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Clinical Biochemistry|July 14, 2009
The significance of the hemoglobin A(2) value in screening for hemoglobinopathiesAntonino Giambona, Cristina Passarello, Disma Renda, et al.Expert Review of Cardiovascular Therapy|March 20, 2004
Cardiac complications in thalassemia: noninvasive detection methods and new directions in the clinical managementLuigi Mancuso, Gaetano Panzarella, Tommaso Vincenzo Bartolotta, et al.Haematologica|December 6, 2006
Analysis of delta-globin gene alleles in the Sicilian population: identification of five new mutationsAntonino Giambona, Cristina Passarello, Gaetano Ruggeri, et al.British Journal of Haematology|August 12, 2008
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 geneCristina Passarello, Antonino Giambona, Luciano Prossomariti, et al.Hemoglobin|November 25, 2017
HBB: c.316-125A>G and HBB: c.316-42delC: Phenotypic Evaluations of Two Rare Changes in the Second Intron of the HBB GeneMargherita Vinciguerra, Monica Cannata, Filippo Cassarà, et al.Journal of Clinical Pathology|August 11, 2017
Phenotypic evaluations of <i>HBB</i>:c.93-23T>C, a nucleotide substitution in the IVS I nt 108 of β-globin geneMargherita Vinciguerra, Filippo Cassarà, Monica Cannata, et al.International Journal of Molecular Sciences|March 3, 2018
Chronic Administration of Hydroxyurea (HU) Benefits Caucasian Patients with Sickle-Beta ThalassemiaRosario Di Maggio, Matthew M Hsieh, Xiongce Zhao, et al.Haematologica|July 8, 2008
Significance of borderline hemoglobin A2 values in an Italian population with a high prevalence of beta-thalassemiaAntonino Giambona, Cristina Passarello, Margherita Vinciguerra, et al.British Journal of Haematology|October 20, 2010
Desensitization to hydroxycarbamide following long-term treatment of thalassaemia intermedia as observed in vivo and in primary erythroid cultures from treated patientsPaolo Rigano, Alice Pecoraro, Roberta Calzolari, et al.Blood Cells, Molecules & Diseases|March 1, 2011
The genetic heterogeneity of β-globin gene defects in Sicily reflects the historic population migrations of the islandAntonino Giambona, Margherita Vinciguerra, Monica Cannata, et al.Pageof 2