All Stories

  1. Hematological and Molecular Findings in the First Case of Hb J-Norfolk [HBA2: c.173G>A (or HBA1] in an Indian Patient
  2. Molecular Pathology of Rare Bleeding Disorders (RBDs) in India: A Systematic Review
  3. Confirmation of Hb S detected on HPLC involves a three-tier process
  4. Liquid nitrogen or laboratory freezers for storage of samples: several factors affect the choice
  5. Hb Koln [β98(FG5) [GTG → ATG, Val → Met]: The first report from India
  6. Variable Presentation of HB H Disease Due to Homozygosity for the Rare Polyadenylation Signal A TIndian(AATAAA>AATA– –) Mutation in Four Indian Families
  7. Hemoglobin Fontainebleau [a21(B2)Ala>Pro]: The second report from India
  8. Research update for articles published in EJCI in 2010
  9. SRY sequence in maternal plasma: Implications for non-invasive prenatal diagnosis: First report from India
  10. Hb H Disease Due to Homozygosity for a Rare α2-Globin Variant, Hb Sallanches
  11. Response to hydroxyurea in β thalassemia major and intermedia: Experience in western India
  12. Hematological and Molecular Analysis of Novel and Rare β-Thalassemia Mutations in the Indian Population
  13. Diagnostic Pitfalls and Fallacies of Measuring Antiplatelet Antibodies
  14. Co-existence of Bernard Soulier syndrome and factor XI deficiency in a family: A unified pathology?
  15. Platelet function tests using platelet aggregometry: need for repetition of the test for diagnosis of defective platelet function
  16. Human platelet alloantigen polymorphism in Glanzmann's thrombasthenia and its impact on the severity of the disease
  17. Glanzmann's thrombasthenia: updated
  18. Glanzmann’s Thrombasthenia
  19. Changes in platelet glycoprotein receptors after smoking – a flow cytometric study
  20. Functional and fibrinogen receptor studies in platelets in pre-eclamptic toxaemia of pregnancy