OLIVIERI, Oliviero

OLIVIERI, Oliviero  

DIPARTIMENTO DI MEDICINA  

Mostra records
Risultati 1 - 20 di 431 (tempo di esecuzione: 0.025 secondi).
Titolo Data di pubblicazione Autore(i) File
11 Beta-Hydroxysteroid Dehydrogenase Type2 Promoter Polymorphisms Determines a Decreased HSD11B2 Expression in Vivo 1-gen-2014 Carvajal, Ca; Tapia Castillo, A; Vidal, A; Valdivia, C; Campino, C; Lagos, Cf; Vecchiola, A; Fuentes, Ca; Martinez Aguayo, A; Aglony, M; Garcia, H; Friso, Simonetta; Olivieri, Oliviero; Fardella, Ce
The -1131 T > C and S19W APOA5 gene polymorphisms are associated with high levels of triglycerides and apolipoprotein C-III, but not with coronary artery disease: an angiographic study 1-gen-2007 Martinelli, Nicola; Trabetti, Elisabetta; Bassi, A; Girelli, Domenico; Friso, Simonetta; Pizzolo, Francesca; Sandri, M; Malerba, Giovanni; Pignatti, Pierfranco; Corrocher, Roberto; Olivieri, Oliviero
11beta-hydroxysteroid dehydrogenase type 2 promoter methylation is increased in adults essential hypertensive patients 1-gen-2012 Cristian, Carvajal; Friso, Simonetta; Carolina, Valdivia; Alejandra, Tapia; Carmen, Campino; Udali, Silvia; Pattini, Patrizia; Guarini, Patrizia; Olivieri, Oliviero; Carlos, Fardella
11beta-hydroxysteroid dehydrogenase type-2 and type-1 (11beta-HSD2 and 11beta-HSD1) and 5beta-reductase activities in the pathogenia of essential hypertension 1-gen-2009 Campino, C.; Carvajal, C. A.; Cornejo, J.; Martín, B. S.; Olivieri, Oliviero; Guidi, Giancesare; Faccini, Giovanni; Pasini, Felice; Sateler, J.; Baudrand, R.; Mosso L., .; Owen, G. I.; Kalergis, A. M.; Padilla, O.; Fardella, C. E.
11beta-hydroxysteroid dehydrogenase type2 promoter methylation is increased in adults essential hypertensive patients 1-gen-2012 Carvajal Cristian, A; Friso, Simonetta; Valdivia, Carolina; Tapia, Alejandra; Campino, Carmen; Udali, Silvia; Pattini, Patrizia; Guarini, Patrizia; Olivieri, Oliviero; Fardella Carlos, E.
11β-Hydroxysteroid Dehydrogenase Type 2 Polymorphisms and Activity in a Chilean Essential Hypertensive and Normotensive Cohort. 1-gen-2012 Campino, C.; Quinteros, H.; Owen, G. I.; Carvajal, C. A.; Morales, M.; Olivieri, Oliviero; Guidi, G.; Faccini, G.; Pasini, F.; Baudrand, R.; Padilla, O.; Valdivia, C.; Thichauer, J.; Lagos, C. F.; Kalergis, A. M.; Fardella, C. E.
A 'desaturase hypothesis' for atherosclerosis: Janus-faced enzymes in omega-6 and omega-3 polyunsaturated fatty acid metabolism. 1-gen-2009 Martinelli, Nicola; Consoli, Letizia; Olivieri, Oliviero
A case of congenital dyserythopoietic anaemia with stomatocytosis, reduced bands 7 and 8 and normal cation transport 1-gen-1992 Olivieri, Oliviero; Girelli, Domenico; Vettore, Luciano; Balercia, Giancarlo; Corrocher, Roberto
A challenging case of abdominal pain associated to Helicobacter pylori infection 1-gen-2011 Delmonte, L; Lunardi, Claudio; Frulloni, Luca; Bason, Caterina; Rossi, A; Busti, F; Trecco, G; Puccetti, A; Olivieri, Oliviero; Friso, Simonetta
