The Classification of Congenital Factor X Deficiency and Abnormalities
Author:
Affiliation:
1. University of Padua Medical School, Second Chair of Medicine, Padua, Italy
Publisher
King Faisal Specialist Hospital and Research Centre
Subject
General Medicine
Reference20 articles.
1. Family with Factor X Variant Defective Only in Factor VII Activation (X + Riyadh)
2. Tentative and updated classification of factor X variants;Girolami A;Acta Hematol (Basel),1986
3. Uber einen neuartigen kongenitalen Gerinnungsdefekt (Mangel and Stuart-Factor);Bachmann F;Thromb Diath Haemorrh,1957
4. Stuart clotting defect: segregation of a hereditary hemorrhagic state from the heterozygous heretofore called “stable factor” (SPCA, proconvertin factor VII deficiency);Hougie C;J Clin Invest,1957
5. A new coagulation defect;Telfer TP;Br J Haematol,1956
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Persistent validity of a classification of congenital factor X defects based on clotting, chromogenic and immunological assays even in the molecular biology era;Haemophilia;2010-12-29
2. Discrepancies between clotting and amidolytic assay in congenital clotting disorders;Thrombosis Research;1990-08
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