Management of an orthognathic surgery patient with factor XI deficiency: review and case report.

[1]  G. Broze,et al.  Factor XI activation in a revised model of blood coagulation , 1991, Science.

[2]  E. Davie,et al.  Factor XI deficiency in Ashkenazi Jews in Israel. , 1991, The New England journal of medicine.

[3]  K. Moos,et al.  Correction of facial deformities in patients with mild bleeding disorders: a report of three cases. , 1990, British Journal of Oral and Maxillofacial Surgery.

[4]  A. Prince,et al.  The use of tri(n‐butyl)phosphate detergent mixtures to inactivate hepatitis viruses and human immunodeficiency virus in plasma and plasma's subsequent fractionation , 1990, Transfusion.

[5]  R M Cook,et al.  Factor XI deficiency disclosed following haemorrhage related to a dental extraction. Brief review and case report. , 1990, Australian dental journal.

[6]  A. McCraw,et al.  Inheritance and bleeding in factor XI deficiency , 1988, British journal of haematology.

[7]  C. Kitchens Prolonged activated partial thromboplastin time of unknown etiology: A prospective study of 100 consecutive cases referred for consultation , 1988, American journal of hematology.

[8]  T. Duffy,et al.  Acquired factor XI inhibitors in congenitally deficient patients , 1987, American journal of hematology/oncology.

[9]  J. Jespersen,et al.  Characterization of Plasminogen Activators in Unstimulated and Stimulated Human Whole Saliva , 1987, Journal of dental research.

[10]  D. Sinha,et al.  Mechanism of activation of coagulation factor XI by factor XIIa studied with monoclonal antibodies. , 1986, Journal of Clinical Investigation.

[11]  S. Sindet‐Pedersen,et al.  Effect of local antifibrinolytic treatment with tranexamic acid in hemophiliacs undergoing oral surgery. , 1986, Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons.

[12]  J. Griffin,et al.  Binding of coagulation factor XI to washed human platelets. , 1986, Biochemistry.

[13]  C. Kitchens Surgery in Hemophilia and Related Disorders: A PROSPECTIVE STUDY OF 100 CONSECUTIVE PROCEDURES , 1986, Medicine.

[14]  D. Sinha,et al.  Comparison of bleeding tendency, factor XI coagulant activity, and factor XI antigen in 25 factor XI-deficient kindreds , 1985 .

[15]  Lewis Jh,et al.  Transfusion support for congenital clotting deficiencies other than haemophilia. , 1984 .

[16]  R. Colman,et al.  Inactivation of factor XIa by plasma protease inhibitors: predominant role of alpha 1-protease inhibitor and protective effect of high molecular weight kininogen. , 1982, The Journal of clinical investigation.

[17]  E. Rosenberg,et al.  Complications of severe bleeding in a patient with undiagnosed Factor XI deficiency. , 1981, Oral surgery, oral medicine, and oral pathology.

[18]  R. Mibashan,et al.  The Measurement of Factor XI (Plasma Thromboplastin Antecedent) , 1966, British Journal of Haematology.

[19]  R. R. Proctor,et al.  The mode of inheritance of PTA deficiency: evidence for the existence of major PTA deficiency and minor PTA deficiency. , 1961, Blood.

[20]  R. Rosenthal,et al.  Plasma thromboplastin antecedent (PTA) deficiency; clinical, coagulation, therapeutic and hereditary aspects of a new hemophilia-like disease. , 1955, Blood.