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2018
Campisciano G, Cason C, Palmisano S, Giuricin M, Rizzardi A, Croce LSaveria, De Manzini N, Comar M. Bariatric surgery drives major rearrangements of the intestinal microbiota including the biofilm composition. Front Biosci (Elite Ed) 2018;10:495-505.
Invernizzi F, Zorzi G, Legati A, Coppola G, d'Adamo P, Nardocci N, Garavaglia B, Ghezzi D. Benign hereditary chorea and deletions outside NKX2-1: What's the role of MBIP?. Eur J Med Genet 2018;61(10):581-584.
Wiel LCortellazz, Pederiva F, Castagnetti M, Barbi E, Pennesi M. Boy with fish-mouth meatus. Arch Dis Child 2018;
Bellazzo A, Di Minin G, Valentino E, Sicari D, Torre D, Marchionni L, Serpi F, Stadler MB, Taverna D, Zuccolotto G, Montagner IMonia, Rosato A, Tonon F, Zennaro C, Agostinis C, Bulla R, Mano M, Del Sal G, Collavin L. Cell-autonomous and cell non-autonomous downregulation of tumor suppressor DAB2IP by microRNA-149-3p promotes aggressiveness of cancer cells. Cell Death Differ 2018;25(7):1224-1238.
Bonin S, Zanotta N, Sartori A, Bratina A, Manganotti P, Trevisan G, Comar M. Cerebrospinal Fluid Cytokine Expression Profile in Multiple Sclerosis and Chronic Inflammatory Demyelinating Polyneuropathy. Immunol Invest 2018;47(2):135-145.
Fichera A, Pagani G, Stagnati V, Cascella S, Faiola S, Gaini C, Lanna M, Pasquini L, Raffaelli R, Stampalija T, Tommasini A, Prefumo F. Cervical-length measurement in mid-gestation to predict spontaneous preterm birth in asymptomatic triplet pregnancy. Ultrasound Obstet Gynecol 2018;51(5):614-620.
Fontana L, Bedeschi MF, Maitz S, Cereda A, Faré C, Motta S, Seresini A, D'Ursi P, Orro A, Pecile V, Calvello M, Selicorni A, Lalatta F, Milani D, Sirchia SM, Miozzo M, Tabano S. Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders. Epigenetics 2018;13(9):897-909.
Fontana L, Bedeschi MF, Maitz S, Cereda A, Faré C, Motta S, Seresini A, D'Ursi P, Orro A, Pecile V, Calvello M, Selicorni A, Lalatta F, Milani D, Sirchia SM, Miozzo M, Tabano S. Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders. Epigenetics 2018;13(9):897-909.
Tamaro G, Pederiva F, Dibello D, Gregori M, Carbone M, Pantaleoni F, Dentici MLisa, Niceta M, Barbi E. A Child with Diminished Linear Growth and Waddling Gait. J Pediatr 2018;201:297-297.e1.
S Sopo M, Romano A, Bersani G, Fantacci C, Badina L, Longo G, Monti G, Viola S, Tripodi S, Barilaro G, Iacono ID, Caffarelli C, Mastrorilli C, Barni S, Mori F, Liotti L, Cuomo B, Franceschini F, Viggiano D, Monaco S. Cooking influence in tolerance acquisition in egg-induced acute food protein enterocolitis syndrome. Allergol Immunopathol (Madr) 2018;
S Sopo M, Romano A, Bersani G, Fantacci C, Badina L, Longo G, Monti G, Viola S, Tripodi S, Barilaro G, Iacono ID, Caffarelli C, Mastrorilli C, Barni S, Mori F, Liotti L, Cuomo B, Franceschini F, Viggiano D, Monaco S. Cooking influence in tolerance acquisition in egg-induced acute food protein enterocolitis syndrome. Allergol Immunopathol (Madr) 2018;
Fetoni ARita, Zorzi V, Paciello F, Ziraldo G, Peres C, Raspa M, Scavizzi F, Salvatore AMaria, Crispino G, Tognola G, Gentile G, Spampinato AGianmaria, Cuccaro D, Guarnaccia M, Morello G, Van Camp G, Fransen E, Brumat M, Girotto G, Paludetti G, Gasparini P, Cavallaro S, Mammano F. Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway. Redox Biol 2018;19:301-317.

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