TAVAZZI, DARIO
TAVAZZI, DARIO
Dipartimento di Scienze Cliniche e di Comunità
A large deletion on chromosome 11 in acute intermittent porphyria
2006 E. Di Pierro, V. Besana, V. Moriondo, V. Brancaleoni, D. Tavazzi, G. Casalgrandi, P. Ventura, E. Rocchi, M.D. Cappellini
A novel mutation in the first italian patient of hereditary coproporphyria
2008 S. Ausenda, E. Di Pierro, V. Besana, V. Brancaleoni, D. Tavazzi, E. Cassinerio, M.D. Cappellini
A novel mutation in the first Italian patient of hereditary coproporphyria
2007 S. Ausenda, E. Di Pierro, V. Besana, V. Brancaleoni, D. Tavazzi, 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
Acute intermittent porphyria : heterogeneity of mutations in the hydroxymethylbilane synthase gene in Italy
2001 F. Martinez di Montemuros, E. Di Pierro, G. Biolcati, E. Rocchi, E. Bissolotti, D. Tavazzi, G. Fiorelli, M.D. Cappellini
Behaviour of glucose-6-phosphate dehydrogenase during erythroid maturation
1991 M.D. Cappellini, S. Villa, A. Gaviraghi, F. Martinez di Montemuros, D. Tavazzi, D. Panzeri, G. Fiorelli
Biochemical and molecular characterization of a new sporadic glucose-6-phosphate dehydrogenase variant described in Italy : G6PD Modena
1994 M.D. Cappellini, M. Sampietro, D. Toniolo, G. Carandina, S. Pittalis, F. Martinez Di Montemuros, D. Tavazzi, G. Fiorelli
C-terminal deletion in the ALAS2 gene and X-linked dominant protoporphyria
2009 E. Di Pierro, V. Brancaleoni, D. Tavazzi, M.D. Cappellini
C-terminal deletion in the ALAS2 gene and X-linked dominant protoporphyria
2009 V. Brancaleoni, E. Di Pierro, D. Tavazzi, C. Cesaretti, M.D. Cappellini
C-terminal deletion in the ALAS2 gene causes X-linked erythropoietic protoporphyria (EPP) despite of wild type fech gene
2009 V. Brancaleoni, E. Di Pierro, D. Tavazzi, M.D. Cappellini
Cell-free DNA (CFDNA) and ineffective erythropoiesis in thalassemia intermedia
2010 M. Sampietro, D. Tavazzi, C. Cesaretti, I. Nava, L. Duca, M.D. Cappellini
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
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
Cholelithiasis in thalassemia major
2009 R. Origa, R. Galanello, L. Perseu, D. Tavazzi, M.D. Cappellini, L. Terenzani, G.L. Forni, G. Quarta, T. Boetti, A. Piga
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
Clinical, biochemical and genetic characteristics of Variegate Porphyria in Italy
2009 E. Di Pierro, P. Ventura, V. Brancaleoni, V. Moriondo, S. Marchini, D. Tavazzi, F. Nascimbeni, M.C. Ferrari, E. Rocchi, M.D. Cappellini
Epidemiological shift of glucose-6-phosphate dehydrogenase mutations in Northern Italy in the last 15 years
2021 L. Duca, I. Nava, D. Tavazzi, A. Marcon, I. Motta, G. Graziadei
Ferrochelatase gene : molecular analysis in Italian patients with erythropoietic protoporphyria
2005 E. Di Pierro, V. Moriondo, D. Tavazzi, P. Bonara, L. Perego, M.D. Cappellini
G6PD Ferrara I has the same two mutations as G6PD A(-) but a distinct biochemical phenotype
1994 M.D. Cappellini, M. Sampietro, D. Toniolo, G. Carandina, F. Martinez Di Montemuros, D. Tavazzi, G. Fiorelli
Gene symbol : G6PD. Disease : Glucose-6-phosphate dehydrogenase deficiency
2008 P. Delbini, L. Duca, I. Nava, D. Tavazzi, M.D. Cappellini