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C
Krauss BS, Calligaris L, Green SM, Barbi E. Current concepts in management of pain in children in the emergency department. Lancet 2016;387(10013):83-92.
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.
Llop S, Tran V, Ballester F, Barbone F, Sofianou-Katsoulis A, Sunyer J, Engström K, Alhamdow A, Love TM, Watson GE, Bustamante M, Murcia M, Iñiguez C, Shamlaye CF, Rosolen V, Mariuz M, Horvat M, Tratnik JS, Mazej D, van Wijngaarden E, Davidson PW, Myers GJ, Rand MD, Broberg K. CYP3A genes and the association between prenatal methylmercury exposure and neurodevelopment. Environ Int 2017;105:34-42.
Zanotta N, Campisciano G, Scrimin F, Blendi U, Marcuzzi A, Vincenti E, Crovella S, Comar M. Cytokine profiles of women with vulvodynia: Identification of a panel of pro-inflammatory molecular targets. Eur J Obstet Gynecol Reprod Biol 2018;226:66-70.
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Wolfler A, Calderoni E, Ottonello G, Conti G, Baroncini S, Santuz P, Vitale P, Salvo I. Daily practice of mechanical ventilation in Italian pediatric intensive care units: a prospective survey. Pediatr Crit Care Med 2011;12(2):141-6.
Zauli G, Voltan R, Bosco R, Melloni E, Marmiroli S, Rigolin GMatteo, Cuneo A, Secchiero P. Dasatinib plus Nutlin-3 shows synergistic antileukemic activity in both p53 wild-type and p53 mutated B chronic lymphocytic leukemias by inhibiting the Akt pathway. Clin Cancer Res 2011;17(4):762-70.
da Silva RCelerino, Tavares Nde Alencar, Moura R, Coelho A, Guimarães RLima, Araújo J, Crovella S, Brandão LAndré Cav, Silva Jde Azevêd. DC-SIGN polymorphisms are associated to type 1 diabetes mellitus. Immunobiology 2014;219(11):859-65.
Fabretto A, Rocca MSanta, Perrone MDolores, Skabar A, Pecile V, Gasparini P. De novo 6.9 Mb interstitial deletion on chromosome 4q31.1-q32.1 in a girl with severe speech delay and dysmorphic features. Am J Med Genet A 2012;158A(4):882-7.
Perrone MD, Rocca MS, Bruno I, Faletra F, Pecile V, Gasparini P. De novo 911 Kb interstitial deletion on chromosome 1q43 in a boy with mental retardation and short stature. Eur J Med Genet 2012;55(2):117-9.
Bonaglia MClara, Kurtas NEdibe, Errichiello E, Bertuzzo S, Beri S, Mehrjouy MM, Provenzano A, Vergani D, Pecile V, Novara F, Reho P, Di Giacomo MCarmela, Discepoli G, Giorda R, Aldred MA, Santos-Rebouças CBarros, Goncalves APereira, Abuelo DN, Giglio S, Ricca I, Franchi F, Patsalis P, Sismani C, Morí MAngeles, Nevado J, Tommerup N, Zuffardi O. De novo unbalanced translocations have a complex history/aetiology. Hum Genet 2018;137(10):817-829.
Taddio A, Rosé C, Lepore L, Ventura A. Dealing with abdominal pain in children affected by systemic lupus erythematosus. Semin Arthritis Rheum 2012;41(4):e3-4.
Bibalo C, Longo G, Ventura A. Decline in Lung Function in Childhood Asthma. N Engl J Med 2016;375(7):e13.

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