PELUCCHI, SARA
PELUCCHI, SARA
DIPARTIMENTO DI MEDICINA E CHIRURGIA (SCHOOL OF MEDICINE AND SURGERY)
Hereditary Hyperferritinemia
2023 Piperno, A; Pelucchi, S; Mariani, R
Intravenous iron therapy improves the hypercapnic ventilatory response and sleep disordered breathing in chronic heart failure
2022 Caravita, S; Faini, A; Vignati, C; Pelucchi, S; Salvioni, E; Cattadori, G; Baratto, C; Torlasco, C; Contini, M; Villani, A; Malfatto, G; Perger, E; Lombardi, C; Piperno, A; Agostoni, P; Parati, G
Ceruloplasmin variants might have different effects in different iron overload disorders
2021 Pelucchi, S; Ravasi, G; Piperno, A
Angiotensin type 2 and mas receptor activation prevents myocardial fibrosis and hypertrophy through the reduction of inflammatory cell infiltration and local sympathetic activity in angiotensin ii‐dependent hypertension
2021 Castoldi, G; Carletti, R; Ippolito, S; Stella, A; Zerbini, G; Pelucchi, S; Zatti, G; Di Gioia, C
Atypical phenotype in a patient with ceruloplasmin mutations in the compound heterozygous state
2021 Ravasi, G; Pelucchi, S; Canonico, F; Mariani, R; Piperno, A
Hif1a: A putative modifier of hemochromatosis
2021 Pelucchi, S; Ravasi, G; Arosio, C; Mauri, M; Piazza, R; Mariani, R; Piperno, A
Prolonged exposure to welding fumes as a novel cause of systemic iron overload
2021 Mariani, R; Pelucchi, S; Paolini, V; Belingheri, M; di Gennaro, F; Faverio, P; Riva, M; Pesci, A; 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
Inherited iron overload disorders
2020 Piperno, A; Pelucchi, S; Mariani, R
Ferroportin disease: A novel SLC40A1 mutation
2020 Ravasi, G; Pelucchi, S; Russo, A; Mariani, R; 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
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
A severe hemojuvelin mutation leading to late onset of HFE2-hemochromatosis
2018 Ravasi, G; Pelucchi, S; Mariani, R; Silvestri, L; Camaschella, C; Piperno, A
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
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
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
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
Does aceruloplasminemia modulate iron phenotype in thalassemia intermedia?
2016 Pelucchi, S; Pelloni, I; Arosio, C; Mariani, R; Piperno, A
Simultaneous liver iron and fat measures by magnetic resonance imaging in patients with hyperferritinemia
2015 Galimberti, S; Trombini, P; Bernasconi, D; Redaelli, I; Pelucchi, S; Bovo, G; Di Gennaro, F; Zucchini, N; Paruccini, N; Piperno, A