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Fyn specifically Regulates the activity of red cell glucose-6-phosphate-dehydrogenase

Redox biology, 2020-09, Vol.36, p.101639, Article 101639

2020

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Pregnancy and beta-thalassemia: an Italian multicenter experience

Haematologica (Roma), 2010-03, Vol.95 (3), p.376

2010

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Management of Iron Overload in Beta-Thalassemia Patients: Clinical Practice Update Based on Case Series

International journal of molecular sciences, 2020-11, Vol.21 (22), p.8771

2020

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CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients

Haematologica (Roma), 2012-12, Vol.97 (12), p.1818

2012

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Special Issue: “Emerging Therapies and Strategies in Thalassemia: Toward a New Era in Management”

Journal of clinical medicine, 2022-09, Vol.11 (17), p.5175

2022

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Safety and efficacy of ketorolac continuous infusion for multimodal analgesia of vaso-occlusive crisis in patients with sickle cell disease

Orphanet journal of rare diseases, 2024-01, Vol.19 (1), p.22-22, Article 22

2024

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A Rapid, Affordable and Feasible Method for Detection of the HBG1: g.-225_-222delAGCA Polymorphism

Hemoglobin, 2018-07, Vol.42 (4), p.283-285

2018

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Stem Cell Modeling of Neuroferritinopathy Reveals Iron as a Determinant of Senescence and Ferroptosis during Neuronal Aging

Stem cell reports, 2019-11, Vol.13 (5), p.832-846

2019

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A pilot trial of deferiprone for neurodegeneration with brain iron accumulation

Haematologica (Roma), 2011-11, Vol.96 (11), p.1708

2011

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Quality of Life and Burden of Disease in Italian Patients with Transfusion-Dependent Beta-Thalassemia

Journal of clinical medicine, 2021-12, Vol.11 (1), p.15

2021

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Complex Modes of Inheritance in Hereditary Red Blood Cell Disorders: A Case Series Study of 155 Patients

Genes, 2021-06, Vol.12 (7), p.958

2021

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Current challenges in the management of patients with sickle cell disease - A report of the Italian experience

Orphanet journal of rare diseases, 2019-05, Vol.14 (1), p.120-120, Article 120

2019

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PB2530: DIXON‐BASED R2 MRI AS AN INTEGRATION/SUBSTITUTE OF STANDARD T2/R2 IN THE EVALUATION OF IRON OVERLOAD IN THE UPPER ABDOMEN

HemaSphere, 2023-08, Vol.7 (S3), p.e9400165-n/a

2023

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Efficacy and safety of deferiprone for the treatment of superficial siderosis: results from a long-term observational study

Neurological sciences, 2019-07, Vol.40 (7), p.1357-1361

2019

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First and Second Level Haemoglobinopathies Diagnosis: Best Practices of the Italian Society of Thalassemia and Haemoglobinopathies (SITE)

Journal of clinical medicine, 2022-09, Vol.11 (18), p.5426

2022

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A phase 2 study of the safety, tolerability, and pharmacodynamics of FBS0701, a novel oral iron chelator, in transfusional iron overload

Blood, 2012-04, Vol.119 (14), p.3263-3268

2012

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P1452: MORTALITY AND CLINICAL COMPLICATIONS AMONG PATIENTS WITH TRANSFUSION‐DEPENDENT BETA‐THALASSEMIA IN ITALY

HemaSphere, 2023-08, Vol.7 (S3), p.e91927ad-n/a

2023

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P1447: MORTALITY AND CLINICAL COMPLICATIONS AMONG PATIENTS WITH SICKLE CELL DISEASE WITH RECURRENT VASO‐OCCLUSIVE CRISES IN ITALY

HemaSphere, 2023-08, Vol.7 (S3), p.e8075902-n/a

2023

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Nephrological Complications in Hemoglobinopathies: SITE Good Practice

Journal of clinical medicine, 2023-12, Vol.12 (23), p.7476

2023

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Management of the Sickle Cell Trait: An Opinion by Expert Panel Members

Journal of clinical medicine, 2023-05, Vol.12 (10), p.3441

2023

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Long-Term Neuroradiological and Clinical Evaluation of NBIA Patients Treated with a Deferiprone Based Iron-Chelation Therapy

Journal of clinical medicine, 2022-08, Vol.11 (15), p.4524

2022

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Real-World Evidence on Disease Burden and Economic Impact of Sickle Cell Disease in Italy

