CORROCHER, Roberto

CORROCHER, Roberto  

DIPARTIMENTO DI MEDICINA CLINICA E SPERIMENTALE  

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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
A 1.1-kb duplication in the p67phox gene causes chronic granulomatous disease 1-gen-2001 Borgato, Lorena; A., Bonizzato; Lunardi, Claudio; Dusi, Stefano; G., Andrioli; A., Scarperi; Corrocher, Roberto
A case of chronic haemolitic anemia induced by cyanidanol 1-gen-1987 M., Casaril; R., Pecci; L., Venturini; 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 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 case of parotideal myeloma in Sjogren's syndrome 1-gen-1987 Casaril, M.; Venturini, L.; Pecci, R.; Bonazzi, L.; Menestrina, F.; Gabrielli, G. B.; 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 double blind placebo controlled comparison of treatment with montelukast and citerezine in patients with chronic urticaria due to food additive and/or ASA. 1-gen-2000 Pacor, Maria Luisa; Di Lorenzo, G.; Corrocher, Roberto
A double blind placebo controlled comparison of treatments with fluticasone dipropionate,ceterizine and montelukast administred as monotherapy and as association in patients with seasonal allergic rhinitis 1-gen-2002 Di Lorenzo, G; Pacor, Maria Luisa; Corrocher, Roberto
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 long term study of hepatitis G virus coinfection in chronic hepatitis B 1-gen-1997 Fattovich, Giovanna; Ribero, A. L.; Favarato, S.; Donato, F.; Giustina, G.; Pantalena, M.; Corrocher, Roberto; A., Tagger
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.