SAMPIETRO, MAURIZIO
SAMPIETRO, MAURIZIO
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
Circulating cell-free DNA and ineffective erythropoiesis in nontransfusion-dependent β-thalassemia
2018 D. Tavazzi, I. Motta, G. Graziadei, M. Sampietro, L. Duca, M.D. Cappellini
Aberrant methylation of oncosuppressor genes detected in the peripheral blood of patients with chronic hepatitis C and hepatocellular carcinoma
2011 M. Sampietro, A.L. Fracanzani, D. Tavazzi, A. Cespiati, C. Bertelli, D. Bignamini, L.V.C. Valenti, S.R. Fargion
Cell-free DNA (CFDNA) and ineffective erythropoiesis in thalassemia intermedia
2010 M. Sampietro, D. Tavazzi, C. Cesaretti, I. Nava, L. Duca, M.D. Cappellini
Hypermethylation of oncosuppressor genes in hereditary hemochromatosis
2010 M. Sampietro, A.L. Fracanzani, D. Tavazzi, C. Bertelli, R. Vaccaroli, R. Rametta, L.V.C. Valenti, S.R. Fargion
Cell-free DNA in HCV-related cirrhosis and small hepatocellular carcinoma
2008 M. Sampietro, A.L. Fracanzani, L. Valenti, C. Bertelli, E. Fatta, D. Bignamini, D. Tavazzi, S. Fargion
Progression of carotic atherosclerotic damage is related to alt values in patients with non alcoholic fatty liver disease
2008 E.A. Pulixi, L. Burdick, L. Valenti, C. Bertelli, E. Fatta, A. Maraschi, M. Sampietro, S. Fargion, A.L. Fracanzani
The risk of severe liver disease in NAFLD with normal amino-transferase levels : a role for insulin and diabetes
2008 A.L. Fracanzani, L. Valenti, E. Bugianesi, M. Andreoletti, A. Colli, E. Vanni, C. Bertelli, E. Fatta, D. Bignamini, G. Marchesini, M. Sampietro, S. Fargion
Cell-free DNA in HCV-related cirrhosis and small hepatocellular carcinoma
2008 M. Sampietro, A.L. Fracanzani, L. Valenti, C. Bertelli, E. Fatta, D. Bignamini, D. Tavazzi, S. Fargion
Liver cancer risk is increased in patients with porphyria cutanea tarda in comparison to matched control patients with chronic liver disease
2001 A.L. Fracanzani, E. Taioli, M. Sampietro, E. Fatta, C. Bertelli, G. Fiorelli, S. Fargion
Tumor necrosis factor alpha-promoter polymorphisms influence the phenotypic expression of hereditary hemochromatosis
2001 S.R. Fargion, L.V.C. Valenti, P. Dongiovanni, P. Scaccabarozzi, A.L. Fracanzani, E. Taioli, M. Mattioli, M. Sampietro, G. Fiorelli
Mutations in the HFE gene and their interaction with exogenous risk factors in hepatocellular carcinoma
2001 S.R. Fargion, M.A. Stazi, A.L. Fracanzani, M. Mattioli, M. Sampietro, D. Tavazzi, C. Bertelli, V. Patriarca, C. Mariani, G. Fiorelli
Hyperferritinemia, iron overload and multiple metabolic alterations identify patients at risk for nonalcoholic steatohepatitis
2001 S.R. Fargion, M. Mattioli, A.L. Fracanzani, M. Sampietro, D. Tavazzi, P. Fociani, E. Taioli, L. Valenti, G. Fiorelli
TT virus infection in adult beta-thalassemia major patients
2001 M. Sampietro, D. Tavazzi, F. Martinez di Montemuros, M. Cerino, S. Zatelli, G. Lunghi, A. Orlandi, S. Fargion, G. Fiorelli, M.D. Cappellini
Autoantibodies to human cytosol : a marker of sporadic porphyria cutanea tarda
2001 Y. Ma, A.L. Fracanzani, M. Sampietro, M. Mattioli, P. Cheeseman, R. Williams, G. Mieli-Vergani, D. Vergani, S.R. Fargion
Hereditary hemochromatosis in a patient with congenital dyserythropoietic anemia
2000 S.R. Fargion, L.V.C. Valenti, A.L. Fracanzani, M. Sampietro, M.D. Cappellini, A. Scaccabarozzi, D. Soligo, C. Mariani, G. Fiorelli
Immunohistochemistry of HFE in the duodenum of C282Y homozygotes with antisera for recombinant HFE protein
2000 L. Zuccon, B. Corsi, S. Levi, M. Mattioli, A.L. Fracanzani, A. Corti, A. Albertini, M. Sampietro, S.R. Fargion, P. Arosio
Molecular analysis of the TFR2 gene : report of a novel polymorphism (1878C*T)
2000 M. Meregalli, A. Pellagatti, E. Bissolotti, A.L. Fracanzani, S.R. Fargion, M. Sampietro
Siderosis in cirrhosis: is genetic hemochromatosis ruled out?
1998 S. Fargion, M. Mattioli, M. Sampietro, G. Fiorelli, L.R. Fassati, G. Rossi, E. David
Nontransfusional iron overload in thalassemia intermedia: role of the hemochromatosis allele
1998 M.D. Cappellini, S. Fargion, M. Sampietro, G. Graziadei, G. Fiorelli
High prevalence of the His63Asp HFE mutation in Italian patients with porphyria cutanea tarda
1998 M. Sampietro, A. Piperno, L. Lupica, C. Arosio, A. Vergani, N. Corbetta, I. Malosio, M. Mattioli, A.L. Fracanzani, M.D. Cappellini, G. Fiorelli, S.R. Fargion