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Letter to the Editor

ACQUIRED VON WILLEBRAND DISEASE IN A TURKISH BOY WITH GAUCHER DISEASE

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Pages 317-319 | Received 31 Oct 2006, Accepted 22 Mar 2007, Published online: 09 Jul 2009

REFERENCES

  • Deghady A, Marzouk I, El-Shayeb A, Wali Y. Coagulation abnormalities in type 1 Gaucher disease in children. Pediatr Hematol Oncol 2006; 23: 411–417
  • Corrigan JJ. Hemorrhagic and thrombotic diseases: von Willebrand disease. Nelson's Textbook of Pediatrics ed. 15, RE Behrman, RM Kliegman, AM Arvin. WB Saunders, Philadelphia 1996; 1428
  • McGovern M M, Desnick R J. Abnormalities of the monocyte-macrophage system: lysosomal storage diseases. Wintrobe's Clinical Hematology, ed. 11, JP Greer, J Foerster, JN Lukens, GM Rodgers, F Paraskevas, B Glader. Lippincott Williams & Wilkins, Philadelphia 2003; 1819–1822
  • Billett H H, Rizvi S, Sawitsky A. Coagulation abnormalities in patients with Gaucher's disease: effect of therapy. Am J Hematol 1996; 51: 234–236
  • Hollak C E, Levi M, Berends F, Aerts J M, van Oers M H. Coagulation abnormalities in type 1 Gaucher disease are due to low-grade activation and can be partly restored by enzyme supplementation therapy. Br J Haematol 1997; 96: 470–476
  • Ozturk G, Kocak U, Gursel T, Ezgu F S. Coagulopathy in Gaucher disease. Indian J Pediatr 1998; 65: 771–772

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