Export 1151 results:
[ Autore(Desc)] Titolo Tipo Anno
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 
B
Badina L, Ferrara G, Guastalla P, Barbi E. A precordial rub in a boy with a severe attack of ulcerative colitis. Pediatr Emerg Care 2014;30(4):268.
Badina L, Barbi E, Berti I, Radillo O, Matarazzo L, Ventura A, Longo G. The dietary paradox in food allergy: yesterday's mistakes, today's evidence and lessons for tomorrow. Curr Pharm Des 2012;18(35):5782-7.
Balduini CL, Pecci A, Savoia A. Recent advances in the understanding and management of MYH9-related inherited thrombocytopenias. Br J Haematol 2011;154(2):161-74.
Barbi E, Longo G, Berti I, Neri E, Saccari A, Rubert L, Matarazzo L, Montico M, Ventura A. Adverse effects during specific oral tolerance induction: in-hospital "rush" phase. Eur Ann Allergy Clin Immunol 2012;44(1):18-25.
Barbi E, Rizzello E, Taddio A. Use of ketamine continuous infusion for pediatric sedation in septic shock. Pediatr Emerg Care 2010;26(9):689-90.
Barbi E, Berti I, Minute M, Zennaro F. Successful treatment of acne with isotretinoin in chronic granulomatous disease. Eur J Dermatol 2011;21(1):111-2.
Barbi E, Longo G, Berti I, Matarazzo L, Rubert L, Saccari A, Lenisa I, Ronfani L, Radillo O, Ventura A. Adverse effects during specific oral tolerance induction: in home phase. Allergol Immunopathol (Madr) 2012;40(1):41-50.
Barbiero C, Lonciari I, Montico M, Monasta L, Penge R, Vio C, Tressoldi PEmanuele, Ferluga V, Bigoni A, Tullio A, Carrozzi M, Ronfani L. The submerged dyslexia iceberg: how many school children are not diagnosed? Results from an Italian study. PLoS One 2012;7(10):e48082.
Barkokebas A, Carvalho Ade Albuque, de Souza PRoberto El, Gomez RSantiago, Xavier GMachado, Ribeiro CMaria Bede, Crovella S, Porter SRoss, Leão JCarneiro. Mannose-binding lectin gene (MBL-2) polymorphism in oral lichen planus. Clin Oral Investig 2011;15(5):699-704.
Barone R, Carrozzi M, Parini R, Battini R, Martinelli D, Elia M, Spada M, Lilliu F, Ciana G, Burlina A, Leuzzi V, Leoni M, Sturiale L, Matthijs G, Jaeken J, Di Rocco M, Garozzo D, Fiumara A. A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation. J Neurol 2015;262(1):154-64.
Barrani M, Massei F, Scaglione M, Paolicchi A, Vitali S, Ciancia EM, Crovella S, Caparello MC, Consolini R. Unusual onset of a case of chronic recurrent multifocal osteomyelitis. Pediatr Rheumatol Online J 2015;13(1):60.
Bastanza G, Gallus R, De Carlini M, Picciotti PM, Muzzi E, Ciciriello E, Orzan E, Conti G. Achieving effective hearing aid fitting within one month after identification of childhood permanent hearing impairment. Acta Otorhinolaryngol Ital 2016;36(1):38-44.

Amministrazione Trasparente