Reference (Apr-21-A8)

  1. Benz, E. (2013). Clinical manifestations and diagnosis of the thalassemias. Up To Date 
  2. Mahdavi, M, Kowsarian, M, Karami, H, Mohseni, A, Vahidshahi, K, Roshan, P, Hojjati, M. & Ebrahimzadeh, M. (2010). Prevalence of hemoglobin alpha-chain gene deletion in neonates in North of Iran. Eur Rev Med Pharmacol Sci, 14(10), 871-875. 
  3. Muncie Jr, H.L. & Campbell, J.S. (2009). Alpha and beta thalassemia. Am Fam Physician, 80(4), 339-344. 
  4. Munkongdee, T, Chen, P, Winichagoon, P, Fucharoen, S. & Paiboonsukwong, K. (2020). Update in laboratory diagnosis of thalassemia. Front Mol Biosci, 7, 74. 
  5. Schrier, S.L. (2002). Pathophysiology of thalassemia. Curr Opin Hematol, 9(2), 123-126. 
  6. Tari, K, Valizadeh Ardalan, P, Abbaszadehdibavar, M, Atashi, A, Jalili, A. & Gheidishahran, M. (2018). Thalassemia an update: molecular basis, clinical features and treatment. Int J Biomed Public Health, 1(1), 48-58. 
  7. Lucarelli, G., Isgrò, A., Sodani, P. & Gaziev, J. (2012). Hematopoietic stem cell transplantation in thalassemia and sickle cell anemia. Cold Spring Harbor perspectives in medicine, 2(5), a011825. 
  8. Hassan, T. & Zakaria, M. (2020). Updates in Thalassemia. In, Beta Thalassemia: IntechOpen.
  9. Braude, P., Pickering, S., Flinter, F. & Ogilvie, C. M. (2002). Preimplantation genetic diagnosis. Nature Reviews Genetics, 3(12), 941-953.
Subscribe for free!Join our community to get full access to our content

Get updates about our magazine release, events and opportunities!