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Titolo Data di pubblicazione Autori Tipo File Abstract
Behaviour of glucose-6-phosphate dehydrogenase during erythroid maturation 1991 M.D. CappelliniD. Tavazzi + Article (author) -
G6PD Ferrara I has the same two mutations as G6PD A(-) but a distinct biochemical phenotype 1994 M.D. CappelliniM. SampietroF. Martinez Di MontemurosD. TavazziG. Fiorelli + Article (author) -
Biochemical and molecular characterization of a new sporadic glucose-6-phosphate dehydrogenase variant described in Italy : G6PD Modena 1994 M.D. CappelliniM. SampietroF. Martinez Di MontemurosD. TavazziG. Fiorelli + Article (author) -
Molecular characterisation of an Italian G6PD variant responsible for chronic non-spherocytic haemolytic anaemia 1994 F. Martinez di MontemurosM.D. CappelliniD. TavazziG. Fiorelli + Article (author) -
Molecular characterisation of the glucose-6-phosphate dehydrogenase (G6PD) Ferrara II variant 1995 M.D. CappelliniF. Martinez Di MontemurosD. TavazziG. Fiorelli + Article (author) -
Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in Italy 1997 F. Martinez Di MontemurosD. TavazziG. FiorelliM.D. Cappellini + Article (author) -
Indices of membrane alterations in beta-thalassemic erythrocytes 1998 D. TavazziM.D. Cappellini + Article (author) -
Acute intermittent porphyria : heterogeneity of mutations in the hydroxymethylbilane synthase gene in Italy 2001 F. Martinez di MontemurosE. Di PierroD. TavazziG. FiorelliM.D. Cappellini + Article (author) -
Membrane-bound iron contributes to oxidative damage of beta-thalassaemia intermedia erythrocytes 2001 D. TavazziL. DucaG. FiorelliM.D. Cappellini + Article (author) -
TT virus infection in adult beta-thalassemia major patients 2001 M. SampietroD. TavazziS. FargionG. FiorelliM.D. Cappellini + Article (author) -
Mutations in the HFE gene and their interaction with exogenous risk factors in hepatocellular carcinoma 2001 S.R. FargionA.L. FracanzaniM. SampietroD. TavazziC. Mariani + Article (author) -
Seven novel point mutations in the uroporphyrinogen decarboxylase (UROD) gene in patients with familial porphyria cutanea tarda (f-PCT) 2001 M.D. CappelliniD. TavazziS. FargionG. Fiorelli + Article (author) -
Hyperferritinemia, iron overload and multiple metabolic alterations identify patients at risk for nonalcoholic steatohepatitis 2001 S.R. FargionA.L. FracanzaniM. SampietroD. TavazziL. Valenti + Article (author) -
Levels of uroporphyrinogen decarboxylase (URO-D) in erythocytes of Italian porphyria cutanea tarda patients 2002 D. TAVAZZIS.R. FARGIONA.L. FRACANZANIM.D. CAPPELLINI + Article (author) -
Red blood cell antioxidant and iron status in alcoholic and nonalcoholic cirrhosis 2002 G. FiorelliD. TavazziS. FargionM.D. Cappellini + Article (author) -
Molecular characterization of porphyrias in Italy : a diagnostic flow-chart 2002 F. Martinez di MontemurosE. Di PierroD. TavazziM.D. Cappellini + Article (author) -
Gene symbol : UROD. Disease : Porphyria, cutanea tarda 2003 D. TavazziM.D. Cappellini + Article (author) -
Human gene mutations. Gene symbol : UROD. Disease : Porphyria, cutanea tarda 2004 D. TavazziM.D. Cappellini + Article (author) -
Ferrochelatase gene : molecular analysis in Italian patients with erythropoietic protoporphyria 2005 D. TavazziM.D. Cappellini + Article (author) -
Large deletion of Cromosome 11 causes acute intermittent porphiryria in an Italian family 2005 E. Di PierroD. TavazziM.D. Cappellini + Article (author) -
Mostrati risultati da 1 a 20 di 54
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