TAVAZZI, DARIO

TAVAZZI, DARIO  

Dipartimento di Scienze Cliniche e di Comunità  

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Risultati 1 - 20 di 54 (tempo di esecuzione: 0.021 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A large deletion on chromosome 11 in acute intermittent porphyria 1-lug-2006 E. Di PierroD. TavazziM.D. Cappellini + Article (author) -
A novel mutation in the first italian patient of hereditary coproporphyria 1-ott-2008 E. Di PierroD. TavazziM.D. Cappellini + Article (author) -
A novel mutation in the first Italian patient of hereditary coproporphyria 1-gen-2007 E. Di PierroD. TavazziM.D. Cappellini + Conference Object -
Aberrant methylation of oncosuppressor genes detected in the peripheral blood of patients with chronic hepatitis C and hepatocellular carcinoma 1-mar-2011 M. SampietroA.L. FracanzaniD. TavazziC. BertelliD. BignaminiL.V.C. ValentiS.R. Fargion + Article (author) -
Acute intermittent porphyria : heterogeneity of mutations in the hydroxymethylbilane synthase gene in Italy 1-gen-2001 F. Martinez di MontemurosE. Di PierroD. TavazziG. FiorelliM.D. Cappellini + Article (author) -
Behaviour of glucose-6-phosphate dehydrogenase during erythroid maturation 1-gen-1991 M.D. CappelliniD. Tavazzi + Article (author) -
Biochemical and molecular characterization of a new sporadic glucose-6-phosphate dehydrogenase variant described in Italy : G6PD Modena 1-mag-1994 M.D. CappelliniM. SampietroF. Martinez Di MontemurosD. TavazziG. Fiorelli + Article (author) -
C-terminal deletion in the ALAS2 gene and X-linked dominant protoporphyria 1-giu-2009 E. Di PierroD. TavazziM.D. Cappellini + Article (author) -
C-terminal deletion in the ALAS2 gene and X-linked dominant protoporphyria 1-ott-2009 E. Di PierroD. TavazziC. CesarettiM.D. Cappellini + Article (author) -
C-terminal deletion in the ALAS2 gene causes X-linked erythropoietic protoporphyria (EPP) despite of wild type fech gene 1-dic-2009 E. Di PierroD. TavazziM.D. Cappellini + Article (author) -
Cell-free DNA (CFDNA) and ineffective erythropoiesis in thalassemia intermedia 1-giu-2010 SAMPIETRO, MAURIZIOD. TavazziC. CesarettiI. NavaL. DucaM. D. Cappellini Article (author) -
Cell-free DNA in HCV-related cirrhosis and small hepatocellular carcinoma 1-ott-2008 M. SampietroA.L. FracanzaniL. ValentiC. BertelliE. FattaD. BignaminiD. TavazziS. Fargion Article (author) -
Cell-free DNA in HCV-related cirrhosis and small hepatocellular carcinoma 1-ott-2008 M. SampietroA.L. FracanzaniL. ValentiC. BertelliE. FattaD. BignaminiD. TavazziS. Fargion Article (author) -
Cholelithiasis in thalassemia major 1-gen-2009 D. TavazziM.D. Cappellini + Article (author) -
Circulating cell-free DNA and ineffective erythropoiesis in nontransfusion-dependent β-thalassemia 1-nov-2018 Tavazzi, DarioMotta, IreneGraziadei, GiovannaSampietro, MaurizioDuca, LorenaCappellini, Maria Domenica Article (author) -
Clinical, biochemical and genetic characteristics of Variegate Porphyria in Italy 1-lug-2009 E. Di PierroD. TavazziM.D. Cappellini + Article (author) -
Epidemiological shift of glucose-6-phosphate dehydrogenase mutations in Northern Italy in the last 15 years 1-nov-2021 Duca L.Nava I.Tavazzi D.Marcon A.Motta I.Graziadei G. Article (author) -
Ferrochelatase gene : molecular analysis in Italian patients with erythropoietic protoporphyria 1-lug-2005 D. TavazziM.D. Cappellini + Article (author) -
G6PD Ferrara I has the same two mutations as G6PD A(-) but a distinct biochemical phenotype 1-feb-1994 M.D. CappelliniM. SampietroF. Martinez Di MontemurosD. TavazziG. Fiorelli + Article (author) -
Gene symbol : G6PD. Disease : Glucose-6-phosphate dehydrogenase deficiency 1-ott-2008 P. DelbiniL. DucaI. NavaD. TavazziM.D. Cappellini Article (author) -