Export 1305 results:
Autore [ Titolo(Desc)] Tipo Anno
Filtri: First Letter Of Last Name è P  [Clear All Filters]
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 
C
Bossi F, Tripodo C, Rizzi L, Bulla R, Agostinis C, Guarnotta C, Munaut C, Baldassarre G, Papa G, Zorzet S, Ghebrehiwet B, Ling GSheng, Botto M, Tedesco F. C1q as a unique player in angiogenesis with therapeutic implication in wound healing. Proc Natl Acad Sci U S A 2014;111(11):4209-14.
De Cunto A, Paviotti G, Ronfani L, Travan L, Bua J, Cont G, Demarini S. Can body mass index accurately predict adiposity in newborns?. Arch Dis Child Fetal Neonatal Ed 2014;99(3):F238-9.
Abate MValentina, Stocco G, Devescovi R, Carrozzi M, Pierobon C, Valencic E, Lucafò M, Di Silvestre A, d'Adamo P, Tommasini A, Decorti G, Ventura A. Carbamazepine-induced thrombocytopenic purpura in a child: Insights from a genomic analysis. Blood Cells Mol Dis 2016;59:97-9.
Paviotti G, Todero S, Demarini S. Cardiac output decreases and systemic vascular resistance increases in newborns placed in the left-lateral position. J Perinatol 2017;37(5):563-565.
Quadrifoglio M, Faletra F, Bussani R, Pecile V, Zennaro F, Grasso A, Zandonà L, Alberico S, Stampalija T. A Case of Prenatal Neurocytoma Associated With ATR-16 Syndrome. J Ultrasound Med 2016;35(6):1359-61.
Tornese G, Marzuillo P, Pellegrin MChiara, Germani C, Faleschini E, Zennaro F, Grandone A, Del Giudice EMiraglia, Perrone L, Ventura A. A case of Rubinstein-Taybi syndrome associated with growth hormone deficiency in childhood. Clin Endocrinol (Oxf) 2015;83(3):437-9.
Tornese G, Marzuillo P, Pellegrin MChiara, Germani C, Faleschini E, Zennaro F, Grandone A, Del Giudice EMiraglia, Perrone L, Ventura A. A case of Rubinstein-Taybi syndrome associated with growth hormone deficiency in childhood. Clin Endocrinol (Oxf) 2015;83(3):437-9.
Toson B, Santos EJosé Dos, Adelino JEduardo, Sandrin-Garcia P, Crovella S, Louzada-Júnior P, Oliveira RDonizete R, Pedroza LSanta Rosa, Sauma Mde Fátima, de Lima CPereira Si, Barbosa FBrasil, Brenol CViegas, Xavier RMachado, Chies JArtur Bogo, Veit TDegani. CCR5Δ32 and the genetic susceptibility to rheumatoid arthritis in admixed populations: a multicentre study. Rheumatology (Oxford) 2017;56(3):495-497.
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.
Zupin L, Polesello V, Alberi G, Moratelli G, Crocè SLory, Masutti F, Pozzato G, Crovella S, Segat L. CD209 promoter polymorphisms associate with HCV infection and pegylated-interferon plus ribavirin treatment response. Mol Immunol 2016;76:49-54.
Zupin L, Polesello V, Alberi G, Moratelli G, Crocè SLory, Masutti F, Pozzato G, Crovella S, Segat L. CD209 promoter polymorphisms associate with HCV infection and pegylated-interferon plus ribavirin treatment response. Mol Immunol 2016;76:49-54.
Parco S, Città A, Vascotto F, Tamaro G. Celiac disease and immigration in Northeastern Italy: the "drawn double nostalgia" of "cozonac" and "panettone" slices. Clin Exp Gastroenterol 2011;4:121-5.

Amministrazione Trasparente