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  1. Relationship Between Single-Nucleotide Polymorphisms of Tumor Necrosis Factor Alpha, Interleukin-10, Factor II and Factor V with Risk of Inhibitor Development in Patients with Severe Hemophilia A
  2. Intracranial hemorrhage in congenital bleeding disorders
  3. von Willebrand Disease
  4. Congenital Factor II Deficiency
  5. Inherited Platelet Function Disorders (IPFDs)
  6. First cases of severe congenital factor XIII deficiency in Southwestern Afghanistan in the vicinity of southeast of Iran
  7. Central nervous system bleeding in pediatric patients with factor XIII deficiency: A study on 23 new cases
  8. Biochezmical Interfering Factors and Blood Cells Indices
  9. Polymorphism of thrombin‐activatable fibrinolysis inhibitor and risk of intracranial haemorrhage in factor XIII deficiency
  10. A Prospective Study of Tubular Dysfunction in Pediatric Patients with Beta Thalassemia Major Receiving Deferasirox