Publications by authors named "Disma Renda"

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HBB: c.316-125A>G and HBB: c.316-42delC: Phenotypic Evaluations of Two Rare Changes in the Second Intron of the HBB Gene.
Margherita Vinciguerra, Monica Cannata, Filippo Cassarà, Cristina Passarello, Filippo Leto, Disma Renda

Hemoglobin· August 2018

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β-Thalassemia heterozygote state detrimentally affects health expectation.
Luciano Graffeo, Angela Vitrano, Salvatore Scondotto, Gabriella Dardanoni, Walter Sebastiano Pollina Addario, Disma Renda

Eur J Intern Med· August 2018

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Chronic Administration of Hydroxyurea (HU) Benefits Caucasian Patients with Sickle-Beta Thalassemia.
Rosario Di Maggio, Matthew M Hsieh, Xiongce Zhao, Giuseppina Calvaruso, Paolo Rigano, Disma Renda

Int J Mol Sci· February 2018

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Phenotypic evaluations of :c.93-23T>C, a nucleotide substitution in the IVS I nt 108 of β-globin gene.
Margherita Vinciguerra, Filippo Cassarà, Monica Cannata, Disma Renda, Giuseppina Calvaruso

J Clin Pathol· August 2017

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Embryo-fetal erythroid cell selection from celomic fluid allows earlier prenatal diagnosis of hemoglobinopathies.
Antonino Giambona, Gianfranca Damiani, Filippo Leto, Cristina Jakil, Disma Renda

Prenat Diagn· April 2016

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Deferiprone versus deferoxamine in sickle cell disease: results from a 5-year long-term Italian multi-center randomized clinical trial.
Giusi Calvaruso, Angela Vitrano, Rosario Di Maggio, Samir Ballas, Martin H Steinberg, Disma Renda

Blood Cells Mol Dis· December 2014

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Iron deficiency does not compromise the diagnosis of high HbA(2) β thalassemia trait.
Cristina Passarello, Antonino Giambona, Monica Cannata, Margherita Vinciguerra, Disma Renda

Haematologica· March 2012

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Marked impact of IL28B genotype in the natural clearance of hepatitis C virus in patients with haemoglobinopathies.
Maria Concetta Renda, Rosario F Ruggeri, Angela Piazza, Emanuela Fecarotta, Disma Renda

Br J Haematol· September 2011

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The genetic heterogeneity of β-globin gene defects in Sicily reflects the historic population migrations of the island.
Antonino Giambona, Margherita Vinciguerra, Monica Cannata, Filippo Cassarà, Germana Fiorentino, Disma Renda

Blood Cells Mol Dis· April 2011

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Feasibility of DNA diagnosis of haemoglobinopathies on coelocentesis.
Antonino Giambona, George Makrydimas, Filippo Leto, Gianfranca Damiani, Maria Cristina Jakil, Disma Renda, Maria Concetta Renda

Br J Haematol· April 2011

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Desensitization to hydroxycarbamide following long-term treatment of thalassaemia intermedia as observed in vivo and in primary erythroid cultures from treated patients.
Paolo Rigano, Alice Pecoraro, Roberta Calzolari, Antonio Troia, Santina Acuto, Disma Renda

Br J Haematol· December 2010

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Embryo-fetal erythroid megaloblasts in the human coelomic cavity.
Maria Concetta Renda, Antonino Giambona, Emanuela Fecarotta, Filippo Leto, George Makrydimas, Disma Renda

J Cell Physiol· November 2010

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Hepatocellular carcinoma in patients with thalassaemia syndromes: clinical characteristics and outcome in a long term single centre experience.
Gaetano Restivo Pantalone, Disma Renda, Franco Valenza, Fabio D'Amato, Angela Vitrano

Br J Haematol· July 2010

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The significance of the hemoglobin A(2) value in screening for hemoglobinopathies.
Antonino Giambona, Cristina Passarello, Disma Renda, Aurelio Maggio

Clin Biochem· December 2009

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Hb Southern Italy: coexistence of two missence mutations (the Hb Sun Prairie alpha2 130 Ala --> Pro and Hb Caserta alpha2 26 Ala --> Thr) in a single HBA2 gene.
Cristina Passarello, Antonino Giambona, Luciano Prossomariti, Massimiliano Ammirabile, Piero Pucci, Disma Renda

Br J Haematol· October 2008

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Significance of borderline hemoglobin A2 values in an Italian population with a high prevalence of beta-thalassemia.
Antonino Giambona, Cristina Passarello, Margherita Vinciguerra, Rita Li Muli, Pietro Teresi, Disma Renda

Haematologica· September 2008

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Analysis of delta-globin gene alleles in the Sicilian population: identification of five new mutations.
Antonino Giambona, Cristina Passarello, Gaetano Ruggeri, Disma Renda, Pietro Teresi

Haematologica· December 2006

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Treatment with hydroxycarbamide for intermedia thalassaemia: decrease of efficacy in some patients during long-term follow up.
Andrea Mancuso, Aurelio Maggio, Disma Renda, Rosalba Di Marzo, Paolo Rigano

Br J Haematol· April 2006

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Hepatocellular carcinoma on cirrhosis-free liver in a HCV-infected thalassemic.
Andrea Mancuso, Paolo Rigano, Disma Renda, Veronica Di Salvo, Caterina Borgna Pignatti

Am J Hematol· February 2005

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Hepatocellular carcinoma in the thalassaemia syndromes.
Caterina Borgna-Pignatti, Gianluca Vergine, Turi Lombardo, Maria Domenica Cappellini, Paolo Cianciulli, Disma Renda

Br J Haematol· January 2004

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Cardiac complications in thalassemia: noninvasive detection methods and new directions in the clinical management.
Luigi Mancuso, Gaetano Panzarella, Tommaso Vincenzo Bartolotta, Massimo Midiri, Disma Renda

Expert Rev Cardiovasc Ther· September 2003

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