Spontaneous aortic thrombosis and embolization: Antithrombin deficiency and the work-up of hypercoagulable states

CMAJ. Canadian Medical Association Journal

Volumn 173, Issue 9, 2005, Pages 1027-1029

  Marcu, Constantin B ^a   Donohue, Thomas J ^b   Ghantous, Andre E ^b  

^a VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^b YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HEPARIN; WARFARIN;

ADULT; ANGIOPLASTY; ANTITHROMBIN DEFICIENCY; AORTA THROMBOSIS; ARTIFICIAL EMBOLISM; CASE REPORT; DIAGNOSTIC PROCEDURE; EMBOLECTOMY; HUMAN; HYPERCOAGULABILITY; LABORATORY TEST; MALE; PHYSICAL EXAMINATION; SHORT SURVEY;

EID: 27544492671     PISSN: 08203946     EISSN: 14882329     Source Type: Journal    
DOI: 10.1503/cmaj.050464     Document Type: Short Survey

References (3)

1. Bauer KA. Hypercoagulable states. In: Hoffman R, Benz EJ, Shattil SJ, editors. Hematology: basic principles and practice. New York: Churchill Livingstone; 2005. p. 2197-224.
2. Egeberg O. Inherited antithrombin deficiency causing thrombophilia. Thromb Diath Haemorrh 1965;13:516.
3. Bick RL. Prothrombin G20210A mutation, antithrombin, heparin cofactor II, protein C, and protein S defects. Hematol Oncol Clin North Am 2003;17(1):9-36.