GIRELLI, Domenico

GIRELLI, Domenico  

DIPARTIMENTO DI MEDICINA  

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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; Lunghi, B; Girelli, Domenico; Pinotti, M; Marchetti, G; Bisi, M; Olivieri, Oliviero; Corrocher, Roberto; 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 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, 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 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