A common mutation in the 5, 10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status 1-gen-2002 Friso, Simonetta; Choi S., W; Girelli, Domenico; Mason, Jb; Dolnikowski, Gg; Bagley, J; Jacques, Pf; Olivieri, Oliviero; Rosenberg, Ih; Corrocher, Roberto; Selhub, J.
A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status. 1-gen-2002 Friso, Simonetta; Choi, S. w.; Girelli, Domenico; Mason, J. b.; Dolnikoski, G. b.; Bagley, P. j.; Olivieri, Oliviero; Jacques, P. f.; Rosenberg, I. h.; Corrocher, Roberto; Selhub, A. j.
A common polymorphism in LDL-receptor gene is a predictor of factor VIII activity and is associated with coronary artery disease. 1-gen-2010 Martinelli, Nicola; Lunghi, B; Girelli, Domenico; Pinotti, M; Marchetti, G; Bisi, M; Manzato, F; Corrocher, Roberto; Olivieri, Oliviero; Bernardi, F.
A common polymorphism in low-density lipoprotein receptor gene is a predictor of factor VIII activity levels and is associated with coronary artery disease. 1-gen-2009 Martinelli, Nicola; B., Lunghi; Girelli, Domenico; M., Pinotti; G., Marchetti; M., Bisi; Olivieri, Oliviero; F., Manzato; Corrocher, Roberto; F., Bernardi
A common polymorphism in low-density lipoprotein receptor gene is a predictor of factor VIII activity levels and is associated with coronary artery disease. 1-gen-2009 Martinelli, Nicola; Lunghi, B; Girelli, Domenico; Pinotti, M; Marchetti, G; Bisi, M; Olivieri, Oliviero; Corrocher, Roberto; Bernardi, F.
A comparative study on inter and intralaboratory reproducibility of renin measurement with a conventional enzymatic method and a new chemiluminescent assay of immunoreactive renin. 1-gen-2010 Morganti, A.; Accetto, R; Azizi, M; Bidlingmaier, M; Danser, J; Mcgregor, Ga; Manterof, ; Ménard, J; Nussberger, J; Olivieri, Oliviero; Persu, A; Ruilope, Lm; Salvetti, A.
A genetic risk factor for vascular disease which leads to mild hyperhomocysteinemia is common in northern Italy. 1-gen-1996 Friso, Simonetta; Girelli, Domenico; Olivieri, Oliviero; Azzini, M.; Faccini, Giovanni; Pessotto, R.; Russo, C.; Guarini, Patrizia; Minguzzi, Diego; Mazzucco, Alessandro; Pignatti, Pierfranco; Corrocher, Roberto
A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract 1-gen-1995 Girelli, Domenico; Olivieri, Oliviero; DE FRANCESCHI, Lucia; Corrocher, Roberto; G., Bergamaschi; M., Cazzola
A mutation in the iron responsive element of ferritin L-subunit gene is associated with the recently described ''hereditary hyperferritinemia-cataract syndrome''. 1-gen-1995 Girelli, Domenico; Corrocher, Roberto; Olivieri, Oliviero; L., Bisceglia; DE FRANCESCHI, Lucia; L., Zelante; P., Gasparini
A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: Relationships with C677T polymorphism and homocysteine/folate metabolism 1-gen-2002 Friso, S.; Girelli, D.; Trabetti, E.; Stranieri, C.; Olivieri, O.; Tinazzi, E.; Martinelli, N.; Faccini, G.; Pignatti, P. F.; Corrocher, R.
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism 1-gen-2002 Friso, Simonetta; Girelli, Domenico; Trabetti, Elisabetta; Stranieri, C; Olivieri, Oliviero; Tinazzi, Elisa; Martinelli, Nicola; Faccini, G; Pignatti, Pierfranco; Corrocher, Roberto