Journal of clinical medicine, 2022-12, Vol.12 (1), p.117

2022

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P1449: SAFETY PROFILE OF KETOROLAC CONTINUOUS INFUSION IN SICKLE CELL RELATED ACUTE VASO‐OCCLUSIVE CRISIS

HemaSphere, 2023-08, Vol.7 (S3), p.e2003822-n/a

2023

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P1472: COINHERITANCE OF PIEZO1 VARIANTS AND MULTI‐LOCUS RED BLOOD CELL DEFECTS ACCOUNT FOR THE SYMPTOMATIC PHENOTYPE IN BETA‐THALASSEMIA CARRIERS

HemaSphere, 2023-08, Vol.7 (S3), p.e8562808-n/a

2023

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PB2535: TRIAL IN PROGRESS: A PHASE 2, DOUBLE‐BLIND, RANDOMIZED, PLACEBO‐CONTROLLED, MULTICENTER STUDY TO EVALUATE THE EFFICACY AND SAFETY OF LUSPATERCEPT TO TREAT ANEMIA IN ADULTS WITH ALPHA‐THALASSEMIA

HemaSphere, 2023-08, Vol.7 (S3), p.e19231b2-n/a

2023

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Fyn specifically Regulates the activity of red cell glucose-6-phosphate-dehydrogenase

Pregnancy and beta-thalassemia: an Italian multicenter experience

Management of Iron Overload in Beta-Thalassemia Patients: Clinical Practice Update Based on Case Series

CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients

Special Issue: “Emerging Therapies and Strategies in Thalassemia: Toward a New Era in Management”

Safety and efficacy of ketorolac continuous infusion for multimodal analgesia of vaso-occlusive crisis in patients with sickle cell disease

A Rapid, Affordable and Feasible Method for Detection of the HBG1: g.-225_-222delAGCA Polymorphism

Stem Cell Modeling of Neuroferritinopathy Reveals Iron as a Determinant of Senescence and Ferroptosis during Neuronal Aging

A pilot trial of deferiprone for neurodegeneration with brain iron accumulation

Quality of Life and Burden of Disease in Italian Patients with Transfusion-Dependent Beta-Thalassemia

Complex Modes of Inheritance in Hereditary Red Blood Cell Disorders: A Case Series Study of 155 Patients

Current challenges in the management of patients with sickle cell disease - A report of the Italian experience

PB2530: DIXON‐BASED R2 MRI AS AN INTEGRATION/SUBSTITUTE OF STANDARD T2/R2 IN THE EVALUATION OF IRON OVERLOAD IN THE UPPER ABDOMEN

Efficacy and safety of deferiprone for the treatment of superficial siderosis: results from a long-term observational study

First and Second Level Haemoglobinopathies Diagnosis: Best Practices of the Italian Society of Thalassemia and Haemoglobinopathies (SITE)

A phase 2 study of the safety, tolerability, and pharmacodynamics of FBS0701, a novel oral iron chelator, in transfusional iron overload

P1452: MORTALITY AND CLINICAL COMPLICATIONS AMONG PATIENTS WITH TRANSFUSION‐DEPENDENT BETA‐THALASSEMIA IN ITALY

P1447: MORTALITY AND CLINICAL COMPLICATIONS AMONG PATIENTS WITH SICKLE CELL DISEASE WITH RECURRENT VASO‐OCCLUSIVE CRISES IN ITALY

Nephrological Complications in Hemoglobinopathies: SITE Good Practice

Management of the Sickle Cell Trait: An Opinion by Expert Panel Members

Long-Term Neuroradiological and Clinical Evaluation of NBIA Patients Treated with a Deferiprone Based Iron-Chelation Therapy

Real-World Evidence on Disease Burden and Economic Impact of Sickle Cell Disease in Italy

P1449: SAFETY PROFILE OF KETOROLAC CONTINUOUS INFUSION IN SICKLE CELL RELATED ACUTE VASO‐OCCLUSIVE CRISIS

P1472: COINHERITANCE OF PIEZO1 VARIANTS AND MULTI‐LOCUS RED BLOOD CELL DEFECTS ACCOUNT FOR THE SYMPTOMATIC PHENOTYPE IN BETA‐THALASSEMIA CARRIERS

PB2535: TRIAL IN PROGRESS: A PHASE 2, DOUBLE‐BLIND, RANDOMIZED, PLACEBO‐CONTROLLED, MULTICENTER STUDY TO EVALUATE THE EFFICACY AND SAFETY OF LUSPATERCEPT TO TREAT ANEMIA IN ADULTS WITH ALPHA‐THALASSEMIA

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