Sfoglia per Autore
A severe hemojuvelin mutation leading to late onset of HFE2-hemochromatosis
2018 Ravasi, G; Pelucchi, S; Mariani, R; Silvestri, L; Camaschella, C; 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
Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemia
2018 Zanardi, A; Conti, A; Cremonesi, M; D'Adamo, P; Gilberti, E; Apostoli, P; Cannistraci, C; Piperno, A; David, S; Alessio, M
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
Aceruloplasminemia: Waiting for an Efficient Therapy
2018 Piperno, A; Alessio, M
Therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr (C282Y/C282Y) homozygous genotype
2018 Adams, P; Altes, A; Brissot, P; Butzeck, B; Cabantchik, I; Cançado, R; Distante, S; Evans, P; Evans, R; Ganz, T; Girelli, D; Hultcrantz, R; Mclaren, G; Marris, B; Milman, N; Nemeth, E; Nielsen, P; Pineau, B; Piperno, A; Porto, G; Prince, D; Ryan, J; Sanchez, M; Santos, P; Swinkels, D; Teixeira, E; Toska, K; Vanclooster, A; White, D
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
Myelodysplastic Syndromes and Iron Chelation Therapy
2017 Angelucci, E; Urru, S; Pilo, F; Piperno, A
Novel mutation in the Transferrin receptor-2 in a patient with Hereditary Hemochromatosis type 3
2017 Achi, H; Moukalled, N; Mahfouz, R; Piperno, A; Taher, 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
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
Does aceruloplasminemia modulate iron phenotype in thalassemia intermedia?
2016 Pelucchi, S; Pelloni, I; Arosio, C; Mariani, R; 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
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
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
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
Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis
2015 de Tayrac, M; Roth, M; Jouanolle, A; Coppin, H; le Gac, G; Piperno, A; Férec, C; Pelucchi, S; Scotet, V; Bardou Jacquet, E; Ropert, M; Bouvet, R; Génin, E; Mosser, J; Deugnier, Y
Movement disorders and brain iron overload in a new subtype of aceruloplasminemia
2015 Melgari, J; Marano, M; Quattrocchi, C; Piperno, A; Arosio, C; Frontali, M; Nuovo, S; Siotto, M; Salomone, G; Altavilla, R; di Biase, L; Scrascia, F; Squitti, R; Vernieri, F
Iron chelation with deferasirox in a patient with de-novo ferroportin mutation
2015 Unal, S; Piperno, A; Gumruk, F
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