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Journal of Clinical Medicine|December 9, 2023
Nephrological Complications in Hemoglobinopathies: SITE Good PracticeGiovan Battista Ruffo, Rodolfo Russo, Tommaso Casini, et al.European Radiology|February 14, 2020
CMR for myocardial iron overload quantification: calibration curve from the MIOT NetworkAntonella Meloni, Aurelio Maggio, Vincenzo Positano, et al.Hemoglobin|June 5, 2003
Potential myocardial iron content evaluation by magnetic resonance imaging in thalassemia major patients treated with Deferoxamine or Deferiprone during a randomized multicenter prospective clinical studyMassimo Galia, Massimo Midiri, Vincenzo Bartolotta, et al.Blood Cells, Molecules & Diseases|March 18, 2019
Cardiac involvement by CMR in different genotypic groups of thalassemia major patientsLaura Pistoia, Antonella Meloni, Stefano Salvadori, et al.Genes|June 27, 2024
Prenatal Diagnosis of Cystic Fibrosis by CelocentesisAntonino Giambona, Margherita Vinciguerra, Filippo Leto, et al.NMR in Biomedicine|January 6, 2007
Standardized T2* map of normal human heart in vivo to correct T2* segmental artefactsVincenzo Positano, Alessia Pepe, Maria Filomena Santarelli, et al.British Journal of Haematology|March 10, 2011
Feasibility of DNA diagnosis of haemoglobinopathies on coelocentesisAntonino Giambona, George Makrydimas, Filippo Leto, et al.European Journal of Internal Medicine|June 24, 2018
β-Thalassemia heterozygote state detrimentally affects health expectationLuciano Graffeo, Angela Vitrano, Salvatore Scondotto, et al.Haematologica|September 18, 2012
Mosaic segmental uniparental isodisomy and progressive clonal selection: a common mechanism of late onset β-thalassemia majorCornelis L Harteveld, Chiara Refaldi, Antonino Giambona, et al.Journal of Clinical Medicine|April 9, 2024
Prognostic Role of Multiparametric Cardiac Magnetic Resonance in Neo Transfusion-Dependent ThalassemiaAntonella Meloni, Laura Pistoia, Paolo Ricchi, et al.Pageof 13