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2015
Schreiber S, Zanchi C, Ronfani L, Delise A, Corbelli A, Bortoluzzi R, Taddio A, Barbi E. Normal saline flushes performed once daily maintain peripheral intravenous catheter patency: a randomised controlled trial. Arch Dis Child 2015;100(7):700-3.
Schreiber S, Zanchi C, Ronfani L, Delise A, Corbelli A, Bortoluzzi R, Taddio A, Barbi E. Normal saline flushes performed once daily maintain peripheral intravenous catheter patency: a randomised controlled trial. Arch Dis Child 2015;100(7):700-3.
Marzuillo P, Rabach I, Barbi E. Ondasetron Is More Likely Than Ketamine to Cause Ventricular Tachycardia. Pediatr Emerg Care 2015;31(8):e4.
Lazzerini M, Martelossi S, Cont G, Bersanini C, Ventura G, Fontana M, Zuin G, Ventura A, Taddio A. Orofacial granulomatosis in children: think about Crohn's disease. Dig Liver Dis 2015;47(4):338-41.
Bembich S, Brovedani P, Cont G, Travan L, Grassi V, Demarini S. Pain activates a defined area of the somatosensory and motor cortex in newborn infants. Acta Paediatr 2015;104(11):e530-3.
Bembich S, Brovedani P, Cont G, Travan L, Grassi V, Demarini S. Pain activates a defined area of the somatosensory and motor cortex in newborn infants. Acta Paediatr 2015;104(11):e530-3.
Zonta F, Girotto G, Buratto D, Crispino G, Morgan A, Abdulhadi K, Alkowari M, Badii R, Gasparini P, Mammano F. The p.Cys169Tyr variant of connexin 26 is not a polymorphism. Hum Mol Genet 2015;24(9):2641-8.
Zonta F, Girotto G, Buratto D, Crispino G, Morgan A, Abdulhadi K, Alkowari M, Badii R, Gasparini P, Mammano F. The p.Cys169Tyr variant of connexin 26 is not a polymorphism. Hum Mol Genet 2015;24(9):2641-8.
Caracciolo I, Bassetti M, Paladini G, Luzzati R, Santon D, Merelli M, De Sabbata G, Carletti T, Marcello A, D'Agaro P. Persistent viremia and urine shedding of tick-borne encephalitis virus in an infected immunosuppressed patient from a new epidemic cluster in North-Eastern Italy. J Clin Virol 2015;69:48-51.
Iossa S, Costa V, Corvino V, Auletta G, Barruffo L, Cappellani S, Ceglia C, Cennamo G, d'Adamo APio, D'Amico A, Di Paolo N, Forte R, Gasparini P, Laria C, Lombardo B, Malesci R, Vitale A, Marciano E, Franzè A. Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss. Mol Cytogenet 2015;8:18.
Calligaris L, Berti I, Barbi E. Phleboliths as a marker of slow-flow venous malformation. Arch Dis Child 2015;100(11):1012.
Calligaris L, Berti I, Barbi E. Phleboliths as a marker of slow-flow venous malformation. Arch Dis Child 2015;100(11):1012.

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