Da Lozzo P, Magnolato A, Del Rizzo I, Sirchia F, Bruno I, Barbi E. When Long-Lasting Food Selectivity Leads to an Unusual Genetic Diagnosis: A Case Report. J Adolesc Health 2019;64(1):137-138.

Fucile C, Mattioli F, Marini V, Gregori M, Sonzogni A, Martelli A, Maximova N. What is known about deferasirox chelation therapy in pediatric HSCT recipients: two case reports of metabolic acidosis. Ther Clin Risk Manag 2018;14:1649-1655.

Bacci A, Hodorogea S, Khachatryan H, Babojonova S, Irsa S, Jansone M, Dondiuc I, Matarazde G, Lazdane G, Lazzerini M. What is the quality of the maternal near-miss case reviews in WHO European Region? Cross-sectional study in Armenia, Georgia, Latvia, Republic of Moldova and Uzbekistan. BMJ Open 2018;8(4):e017696.

Littooij AS, Kwee TC, Enríquez G, Verbeke JIML, Granata C, Beishuizen A, de Lange C, Zennaro F, Bruin MCA, Nievelstein RAJ. Whole-body MRI reveals high incidence of osteonecrosis in children treated for Hodgkin lymphoma. Br J Haematol 2017;176(4):637-642.

Tachmazidou I, Süveges D, Min JL, Ritchie GRS, Steinberg J, Walter K, Iotchkova V, Schwartzentruber J, Huang J, Memari Y, McCarthy S, Crawford AA, Bombieri C, Cocca M, Farmaki A-E, Gaunt TR, Jousilahti P, Kooijman MN, Lehne B, Malerba G, Männistö S, Matchan A, Medina-Gomez C, Metrustry SJ, Nag A, Ntalla I, Paternoster L, Rayner NW, Sala C, Scott WR, Shihab HA, Southam L, St Pourcain B, Traglia M, Trajanoska K, Zaza G, Zhang W, Artigas MS, Bansal N, Benn M, Chen Z, Danecek P, Lin W-Y, Locke A, Luan J'an, Manning AK, Mulas A, Sidore C, Tybjaerg-Hansen A, Varbo A, Zoledziewska M, Finan C, Hatzikotoulas K, Hendricks AE, Kemp JP, Moayyeri A, Panoutsopoulou K, Szpak M, Wilson SG, Boehnke M, Cucca F, Di Angelantonio E, Langenberg C, Lindgren C, McCarthy MI, Morris AP, Nordestgaard BG, Scott RA, Tobin MD, Wareham NJ, Burton P, Chambers JC, Smith GDavey, Dedoussis G, Felix JF, Franco OH, Gambaro G, Gasparini P, Hammond CJ, Hofman A, Jaddoe VWV, Kleber M, Kooner JS, Perola M, Relton C, Ring SM, Rivadeneira F, Salomaa V, Spector TD, Stegle O, Toniolo D, Uitterlinden AG, Barroso I, Greenwood CMT, Perry JRB, Walker BR, Butterworth AS, Xue Y, Durbin R, Small KS, Soranzo N, Timpson NJ, Zeggini E. Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. Am J Hum Genet 2017;100(6):865-884.

Amigoni A, Mondardini MCristina, Vittadello I, Zaglia F, Rossetti E, Vitale F, Ferrario S, Savron F, Coffaro G, Brugnaro L, Amato R, Wolfler A, Franck LS. Withdrawal Assessment Tool-1 Monitoring in PICU: A Multicenter Study on Iatrogenic Withdrawal Syndrome. Pediatr Crit Care Med 2017;18(2):e86-e91.

Guida E, Di Grazia M, Cattaruzzi E, Bussani R, Rigamonti W, Lembo MAntonietta. When a lymphatic malformation determines a bowel volvulus: Are clinical status and images always reliable?. Int J Surg Case Rep 2016;25:192-5.

Frausin S, Viventi S, Falzacappa LVerga, Quattromani MJlenia, Leanza G, Tommasini A, Valencic E. Wharton's jelly derived mesenchymal stromal cells: Biological properties, induction of neuronal phenotype and current applications in neurodegeneration research. Acta Histochem 2015;117(4-5):329-38.

Travan L, Rocca MSanta, Buonomo F, Cleva L, Pecile V, De Cunto A. When Feeding Difficulties Are due to Genetics: The Case of Familial Partial 9q Duplication. J Investig Med High Impact Case Rep 2015;3(1):2324709615574949.

De Cunto A, Paviotti G, Demarini S. When does postnatal catch-up fat occur in late preterm infants?. Acta Paediatr 2014;103(8):e325.

Bava M, Bradashia F, Rovere F, Maestro A, Brumatti LVecchi, Accardo A, Paparazzo R, Zanon D. A web-based system for total parenteral nutrition prescription in a pediatric hospital - biomed 2010. Biomed Sci Instrum 2010;46:351-6.

Castiello U, Becchio C, Zoia S, Nelini C, Sartori L, Blason L, D'Ottavio G, Bulgheroni M, Gallese V. Wired to be social: the ontogeny of human interaction. PLoS One 2010;5(10):e13199.