Export 916 results:
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2016
Crevatin F, Cozzi G, Braido E, Bertossa G, Rizzitelli P, Lionetti D, Matassi D, Calusa D, Ronfani L, Barbi E. Hand-held computers can help to distract children undergoing painful venipuncture procedures. Acta Paediatr 2016;105(8):930-4.
Wolfler A, Osello R, Gualino J, Calderini E, Vigna G, Santuz P, Amigoni A, Savron F, Caramelli F, Rossetti E, Cecchetti C, Corbari M, Piastra M, Testa R, Coffaro G, Stancanelli G, Gitto E, Amato R, Prinelli F, Salvo I. The Importance of Mortality Risk Assessment: Validation of the Pediatric Index of Mortality 3 Score. Pediatr Crit Care Med 2016;17(3):251-6.
Molini E, Cristi MC, Lapenna R, Calzolaro L, Muzzi E, Ciciriello E, A Volpe D, Orzan E, Ricci G. Improving regional universal newborn hearing screening programmes in Italy. Acta Otorhinolaryngol Ital 2016;36(1):10-4.
Morassutto C, Monasta L, Ricci G, Barbone F, Ronfani L. Incidence and Estimated Prevalence of Endometriosis and Adenomyosis in Northeast Italy: A Data Linkage Study. PLoS One 2016;11(4):e0154227.
Morassutto C, Monasta L, Ricci G, Barbone F, Ronfani L. Incidence and Estimated Prevalence of Endometriosis and Adenomyosis in Northeast Italy: A Data Linkage Study. PLoS One 2016;11(4):e0154227.
Di Sabatino A, Giuffrida P, Fornasa G, Salvatore C, Vanoli A, Naviglio S, De Leo L, Pasini A, De Amici M, Alvisi C, Not T, Rescigno M, Corazza GRoberto. Innate and adaptive immunity in self-reported nonceliac gluten sensitivity versus celiac disease. Dig Liver Dis 2016;48(7):745-52.
Rocca MS, Pecile V, Cleva L, Speltra E, Selice R, Di Mambro A, Foresta C, Ferlin A. The Klinefelter syndrome is associated with high recurrence of copy number variations on the X chromosome with a potential role in the clinical phenotype. Andrology 2016;4(2):328-34.
Rabach I, Salis S, Bruno I, Ventura A. Macrocephaly and palmoplantar pitting. Arch Dis Child 2016;
Russo S, Calzari L, Mussa A, Mainini E, Cassina M, Di Candia S, Clementi M, Guzzetti S, Tabano S, Miozzo M, Sirchia S, Finelli P, Prontera P, Maitz S, Sorge G, Calcagno A, Maghnie M, Divizia MTeresa, Melis D, Manfredini E, Ferrero GBattista, Pecile V, Larizza L. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes. Clin Epigenetics 2016;8:23.
Pirastu N, Kooyman M, Robino A, van der Spek A, Navarini L, Amin N, Karssen LC, van Duijn CM, Gasparini P. Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption. Sci Rep 2016;6:31590.
Kostevsek N, Locatelli E, Garrovo C, Arena F, Monaco I, Nikolov IPetrov, Sturm S, Rozman KZuzek, Lorusso V, Giustetto P, Bardini P, Biffi S, Franchini MComes. The one-step synthesis and surface functionalization of dumbbell-like gold-iron oxide nanoparticles: a chitosan-based nanotheranostic system. Chem Commun (Camb) 2016;52(2):378-81.
Pascolo L, Bedolla DE, Vaccari L, Venturin I, Cammisuli F, Gianoncelli A, Mitri E, Giolo E, Luppi S, Martinelli M, Zweyer M, Ricci G. Pitfalls and promises in FTIR spectromicroscopy analyses to monitor iron-mediated DNA damage in sperm. Reprod Toxicol 2016;61:39-46.

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