MARIANI, RAFFAELLA
MARIANI, RAFFAELLA
DIPARTIMENTO DI MEDICINA CLINICA E PREVENZIONE (attivo dal 10/07/2006 al 30/09/2012)
Haemochromatosis in children: A national retrospective cohort promoted by the A.I.E.O.P. (Associazione Italiana Emato-Oncologia Pediatrica) study group
2024 Corti, P; Ferrari, G; Faraguna, M; Capitoli, G; Longo, F; Corradini, E; Casini, T; Boscarol, G; Pinto, V; Ghilardi, R; Russo, G; Colombatti, R; Mariani, R; Piperno, A
Hereditary Hyperferritinemia
2023 Piperno, A; Pelucchi, S; Mariani, R
Hif1a: A putative modifier of hemochromatosis
2021 Pelucchi, S; Ravasi, G; Arosio, C; Mauri, M; Piazza, R; 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
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
Inherited iron overload disorders
2020 Piperno, A; Pelucchi, S; Mariani, R
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
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
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
Alterations in sympathetic nerve traffic in genetic haemochromatosis before and after iron depletion therapy: A microneurographic study
2016 Seravalle, G; Piperno, A; Mariani, R; Pelloni, I; Facchetti, R; Dell'Oro, R; Cuspidi, C; Mancia, G; Grassi, G
Does aceruloplasminemia modulate iron phenotype in thalassemia intermedia?
2016 Pelucchi, S; Pelloni, I; Arosio, C; Mariani, R; 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
Serum ferritin and liver features in a cohort of 15 patients affected by Gaucher disease
2016 Rigoldi, M; Borin, L; Mariani, R; Pelloni, I; Greni, F; Arosio, C; 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
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
CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients
2012 Pelucchi, S; Mariani, R; Calza, S; Fracanzani, A; Litta Modignani, G; Bertola, F; Busti, F; Trombini, P; Fraquelli, ; M:, F; Gl, ; Girelli, D; Fargion, S; Specchia, C; Piperno, A