RAVASI, GIULIA
RAVASI, GIULIA
DIPARTIMENTO DI MEDICINA E CHIRURGIA (SCHOOL OF MEDICINE AND SURGERY)
Modulation of hepcidin production during hypoxia-induced erythropoiesis in humans in vivo: data from the HIGHCARE project
2011 Piperno, A; Galimberti, S; Mariani, R; Pelucchi, S; Ravasi, G; Lombardi, C; Bilo, G; Revera, M; Giuliano, A; Faini, A; Mainini, V; Westerman, M; Ganz, T; Valsecchi, M; Mancia, G; Parati, G
Hepcidin expression in iron overload diseases is variably modulated by circulating factors
2012 Ravasi, G; Pelucchi, S; Trombini, P; Mariani, R; Tomosugi, N; Modignani, G; Pozzi, M; Nemeth, E; Ganz, T; Hayashi, H; Barisani, D; Piperno, A
IRON AND HYPOXIA LINK: DOWNREGULATION OF LUCIFERASE ACTIVITY OF HEPCIDIN PROMOTER BY HYPOXIC SERA IN HUH-7 CELLS
2013 Greni, F; Ravasi, G; Pelucchi, S; Silvestri, L; Cappellini, M; Barisani, D; Camaschella, C; Piperno, A
UNEXPLAINED ISOLATED HYPERFERRITINEMIA IN PATIENTS WITHOUT MUTATIONS IN FERRITIN GENE AND L-FERRITIN IRES REGIONS
2013 Ravasi, G; Pelucchi, S; Trombini, P; Mariani, R; Greni, F; Arosio, C; Majore, S; Piperno, A
Hypoxia-dependent hepcidin down-regulation: an in vitro study
2014 Ravasi, G; Greni, F; Mariani, R; Giuliano, A; Cappellini, M; Parati, G; Pelucchi, S; Piperno, A
Circulating factors are involved in hypoxia-induced hepcidin suppression
2014 Ravasi, G; Pelucchi, S; Greni, F; Mariani, R; Giuliano, A; Parati, G; Silvestri, L; Piperno, A
Transferrin receptor 2 mutations in patients with juvenile hemochromatosis phenotype
2015 Ravasi, G; Rausa, M; Pelucchi, S; Arosio, C; Greni, F; Mariani, R; Pelloni, I; Silvestri, L; Pineda, P; Camaschella, C; Piperno, A
GNPAT rs11558492 is not associated to iron overload in Italian HFE p.C282Y homozygotes
2016 Greni, F; Valenti, L; Mariani, R; Pelloni, I; Rametta, R; Busti, F; Ravasi, G; Girelli, D; Piperno, A; Pelucchi, S
Hepcidin regulation in a mouse model of acute hypoxia
2016 Ravasi, G; Pelucchi, S; BUOLI COMANI, G; Greni, F; Mariani, R; Pelloni, I; Rivolta, I; Barisani, D; Piperno, A
Proprotein convertase 7 rs236918 associated with liver fibrosis in Italian patients with HFE-related hemochromatosis
2016 Pelucchi, S; Galimberti, S; Greni, F; Rametta, R; Mariani, R; Pelloni, I; Girelli, D; Busti, F; Ravasi, G; Valsecchi, M; Valenti, L; Piperno, A
Hypoxia-Dependent Hepcidin Down-Regulation: In Vitro and In Vivo Studies
2016 Ravasi, G
GNPAT rs11558492 is not a major modifier of iron status: Study of Italian hemochromatosis patients and blood donors
2017 Greni, F; Valenti, L; Mariani, R; Pelloni, I; Rametta, R; Busti, F; Ravasi, G; Girelli, D; Fargion, S; Galimberti, S; Piperno, A; Pelucchi, S
Unexplained isolated hyperferritinemia without iron overload
2017 Ravasi, G; Pelucchi, S; Mariani, R; Casati, M; Greni, F; Arosio, C; Pelloni, I; Majore, S; Santambrogio, P; Levi, S; Piperno, A
Phenotypic heterogeneity in seven Italian cases of aceruloplasminemia
2018 Pelucchi, S; Mariani, R; Ravasi, G; Pelloni, I; Marano, M; Tremolizzo, L; Alessio, M; Piperno, A
A severe hemojuvelin mutation leading to late onset of HFE2-hemochromatosis
2018 Ravasi, G; Pelucchi, S; Mariani, R; Silvestri, L; Camaschella, C; Piperno, A
Hepcidin regulation in a mouse model of acute hypoxia
2018 Ravasi, G; Pelucchi, S; Buoli Comani, G; Greni, F; Mariani, R; Pelloni, I; Bombelli, S; Perego, R; Barisani, D; Piperno, A
Ferroportin disease: A novel SLC40A1 mutation
2020 Ravasi, G; Pelucchi, S; Russo, A; Mariani, R; Piperno, A
Atypical phenotype in a patient with ceruloplasmin mutations in the compound heterozygous state
2021 Ravasi, G; Pelucchi, S; Canonico, F; Mariani, R; Piperno, A
Mental well-being in patients with transfusion-dependent anemias and hemochromatosis during the SARS-CoV-2 pandemic
2021 Piperno, R; Bertazioli, G; Ravasi, G; Mariani, R; Piperno, A
Identification of novel mutations by targeted NGS panel in patients with hyperferritinemia
2021 Ravasi, G; Pelucchi, S; Bertola, F; Capelletti, M; Mariani, R; Piperno, A