GIRELLI, Domenico

GIRELLI, Domenico  

DIPARTIMENTO DI MEDICINA  

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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 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 polymorphism in the chromosome 9p21 ANRIL locus is associated to Philadelphia positive acute lymphoblastic leukemia 1-gen-2011 Iacobucci, I; Sazzini, M; Garagnani, P; Ferrari, A; Boattini, A; Lonetti, A; Papayannidis, C; Mantovani, V; Marasco, E; Ottaviani, E; Soverini, S; Girelli, Domenico; Luiselli, D; Vignetti, M; Baccarani, M; Martinelli, G.
A time course of hepcidin response to iron challenge in HFE and TfR2 Haemochromatosis patients 1-gen-2010 Girelli, Domenico; Trombini, P; Busti, Fabiana; Campostrini, Natascia; Sandri, Marco; Pelucchi, S; Westerman, M; Ganz, T; Nemeth, E; Piperno, A; Camaschella, C.
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
The A736V TMPRSS6 polymorphism influences hepcidin and iron metabolism in chronic hemodialysis patients: TMPRSS6 and hepcidin in hemodialysis. 1-gen-2013 Pelusi, S; Girelli, Domenico; Rametta, R; Campostrini, Natascia; Alfieri, C; Traglia, M; Dongiovanni, P; Como, G; Toniolo, D; Camaschella, C; Messa, P; Fargion, S; Valenti, L.
Aceruloplasminemia: A Severe Neurodegenerative Disorder Deserving an Early Diagnosis 1-gen-2019 Marchi, Giacomo; Busti, Fabiana; LIRA ZIDANES, Acaynne; Castagna, Annalisa; Girelli, Domenico
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