Low plasma heparin cofactor II levels in thalassaemia syndromes are corrected by chronic blood transfusion
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1995.tb03381.x/fullpdf
Reference30 articles.
1. Hereditary Heparin Cofactor II Deficiency and the Risk of Development of Thrombosis
2. Screening Coagulation Tests and Clotting Factors in Homozygous β-Thalassemia
3. Plasma dermatan sulfate proteoglycan in a patient on chronic hemodialysis
4. PADGEM/GMP-140 expression on platelet membranes from homozygous beta thalassaemic patients
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