MARIANI, RAFFAELLA
MARIANI, RAFFAELLA
DIPARTIMENTO DI MEDICINA CLINICA E PREVENZIONE (attivo dal 2006 al 2012)
Haemochromatosis in patients with β-thalassaemia trait
2000 Piperno, A; Mariani, R; Arosio, C; Vergani, A; Bosio, S; Fargion, S; Sampietro, M; Girelli, D; Fraquelli, M; Conte, D; Fiorelli, G; Camaschella, C
Natural history of juvenile haemochromatosis
2002 De Gobbi, M; Roetto, A; Piperno, A; Mariani, R; Alberti, F; Papanikolaou, G; Politou, M; Lockitch, G; Girelli, D; Fargion, S; Cox, T; Gasparini, P; Cazzola, M; Camaschella, C
Increased serum ferritin is common in men with essential hypertension
2002 Piperno, A; Trombini, P; Gelosa, M; Mauri, V; Pecci, V; Vergani, A; Salvioni, A; Mariani, R; Mancia, G
Prevalence of HFE mutations in upper northern Italy: study of 1132 unrelated blood donors
2003 Mariani, R; Salvioni, A; Corengia, C; Erba, N; Lanzafame, C; De Micheli, V; Baldini, V; Arosio, C; Fossati, L; Trombini, P; Oberkanins, C; Piperno, A
Prevalence of C282Y and E168X HFE mutations in an italian population of northern european ancestry
2003 Salvioni, A; Mariani, R; Oberkanins, C; Moritz, A; Mauri, V; Pelucchi, S; Riva, A; Arosio, C; Cerutti, P; Piperno, A
Type 3 hemochromatosis and beta-thalassemia trait
2004 Riva, A; Mariani, R; Bovo, G; Pelucchi, S; Arosio, C; Salvioni, A; Vergani, A; Piperno, A
Homozygosity for transferrin receptor-2 y250x mutation induces early iron overload
2004 Piperno, A; Roetto, A; Mariani, R; Pelucchi, S; Corengia, C; Daraio, F; Piga, A; Garozzo, G; Camaschella, C
Iron chelation therapy in aceruloplasminaemia: study of a patient with a novel missense mutation
2004 Mariani, R; Arosio, C; Pelucchi, S; Grisoli, M; Piga, A; Trombini, P; Piperno, A
Erythrocytapheresis plus erythropoietin: An alternative therapy for selected patients with hemochromatosis and severe organ damage
2005 Mariani, R; Pelucchi, S; Perseghin, P; Corengia, C; Piperno, A
MR imaging of cerebral cortical involvement in aceruloplasminemia
2005 Grisoli, M; Piperno, A; Chiapparini, L; Mariani, R; Savoiardo, M
Iron accumulation in chronic hepatitis C: relation of hepatic iron distribution, HFE genotype, and disease course
2005 Corengia, C; Galimberti, S; Bovo, G; Vergani, A; Arosio, C; Mariani, R; Redaelli, A; Riva, A; Cestari, C; Pozzi, M; Valsecchi, M; Piperno, A
HFE and SLC40A1 polymorphisms in patients with unexplained iron overload
2006 Trombini, P; Pelucchi, S; Maldini, F; Salvioni, A; Riva, A; Mariani, R; Casati, G; Piperno, A
Heterogeneity of iron overload: Clinical, biochemical, histopathologic and genetic study of 70 patients
2006 Riva, A; Pelucchi, S; Bovo, G; Trombini, P; Salvioni, A; Mariani, R; Vergani, A; Casati, G; Fargion, S; Piperno, A
Effects of plasma transfusion on hepcidin production in human congenital hypotransferrinemia
2007 Trombini, P; Coliva, T; Nemeth, E; Mariani, R; Ganz, T; Biondi, A; Piperno, A
Hepcidin and iron-related gene expression in subjects with Dysmetabolic Hepatic Iron Overload
2008 Barisani, D; Pelucchi, S; Mariani, R; Galimberti, S; Trombini, P; Fumagalli, D; Meneveri, R; Nemeth, E; Ganz, T; Piperno, A
Novel mutations of the ferroportin gene (SLC40A1): Analysis of 56 consecutive patients with unexplained iron overload
2008 Pelucchi, S; Mariani, R; Salvioni, A; Bonfadini, S; Riva, A; Bertola, F; Trombini, P; Piperno, A
Reduced expression of hepcidin in patients with myelodysplastic syndrome and myelofibrosis: the causes might be more heterogeneous than in thalassaemia.
2008 Mariani, R; Pelucchi, S; Pozzi, M; Paolini, V; Piperno, A
The presence of two or more metabolic alterations and hepatic steatosis characterizes the dysmetabolic iron overload syndrome
2008 Riva, A; Trombini, P; Mariani, R; Salvioni, A; Coletti, S; Bonfadini, S; Paolini, V; Pozzi, M; Bovo, G; Piperno, A
Re-evaluation of clinical and histological criteria for diagnosis of dysmetabolic iron overload syndrome
2008 Riva, A; Trombini, P; Mariani, R; Salvioni, A; Coletti, S; Bonfadini, S; Paolini, V; Pozzi, M; Facchetti, R; Bovo, G; Piperno, A
Il sovraccarico di ferro: modulatore della risposta adrenergica
2009 Mariani, R