All Stories

  1. Effect of Aging on Deferasirox Therapy in Transfusion-dependent Patients. A Prospective- Retrospective, Cohort-study
  2. Daily alternating deferasirox and deferiprone therapy successfully controls iron accumulation in untreatable transfusion-dependent thalassemia patients
  3. A Rapid, Affordable and Feasible Method for Detection of the HBG1: g.-225_-222delAGCA Polymorphism
  4. Renal safety under long-course deferasirox therapy in iron overloaded transfusion-dependent β-thalassemia and other anemias
  5. Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias
  6. Pseudoxanthoma Elasticum-Like in β-Thalassemia Major, a matter of α-Klotho and Parathyroid Hormone?
  7. Noninvasive monitoring of liver fibrosis in sickle cell disease: Longitudinal observation of a cohort of adult patients
  8. Treatment of hepatitis C virus infection with direct-acting antiviral drugs is safe and effective in patients with hemoglobinopathies
  9. Hydroxyurea prescription, availability and use for children with sickle cell disease in Italy: Results of a National Multicenter survey
  10. Hepatocellular carcinoma in thalassaemia: an update of the Italian Registry
  11. Development of interactive algorithm for clinical management of acute events related to sickle cell disease in emergency department
  12. Efficacy and safety of deferiprone for the treatment of pantothenate kinase-associated neurodegeneration (PKAN) and neurodegeneration with brain iron accumulation (NBIA): Results from a four years follow-up
  13. Diagnostic value of real-time elastography in the assessment of hepatic fibrosis in patients with liver iron overload
  14. Transferrin‐immune complex disease: A potentially overlooked gammopathy mediated by IgM and IgG
  15. Assessment and management of iron overload in β‐thalassaemia major patients during the 21st century: a real‐life experience from the Italian Webthal project
  16. Neridronate improves bone mineral density and reduces back pain in β‐thalassaemia patients with osteoporosis: results from a phase 2, randomized, parallel‐arm, open‐label study
  17. Congenital Dyserythropoietic Anemia Type II: molecular analysis and expression of the SEC23B Gene
  18. Changing patterns of splenectomy in transfusion‐dependent thalassemia patients
  19. Response of iron overload to deferasirox in rare transfusion‐dependent anaemias: equivalent effects on serum ferritin and labile plasma iron for haemolytic or production anaemias
  20. Risk factors for cholangiocarcinoma
  21. Long‐term safety and efficacy of deferasirox (Exjade®) for up to 5 years in transfusional iron‐overloaded patients with sickle cell disease
  22. Worldwide survey of T2* cardiovascular magnetic resonance in Thalassaemia
  23. Analysis of Nucleotide Variations in Genes of Iron Management in Patients of Parkinson's Disease and Other Movement Disorders
  24. Sequence Variations in Mitochondrial Ferritin: Distribution in Healthy Controls and Different Types of Patients
  25. Manual erythroexchange for chronic transfusion therapy in patients with sickle cell syndromes unresponsive to hydroxyurea: A long‐term follow‐up
  26. Mutational spectrum in congenital dyserythropoietic anemia type II: Identification of 19 novel variants in SEC23B gene
  27. Venous-Like Leg Ulcers without Venous Insufficiency in Congenital Anemia: Successful Treatment Using Compression Bandages
  28. Daily alternating deferasirox and deferiprone therapy for “hard‐to‐chelate” β‐thalassemia major patients
  29. The influence of treatment in specialized centers on survival of patients with thalassemia major
  30. Calibration of myocardial iron concentration against T2-star Cardiovascular Magnetic Resonance
  31. Cholelithiasis in thalassemia major
  32. Acquired iron overload associated with antitransferrin monoclonal immunoglobulin: A case report
  33. Regression of symptoms after selective iron chelation therapy in a case of neurodegeneration with brain iron accumulation
  34. Effect of Food, Type of Food, and Time of Food Intake on Deferasirox Bioavailability: Recommendations for an Optimal Deferasirox Administration Regimen
  35. Patient-Reported Outcomes of Deferasirox (Exjade®, ICL670) versus Deferoxamine in Sickle Cell Disease Patients with Transfusional Hemosiderosis
  36. Standardized T2* Map of a Normal Human Heart to Correct T2* Segmental Artefacts; Myocardial Iron Overload and Fibrosis in Thalassemia IntermediaVersusThalassemia Major Patients and Electrocardiogram Changes in Thalassemia Major Patients
  37. Relative response of patients with myelodysplastic syndromes and other transfusion‐dependent anaemias to deferasirox (ICL670): a 1‐yr prospective study
  38. Standardized T2* map of normal human heart in vivo to correct T2* segmental artefacts
  39. A randomised comparison of deferasiroxversusdeferoxamine for the treatment of transfusional iron overload in sickle cell disease
  40. Therapeutic Approaches to Pulmonary Hypertension in Hemoglobinopathies: Efficacy and Safety of Sildenafil in the Treatment of Severe Pulmonary Hypertension in Patients with Hemoglobinopathy
  41. Genetic and clinical heterogeneity of ferroportin disease
  42. Lack of Prognostic Value of Normalized Integrated Backscatter Analysis of Myocardium in Patients with Thalassemia Major: A Long‐Term Follow‐Up Study
  43. Hepatocellular carcinoma in the thalassaemia syndromes
  44. Typical manifestation of acute congestive heart failure in patients with Thalassaemia major causing diagnostic delay in the emergency room
  45. Pulmonary hypertension in patients with thalassemia major
  46. Nonrandom X‐Chromosome Inactivation in Hemopoietic Cells from Carriers of Dyskeratosis Congenita
  47. Nonrandom X-Chromosome Inactivation in Hemopoietic Cells from Carriers of Dyskeratosis Congenita
  48. Quantitative Texture Analysis in Two‐Dimensional Echocardiography
  49. G6PD deficiency‐related chronic hemolysis treated with splenectomy: A case report
  50. Dyskeratosis Congenita: Unusual Presenting Features Within a Kindred
  51. Increased ultrasonic myocardial reflectivity in patients with thalassemia major and iron overload
  52. Widespread multitissue deletions of the mitochondrial genome in the Pearson marrow-pancreas syndrome
  53. A new glucose-6-phosphate dehydrogenase variant with congenital nonspherocytic hemolytic anemia (G6PD Genova)