GIRELLI, Domenico
GIRELLI, Domenico
DIPARTIMENTO DI MEDICINA
["Hyperferritinemia-cataract syndrome". Description of a new hereditary disease, from anamnesis to molecular diagnosis]
1997-01-01 Girelli, Domenico; P., Piccoli; Corrocher, Roberto
[Effectiveness of loratadine vs. placebo in the treatment of urticaria-angioedema syndrome in patients with food allergy]
1993-01-01 Pacor, Maria Luisa; Biasi, Domenico; Girelli, Domenico; P., Cortina; Corrocher, Roberto
[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
[Genetic risk factors in ischemic cardiopathy]
2001-01-01 Girelli, Domenico; Martinelli, Nicola
[Ion transport in erythrocytes: a universal physiological model. Reflections on the pathogenesis of hypertension (editorial)]
1991-01-01 Olivieri, Oliviero; Girelli, Domenico; Corrocher, Roberto
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, 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.
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 common polymorphism in LDL-receptor gene is a predictor of factor VIII activity and is associated with coronary artery disease.
2010-01-01 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.
2009-01-01 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.
2009-01-01 Martinelli, Nicola; Lunghi, B; Girelli, Domenico; Pinotti, M; Marchetti, G; Bisi, M; Olivieri, Oliviero; Corrocher, Roberto; Bernardi, F.
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 Five-Step Vascular Ultrasound Examination in Heart Failure: The First Two Years of the "ABCDE" G-SIUMB Multicenter Study 2018-2022
2020-01-01 Mozzini, Chiara; Soresi, Maurizio; Pesce, Giancarlo; Girelli, Domenico
A genetic risk factor for vascular disease which leads to mild hyperhomocysteinemia is common in northern Italy.
1996-01-01 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
1995-01-01 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''.
1995-01-01 Girelli, Domenico; Corrocher, Roberto; Olivieri, Oliviero; L., Bisceglia; DE FRANCESCHI, Lucia; L., Zelante; P., Gasparini
A new mutation in the trnsferrin receptor 2 gene in hemochromatosis type 3
2001-01-01 Girelli, Domenico; Bozzini, Claudia; Roetto, A.; Daraio, F.; Colombari, R.; Corrocher, Roberto; Camaschella, C.
A new mutation in transferrin receptor 2 gene in hemochromatosis type 3
2001-01-01 Girelli, Domenico; Bozzini, C; Roetto, A; Daraio, F; Colombari, R; Corrocher, Roberto; Camaschella, C.
A new mutation in transferrin receptor 2 gene in hemochromatosis type 3
2001-01-01 Girelli, Domenico; Bozzini, Claudia; Roetto, A.; Daraio, F.; Colombari, R.; Corrocher, Roberto; Camaschella, C.
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
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| ["Hyperferritinemia-cataract syndrome". Description of a new hereditary disease, from anamnesis to molecular diagnosis] | 1-gen-1997 | Girelli, Domenico; P., Piccoli; Corrocher, Roberto | |
| [Effectiveness of loratadine vs. placebo in the treatment of urticaria-angioedema syndrome in patients with food allergy] | 1-gen-1993 | Pacor, Maria Luisa; Biasi, Domenico; Girelli, Domenico; P., Cortina; Corrocher, Roberto | |
| [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 | |
| [Genetic risk factors in ischemic cardiopathy] | 1-gen-2001 | Girelli, Domenico; Martinelli, Nicola | |
| [Ion transport in erythrocytes: a universal physiological model. Reflections on the pathogenesis of hypertension (editorial)] | 1-gen-1991 | Olivieri, Oliviero; Girelli, Domenico; Corrocher, Roberto | |
| 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, 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 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 Five-Step Vascular Ultrasound Examination in Heart Failure: The First Two Years of the "ABCDE" G-SIUMB Multicenter Study 2018-2022 | 1-gen-2020 | Mozzini, Chiara; Soresi, Maurizio; Pesce, Giancarlo; Girelli, Domenico | |
| 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 | |
| A new mutation in the trnsferrin receptor 2 gene in hemochromatosis type 3 | 1-gen-2001 | Girelli, Domenico; Bozzini, Claudia; Roetto, A.; Daraio, F.; Colombari, R.; Corrocher, Roberto; Camaschella, C. | |
| A new mutation in transferrin receptor 2 gene in hemochromatosis type 3 | 1-gen-2001 | Girelli, Domenico; Bozzini, C; Roetto, A; Daraio, F; Colombari, R; Corrocher, Roberto; Camaschella, C. | |
| A new mutation in transferrin receptor 2 gene in hemochromatosis type 3 | 1-gen-2001 | Girelli, Domenico; Bozzini, Claudia; Roetto, A.; Daraio, F.; Colombari, R.; Corrocher, Roberto; Camaschella, C. | |
| 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 |