Export 8 results:
Autore Titolo Tipo [ Anno(Asc)]
Filtri: Autore è Marchetti, Federico  [Clear All Filters]
2018
De Zen L, Marchetti F, Barbi E, Benini F. Off-label drugs use in pediatric palliative care. Ital J Pediatr 2018;44(1):144.
2017
Caorsi R, Penco F, Grossi A, Insalaco A, Omenetti A, Alessio M, Conti G, Marchetti F, Picco P, Tommasini A, Martino S, Malattia C, Gallizi R, Podda RAnna, Salis A, Falcini F, Schena F, Garbarino F, Morreale A, Pardeo M, Ventrici C, Passarelli C, Zhou Q, Severino M, Gandolfo C, Damonte G, Martini A, Ravelli A, Aksentijevich I, Ceccherini I, Gattorno M. ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national study. Ann Rheum Dis 2017;76(10):1648-1656.
2012
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.
Marchetti F, Bua J, Tornese G, Piras G, Toffol G, Ronfani L. Management of cryptorchidism: a survey of clinical practice in Italy. BMC Pediatr 2012;12:4.
Zanchi C, Paloni G, Marchetti F. Recurrent fever and fitful abdominal pain in a child. Gastroenterology 2012;143(2):e11-2.
Amaddeo A, Ventura A, Marchetti F, Benettoni A, Londero M. Should cardiac involvement be included in the criteria for diagnosis of Churg Strauss syndrome?. J Pediatr 2012;160(4):707.
2011
Faletra F, Athanasakis E, Minen F, Fornasier F, Marchetti F, Gasparini P. Vertebral defects in patients with Peters plus syndrome and mutations in B3GALTL. Ophthalmic Genet 2011;32(4):256-8.
2010
Bua J, Marchetti F, Faleschini E, Ventura A, Bussani R. Hepatic glycogenosis in an adolescent with diabetes. J Pediatr 2010;157(6):1042.

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