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  1. Association between expression of MMP-2 and MMP-9 genes and pathogenesis of intracranial hemorrhage in severe coagulation factor XIII deficiency
  2. Central nervous system bleeding in pediatric patients with factor XIII deficiency: A study on 23 new cases
  3. C0105: Plasminogen Activator Inhibitor-1 Polymorphism is Not Associated with Central Nervous System Bleeding in Pediatric Patients with Factor XIII Deficiency
  4. Biochezmical Interfering Factors and Blood Cells Indices
  5. Evaluation of complement regulatory components in patients with atypical hemolytic uremic syndrome
  6. Frequency of β-Thalassemia or β-Hemoglobinopathy Carriers Simultaneously Affected with α-Thalassemia in Iran
  7. Polymorphism of thrombin‐activatable fibrinolysis inhibitor and risk of intracranial haemorrhage in factor XIII deficiency
  8. A Prospective Study of Tubular Dysfunction in Pediatric Patients with Beta Thalassemia Major Receiving Deferasirox
  9. Safety of human blood products in rare bleeding disorders in southeast of Iran