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2012
Ammenti A, Cataldi L, Chimenz R, Fanos V, La Manna A, Marra G, Materassi M, Pecile P, Pennesi M, Pisanello L, Sica F, Toffolo A, Montini G. Febrile urinary tract infections in young children: recommendations for the diagnosis, treatment and follow-up. Acta Paediatr 2012;101(5):451-7.
Di Lorenzo G, Ceccarello M, Cecotti V, Ronfani L, Monasta L, L Brumatti V, Montico M, D'Ottavio G. First trimester maternal serum PIGF, free β-hCG, PAPP-A, PP-13, uterine artery Doppler and maternal history for the prediction of preeclampsia. Placenta 2012;33(6):495-501.
Miorin L, Albornoz A, Baba MM, D'Agaro P, Marcello A. Formation of membrane-defined compartments by tick-borne encephalitis virus contributes to the early delay in interferon signaling. Virus Res 2012;163(2):660-6.
da Silva MFPTBald, Guimarães V, Silva MAR, Amaral CMMedeiros, Beçak W, Stocco RC, Freitas AC, Crovella S. Frequency of human papillomavirus types 16, 18, 31, and 33 and sites of cervical lesions in gynecological patients from Recife, Brazil. Genet Mol Res 2012;11(1):462-6.
Taddio A, Biondi A, Piscianz E, Valencic E, Biagi E, Badolato R. From bone marrow transplantation to cellular therapies: possible therapeutic strategies in managing autoimmune disorders. Curr Pharm Des 2012;18(35):5776-81.
Sandrin-Garcia P, Brandão LAC, Guimarães RL, Pancoto JAT, Donadi EA, de Lima-Filho JL, Segat L, Crovella S. Functional single-nucleotide polymorphisms in the DEFB1 gene are associated with systemic lupus erythematosus in Southern Brazilians. Lupus 2012;21(6):625-31.
2011
Marcuzzi A, De Leo L, Decorti G, Crovella S, Tommasini A, Pontillo A. The farnesyltransferase inhibitors tipifarnib and lonafarnib inhibit cytokines secretion in a cellular model of mevalonate kinase deficiency. Pediatr Res 2011;70(1):78-82.
Bosco R, Melloni E, Celeghini C, Rimondi E, Vaccarezza M, Zauli G. Fine tuning of protein kinase C (PKC) isoforms in cancer: shortening the distance from the laboratory to the bedside. Mini Rev Med Chem 2011;11(3):185-99.
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.
Passerini L, Olek S, Di Nunzio S, Barzaghi F, Hambleton S, Abinun M, Tommasini A, Vignola S, Cipolli M, Amendola M, Naldini L, Guidi L, Cecconi M, Roncarolo MG, Bacchetta R. Forkhead box protein 3 (FOXP3) mutations lead to increased TH17 cell numbers and regulatory T-cell instability. J Allergy Clin Immunol 2011;128(6):1376-1379.e1.
Castro-Antunes MMaria, Crovella S, Brandão LAndré Cav, Guimarães RLima, Motta MEugênia F, da Silva GAlves Pont. Frequency distribution of HLA DQ2 and DQ8 in celiac patients and first-degree relatives in Recife, northeastern Brazil. Clinics (Sao Paulo) 2011;66(2):227-31.

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