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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.
Bucci S, Umari P, Rizzo M, Pavan N, Liguori G, Barbone F, Trombetta C. Emergency extracorporeal shockwave lithotripsy as opposed to delayed shockwave lithotripsy for the treatment of acute renal colic due to obstructive ureteral stone: a prospective randomized trial. Minerva Urol Nefrol 2018;70(5):526-533.
Ciciriello E, Bolzonello P, Marchi R, Falzone C, Muzzi E, Orzan E. Empowering the family during the first months after identification of permanent hearing impairment in children. Acta Otorhinolaryngol Ital 2016;36(1):64-70.
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.
Ferlin A, Selice R, Angelini S, Di Grazia M, Caretta N, Cavalieri F, Di Mambro A, Foresta C. Endocrine and psychological aspects of sexual dysfunction in Klinefelter patients. Andrology 2018;6(3):414-419.
Pennesi M, L'erario I, Barbi E. Endoscopic treatment of primary vesicoureteral reflux. N Engl J Med 2012;367(1):88; author reply 89.
Tisato V, Zauli G, Voltan R, Gianesini S, di Iasio MGrazia, Volpi I, Fiorentini G, Zamboni P, Secchiero P. Endothelial cells obtained from patients affected by chronic venous disease exhibit a pro-inflammatory phenotype. PLoS One 2012;7(6):e39543.
Paviotti G, Fadini GPaolo, Boscaro E, Agostini C, Avogaro A, Chiandetti L, Baraldi E, Filippone M. Endothelial progenitor cells, bronchopulmonary dysplasia and other short-term outcomes of extremely preterm birth. Early Hum Dev 2011;87(7):461-5.
Biolo G, Secchiero P, De Giorgi S, Tisato V, Zauli G. The energy balance positively regulates the levels of circulating TNF-related apoptosis inducing ligand in humans. Clin Nutr 2012;31(6):1018-21.
Xue Y, Mezzavilla M, Haber M, McCarthy S, Chen Y, Narasimhan V, Gilly A, Ayub Q, Colonna V, Southam L, Finan C, Massaia A, Chheda H, Palta P, Ritchie G, Asimit J, Dedoussis G, Gasparini P, Palotie A, Ripatti S, Soranzo N, Toniolo D, Wilson JF, Durbin R, Tyler-Smith C, Zeggini E. Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations. Nat Commun 2017;8:15927.
Byrne S, Jansen L, U-King-Im J-M, Siddiqui A, Lidov HGW, Bodi I, Smith L, Mein R, Cullup T, Dionisi-Vici C, Al-Gazali L, Al-Owain M, Bruwer Z, Thihli KAl, El-Garhy R, Flanigan KM, Manickam K, Zmuda E, Banks W, Gershoni-Baruch R, Mandel H, Dagan E, Raas-Rothschild A, Barash H, Filloux F, Creel D, Harris M, Hamosh A, Kölker S, Ebrahimi-Fakhari D, Hoffmann GF, Manchester D, Boyer PJ, Manzur AY, Lourenco CMarques, Pilz DT, Kamath A, Prabhakar P, Rao VK, R Rogers C, Ryan MM, Brown NJ, McLean CA, Said E, Schara U, Stein A, Sewry C, Travan L, Wijburg FA, Zenker M, Mohammed S, Fanto M, Gautel M, Jungbluth H. EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy. Brain 2016;139(Pt 3):765-81.
D'Agaro P, Dal Molin G, Gallo T, Rossi T, Santon D, Busetti M, Comar M, Campello C. Epidemiological and molecular assessment of a measles outbreak in a highly vaccinated population of northeast Italy. Epidemiol Infect 2011;139(11):1727-33.

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