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Monasta L, Ronfani L, Marchetti F, Montico M, Brumatti LVecchi, Bavcar A, Grasso D, Barbiero C, Tamburlini G. Burden of disease caused by otitis media: systematic review and global estimates. PLoS One 2012;7(4):e36226.
C
Bulla R, Tripodo C, Rami D, Ling GSheng, Agostinis C, Guarnotta C, Zorzet S, Durigutto P, Botto M, Tedesco F. C1q acts in the tumour microenvironment as a cancer-promoting factor independently of complement activation. Nat Commun 2016;7:10346.
Bossi F, Tripodo C, Rizzi L, Bulla R, Agostinis C, Guarnotta C, Munaut C, Baldassarre G, Papa G, Zorzet S, Ghebrehiwet B, Ling GSheng, Botto M, Tedesco F. C1q as a unique player in angiogenesis with therapeutic implication in wound healing. Proc Natl Acad Sci U S A 2014;111(11):4209-14.
De Cunto A, Paviotti G, Ronfani L, Travan L, Bua J, Cont G, Demarini S. Can body mass index accurately predict adiposity in newborns?. Arch Dis Child Fetal Neonatal Ed 2014;99(3):F238-9.
Murina F, Graziottin A, Vicariotto F, De Seta F. Can Lactobacillus fermentum LF10 and Lactobacillus acidophilus LA02 in a slow-release vaginal product be useful for prevention of recurrent vulvovaginal candidiasis?: A clinical study. J Clin Gastroenterol 2014;48 Suppl 1:S102-5.
Zanotta N, Tornesello MLina, Annunziata C, Stellato G, Buonaguro FMaria, Comar M. Candidate Soluble Immune Mediators in Young Women with High-Risk Human Papillomavirus Infection: High Expression of Chemokines Promoting Angiogenesis and Cell Proliferation. PLoS One 2016;11(3):e0151851.
Abate MValentina, Stocco G, Devescovi R, Carrozzi M, Pierobon C, Valencic E, Lucafò M, Di Silvestre A, d'Adamo P, Tommasini A, Decorti G, Ventura A. Carbamazepine-induced thrombocytopenic purpura in a child: Insights from a genomic analysis. Blood Cells Mol Dis 2016;59:97-9.
Paviotti G, Todero S, Demarini S. Cardiac output decreases and systemic vascular resistance increases in newborns placed in the left-lateral position. J Perinatol 2017;37(5):563-565.
De Cunto A, Bensa M, Tonelli A. A case of familial hemiplegic migraine associated with a novel ATP1A2 gene mutation. Pediatr Neurol 2012;47(2):133-6.
Fabretto A, Shardlow A, Faletra F, Lepore L, Hladnik U, Gasparini P. A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation. Ophthalmic Genet 2010;31(2):98-100.
Quadrifoglio M, Faletra F, Bussani R, Pecile V, Zennaro F, Grasso A, Zandonà L, Alberico S, Stampalija T. A Case of Prenatal Neurocytoma Associated With ATR-16 Syndrome. J Ultrasound Med 2016;35(6):1359-61.
Tornese G, Marzuillo P, Pellegrin MChiara, Germani C, Faleschini E, Zennaro F, Grandone A, Del Giudice EMiraglia, Perrone L, Ventura A. A case of Rubinstein-Taybi syndrome associated with growth hormone deficiency in childhood. Clin Endocrinol (Oxf) 2015;83(3):437-9.

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