Search Results - "MAGGIO, Aurelio"
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The New Voice for the New Era of Thalassemia Reports
Published in Thalassemia reports (01-03-2022)“…The recent transfer of Thalassemia Reports, the only journal fully dedicated on Thalassemia, from PagePress to MDPI was great news for those who contributed to…”
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Antioxidant, Pro-Survival and Pro-Regenerative Effects of Conditioned Medium from Wharton’s Jelly Mesenchymal Stem Cells on Developing Zebrafish Embryos
Published in International journal of molecular sciences (01-09-2023)“…Conditioned media harvested from stem cell culturing have the potential to be innovative therapeutic tools against various diseases, due to their high content…”
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Lentiviral globin gene therapy with reduced-intensity conditioning in adults with β-thalassemia: a phase 1 trial
Published in Nature medicine (01-01-2022)“…β-Thalassemias are inherited anemias that are caused by the absent or insufficient production of the β chain of hemoglobin. Here we report 6–8-year follow-up…”
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Wharton’s Jelly Mesenchymal Stromal Cells Support the Expansion of Cord Blood–derived CD34+ Cells Mimicking a Hematopoietic Niche in a Direct Cell–cell Contact Culture System
Published in Cell transplantation (01-01-2018)“…Wharton’s jelly mesenchymal stromal cells (WJ-MSCs) have been recently exploited as a feeder layer in coculture systems to expand umbilical cord…”
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2021 Thalassaemia International Federation Guidelines for the Management of Transfusion‐dependent Thalassemia
Published in HemaSphere (01-08-2022)“…Beta‐thalassemia and particularly its transfusion‐dependent form (TDT) is a demanding clinical condition, requiring life‐long care and follow‐up, ideally in…”
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CMR for myocardial iron overload quantification: calibration curve from the MIOT Network
Published in European radiology (01-06-2020)“…Objectives R2* cardiac magnetic resonance (CMR) allows the non-invasive measurement of myocardial iron. We calibrated cardiac R2* values against myocardial…”
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Survival and causes of death in 2,033 patients with non-transfusion-dependent β-thalassemia
Published in Haematologica (Roma) (01-09-2021)Get full text
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Current challenges in the management of patients with sickle cell disease - A report of the Italian experience
Published in Orphanet journal of rare diseases (30-05-2019)“…Sickle cell disease (SCD) is an inherited red blood cell disorder caused by a structural abnormality of hemoglobin called sickle hemoglobin (HbS). Clinical…”
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An optimized procedure for preparation of conditioned medium from Wharton’s jelly mesenchymal stromal cells isolated from umbilical cord
Published in Frontiers in molecular biosciences (02-10-2023)“…Cell-free therapy based on conditioned medium derived from mesenchymal stromal cells (MSCs) has gained attention in the field of protective and regenerative…”
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Bone Marrow Transplantation in Nonmalignant Haematological Diseases: What Have We Learned about Thalassemia?
Published in Thalassemia reports (01-06-2023)“…Allogeneic stem cell transplantation remains the only therapy for congenital, severe haemoglobinopathies that is able to reverse the pathological phenotype. In…”
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Antimicrobial prophylaxis in patients with immune thrombocytopenia treated with rituximab: a retrospective multicenter analysis
Published in Annals of hematology (01-03-2021)“…The primary aim of this study was to describe the use of primary anti-infective prophylaxis (AP) in common clinical practice in patients affected by immune…”
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Deferasirox, deferiprone and desferrioxamine treatment in thalassemia major patients: cardiac iron and function comparison determined by quantitative magnetic resonance imaging
Published in Haematologica (Roma) (01-01-2011)“…Oral deferiprone was suggested to be more effective than subcutaneous desferrioxamine for removing heart iron. Oral once-daily chelator deferasirox has…”
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Cystic Fibrosis assessment in infertile couples: genetic analysis trough the Next Generation Sequencing technique
Published in Clinical and experimental obstetrics & gynecology (01-05-2022)“…Background: Cystic Fibrosis (CF) is a genetic disease which is responsible for different systemic conditions. In particular, CF could be responsible for…”
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Multicenter validation of the magnetic resonance t2 technique for segmental and global quantification of myocardial iron
Published in Journal of magnetic resonance imaging (01-07-2009)“…Purpose To assess the transferability of the magnetic resonance imaging (MRI) multislice multiecho T2* technique for global and segmental measurement of iron…”
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RP1 Dominant p.Ser740 Pathogenic Variant in 20 Knowingly Unrelated Families Affected by Rod-Cone Dystrophy: Potential Founder Effect in Western Sicily
Published in Medicina (Kaunas, Lithuania) (01-02-2024)“… Retinitis pigmentosa (RP) is the most common inherited rod-cone dystrophy (RCD), resulting in nyctalopia, progressive visual field, and visual acuity decay…”
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Chronic Administration of Hydroxyurea (HU) Benefits Caucasian Patients with Sickle-Beta Thalassemia
Published in International journal of molecular sciences (28-02-2018)“…In sickle cell disease (SCD), hydroxyurea (HU) treatment decreases the number of vaso-occlusive crisis (VOC) and acute chest syndrome (ACS) by increasing fetal…”
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Multislice multiecho T2 cardiovascular magnetic resonance for detection of the heterogeneous distribution of myocardial iron overload
Published in Journal of magnetic resonance imaging (01-05-2006)“…Purpose To assess the tissue iron concentration of the left ventricle (LV) using a multislice, multiecho T2* MR technique and a segmental analysis. Materials…”
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Incidental Detection of a Chromosomal Aberration by Array-CGH in an Early Prenatal Diagnosis for Monogenic Disease on Coelomic Fluid
Published in Life (Basel, Switzerland) (21-12-2022)“…Turner syndrome is a rare genetic condition in which a female is partly or completely missing an X chromosome. Signs and symptoms vary among those affected. In…”
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A Patient with Sickle Cell Disease and Recurrent Venous Thromboembolism after Renal Transplantation
Published in Thalassemia reports (01-09-2022)“…Venous thromboembolism (VTE) is a life-threatening complication, especially in case of recurrence. The appropriate duration of anticoagulant treatment…”
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