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Berton E, Vitali-Serdoz L, Vallon P, Maschio M, Gortani G, Benettoni A. Young girl with apical ballooning heart syndrome. Int J Cardiol 2012;161(1):e4-6.
Bertozzi M, Esposito C, Vella C, Briganti V, Zampieri N, Codrich D, Ubertazzi M, Trucchi A, Magrini E, Battaglia S, Bini V, Conighi MLuisa, Gulia C, Farina A, Camoglio FSaverio, Rigamonti W, Gamba P, Riccipetitoni G, Chiarenza SFabio, Inserra A, Appignani A. Pediatric Ovarian Torsion and its Recurrence: A Multicenter Study. J Pediatr Adolesc Gynecol 2017;30(3):413-417.
Betterle C, Ghizzoni L, Cassio A, Baronio F, Cervato S, Garelli S, Barbi E, Tonini G. Autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy in Calabria: clinical, immunological and genetic patterns. J Endocrinol Invest 2012;35(10):877-81.
Bettinelli MEnrica, Chapin EM, Cattaneo A. Establishing the Baby-Friendly Community Initiative in Italy: development, strategy, and implementation. J Hum Lact 2012;28(3):297-303.
Bevilacqua L, Navarra CO, Pirastu N, Di Lenarda R, Gasparini P, Robino A. A genome-wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population. J Periodontal Res 2018;53(6):992-998.
Bezzerri V, d'Adamo P, Rimessi A, Lanzara C, Crovella S, Nicolis E, Tamanini A, Athanasakis E, Tebon M, Bisoffi G, Drumm ML, Knowles MR, Pinton P, Gasparini P, Berton G, Cabrini G. Phospholipase C-β3 is a key modulator of IL-8 expression in cystic fibrosis bronchial epithelial cells. J Immunol 2011;186(8):4946-58.
Bianco AMonica, Zanin V, Marcuzzi A, Crovella S. Clarification of the pleiotropic effects of statins on mevalonate pathway and the feedback regulation of isoprenoids requires more comprehensive investigation. Cell Biochem Funct 2012;30(2):176.
Bianco AMonica, Girardelli M, Vozzi D, Crovella S, Kleiner G, Marcuzzi A. Mevalonate kinase deficiency and IBD: shared genetic background. Gut 2014;63(8):1367-8.
Bianco AMonica, Girardelli M, Tommasini A. Genetics of inflammatory bowel disease from multifactorial to monogenic forms. World J Gastroenterol 2015;21(43):12296-310.
Bianco AMonica, Faletra F, Vozzi D, Girardelli M, Knowles A, Tommasini A, Zauli G, Marcuzzi A. Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome results. Mol Med Rep 2015;12(4):6128-32.
Bianco AMonica, Zanin V, Monasta L, Martelossi S, Marcuzzi A, Crovella S. Family history in early-onset inflammatory bowel disease. J Gastroenterol 2013;48(1):144.
Bianco AMonica, Zanin V, Girardelli M, Magnolato A, Martelossi S, Martellossi S, Tommasini A, Marcuzzi A, Crovella S. A common genetic background could explain early-onset Crohn's disease. Med Hypotheses 2012;78(4):520-2.

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