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2010
Floridia M, Tamburrini E, Anzidei G, Tibaldi C, Muggiasca ML, Guaraldi G, Fiscon M, Vimercati A, Martinelli P, Donisi A, Dalzero S, Ravizza M. Declining HCV seroprevalence in pregnant women with HIV. Epidemiol Infect 2010;138(9):1317-21.
Floridia M, Tamburrini E, Anzidei G, Tibaldi C, Muggiasca ML, Guaraldi G, Fiscon M, Vimercati A, Martinelli P, Donisi A, Dalzero S, Ravizza M. Declining HCV seroprevalence in pregnant women with HIV. Epidemiol Infect 2010;138(9):1317-21.
Pecci A, Gresele P, Klersy C, Savoia A, Noris P, Fierro T, Bozzi V, Mezzasoma AMaria, Melazzini F, Balduini CL. Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations. Blood 2010;116(26):5832-7.
Brancaccio M, Pivetta C, Granzotto M, Filippis C, Mallamaci A. Emx2 and Foxg1 inhibit gliogenesis and promote neuronogenesis. Stem Cells 2010;28(7):1206-18.
Ruperto N, Ozen S, Pistorio A, Dolezalova P, Brogan P, Cabral DA, Cuttica R, Khubchandani R, Lovell DJ, O'Neil KM, Quartier P, Ravelli A, Iusan SM, Filocamo G, Magalhães CSaad, Unsal E, Oliveira S, Bracaglia C, Bagga A, Stanevicha V, Manzoni SMagni, Pratsidou P, Lepore L, Espada G, Kone-Paut I, Paut IKone, Zulian F, Barone P, Bircan Z, Maldonado Mdel Rocio, Russo R, Vilca I, Tullus K, Cimaz R, Horneff G, Anton J, Garay S, Nielsen S, Barbano G, Martini A. EULAR/PRINTO/PRES criteria for Henoch-Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part I: Overall methodology and clinical characterisation. Ann Rheum Dis 2010;69(5):790-7.
Campanini G, Piralla A, Rovida F, Puzelli S, Facchini M, Locatelli F, Minoli L, Percivalle E, Donatelli I, Baldanti F. First case in Italy of acquired resistance to oseltamivir in an immunocompromised patient with influenza A/H1N1v infection. J Clin Virol 2010;48(3):220-2.
Zadro C, Ciorba A, Fabris A, Morgutti M, Trevisi P, Gasparini P, Martini A. Five new OTOF gene mutations and auditory neuropathy. Int J Pediatr Otorhinolaryngol 2010;74(5):494-8.
Vettore S, De Rocco D, Gerber B, Scandellari R, Bianco AMonica, Balduini CL, Pecci A, Fabris F, Savoia A. A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defect. Eur J Med Genet 2010;53(5):256-60.
Bua J, Marchetti F, Faleschini E, Ventura A, Bussani R. Hepatic glycogenosis in an adolescent with diabetes. J Pediatr 2010;157(6):1042.
Segat L, Catamo E, Fabris A, Morgutti M, D'Agaro P, Campello C, Crovella S. HLA-G*0105N allele is associated with augmented risk for HIV infection in white female patients. AIDS 2010;24(12):1961-4.
de Mendonça VGuimarães, Guimarães MJosé Beze, Filho JLuiz de Li, de Mendonça CGuimarães, Martins DBruneska G, Crovella S, de Alencar LCláudio A. [Human papillomavirus cervical infection: viral genotyping and risk factors for high-grade squamous intraepithelial lesion and cervix cancer]. Rev Bras Ginecol Obstet 2010;32(10):476-85.
Castagnola E, Rossi MR, Cesaro S, Livadiotti S, Giacchino M, Zanazzo G, Fioredda F, Beretta C, Ciocchello F, Carli M, Putti MCaterina, Pansini V, Berger M, Licciardello M, Farina S, Caviglia I, Haupt R. Incidence of bacteremias and invasive mycoses in children with acute non-lymphoblastic leukemia: results from a multi-center Italian study. Pediatr Blood Cancer 2010;55(6):1103-7.

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