References

  1. Alamelu J, Liesner R. Modern management of severe platelet function disorders. British Journal of Haematology. 2010; 149(6):813-823. PubMed | Google Scholar

  2. Nurden AT. Glanzmann thrombasthenia. Orphanet J Rare Dis. 2006; 1:10. PubMed | Google Scholar

  3. Elalamy I. Thrombopathies acquises et congénitales. EMC elsevier. 2006; 13-021-A-10. PubMed | Google Scholar

  4. Ben Aribia N, Mseddi S, Elloumi M, Kallel C, Kastally R, Souissi T. Genetic profile of Glanzmann's thrombasthenia in south Tunisia: report of 17 cases (11 families). Tunis Med. 2005; 83(4):208-12. PubMed | Google Scholar

  5. George JN, Caen JP, Nurden AT. Glanzmann's thrombasthenia: the spectrum of clinical disease. Blood. 1990; 75(7):1383-95. PubMed | Google Scholar

  6. Bolton-Maggs PH, Chalmers EA, Collins PW, Harrison P, Kitchen S, Liesner RJ et al. A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO. Br J Haematol. 2006; 135(5):603-33. PubMed | Google Scholar

  7. Jaouad IC, Elalaoui SC, Sbiti A, Elkerh F, Belmahi L, Sefiani A. Consanguineous marriages in Morocco and the consequence for the incidence of autosomal recessive disorders. J Biosoc Sci. 2009; 41(5):575-81. PubMed | Google Scholar

  8. Ali N, Moiz B, Shaikh U, Adil S, Rizvi B, Rahman Y. Diagnostic tool for Glanzmann's thrombasthenia clinicopathologic spectrum. J Coll Physicians Surg Pak. 2008; 18(2):91-4. PubMed | Google Scholar

  9. Toogeh G, Sharifian R, Lak M, Safaee R, Artoni A, Peyvandi F. Presentation and pattern of symptoms in 382 patients with Glanzmann thrombasthenia in Iran. Am J Hematol. 2004; 77(2):198-9. PubMed | Google Scholar

  10. Saraya AK, Saxena R, Dhot PS, Choudhry VP, Pati H. Platelet function disorders in north India. Natl Med J India. 1994; 7(1):5-7. PubMed | Google Scholar

  11. Karimi M, Ravanbod S, Cohan N, Ala F. How to deal with medical and social aspects of bleeding disorders--preparing women and the family in developing countries. Haemophilia. 2011; 17(s1):42-4. PubMed | Google Scholar

  12. Franchini M, Favaloro EJ, Lippi G. Glanzmann thrombasthenia: an update. Clin Chim Acta. 2010; 411(1-2):1-6. PubMed | Google Scholar

  13. Harrison P, Mackie I, Mumford A, Briggs C, Liesner R, Winter M et al. Guidelines for the laboratory investigation of heritable disorders of platelet function. Br J Haematol. 2011; 155(1):30-44. PubMed | Google Scholar

  14. Elalamy I, Gkalea V, Gerotziafas G, Ketatni H, Hatmi M. The usefulness of platelet function evaluation in clinical practice. Ann Biol Clin. 2013; 71:47-57. PubMed | Google Scholar

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