OLIVIERI, Oliviero
OLIVIERI, Oliviero
DIPARTIMENTO DI MEDICINA
11 Beta-Hydroxysteroid Dehydrogenase Type2 Promoter Polymorphisms Determines a Decreased HSD11B2 Expression in Vivo
2014-01-01 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 and type-1 (11beta-HSD2 and 11beta-HSD1) and 5beta-reductase activities in the pathogenia of essential hypertension
2009-01-01 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.
11β-Hydroxysteroid Dehydrogenase Type 2 Polymorphisms and Activity in a Chilean Essential Hypertensive and Normotensive Cohort.
2012-01-01 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.
[Endogenous erythrocyte proteolysis: a new approach to the study of membrane physiopathology]
1991-01-01 L., Vettore; M. C., De Mattels; E., Bonollo; V., De Angelis; F., Sorrentino; T., Trevisan; Guarini, Patrizia; Girelli, Domenico; Olivieri, Oliviero
[Ion transport in erythrocytes: a universal physiological model. Reflections on the pathogenesis of hypertension (editorial)]
1991-01-01 Olivieri, Oliviero; Girelli, Domenico; Corrocher, Roberto
[Paroxysmal nocturnal hemoglobinuria. Recent findings]
1988-01-01 G., De Sandre; Olivieri, Oliviero
A 'desaturase hypothesis' for atherosclerosis: Janus-faced enzymes in omega-6 and omega-3 polyunsaturated fatty acid metabolism.
2009-01-01 Martinelli, Nicola; Consoli, Letizia; Olivieri, Oliviero
A case of congenital dyserythopoietic anaemia with stomatocytosis, reduced bands 7 and 8 and normal cation transport
1992-01-01 Olivieri, Oliviero; Girelli, Domenico; Vettore, Luciano; Balercia, Giancarlo; Corrocher, Roberto
A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status.
2002-01-01 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 comparative study on inter and intralaboratory reproducibility of renin measurement with a conventional enzymatic method and a new chemiluminescent assay of immunoreactive renin.
2010-01-01 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 dangerous onychodystrophy
2020-01-01 Martinelli, Nicola; Olivieri, Oliviero
A decade of progress on the genetic basis of coronary artery disease. Practical insights for the internist
2017-01-01 Girelli, Domenico; Piubelli, Chiara; Martinelli, Nicola; Corrocher, Roberto; Olivieri, Oliviero
A late diagnosis of Primary Aldosteronism
2017-01-01 Zorzi, Francesco; Olivieri, Oliviero; Brazzarola, Paolo; Pizzolo, Francesca
A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract
1995-01-01 Girelli, Domenico; Olivieri, Oliviero; DE FRANCESCHI, Lucia; Corrocher, Roberto; G., Bergamaschi; M., Cazzola
A Novel ALAS2 Missense Mutation in Two Brothers With Iron Overload and Associated Alterations in Serum Hepcidin/Erythroferrone Levels
2020-01-01 Lira Zidanes, Acaynne; Marchi, Giacomo; Busti, Fabiana; Marchetto, Alessandro; Fermo, Elisa; Giorgetti, Alejandro; Vianello, Alice; Castagna, Annalisa; Olivieri, Oliviero; Bianchi, Paola; Girelli, Domenico
A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene.
2014-01-01 Shen, Gq; Girelli, Domenico; Li, L; Rao, S; Archacki, S; Olivieri, Oliviero; Martinelli, Nicola; Park, Je; Chen, Q; Topol, Ej; Wang, Qk
A relative ADAMTS13 deficiency supports the presence of a secondary microangiopathy in COVID 19
2020-01-01 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
2002-01-01 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
2002-01-01 Friso, Simonetta; Girelli, Domenico; Trabetti, Elisabetta; Stranieri, C; Olivieri, Oliviero; Tinazzi, Elisa; Martinelli, Nicola; Faccini, G; Pignatti, Pierfranco; Corrocher, Roberto
Abnormal modulation of cell protective systems in response to ischemic/reperfusion injury is important in the development of mouse sickle cell hepatopathy
2011-01-01 Siciliano, Angela; Malpeli, Giorgio; Platt, O; Lebouef, C; Janin, A; Scarpa, Aldo; Olivieri, Oliviero; Amato, Eliana; Corrocher, Roberto; Beuzard, Y; DE FRANCESCHI, Lucia
| 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 | |
| 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. | |
| 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. | |
| [Endogenous erythrocyte proteolysis: a new approach to the study of membrane physiopathology] | 1-gen-1991 | L., Vettore; M. C., De Mattels; E., Bonollo; V., De Angelis; F., Sorrentino; T., Trevisan; Guarini, Patrizia; Girelli, Domenico; Olivieri, Oliviero | |
| [Ion transport in erythrocytes: a universal physiological model. Reflections on the pathogenesis of hypertension (editorial)] | 1-gen-1991 | Olivieri, Oliviero; Girelli, Domenico; Corrocher, Roberto | |
| [Paroxysmal nocturnal hemoglobinuria. Recent findings] | 1-gen-1988 | G., De Sandre; Olivieri, Oliviero | |
| 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 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 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 dangerous onychodystrophy | 1-gen-2020 | Martinelli, Nicola; Olivieri, Oliviero | |
| A decade of progress on the genetic basis of coronary artery disease. Practical insights for the internist | 1-gen-2017 | Girelli, Domenico; Piubelli, Chiara; Martinelli, Nicola; Corrocher, Roberto; Olivieri, Oliviero | |
| A late diagnosis of Primary Aldosteronism | 1-gen-2017 | Zorzi, Francesco; Olivieri, Oliviero; Brazzarola, Paolo; Pizzolo, Francesca | |
| 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 Novel ALAS2 Missense Mutation in Two Brothers With Iron Overload and Associated Alterations in Serum Hepcidin/Erythroferrone Levels | 1-gen-2020 | Lira Zidanes, Acaynne; Marchi, Giacomo; Busti, Fabiana; Marchetto, Alessandro; Fermo, Elisa; Giorgetti, Alejandro; Vianello, Alice; Castagna, Annalisa; Olivieri, Oliviero; Bianchi, Paola; Girelli, Domenico | |
| A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene. | 1-gen-2014 | Shen, Gq; Girelli, Domenico; Li, L; Rao, S; Archacki, S; Olivieri, Oliviero; Martinelli, Nicola; Park, Je; Chen, Q; Topol, Ej; Wang, Qk | |
| 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 | |
| Abnormal modulation of cell protective systems in response to ischemic/reperfusion injury is important in the development of mouse sickle cell hepatopathy | 1-gen-2011 | Siciliano, Angela; Malpeli, Giorgio; Platt, O; Lebouef, C; Janin, A; Scarpa, Aldo; Olivieri, Oliviero; Amato, Eliana; Corrocher, Roberto; Beuzard, Y; DE FRANCESCHI, Lucia |