevers and in healthy controls 1-gen-2014 VUCH, JOSEFATHANASAKIS, EMMANOUILSEVERINI, GIOVANNI MARIACROVELLA, SERGIOBIANCO, ANNA MONICA ROSARIATOMMASINI, ALBERTO +
Novel Missense Mutation in the NOD2 Gene in a Patient with Early Onset Ulcerative Colitis: Causal or Chance Association? 1-gen-2014 GIRARDELLI, MARTINAVUCH, JOSEFA. TommasiniCROVELLA, SERGIO +
Clinical significance of hyper-IgA in a paediatric laboratory series 1-gen-2014 PASTORE, SERENATADDIO, ANDREAVENTURA, ALESSANDROTOMMASINI, ALBERTO +
Mostrati risultati da 101 a 120 di 246
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