Neonatal onset of congenital factor X deficiency
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Hematology,General Medicine
Reference13 articles.
1. Factor X deficiency.;Menegatti;Semin Thromb Hemost,2009
2. Recessively inherited coagulation disorders.;Mannucci;Blood,2004
3. 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
4. Simultaneous purification of bovine prothrombin and factor X. Activation of prothrombin by trypsin-activated factor X.;Bajaj;J Biol Chem,1973
5. Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34).;Pfeiffer;Hum Genet,1982
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1. Molecular basis of rare congenital bleeding disorders;Blood Reviews;2023-05
2. Occurrence and management of severe bleeding episodes in patients with hereditary factor X deficiency;Haemophilia;2021-05-22
3. Genotype analysis and identification of novel mutations in a multicentre cohort of patients with hereditary factor X deficiency;Blood Coagulation & Fibrinolysis;2019-01
4. Intracranial Hemorrhage as the First Manifestation of Severe Congenital Factor X Deficiency in a 20-Month-Old Male: Case Report and Review of the Literature;Pediatric Blood & Cancer;2016-04-21
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