Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years)
Author:
Affiliation:
1. Department of Medicine; University of Padua Medical School; Padua Italy
2. Division of Medicine; Padua City Hospital; Padua Italy
Funder
Associazione Emofilia ed altre Coagulopatie delle Tre Venezie
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ejh.12767/fullpdf
Reference33 articles.
1. A new coagulation defect;Telfer;Br J Haematol,1956
2. Stuart clotting defect I. segregation of an hereditary hemorrhagic state from the heterogeneous group heretofore called stable factor (SPCA, Proconvertin, Factor VII) deficiency;Hougie;J Clin Invest,1957
3. Stuart clotting defect. II. Genetic aspects of a new hemorrhagic state;Graham;J Clin Invest,1957
4. Uber einen neuartigen kongenitalen gerinnungs defect (Mangel an Stuart Faktor);Bachmann;Thromb Diath Haemorrh,1957
5. A “new” congenital haemorrhagic condition due to the presence of an abnormal factor X (factor X Friuli): study of a large kindred;Girolami;Br J Haematol,1970
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