FRISO, Simonetta

FRISO, Simonetta  

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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
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 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.
A case of Listeria murray/grayi bacteremia in a patient with advanced Hodgking's disease 1-gen-1998 Todeschini, Giuseppe; Friso, Simonetta; S., Lombardi; M., Casaril; Fontana, Roberta; 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 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 lifelong exposure to a Western-style diet, but not aging, alters global DNA methylation in mouse colon 1-gen-2015 Choi, Sang Woon; Tammen, Stephanie A; Liu, Zhenhua; Friso, Simonetta
A method to assess genomic DNA methylation using high-performance liquid chromatography/electrospray ionization mass spectrometry. 1-gen-2002 Friso, Simonetta; Choi, S. W.; Dolninowski, G. C.; J., Selhub
A Method to Assess Genomic DNA MethylationUsing High-Performance Liquid Chromatography/Electrospray Ionization Mass Spectrometry 1-gen-2004 Friso, Simonetta; Choi, Sw; Dolnikowski, Gg; Selhub, J.
A relative ADAMTS13 deficiency supports the presence of a secondary microangiopathy in COVID 19 1-gen-2020 Martinelli, Nicola; Montagnana, Martina; Pizzolo, Francesca; Friso, Simonetta; Salvagno, Gian Luca; Forni, Gian Luca; Gianesin, Barbara; Morandi, Matteo; Lunardi, Claudio; Lippi, Giuseppe; Polati, Enrico; Olivieri, Oliviero; De Franceschi, Lucia
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
Acquired and genetic determinants of homocysteine in atheromatous renel artery stenosis with mild renal insufficiency 1-gen-1999 Olivieri, Oliviero; Grazioli, S.; Trabetti, Elisabetta; Faccini, Giovanni; Pizzolo, Francesca; Stranieri, Chiara; Friso, Simonetta; Girelli, Domenico; Pignatti, Pierfranco; Russo, C.; Minguzzi, Diego; Corrocher, Roberto
Acquired form of activated protein C resistance in healthy women taking oestrogen therapy. 1-gen-1995 Friso, Simonetta; A., Guella; Olivieri, Oliviero; F., Manzato; F., Bernardi; G., Brocco; Girelli, Domenico; M., Azzini; C., Russo; Corrocher, Roberto
Activation of K+/Cl- cotransport in human erythrocytes exposed to oxidative agents 1-gen-1993 Olivieri, Oliviero; M., Bonollo; Friso, Simonetta; Girelli, Domenico; Corrocher, Roberto; L., Vettore
Activation of the pump and cotransport Na/K system on membranes of red blood cells in a patients affected by myolysis for abuse of glicerizinic acid 1-gen-1993 Stanzial, Annamaria; Menini, C; Friso, Simonetta; Olivieri, Oliviero; Tessitore, N.; Bertoloni, A.; Corrocher, Roberto
Acute haemolysis by cold antibody during SARS-CoV-2 infection in a patient with Evans syndrome: a case report and literature review 1-gen-2022 Osti, Nicola; Ceolan, Jacopo; Piccoli, Pierluigi; Mazzi, Filippo; Montemezzi, Rachele; Dima, Francesco; Friso, Simonetta; Pizzolo, Francesca; Martinelli, Nicola; Rizzi, Monica; Moruzzi, Sara; Olivieri, Oliviero; De Franceschi, Lucia
Additive effect of LRP8/APOER2 R952Q variant to APOE epsilon2/epsilon3/epsilon4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study. 1-gen-2009 Martinelli, Nicola; Olivieri, Oliviero; Gong Qing, Shen; Trabetti, Elisabetta; Pizzolo, Francesca; Busti, Fabiana; Friso, Simonetta; Bassi, Antonella; Lin, Li; Ying, Hu; Pignatti, Pierfranco; Corrocher, Roberto; Qing Kenneth, Wang; Girelli, Domenico