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Hemoglobin|June 3, 2016
Hb San Cataldo [β144(HC1)Lys→Thr; HBB: C.434A > C]: A New Hemoglobin Variant with Increased Affinity for OxygenMargherita Vinciguerra, Cristina Passarello, Filippo Cassarà, et al.Hemoglobin|May 29, 2015
Efficacy of Rapamycin as Inducer of Hb F in Primary Erythroid Cultures from Sickle Cell Disease and β-Thalassemia PatientsAlice Pecoraro, Antonio Troia, Roberta Calzolari, et al.Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology|January 10, 2022
Very early prenatal diagnosis of Cockayne's syndrome by coelocentesisAntonino Giambona, Margherita Vinciguerra, Filippo Leto, et al.International Journal of Laboratory Hematology|March 25, 2022
Early prenatal diagnosis of Hb Lepore Boston-Washington and β-thalassemia on fetal celomatic DNAAntonino Giambona, Filippo Leto, Filippo Cassarà, et al.Cell Transplantation|March 23, 2018
Wharton's Jelly Mesenchymal Stromal Cells Support the Expansion of Cord Blood-derived CD34<sup>+</sup> Cells Mimicking a Hematopoietic Niche in a Direct Cell-cell Contact Culture SystemMelania Lo Iacono, Eleonora Russo, Rita Anzalone, et al.Hematology (Amsterdam, Netherlands)|November 22, 2017
Co-inheritance of HBB:c.-106G > C, a rare single nucleotide variation at position -56 relative to transcription initiation site, with other known mutations in the globin clustersMargherita Vinciguerra, Cristina Passarello, Filippo Cassarà, et al.Annals of the New York Academy of Sciences|August 18, 2010
Strategy for a multicenter phase I clinical trial to evaluate globin gene transfer in beta-thalassemiaMichel Sadelain, Isabelle Rivière, Xiuyan Wang, et al.Clinical Chemistry and Laboratory Medicine|October 15, 2009
Nucleated red blood cells and soluble transferrin receptor in thalassemia syndromes: relationship with global and ineffective erythropoiesisPaolo Danise, Giovanni Amendola, Rosanna Di Concilio, 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.Hematology Reports|January 6, 2017
Study on Hydroxyurea Response in Hemoglobinopathies Patients Using Genetic Markers and Liquid Erythroid CulturesSerena Sclafani, Alice Pecoraro, Veronica Agrigento, et al.Pageof 13