Export 1151 results:
Autore Titolo Tipo [ Anno(Asc)]
Filtri: Content è privacy  [Clear All Filters]
2012
Filho CB, Rodrigues FF, Segat L, Fonseca AM, Araujo J, Arahata C, Pontes L, Vilar L, Filho JL de Lima, Crovella S. Association of MBL2 gene exon 1 variants with autoimmune thyroid disease in Brazilian patients. Int J Immunogenet 2012;39(4):357-61.
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.
Parco S, Vascotto F. Autologous cord blood harvesting in North Eastern Italy: ethical questions and emerging hopes for curing diabetes and celiac disease. Int J Gen Med 2012;5:511-6.
Buchini S, Quattrin R. Avoidable interruptions during drug administration in an intensive rehabilitation ward: improvement project. J Nurs Manag 2012;20(3):326-34.
Poropat F, Ventura G, Murru FM, Orzan E, Maschio M. A boy with acute strabismus. J Pediatr 2012;161(6):1178.
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.
De Cunto A, Bensa M, Tonelli A. A case of familial hemiplegic migraine associated with a novel ATP1A2 gene mutation. Pediatr Neurol 2012;47(2):133-6.
Catamo E, Segat L, Lenarduzzi S, Petix V, Morgutti M, Crovella S. CD14 polymorphisms correlate with an augmented risk for celiac disease in Italian patients. Genes Immun 2012;13(6):489-95.
Carlino C, Trotta E, Stabile H, Morrone S, Bulla R, Soriani A, Iannitto MLuisa, Agostinis C, Mocci C, Minozzi M, Aragona C, Perniola G, Tedesco F, Sozzani S, Santoni A, Gismondi A. Chemerin regulates NK cell accumulation and endothelial cell morphogenesis in the decidua during early pregnancy. J Clin Endocrinol Metab 2012;97(10):3603-12.
Gortani G, Maschio M, Ventura A. A child with edema, lower limb deformity, and recurrent diarrhea. J Pediatr 2012;161(6):1177.
Copertino M, Barbi E, Poli F, Zennaro F, Ferrari M, Carrera P, Ventura A. A child with severe pneumomediastinum and ABCA3 gene mutation: a puzzling connection. Arch Bronconeumol 2012;48(4):139-40.
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.

Amministrazione Trasparente